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Unsere wissenschaftlichen Publikationen

P. Koblischek, R. Brückner, „First Total Synthesis of the Benzotropolone/Bis(pulvinone)Natural Product Aurantricholone Exploiting New Strategies forEstablishing Benzotropolones and Z-Configured Pulvinones”, Eur. J. Org. Chem. 2022, e202201120.
216 S. N. Momm, R. Brückner, „Syntheses of 6,7-Benzotropolones by a Sequence of Acylation (or α-Hydroxyalkylation/Oxidation), Ring-Closing Metathesis, and Hydrolysis/β-Elimination”, J. Org. Chem. 2022, 22, 15415-15420.
215) P. Koblischek, R. Brückner, „Syntheses of 7‐, 8‐ and 9‐Bromobenzotropolone, Cross‐Couplings of Their Methyl Ethers, and Deprotection to 7‐, 8‐ or 9‐Substituted Benzotropolones”, Eur. J. Org. Chem. 2022, e202200686.
214) P. Koblischek, R. Brückner, „Syntheses of 6,7‐Benzotropolone by Using Ring‐Closing Metathesis Variants Obviating a Strongly Acidic Hydrolysis Thereafter”, Eur. J. Org. Chem. 2022, e202101070.
213) J. Kopp, R. Brückner, "First total synthesis of the dimeric naphthoquinonopyrano-γ-lactone natural product (−)-crisamicin A. How procrastination may be of help in binaphthyl synthesis" in Strategies and Tactics in Organic Synthesis, Vol. 15, M. Harmata (Edt.), Elsevier / Academic Press, Amsterdam, 2021, S. 281-334 (ISBN 978-0-12-822212-6).
212) C. Drescher, R. Brückner, „Stereostructure Clarifying Total Synthesis of the (Polyenoyl)tetramic Acid Militarinone B. A Highly Acid-Labile N-Protecting Group for Amides”, Org. Lett. 2021, 16, 6194-6199.
211) M. Kreibich, M. Gemander, D. Peter, D. B. Yadav, C. B. de Koning, M. A: Fernandes, I. R. Green, W. A. L. van Otterlo, R. Brückner, „6,7-Benzotropolone Syntheses Based on Ring-Closing Metatheses and Four-Electron Oxidations”, Eur. J. Org. Chem. 2020, 2929-2955.
J. Kopp, R. Brückner, „Stereoselective Total Synthesis of the Dimeric Naphthoquinonopyrano-y-lactone (–)-Crisamicin A: Introducing the Dimerization Site by a Late-Stage Hartwig Borylation”, Org. Lett. 2020, 22, 3607-3612.
C. Drescher, M. Keller, O. Potterat, M. Hamburger, R. Brückner, „Structure-Elucidating Total Synthesis of the (Polyenoyl)tetramic Acid Militarinone C§”, Org. Lett. 2020, 22, 2559-2563.
F. Bäuerle, R. Brückner, „Atropselective Synthesis of N,C-Bis(diphenylphosphanes) from Bridged 2-Arylindoles Based on Effective Point-to-Axial Asymmetric Inductions after an Unusal Dilithiation”, Org. Lett. 2019, 21, 9970-9975.
R. Brückner, „Pioneering Work on Catenanes, Rotaxanes, and a Knotane in the University of Freiburg 1958-1988”, Eur. J. Org. Chem. 2019, 3289-3319.
T. Engesser, R. Brückner, „Stereoselective Aldol Additions of Glycolic Acid and Its Derivatives”, Synthesis 2019, 51, 1715-1745.
T. Baumann, R. Brückner, „Atropselektive Dibromierungen eines 1,1′‐disubstituierten 2,2′‐Biindolyls mit divergierender zentral‐zu‐axialer asymmetrischer Induktion. Ableitung von 2,2′‐Biindolyl‐3,3′‐diphosphan‐Liganden für asymmetrische Katalysen”, Angew. Chem. 2019, 131, 4762-4768.
A.-C. Loesche, R. Brückner, „Dienolates of Cycloalkenones and α,β-Unsaturated Esters Form Diels-Alder Adducts by a Michael/Michael-Tandem Reaction Rather Than in One Step”, Eur. J. Org. Chem. 2019, 562-573.
D. Hermann, R. Brückner, „Silver-Catalyzed tert-Butyl 3-Oxopent-4-ynoate π-Cyclizations: Controlling the Ring-Size − Hydroxypyrone or Pulvinone Formation − by Counter-Ion and Additive Optimization”, Org. Lett. 2018, 20, 7455-7460.
D. Peter, R. Brückner, „Syntheses of a Pair of Simplified Model Compounds of the Dihydroxycyclopentenone Core of the Kodaistatins A-D”, Eur. J. Org. Chem. 2018, 6256-6273.
S. Ruppenthal, R. Brückner, „Asymmetric Sulfinylations of N-Methylephedrine-Modified Tri- or Tetraalkyl Zincates by Symmetric Diaryl Sulfoxides”, Eur. J. Org. Chem. 2018, 2518-2530.
E. Diehl (née Knobloch), R. Brückner, „Turning the Nitrogen Atoms of an Ar₂P−CH₂−N−N−CH₂−PAr₂ Motif Into Uniquely Configured Stereocenters: A Novel Diphosphane Design for Asymmetric Catalysis”, Chem. Eur. J. 2018, 24, 3429-3433.
S. Ruppenthal, R. Brückner, „Asymmetric  Sulfinylations  of  N -Methylephedrine-Modified  Tri-  or  Tetraalkyl Zincates by Symmetric Diaryl Sulfoxides ", Eur. J. Org. Chem. 2018, accepted article (DOI: 10.1002/ejoc.201701603).
M. Kreibich, D. Petrović, R. Brückner, „Mechanistic Studies of the Deslongchamps Annulation", J. Org. Chem. 2018, 83, 1116-1133.
S. Ruppenthal, R. Brückner, „Prochiral Diheteroaryl Sulfoxides and Their Reactions With (S)-Li2-BINOLate-Activated Diisobutylmagnesium", Eur. J. Org. Chem. 2018, 1, 89-98.
T. Engesser, R. Brückner, „Synthesis of trans-Configured Enol Ethers by a Sequence of syn-Selective Glycolate Aldol Addition, Hydrolysis, and Grob Fragmentation", Eur. J. Org. Chem. 2017, 38, 5789-5794.
D. Peter, R. Brückner, „A New Approach to Models of the 4,5-Dihydroxycyclopentenone Core of the Kodaistatins A-D. Elucidation of the Diol Configuration in Kodaistatin A”, Chem. Eur. J. 2017, 23, 12104-12109.
T. Hampel, R. Brückner, „Towards a Total Synthesis of Phenalinolactone Core Diterpenoid 6: Synthesis of a Racemic Decahydrobenzocyclobutaisobenzofuran with a trans-anti-cis Junction of the Isocyclic Rings”, Eur. J. Org. Chem. 2017, 2950-2963.
M. Neumeyer, J. Kopp, R. Brückner, „Controlling the Substitution Pattern of Hexasubstituted Naphthalenes by Aryne/Siloxyfuran Diels-Alder Additions: Regio- and Stereocontrolled Synthesis of Arizonin C1 Analogs”, Eur. J. Org. Chem. 2017, 2883-2915.
