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Reinhard Brückner, Dr. - Publications

Affiliations: 
Institut für Organische Chemie Julius-Maximilians-Universität Würzburg, Würzburg, Bayern, Germany 
 Georg-August-Universität Göttingen, Göttingen, Niedersachsen, Germany 
 Institut für Chemie und Biochemie Albert-Ludwigs-Universität Freiburg, Freiburg im Breisgau, Baden-Württemberg, Germany 
Website:
http://www.brueckner.uni-freiburg.de/brueckner
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Year Citation  Score
2022 Momm SN, Brückner R. Syntheses of 6,7-Benzotropolones by a Sequence of Acylation (or α-Hydroxyalkylation/Oxidation), Ring-Closing Metathesis, and Hydrolysis/β-Elimination. The Journal of Organic Chemistry. 87: 15415-15420. PMID 36318761 DOI: 10.1021/acs.joc.2c01968  0.312
2020 Kopp J, Brückner R. Stereoselective Total Synthesis of the Dimeric Naphthoquinonopyrano-γ-lactone (-)-Crisamicin A: Introducing the Dimerization Site by a Late-Stage Hartwig Borylation. Organic Letters. PMID 32298125 DOI: 10.1021/acs.orglett.0c01078  0.39
2020 Kopp J, Brückner R. Stereoselective Total Synthesis of the Dimeric Naphthoquinonopyrano-γ-lactone (-)-Crisamicin A: Introducing the Dimerization Site by a Late-Stage Hartwig Borylation. Organic Letters. PMID 32298125 DOI: 10.1021/acs.orglett.0c01078  0.39
2020 Kopp J, Brückner R. Stereoselective Total Synthesis of the Dimeric Naphthoquinonopyrano-γ-lactone (-)-Crisamicin A: Introducing the Dimerization Site by a Late-Stage Hartwig Borylation. Organic Letters. PMID 32298125 DOI: 10.1021/acs.orglett.0c01078  0.39
2020 Drescher C, Keller M, Potterat O, Hamburger M, Brückner R. Structure-Elucidating Total Synthesis of the (Polyenoyl)tetramic Acid Militarinone C§. Organic Letters. PMID 32191484 DOI: 10.1021/acs.orglett.0c00431  0.307
2019 Bäuerle F, Brückner R. Atropselective Synthesis of -Bis(diphenylphosphanes) from Bridged 2-Arylindoles Based on Effective Point-to-Axial Asymmetric Inductions after an Unusual Dilithiation ⊥. Organic Letters. PMID 31790259 DOI: 10.1021/acs.orglett.9b03896  0.38
2019 Engesser T, Brückner R. Stereoselective Aldol Additions of Glycolic Acid and Its Derivatives Synthesis. 51: 1715-1745. DOI: 10.1055/s-0037-1611721  0.31
2019 Engesser T, Brückner R. Stereoselective Aldol Additions of Glycolic Acid and Its Derivatives Synthesis. 51: 1715-1745. DOI: 10.1055/s-0037-1611721  0.31
2019 Engesser T, Brückner R. Stereoselective Aldol Additions of Glycolic Acid and Its Derivatives Synthesis. 51: 1715-1745. DOI: 10.1055/s-0037-1611721  0.31
2019 Engesser T, Brückner R. Stereoselective Aldol Additions of Glycolic Acid and Its Derivatives Synthesis. 51: 1715-1745. DOI: 10.1055/s-0037-1611721  0.31
2019 Engesser T, Brückner R. Stereoselective Aldol Additions of Glycolic Acid and Its Derivatives Synthesis. 51: 1715-1745. DOI: 10.1055/s-0037-1611721  0.31
2017 Sartorius F, Trebing M, Brückner C, Brückner R. Reducing Diastereomorphous Bis(phosphane oxide) Atropisomers to One Atropisomerically Pure Diphosphane: A New Ligand and a Novel Ligand-Preparation Design. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29154471 DOI: 10.1002/chem.201704800  0.314
2017 Sartorius F, Trebing M, Brückner C, Brückner R. Reducing Diastereomorphous Bis(phosphane oxide) Atropisomers to One Atropisomerically Pure Diphosphane: A New Ligand and a Novel Ligand-Preparation Design. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29154471 DOI: 10.1002/chem.201704800  0.314
2017 Neumeyer M, Brückner R. First Stereoselective Total Synthesis of a Dimeric Naphthoquinonopyrano-γ-lactone: (+)-γ-Actinorhodin. Angewandte Chemie (International Ed. in English). PMID 28211203 DOI: 10.1002/anie.201611183  0.373
2017 Brückner R, Arican D, Braukmüller S. Regioselective Bromination of Benzocycloheptadienones for the Synthesis of Substituted 3,4-Benzotropolones Including Goupiolone A. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28187235 DOI: 10.1002/chem.201700622  0.418