D. Arican, S. Braukmüller, R. Brückner, "Regioselective Bromination of Benzocycloheptadienones for the Synthesis of Substituted 3,4-Benzotropolones Including Goupiolone A", Chem. Eur. J. 2017, 23, 4537-4541.
191) M. Neumeyer, R. Brückner, „Consensus Stereostructures for the Naphthoquinonopyrano-γ-lactone Natural Products (–)-Arizonin B1 and (–)-Arizonin C1. Diastereocontrol of Oxa-Pictet-Spengler Cyclizations", Eur. J. Org. Chem. 2017, 2512-2539.
190) M. Neumeyer, R Brückner, "Die erste stereoselektive Totalsynthese eines dimeren γ-Lactonanellierten Pyranonaphtochinons: γ-Actinorhodin", "First Stereoselective Total Synthesis of a Dimeric Naphthoquinonopyrano-γ-lactone: (+)-γ-Actinorhodin", Angew. Chem. 2017, 129, 3432-3437; Angew. Chem. Int. Ed. 2017, 56, 3383-3388.
189) D. Hermann, D. Arican, R. Brückner, "Two-Step Synthesis of (Z)-3-Aryl-5-(arylmethylidene)butenolides by an Ivanov Reaction/Silver(I)-Catalyzed Lactonization/In Situ Dehydration Sequence", Synthesis 2017, 49, 326-352.
188) J. Diehl, R. Brückner, "Synthesis of Enantiomerically Pure β-Hydroxy Ketones via β-Keto Weinreb Amides by a Condensation/Asymmetric-Hydrogenation/Acylation Sequence", Eur. J. Org. Chem. 2017, 278-286.
M. L. Hofferberth, R. Brückner, "The Tetramic Acid Antibiotics α- and β-Lipomycin: Total Synthesis and Assignment of the Absolute Configuration of all Stereogenic Centers. Making Doubly Sure" in Strategies and Tactics in Organic Synthesis, Vol. 12, M. Harmata (Edt.), Elsevier / Academic Press, Amsterdam, 2017, S. 37-93 (ISBN 978-0-08-100756-3).
M. Neumeyer, R. Brückner, "Nonracemic γ-Lactones from the Sharpless Asymmetric Dihydroxylation of β,γ-Unsaturated Carboxylic Esters", Eur. J. Org. Chem. 2016, 30, 5060-5087
185)  F. Weber, F. Becker, M. Keller, H. Hillebrecht, R. Brückner, "Aldol Additions of Titanium and Boron Enolates of Achiral and Chiral δ-Lactones to Achiral Model Aldehydes: Simple and Induced Diastereoselectivities", Eur. J. Org. Chem. 2015, 7892-7918.
184) F. Weber, R. Brückner, "Asymmetric Dihydroxylation of Esters and Amides of Methacrylic, Tiglic, and Angelic Acid: No Exception to the Sharpless Mnemonic!", Eur. J. Org. Chem. 2015, 2428-2449.
183) S. Ruppenthal, R. Brückner, "Symmetric Diarylsulfoxides as Asymmetric Sulfinylating Reagents for Dialkylmagnesium Compounds", J. Org. Chem. 2015, 80, 897-910.
182) J. Aucktor, R. Brückner, "Total Synthesis of Quercitols: (+)-allo-, (–)-proto-, (+)-talo-, (–)-gala-, (+)-gala-, neo-, and (–)-epi-Quercitol", Synlett 2015, 26, 250-258.
181) F. Weber, R. Brückner, "Total Syntheses of the Dihydrofuranonecarboxylate Natural Products Gregatin B and E: Gram-Scale Synthesis of (+)-Gregatin B and Unambiguous Assignment of the Stereostructure of (+)-Gregatin E", Org. Lett. 2014, 16, 6428-6431.
180) M. L. Hofferberth, R. Brückner, "α- und β-Lipomycin:Totalsynthesen auf der Grundlage sequentieler Stille-Kupplungen und Zuordnung der absoluten Konfiguration aller stereogenen Zentren", Angew. Chem. 2014, 126, 7456-7462; "a- and β-Lipomycin: Total Syntheses by Sequential Stille Couplings and Assignment of the Abolsute Configuration of all Stereogenic Centers", Angew. Chem. Int. Ed. 2014, 53, 7328-7334.
P. Walleser, R. Brückner, „Stereocontrolled Synthesis of a C1-C10 Building Block (“Southwestern Moiety”) for the Unnatural Enantiomers of the Poly­ene,Poly­ol Antibiotics Filipin III and Pentamycin. A Sultone Forming Ring-Closing Metathesis for a Novel Pro­tec­tion of Homoallylic Alcohols”, Eur. J. Org. Chem. 2014, 3210-3224.
T. Hampel, M. Bruns, M. Bayer, R. Handgretinger, G. Bruchelt, R. Brückner, „Synthesis and biological effects of new hybrid compounds composed of benzylguanidines and the alkylating group of busulfan on neuroblastoma cells“, Bioorg. Med. Chem. Lett. 201424, 2728-2733.
J. Aucktor, C. Anselmi, R. Brückner, M. Keller, „The Synthesis of Tricyclic Precursors of Cyclitols“, Synlett 2014, 1312-1318.
J. Diehl, R. Brückner, „Unexpected Rearrangements of Rhodium Carbenoids Containing a Pyrrolidin-1-yl Group“, Tetrahedron Lett. 201455, 2629-2632.
S. B. Kamptmann, R. Brückner, „Stereocontrolled Synthesis of a Cn-Cn+7 Building Block (“Eastern Moiety”) for the Unnatural Enantiomers of Important Poly­ol,Poly­ene Antibiotics Based on a Ring-Closing Meta­the­sis and an Aldol Addition of a Lactone Enolate”, Eur. J. Org. Chem. 2013, 6584-6600.
R. Kramer, R. Brückner, „Stereocontrolled Synthesis of a Cn-Cn+6 Building Block Common to the Unnatural Enantiomers of Important Poly­ol,Poly­ene Antibiotics From an Ep­oxyalcohol by a Reduction / Conjugate Addition / Hydroxyla­tion Sequence”, Eur. J. Org. Chem. 2013, 6563-6583.
L. Nachbauer, R. Brückner, „Synthesis of a Cn-Cn+6 Building Block Common to Important Poly­ol,Poly­ene Antibiotics From a Divinylcarbinol by a Desym­metrizing Sharp­less Epoxidation”, Eur. J. Org. Chem. 2013, 6545-6562.
T. Wüster, N. Kaczybura, R. Brückner, M. Keller, „Synthesis of enantiomerically pure model compounds of the glucose-6-phosphate-T1-translocase inhibitors kodaistatins A-D. Inferences with regard to the stereostructure of the natural products“, Tetrahedron 201369, 7785-7809.
D. Arican, R. Brückner, „Syntheses of 3,4-Benzotropolones by Ring-Closing Metatheses“, Org. Lett. 201315, 2582-2585.
P. Walleser, R. Brückner, „Enantioselective Synthesis of (+)-Obolactone Based on a Symmetry-Breaking Wacker Monooxidation of a Diene“, Org. Lett. 201315, 1294-1297.
B. Breit, R. Brückner, „Horst Prinzbach (1931-2012)“, Nachr. Chem. 201361, 163-163.
F. Weber, R. Brückner, „Conformational Analyses of δ-Lactones by DFT Calculations: The Parent Compound and its Monomethyl and Selected Dimethyl Derivatives“, Chem. Eur. J. 201319, 1288-1302.
L. Nachbauer, R. Brückner, „Converting a Birch Reduction Product into a Polyketide: An Application to the Synthesis of a C1-C11 Building Block of Rimocidin“, Eur. J. Org. Chem. 2012, 6904-6923.
C. Stock, R. Brückner, „Mild and High-Yielding Molybdenum(VI) Dichloride Dioxide Catalyzed Formation of Mono- and Oligo¬carbamates from Alcohols and Aromatic or Aliphatic Isocyanates“, Adv. Synth. Catal. 2012, 354, 2309-2330.
H. Burghart-Stoll, R. Brückner, „Total Syntheses of the Gregatins A-D and Aspertetronin A. Structure Revision of these Compounds and Aspertetronin B and Plausible Structure Revisions of Gregatin E, Cyclogregatin, Graminin A, the Penicilliols A and B, and the Huaspenones A and B“, Eur. J. Org. Chem. 2012, 3978-4017.
T. Hampel, S. Ruppenthal, D. Sälinger, R. Brückner, „Desymmetrization of Prochiral Diaryl Sulfoxides by an Asymmetric Sulfoxide-Magnesium Exchange“, Chem. Eur. J. 2012, 18, 3136-3140.
D. Petrović, R. Brückner, „Deslongchamps Annulations with Benzoquinone Monoketals“, Org. Lett. 2011, 13, 6524-6527.
M. Mahlau, R. A. Fernandes, R. Brückner, „First Synthesis of the Pyranonaphthoquinone Lactone (-)-Arizonin C1“, Eur. J. Org. Chem. 2011, 4765-4772.
J. Burghart, A. Sorg, R. Brückner, „Stereocomplementary Syntheses of 1,ω-Distannylated E,Z-Isomeric Conjugated Trienes, Tetraenes, and Pentaenes“, Chem. Eur. J. 201117, 6469-6483.
H. Burghart-Stoll, R. Brückner, „A Serendipitous Synthesis of (+)-Gregatin B. Second Structure Revision of the Aspertetronins, Gregatins, and Graminin A. Structure Revision of the Penicilliols“, Org. Lett. 201113, 2730-2733.
H. Burghart-Stoll, O. Böhnke, R. Brückner, „Asymmetric Dihydroxylations of 1-Substituted (E)- and (Z)-3-Methylpent-2-en-4-ynes: Full Compliance with the Sharpless Mnemonic Re-established and Embellished“, Org. Lett. 201113, 1020-1023.
H. Burghart-Stoll, T. Kapferer, R. Brückner, „Asymmetric Dihydroxylations of Enynes with a Trisubstituted C=C Bond. An Unprecedented Route to γ Lactone Building Blocks with a Quaternary Stereocenter“, Org. Lett. 201113, 1016-1019.
J. Burghart, R. Brückner, „Sn/Li Exchange Reactions in 1,ω-Distannylated Conjugated Trienes and Tetraenes: An Enabling Step for Polyene Synthesis“, Eur. J. Org. Chem. 2011, 150-165.
C. Stock, R. Brückner, „Exceptionally Active Catalysts for the Formation of Carbamates from Alcohols and Isocyanates: Molybdenum(VI) Dichloride Dioxide and its DMF Complex“, Synlett 2010, 2429-2434.
P. Walleser, R. Brückner, „Stereocontrolled Synthesis of 1,3,5-Triols by an Iteration of Asymmetric Dihydroxylation and Desoxygenation”, Eur. J. Org. Chem. 2010, 4802-4822.
A. Zörb, R. Brückner, „Conversion of Conjugated Enones into Enantiomerically Pure β-Hydroxyketones or 1,3-Diols. Samarium(II)-Bromide Reductions of Protected α,β-Dihydroxyketones“, Eur. J. Org. Chem. 2010, 4785-4801.
E. Haug-Schifferdecker, D. Arican, R. Brückner, L. Heide, „A new group of aromatic prenyltransferases in fungi, catalyzing a 2,7-dihydroxynaphthalene dimethylallyltransferase reaction“, J. Biol. Chem. 2010285, 16487-16494.
R. Brückner, „Organic Mechanisms. Reactions, Stereochemistry and Synthesis“ (Übersetzungs-Herausgeber: M. Harmata), Springer, Heidelberg, New York, 2010, 856 p.
T. Hampel, R. Brückner, „A Novel Cis-Selective Cyclohexanone Annulation as the Key Step of a Total Synthesis of the Sesquiterpene Isoacanthodoral“, Org. Lett. 200911, 4842-4845.
D. Sälinger, R. Brückner, „The First Asymmetric Halogen/Metal Exchange Reaction: Desymmetrization of Alcohols with Enantiotopic Bromoarene Substituents”, Chemistry 2009, 15, 6688-6703.
D. Sälinger, R. Brückner, „High-Yielding Large-Scale Syntheses of Enantiomerically Pure NOBIN and a NOBIN-Based Enantiomerically Pure NHC Precursor”, Synlett 2009, 109-111.
R. Brückner, S. Braukmüller, H.-D. Beckhaus, J. Dirksen, D. Goeppel, M. Oestreich, „Praktikum Präparative Organische Chemie - Organisch-Chemisches Fortgeschrittenenpraktikum”, Spektrum Akademischer Verlag, Heidelberg, 2008, 373 S.
J. Burghart, R. Brückner, "Totalsynthese von natürlich konfiguriertem Pyrrhoxanthin, einem Carotinoid-Butenolid aus Plankton", Angew. Chem. 2008, 120, 7777-7782; "Total Synthesis of Naturally Configured Pyrrhoxanthin, a Carotenoid Butenolide from Plankton", Angew. Chem. Int. Ed. 2008, 47, 7664-7668.
E. Knobloch, R. Brückner, "β-Ketoesters Derived from 2-(Trimethylsilyl)ethanol: Orthogonal Protection vs. β-Ketoesters Derived from Other Alcohols", Synthesis 2008, 2229-2246.
E. Knobloch, R. Brückner, "Selective Cleavage/Decarboxylation of β-Ketoesters Derived from (Trimethylsilyl)ethanol in the Presence of β-Ketoesters Derived from Other Alcohols", Synlett 2008, 1865-1869
R. Brückner, S. Braukmüller, H.-D. Beckhaus, J. Dirksen, D. Goeppel, M. Oestreich, "Praktikum Präparative Organische Chemie - Organisch-Chemisches Grundpraktikum", Spektrum Akademischer Verlag, Heidelberg, 2008, S. 394.
R. Kramer, T. Berkenbusch, R. Brückner, "Stereocomplementary Desymmetrizations of Divinylcarbinols by Zr(IV)- vs. Ti(IV)-Mediated Asymmetric Epoxidations", Adv. Synth. Catal. 2008, 350, 1131-1148.
R. Kramer, R. Brückner, "Asymmetric Hydrogenations One by One: Differentiation of up to Three β-Ketocarboxylic Acid Derivatives Based on Ruthenium(II)-BINAP Catalysis", Chem. Eur. J. 2007, 13, 9076-9086.
R. Kramer, R. Brückner, "Kinetische Differenzierung von β-Ketoestern durch Ruthenium(II)-BINAP-katalysierte Asymmetrische Hydrierung", Angew. Chem. 2007, 119, 6657-6661, Angew. Chem. Int. Ed. 2007, 46, 6537-6541.
D. Bernier, R. Brückner, "Novel Synthesis of Naturally Occurring Pulvinones: A Heck Coupling, Transesterification, and Dieckmann Condensation Strategy", Synthesis 2007, 2249-2272.
D. Bernier, F. Moser, R. Brückner, "Synthesis and Cyclization of 3-Aryl-2-(arylacetoxy)acrylates: A 3-Step Access to Pulvinones", Synthesis 2007, 2240-2248.
T. Tricotet, R. Brückner, "Enantio- and Diastereomerically Pure Decalins by Deslongchamps-Type Annulation of Dienolates Containing a Chiral Lactone Substituent", Eur. J. Org. Chem. 2007, 1069-1074.
R. Brückner, "Introduction to Aldehydes", in "Aldehydes", Science of Synthesis - Houben-Weyl Methods of Organic Chemistry, Bd. 25 (Hrsg. R. Brückner), Thieme, Stuttgart, New York, 2007, 1-16.
R. Brückner (Herausgeber), "Aldehydes", Science of Synthesis -Houben-Weyl Methods of Organic Chemistry, Bd. 25, Thieme, Stuttgart, New York, 2007, S. 902 (ISBN 978-3-13-118761-1).
K. L. Dormann, R. Brückner, "Variationsfähige Synthese der optisch aktiven Thiotetronsäure-Antibiotika Thiolactomycin, Thiotetromycin und 834- B1", Angew. Chem. 2007119, 1178-1182; Angew. Chem. Int. Ed. 200746, 1160-1163.
N. Kaczybura, R. Brückner, "Tandem Claisen Condensations / Transesterifications Between Arylacetate Enolates and Arylmethylene-Substituted 2,2-Dimethyl-1,3-dioxolan-4-ones: An Improved Synthesis of Z- Configured Pulvinones", Synthesis 2007, 118-130.
R. Brückner, "Asymmetric Epoxidation of Pentadienols" in "Asymmetric Synthesis - The Essentials" (Hrsg. M. Christmann, S. Bräse), Wiley-VCH, Weinheim, 2006, 10-15 (ISBN 978-3-527-31399-0).
T. Tricotet, R. Brückner, "[4+2]-Annulations Leading to Configurationally Homogeneous Bicyclo[4.4.0]decanediones with five new Stereocenters", Tetrahedron Lett. 200647, 8499-8502.
J. Schmidt-Leithoff, R. Brückner, "Regioselective Cis-vic-Dihydroxylation of α,β,γ,δ-Unsaturated Carboxylic Esters: Enhanced γ,δ-Selectivity by Employing Trifluoroethyl or Hexafluoroisopropyl Esters", Synlett 2006, 641- 2645.
T. Olpp, R. Brückner, "Total Synthesis of the Light-Harvesting Carotenoid Peridinin", Angew. Chem. 2006118, 4128-4132; Angew. Chem. Int. Ed. 200645, 4023-4027.
T. Kapferer, R. Brückner, "Asymmetric Dihydroxylation of β,γ-Unsaturated Carboxylic Esters with Trisubstituted C=C Bonds - Enantioselective Syntheses of Trisubstituted γ-Butyrolactones", Eur. J. Org. Chem. 2006, 2119-2133.
S. Braukmüller, R. Brückner, "Enantioselective Butenolide Preparations for Straightforward Syntheses of γ-Lactones - Paraconic Acids, Avenaciolide, and Hydroxylated Eleutherol", Eur. J. Org. Chem. 2006, 2110-2118.
R. Kramer, R. Brückner, "Desymmetrizing Asymmetric Epoxidations of Bis(cis-Configured) Divinylcarbinols: Unusual syn-Selectivity Combined with ee-Enhancement through Kinetic Resolution", Synlett 2006, 33-38.
K. Körber, P. Risch, R. Brückner, "A Novel Strategy for the Convergent Synthesis of 1,3,5,...-Polyols: Enone Formation / Asymmetric Dihydroxylation / Reductive Cleavage / Hydride Addition", Synlett 2005, 2905-2910.
J. Schmidt-Leithoff, R. Brückner, "Synthesis of the 2-Alkenyl-4-alkylidenebut- 2-eno-4-lactone (= α-Alkenyl-γ-alkylidenebutenolide) Core Structure of the Carotenoid Pyrrhoxanthin via the Regioselective Dihydroxylation of Hepta- 2,4-diene-5-ynoic Acid Esters", Helv. Chim. Acta 200588, 1943-1959.
A. Sorg, F. Blank, R. Brückner, "Stepwise Cross-Couplings of a Dibromo-γ-methylenebutenolide as an Access to Z-Configured α-Alkenyl-γ-alkylidenebutenolides. Straightforward Synthesis of the Antibiotic Lissoclinolide", Synlett 2005, 1286-1290.
R. A. Fernandes, R. Brückner, "Efficient Synthesis of (+)-Kalafungin and (-)-Nanaomycin D by Asymmetric Dihydroxylation, Oxa-Pictet-Spengler Cyclization, and H2SO4-Mediated Isomerization", Synlett 2005, 1281-1285.
T. Kapferer, R. Brückner, A. Herzig, M. Junge, W. A. König, "Enantioselective Syntheses and Configurational Assignments of γ-Chiral Butenolides from Plagiomnium Undulatum. Butenolide Synthesis from Tetronic Acids", Chem. Eur. J. 200511, 2154-2162.
R. Brückner (Koordinator) et al., "Organische Chemie 2004 (Trendbericht)", Nachr. Chem. 2005, 53, 251-272.
A. Sorg, K. Siegel, R. Brückner, "Stereoselective Syntheses of Dihydroxerulin and Xerulinic Acid, Anti-Hypocholesterolemic Dyes from the Fungus Xerula melanotricha", Chem. Eur. J. 200511, 1610-1624.
T. Olpp, R. Brückner, "Novel Strategy for the Synthesis of the Butenolide Moiety of Peridinin", Angew. Chem. 2005117, 1577-1581; Angew. Chem. Int. Ed. 200544, 1610-1624.
B. Vaz, R. Alvarez, R. Brückner, A. R. de Lera, "The Stille Reaction in the Synthesis of Carotenoid Butenolides: Synthesis of 6'-epi-Peridinin", Org. Lett. 20057, 545-548.
A. Sorg, R. Brückner, "Unexpected cis-Selectivity in (Sylvestre) Julia Olefinations with Bu3Sn-Containing Allyl Benzothiazolyl Sulfones: Stereoselective Synthesis of 1,3-Butadienyl- and 1,3,5- Hexatrienylstannanes", Synlett 2005, 289-293.
T. Berkenbusch, A. Ch. Laungani, R. Brückner, M. Keller, Serendipitous Synthesis of a Ditwistane: A One-Step Access!", Tetrahedron Lett. 200445, 9517-9520.
R. Brückner, "Reaktionsmechanismen • Organische Reaktionen, Stereochemie, moderne Synthesemethoden", 3. Aufl., Elsevier - Spektrum Akademischer Verlag, Heidelberg, Berlin, Oxford, 2004, S. 863.
T. Olpp, R. Brückner, "Stereoselective Preparation of (E)-α- Bromoacrylates from Mixtures of Brominated Ando Phosphonates", Synthesis 2004, 2135-2152.
A. Sorg, R. Brückner, "Totalsynthese von Xerulinsäure", Angew. Chem. 2004116, 4623-4626; "Total Synthesis of Xerulinic Acid", Angew. Chem. Int. Ed. Engl. 200443, 4523-4526.
R. Brückner, K. Siegel, A. Sorg, "Stereoselective Synthesis of Polyunsaturated γ-Alkylidenebutenolides: The Total Synthesis of the Xerulins" in Strategies and Tactics in Organic Synthesis, Vol. 5, M. Harmata (Ed.), Elsevier, Amsterdam, 2004, 437-473.
R. Brückner (coordinator) et al., "Organische Chemie 2003 (Trendbericht)", Nachr. Chem. 200452, 267-291.
T. Berkenbusch, R. Brückner, "Stereocontrolled Synthesis of the C21-C38 Fragment of the Unnatural Enantiomer of the Antibiotic Nystatin A1", Chem. Eur. J. 200410, 1545-1557.
A. Sorg, K. Siegel, R. Brückner, "A Novel Access to γ-Alkylidenebutenolides: Sequential Stille Couplings of Dibromomethylenebutenolides", Synlett 2004, 321-325.
T. Berkenbusch, R. Brückner, "Concise Synthesis of Optically Puresyn-1,3-Diols by Stereoselective Desymmetrization of a Divinylcarbinol", Synlett 2003, 1813-1816.
R. Brückner (coordinator) et al., "Organische Chemie 2002 (Trendbericht)", Nachr. Chem. 200351, 286-311.
R. Brückner, "Reaktionsmechanismen • Organische Reaktionen, Stereochemie, moderne Synthesemethoden", 2nd Ed., Spektrum Akademischer Verlag, Heidelberg, Berlin, Oxford, 2002, 857 pp.
R. Brückner, "Advanced Organic Chemistry", Harcourt / Academic Press, 2001, 636 pp.
C. Harcken, R. Brückner, Stereopure 1,3-Butadiene-2-carboxylates and their Conversion into - α-Alkylidenebutyrolactone Natural Products by Asymmetric Dihydroxylation", Tetrahedron Lett. 2001, 42, 3967-3971.
R. Brückner, "The Synthesis of γ-Alkylidenebutenolides", Curr. Org. Chem. 20014, 679-718.
C. Harcken, R. Brückner, "A 4-Step Route from Aldehydes to C2-Elongated Enantiomerically Pure α,β-Unsaturated γ-Hydroxyesters", Synlett 2001, 718-721.
R. Brückner, "The β-Elimination Route to Stereodefined γ-Alkylidenebutenolides", J. Chem. Soc. Chem. Comm. 2001, 141-152.
C. Harcken, R. Brückner, "Elucidation of the Stereostructure of the Annonaceous Acetogenin (+)-Montecristin through Total Synthesis", New J. Chem. 2001, 40-45.
F. v. d. Ohe, R. Brückner, "Stereoselective Synthesis of Freelingyne and Related γ-Alkylidenebutenolides via Vinylogous Mukaiyama Aldol Additions", New J. Chem. 2000, 659-669.
F. Görth, M. Rucker, M. Eckhardt, R. Brückner, "Decagram-Scale Synthesis of the Neocarzinostatin Carboxylic Acid", Eur. J. Org. Chem. 2000, 2605-2611.
O. Gebauer, R. Brückner, "β-Alkoxycarbonyl Enol Triflates as Precursors of Stereopure 3-Ene-1,5-diyne Building Blocks for the Chromophores of Neocarzinostatin, C-1027, and Maduropeptin", Synthesis 2000, 588-602.
I. Hanisch, R. Brückner, "Sequential Suzuki/Suzuki Couplings with a Dibromoiododiene - A Versatile Strategy for the Stereocontrolled Synthesis of Polyunsaturated Butenolides", Synlett 2000, 374-378.
R. Brückner, "Mécanismes Réactionnels en Chimie Organique", DeBoeck Université, 1999, S. 614.
F. Görth, R. Brückner, "Stereoselective Synthesis of Lissoclinolide and Proof that ´Tetrenolin´ is Identical with Lissoclinolide", Synthesis 1999, 1520-1528.
K. Siegel, R. Brückner, "First Synthesis of Xerulin, an Inhibitor of the Biosynthesis of Cholesterol", Synlett 1999, 1227-1230.
R. Brückner, J. Suffert, "The Bis(enol triflate) Route to Dienediyne Models of the Biradical Forming and DNA-Cleaving Natural Product Neocarzinostatin Chromophore", Synlett 1999, 657-679.
C. Harcken, T. Berkenbusch, S. Braukmüller, A. Umland, K. Siegel, F. Görth, F. von der Ohe, R. Brückner, "Stereoselective Syntheses of γ-Lactones and γ-Alkylidenebutenolides", in "Current Trends in Organic Synthesis" (C. Scolastico, F. Nicotra, Hrsg.), Plenum Press, 1999, 153-161.
T. Berkenbusch, R. Brückner, "Synthesis of (+)-Ginnol, a Type Rlong-CH(OH)- R'long Alcohol, by an Asymmetric β,γ-Unsaturated Ester →Butyrolactone Conversion", Tetrahedron 199854, 11471-11480.
T. Berkenbusch, R. Brückner, "Brief Syntheses of (+)-Blastmycinone and Related γ -Lactones from an Asymmetrically Dihydroxylated Carboxylic Ester", Tetrahedron 199854, 11461-11470.
C. Harcken, E. Rank (in part), R. Brückner, "Total Syntheses of (+)-Grandinolid and (-)-Sapranthin via the Sharpless Asymmetric Dihydroxylation of Methyl trans-3-Pentenoate. Elucidation of the Stereostructure of (-)-Sapranthin", Chem. Eur. J. 19983, 2342-2352.
F. C. Görth, A. Umland, R. Brückner, "From Sugar Lactones to Stereodefined γ-Alkylidenebutenolides. Synthesis of Analogs of the γ-Alkylidenebutenolide Antibiotics Lissoclinolid and Tetrenolin", Eur. J. Org. Chem. 1998, 1055-1062.
E. Rank, R. Brückner, "A McMurry Route to the Dienediyne Portion of Models of the Neocarzinostatin Chromophore", Eur. J. Org. Chem. 1998, 1045-1053.
D. Muñoz-Torrero, R. Brückner, "Synthesis of a Key Building Block for a Butyrolactone → 1,3-Diol Approach to the Polyol Part of Roflamycoin", Eur. J. Org. Chem. 1998, 1031-1043.
M. Menges, R. Brückner, "Synthesis of a Butyrolactone Precursor of an Algae Nonaether from an Enantiopure Glycol Obtained by Hoppe's Chemistry", Eur. J. Org. Chem. 1998, 1023-1030.
F. Ferri, R. Brückner, R. Herges, "Straightforward Syntheses of Biradical-Producing Bicyclic Dienediynes - Dienediyne Ketones Cycloaromatize via the Saito-Myers and not the Neocarzinostatin Pathway", New J. Chem. 199822, 531-545.
K. Siegel, R. Brückner, "First Total Synthesis of Dihydroxerulin, a Potent Inhibitor of the Biosynthesis of Cholesterol", Chem. Eur. J. 19983, 1116-1122.
F. v. d. Ohe, R. Brückner, "Z- or E-Configurated γ-Alkylidenebutenolides from a 2-(Trialkylsilyloxy)furan and Iodomethacrolein - Stereoselective Synthesis of Z- and E-Freelingyne", Tetrahedron Lett. 199839, 1909-1910.
C. Gibson, T. Buck, M. Walker, R. Brückner, "Approaching the C33-C38 Fragment of Amphotericin B and Nystatin by a Retro-[1,4]-Brook Rearrangement and the Stereoselective Manipulation of the Resulting Allylsilane", Synlett 1998, 201-205.
M. Rucker, R. Brückner, "First Generation of the Dienediyne Portion of a Dienediyne Model of the Neocarzinostatin Chromophore by a McMurry Reaction", Tetrahedron Lett. 199738, 7353-7356.
C. Harcken, R. Brückner, "Synthesis of Optically Active Butenolides and γ-Lactones via the Sharpless Asymmetic Dihydroxylation of β,γ-Unsaturated Carboxylic Esters", Angew. Chem. 1997, 109, 2866-2868; Angew. Chem. Int. Ed. Engl. 199736, 2750-2752.
M. Rucker, R. Brückner, "Practical Synthesis of the Trisubstituted Naphthalene Carboxylic Acid from Neocarzinostatin Chromophore", Synlett 1997, 1187-1189.
S. Allerheiligen, R. Brückner, "Total Synthesis of the TolypothrixPentaether via a Bis(γ-butyrolactone) → 1,3,7,9-Tetraol Route", Liebigs Ann. Recueil 1997, 1667-1676.
S. Weigand, R. Brückner, "Total Synthesis of the TolypothrixPentaether from Enantiomerically Pure Homoallyl Alcohols via a Butyrolactone → 1,3-Diol Strategy", Liebigs Ann. Recueil 1997, 1657-1666.
H. Priepke, R. Brückner, "A Butyrolactone → 1,3-Diol Strategy for the Obtention of Tolypothrix Pentaethers - Total Synthesis of theTolypothrix Pentaether from Enantiomerically Enriched S-Glycidol", Liebigs Ann. Recueil 1997, 1645-1655.
H. Priepke, S. Weigand, R. Brückner, "A Butyrolactone → 1,3-Diol Strategy for the Obtention of Tolypothrix Pentaethers - Stereoselective Synthesis of a Key Lactone Precursor", Liebigs Ann. Recueil 1997, 1635-1644.
F. Sammtleben, M. Noltemeyer, R. Brückner, "1,3-Asymmetric Induction in Retro-[1,4]-Brook Rearrangements of Propargyl Lithium Compounds", Tetrahedron Lett. 199738, 3893-3896.
D. Goeppel, R. Brückner, "1,3-Asymmetric Induction in Retro-[1,4]-Brook Rearrangements of Lithiated Allyl Methyl Ethers and Lithiated Allyl MOM Ethers", Tetrahedron Lett. 199738, 2937-2938.
C. Gibson, T. Buck, M. Noltemeyer, R. Brückner, "Metal Dependent 1,3-Asymmetric Induction in the Retro-[1,4]-Brook Rearrangement of a Silylated Tiglyl Alkalimetal Compound", Tetrahedron Lett. 1997, 38, 2933-2936.
F. Ferri, R. Brückner, "Synthesis of an Epoxide- and Carbonate-Containing 6-Ring/10-Ring Dienediyne Model of the Neocarzinostatin Chromophore", Liebigs Ann. Recueil 1997, 961-965.
M. Eckhardt, R. Brückner, "Strategy for the Synthesis of Epoxide- and Carbonate-Containing Dienediyne Models of the Neocarzinostatin Chromophore. Application to the 6-Ring/11-Ring Case", Liebigs Ann. Recueil 1997, 947-959.
S. Weigand, R. Brückner, "Building Blocks for the Stereocontrolled Synthesis of 1,3-Diols of Various Configurations", Synlett 1997, 225-228.
K. Peters, E.-M. Peters, J. Fischer, R. Brückner, "Crystal Structure of 5-tert-butyl-3-ethinyl-2,2-dimethyl-1-(2-trimethylsilylethinyl)-cyclohexane-1,3-diol", Z. Krist. 1996211, 965-966.
K. Peters, E.-M. Peters, J. Fischer, R. Brückner, "Crystal Structure of 5-tert-butyl-2,2-dimethyl-1,3-bis-(2-trimethylsilylethinyl)-cyclohexane-1,3-diol", Z. Krist. 1996211, 957-960.
O. Gebauer, R. Brückner, "A Practical Synthesis of Enantiopure R-4-Hydroxy-2-cyclohexen-1-one", Liebigs Ann. 1996, 1559-1563.
R. Brückner, "Reaktionsmechanismen - Organische Reaktionen, Stereochemie, moderne Synthesemethoden", Spektrum Akademischer Verlag, Heidelberg, Berlin, Oxford, 1996, S. 570.
S. Weigand, R. Brückner, "BINOL/Ti(OR)4-Catalyzed Highly Enantioselective Additions of β-Substituted Allylstannanes to Aldehydes", Chemistry Eur. J. 19962, 1077-1084.
M. Eckhardt, R. Brückner, "Die erste Modellverbindung des Neocarzinostatin-Chromophors, die Epoxid- und Carbonatring enthält", Angew. Chem. 1996, 108, 1185-1188; Angew. Chem. Int. Ed. Engl. 199635, 1093-1096.
J. Suffert, R. Brückner, "Diènediynes analogues cycliques et acycliques de la néocarzinostatine, puissant antibiotique anticancéreux", Lettre des Sciences Chimiques, février-avril 1996, 25-29.
M. Eckhardt, R. Brückner, "The First Syntheses of 6-Ring/10-Ring Analogs and of a 6-Ring/11-Ring Analog of the Dienediyne Core of Neocarzinostatin Chromophore by the Nozaki-Hiyama Reaction", Liebigs Ann. 1996, 473-488.
K. Brickmann, F. Hambloch, J. Suffert, R. Brückner, "Synthesis of 6-Ring/10-Ring Analogs of the Dienediyne Core of Neocarzinostatin Chromophore Through Palladium(0)-mediated Ring-closure Reactions", Liebigs Ann. 1996, 457-471.
J. Suffert, E. Abraham, S. Raeppel, R. Brückner, "Synthesis of 5-Ring/10-Ring Analogs of the Dienediyne Core of Neocarzinostatin Chromophore Through Palladium(0)-mediated Ring-closure Reactions", Liebigs Ann. 1996, 447-456.
S. Weigand, R. Brückner, "Direct Preparation of Allyl Stannanes from Allyl Alcohols - Convenient Syntheses of ß-Substituted Allylstannanes and of Stereodefined γ-Substituted Allylstannanes", Synthesis 1996, 475-482.
M. Eckhardt, R. Brückner, J. Suffert, "The First 6-Membered/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatin Chromophore", Tetrahedron Lett. 199536, 5167-5170.
I. Kalvinsh, K.-H. Metten, R. Brückner, "A Novel Pathway to Alkenyl (Trifluoromethanesulfonates). Application to the Conversion of Sugar Lactones into Versatile Chirons", Heterocycles 199540, 939-952.
K. Behrens, B. Kneisel, M. Noltemeyer, R. Brückner, "Preparation of α-Chiral Crotylsilanes Through Retro-[1,4]-Brook Rearrangements. A Stereochemical Study", Liebigs Ann. 1995, 385-400.
M. Menges, R. Brückner, "Enantioselective Synthesis of Bis(γ-butyrolactones). Their Oxidative Degradations to Tetraols as a Key Step in Stereoselective Syntheses of 1,3,5,7,9-Pentaol Synthons for Polyhydroxylated Natural Products", Liebigs Ann. 1995, 365-384.
E. Winter, R. Brückner, "High 1,3-Asymmetric Induction in Retro-[1,4]-Brook Rearrangements: Stereocontrolled Synthesis of Chiral Allyl Silanes", Synlett 1994, 1049-1053.
M. Menges, R. Brückner, Oxidative Degradation of a Bis(γ-butyrolactone) into a Stereodefined 1,3,7,9-tetraol. Enantioselective Synthesis of a 1,3,5,7,9-Pentaol Building Block for Polymethoxylated Marine Natural Products", Synlett 1994, 809-813.
P. Keiner, R. Brückner, "The [2,3]-Wittig Rearrangements of Lithioalkyl Allyl Ethers Exhibit Different cis,trans-Selectivities than [2,3] Shifts in their Lithiomethyl Analogues", Tetrahedron 199450, 13417-13424.
H. v. d. Emde, A. Langels, R. Brückner, "1,2-Asymmetric Induction in the [2,3]-Thia-Wittig Rearrangement Applied to a Synthesis of the C17-C22-Subunit of Ionomycin", Tetrahedron Lett. 199435, 7609-7612.
R. Brückner, R. Huisgen, "Diels-Alder Reactions with Bis(trifluoromethyl)ethylene-1,1-dicarbonitrile as Dienophile", Tetrahedron Lett. 199435, 3285-3288.
R. Brückner, R. Huisgen, "Homoallyl Cyanide and N-Allylketene Imine; A [3,3]Sigmatropic Equilibrium", Tetrahedron Lett. 199435, 3281-3284.
K. Brickmann, F. Hambloch, E. Spolaore, R. Brückner, "[2,3]-Thia-Wittig Rearrangments of α-Lithiated Sulfides Via De-aromatized Cyclohexadiene Intermediates Proceed with Inversion of Configuration at the Carbanionic Center", Chem. Ber. 1994127, 1949-1957.
M. Moniatte, M. Eckhardt, K. Brickmann, R. Brückner, J. Suffert, "Study of the Regioselectivity of Palladium-catalyzed Monocouplings between conjugated Bis(enoltriflates) and Trimethylsilylacetylene", Tetrahedron Lett. 199435, 1965-1968.
D. Goeppel, I. Münster, R. Brückner, "The Geometry of the Carbanionic Moiety influences the Non-Induced Diastereoselectivity of the [2,3]-Wittig Rearrangement of Lithiated Diallyl Ethers", Tetrahedron 199450, 3687-3708.
J. Suffert, R. Brückner, "The Synthesis and Acid Induced Cycloaromatization of a Dienediyne Analogue of Neocarzinostatin Chromophore", Synlett 1994, 51-53.
M. Menges, R. Brückner, "Oxidative Degradation of γ-Butyrolactones into 1,3-Diols via a Criegee Rearrangement of Peroxosulfonates. An Enantioselective Synthesis of Compactin Lactone and its Diastereomer", Synlett 1993, 901-905.
S. W. Scheuplein, R. Machinek, J. Suffert, R. Brückner, "Activation of a Dienediyne Model of Neocarzinostatin Chromophore Through an Acid Mediated Solvolysis. Evidence for a New Cyclization Mode of Enyne[3]cumulenes", Tetrahedron Lett. 199334, 6549-6552.
J. Suffert, A. Eggers, S. Scheuplein, R. Brückner, "Contrasteric Regioselectivity of Palladium(0) Catalyzed Couplings of Alkynes with a Bis(enoltriflate). Novel Syntheses of E-Configurated Dienediynes", Tetrahedron Lett. 199334, 4177-4180.
K. Brickmann, R. Brückner, "[2,3]-Thia-Wittig Rearrangements Proceeding with Complete Inversion or Partial Loss of Configuration at the Carbanion Center", Chem. Ber. 1993126, 1227-1239.
R. Hoffmann, T. Rückert, R. Brückner, "[1,2]-Wittig Rearrangement of a Lithioalkyl Benzyl Ether with Inversion of Configuration at the Carbanion C Atom. Diastereoselective Reductions of Cyclohexyl Radicals with Li+ Arene-", Tetrahedron Lett. 199334, 297-300.
H. v. d. Emde, R. Brückner, "[2,3]-Thia-Wittig Rearrangements with a Marked Starting Material Dependence of Stereoselectivity", Tetrahedron Lett. 199233, 7323-7326.
R. Hoffmann, R. Brückner, "Retro [1,4]-Brook Rearrangements of Nonconjugated Secondary α-Lithio Ethers: Proof of Stereospecifity and of Retention of Configuration at the Carbanion Center", Chem. Ber. 1992125, 2731-2739.
R. Hoffmann, R. Brückner, "Ein neuartiger Einstieg in Wittig-Umlagerungen - Eine stereoselektive [1,2]-Wittig-Umlagerung mit Konfigurationsumkehr am Carbanion-Zentrum", Chem. Ber. 1992, 125, 1957-1963.
R. Hoffmann, R. Brückner, "[2,3]-Wittig-Umlagerung von sekundären α-Lithioethern: Nachweis von Stereospezifität und Umkehr der Konfiguration am Carbanion-Kohlenstoff", Angew. Chem. 1992104, 646-648, Angew. Chem. Int. Ed. Engl. 199231, 647-649.
R. Hoffmann, R. Brückner, "Asymmetric Induction in Reductively Initiated [2,3]-Wittig and Retro-[1,4]-Brook Rearrangements of Secondary Carbanions", Chem. Ber. 1992125, 1471-1484.
H. v. d. Emde, P. Keiner, B. Kruse, R. Hoffmann, R. Brückner, "Reductively Initiated [2,3]-Wittig Rearrangements", in "Selective Reactions of Metal Activated Molecules" (H. Werner, A. G. Griesbeck, W. Adam, G. Bringmann, W. Kiefer, Hrsg.), Vieweg, Braunschweig/Wiesbaden, 1992, 207-210.
S. W. Scheuplein, K. Harms, R. Brückner, J. Suffert, "Regiocontrol in Pd(0)-mediated Couplings of a Bis(enoltriflate) with Alkynes - Stereoselective Syntheses of Monocyclic Dienediynes Related to the Neocarzinostatin Chromophore", Chem. Ber. 1992125, 271-278.
R. Brückner, "[2,3]-Wittig Rearrangements in Stereoselective Synthesis", Kontakte (Darmstadt) 19912, 3-14, 19913, 3-15.
R. Brückner, "2,3 Sigmatropic Rearrangement", in: Heteroatom Manipulation (E. Winterfeldt, Edt.), Comprehensive Organic Synthesis (B. M. Trost, I. Fleming, Edts.), Pergamon Press, Oxford, New York, Seoul, Tokyo, 1991, Bd. 6, 873-908.
S. W. Scheuplein, R. Brückner, "1,3-Butadienyltributylphosphonium Bromide as a Conjunctive Reagent for the Synthesis of 1,3-Dienes from Carbonyl Compounds and Gilman Cuprates", Chem. Ber. 1991, 124, 1871-1874.
R. Brückner, R. Huisgen, "Substitutions and Dehydrogenations by 2,2-Bis(trifluoromethyl)ethylene-1,1-dicarbonitrile via Hydride Abstraction", Tetrahedron Lett. 199132, 1875-1878.
R. Brückner, R. Huisgen, "Electrophilic Substitutions by 2,2-Bis(trifluoromethyl)ethylene-1,1-dicarbonitrile via Addition", Tetrahedron Lett. 199132, 1871-1874.
J. Suffert, R. Brückner, "Palladium Catalyzed Couplings of Enol Triflates Under Very Mild Conditions - The Stereoselective Synthesis of Dienediynes from Bis(enoltriflates)", Tetrahedron Lett. 199132, 1453-1457.
R. Brückner, S. W. Scheuplein, J. Suffert, "Rapid and Stereoselective Construction of Dienediynes Related to the Neocarzinostatin Chromophore, Tetrahedron Lett. 199132, 1449-1452.
R. Huisgen, R. Brückner, "2,2-Bis(trifluoromethyl)ethylene-1,1-dicarbonitrile as a Unique Enophile", J. Org. Chem. 199156, 1679-1681.
R. Brückner, R. Huisgen, "The Electron-Deficient Olefin 2,2-Bis(trifluoromethyl)ethylene-1,1-dicarbonitrile: Hydride Abstractions from Allyl and Isobutenyl Ethers and Thioethers", J. Org. Chem. 199156, 1677-1679.
A. Kusche, R. Hoffmann, I. Münster, P. Keiner, R. Brückner, "A Direct Synthesis of O,S-Acetals from Aldehydes", Tetrahedron Lett. 1991, 32, 467-470.
R. Brückner, "Asymmetrische Synthesen: [2,3]-Wittig-Umlagerung, Nachr. Chem. Tech. Lab. 199038, 1506-1510.
R. Brückner, R. Huisgen, "2,2-Bis(trifluoromethyl)ethylene-1,1-dicarbonitrile and Styrenes - The Concertedness of the [2+4]-Cycloaddition", Tetrahedron Lett. 199031, 7133-7136.
R. Brückner, R. Huisgen, J. Schmid, "2,2-Bis(trifluoromethyl)ethylene-1,1-dicarbonitrile and Styrenes - A Dichotomy of Cycloaddition Pathways", Tetrahedron Lett. 199031, 7129-7132.
B. Kruse, R. Brückner, "Does the Wittig-Still Rearrangement Proceed via a Metal Free Carbanion?", Tetrahedron Lett. 199031, 4425-4428.
R. Brückner, R. Huisgen, "[2+2] Cycloadditions of 2,2-Bis(trifluoromethyl)ethylene-1,1-dicarbonitrile with Vinyl Sulfides and Ketene S,S-Acetals", Tetrahedron Lett. 199031, 2561-2565.
R. Brückner, R. Huisgen, "Kinetics of [2+2] Cycloadditions of 2,2-Bis(trifluoromethyl)ethylene-1,1-dicarbonitrile with Enol Ethers, 1,1-Dimethylbutadiene, and Allyltrimethylsilane", Tetrahedron Lett. 1990, 31, 2557-2560.
R. Huisgen, R. Brückner, "[2+2] Cycloadditions of 2,2-Bis(trifluoromethyl)ethylene-1,1-dicarbonitrile with Enol Ethers, 1,1-Dimethylbutadiene, and Allyltrimethylsilane", Tetrahedron Lett. 1990, 31, 2553-2556.
S. W. Scheuplein, A. Kusche, R. Brückner, K. Harms, "Asymmetric Induction in the [2,3] Wittig Rearrangement by Chiral Substituents in the Allyl Moiety: 1,3 Asymmetric Induction", Chem. Ber. 1990123, 917-925.
H. Priepke, R. Brückner, K. Harms, "Asymmetric Induction in the Wittig-Still Rearrangement of Ethers Containing an Allylic Stereocenter - Diastereocontrol by Allylic Nitrogen", Chem. Ber. 1990123, 555-563.
H. Priepke, R. Brückner, "Asymmetric Induction in the Wittig-Still Rearrangement of Ethers Containing an Allylic Stereocenter - Diastereocontrol by Allylic Oxygen", Chem. Ber. 1990123, 153-168.
B. Kruse, R. Brückner, "Reductive Lithiation of Sulfides and Sulfones - A Novel Entry into [2,3] Wittig Rearrangements", Chem. Ber. 1989, 122, 2023-2025.
R. Brückner, "Organisch-chemischer Denksport - Ein Seminar für Fortgeschrittene", Vieweg & Sohn, Braunschweig, Wiesbaden 1989.
R. Brückner, "Asymmetric Induction in the [2,3] Wittig Rearrangement - The Stereoselective Synthesis of Unsaturated Alcohols with Three Contiguous Stereoge-nic Cen-ters", Chem. Ber. 1989122, 193-198.
R. Brückner, "Asymmetric Induction in the [2,3] Wittig Rearrangement - The Stereoselective Synthesis of Unsaturated Alcohols with Three Contiguous Stereogenic Centers", Chem. Ber. 1989122, 193-198.
R. Brückner, "Stereocontrolled Synthesis of a C14-C20 Building Block for Amphotericin B Using a Novel [2,3] Wittig Rearrangement", Tetrahedron Lett. 198829, 5747-5750.
R. Brückner, B. Peiseler, "Synthesis and Reactions of [(Allyloxy)methyl]sulfones - An Equivalent for the [2,3] Wittig Rearrangement of Nonconjugated Secondary Carbanions", Tetrahedron Lett. 198829, 5233-5236.
R. Brückner, H. Priepke, "Asymmetrische Induktion bei der Wittig-Umlagerung durch chirale Substituenten im Allylteil", Angew. Chem. 1988100, 285-286.
H. Nöth, R. Staudigl, R. Brückner, "Untersuchung von Substituenten-Austauschreaktionen mittels 10B-Isotopenmarkierung: Reaktionen zwischen 1,2,4,3,5-Trithiadiborolanen", Chem. Ber. 1981114, 1871-1883.
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