2017 Brückner R, Arican D, Braukmüller S. Regioselective Bromination of Benzocycloheptadienones for the Synthesis of Substituted 3,4-Benzotropolones Including Goupiolone A. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28187235 DOI: 10.1002/chem.201700622  0.418
2017 Brückner R, Arican D, Braukmüller S. Regioselective Bromination of Benzocycloheptadienones for the Synthesis of Substituted 3,4-Benzotropolones Including Goupiolone A. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28187235 DOI: 10.1002/chem.201700622  0.418
2017 Brückner R, Arican D, Braukmüller S. Regioselective Bromination of Benzocycloheptadienones for the Synthesis of Substituted 3,4-Benzotropolones Including Goupiolone A. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28187235 DOI: 10.1002/chem.201700622  0.418
2017 Hampel T, Brückner R. Towards a Total Synthesis of Phenalinolactone Core Diterpenoid 6: Synthesis of a Racemic Decahydrobenzocyclobutaisobenzofuran with a trans-anti-cis Junction of the Isocyclic Rings European Journal of Organic Chemistry. 2017: 2950-2963. DOI: 10.1002/ejoc.201700198  0.327
2017 Hampel T, Brückner R. Towards a Total Synthesis of Phenalinolactone Core Diterpenoid 6: Synthesis of a Racemic Decahydrobenzocyclobutaisobenzofuran with a trans-anti-cis Junction of the Isocyclic Rings European Journal of Organic Chemistry. 2017: 2950-2963. DOI: 10.1002/ejoc.201700198  0.327
2017 Hampel T, Brückner R. Towards a Total Synthesis of Phenalinolactone Core Diterpenoid 6: Synthesis of a Racemic Decahydrobenzocyclobutaisobenzofuran with a trans-anti-cis Junction of the Isocyclic Rings European Journal of Organic Chemistry. 2017: 2950-2963. DOI: 10.1002/ejoc.201700198  0.327
2017 Hampel T, Brückner R. Towards a Total Synthesis of Phenalinolactone Core Diterpenoid 6: Synthesis of a Racemic Decahydrobenzocyclobutaisobenzofuran with a trans-anti-cis Junction of the Isocyclic Rings European Journal of Organic Chemistry. 2017: 2950-2963. DOI: 10.1002/ejoc.201700198  0.327
2017 Hampel T, Brückner R. Towards a Total Synthesis of Phenalinolactone Core Diterpenoid 6: Synthesis of a Racemic Decahydrobenzocyclobutaisobenzofuran with a trans-anti-cis Junction of the Isocyclic Rings European Journal of Organic Chemistry. 2017: 2950-2963. DOI: 10.1002/ejoc.201700198  0.327
2017 Neumeyer M, Kopp J, Brückner R. Controlling the Substitution Pattern of Hexasubstituted Naphthalenes by Aryne/Siloxyfuran Diels-Alder Additions: Regio- and Stereocontrolled Synthesis of Arizonin C1 Analogs European Journal of Organic Chemistry. 2017: 2883-2915. DOI: 10.1002/ejoc.201700195  0.309
2017 Neumeyer M, Kopp J, Brückner R. Controlling the Substitution Pattern of Hexasubstituted Naphthalenes by Aryne/Siloxyfuran Diels-Alder Additions: Regio- and Stereocontrolled Synthesis of Arizonin C1 Analogs European Journal of Organic Chemistry. 2017: 2883-2915. DOI: 10.1002/ejoc.201700195  0.309
2016 Brückner R, Hermann D, Arican D. Two-Step Synthesis of (Z)-3-Aryl-5-(arylmethylidene)butenolides by an Ivanov Reaction/Silver(I)-Catalyzed Lactonization/In Situ Dehydration Sequence Synthesis. 49: 326-352. DOI: 10.1055/s-0036-1588338  0.31
2016 Brückner R, Hermann D, Arican D. Two-Step Synthesis of (Z)-3-Aryl-5-(arylmethylidene)butenolides by an Ivanov Reaction/Silver(I)-Catalyzed Lactonization/In Situ Dehydration Sequence Synthesis. 49: 326-352. DOI: 10.1055/s-0036-1588338  0.31
2016 Brückner R, Hermann D, Arican D. Two-Step Synthesis of (Z)-3-Aryl-5-(arylmethylidene)butenolides by an Ivanov Reaction/Silver(I)-Catalyzed Lactonization/In Situ Dehydration Sequence Synthesis. 49: 326-352. DOI: 10.1055/s-0036-1588338  0.31
2016 Brückner R, Hermann D, Arican D. Two-Step Synthesis of (Z)-3-Aryl-5-(arylmethylidene)butenolides by an Ivanov Reaction/Silver(I)-Catalyzed Lactonization/In Situ Dehydration Sequence Synthesis. 49: 326-352. DOI: 10.1055/s-0036-1588338  0.31
2015 Aucktor J, Brückner R. Total Synthesis of Quercitols: (+)- allo -, (-)- proto -, (+)- talo -, (-)- gala -, (+)- gala -, neo -, and (-)- epi -Quercitol Synlett. 25. DOI: 10.1055/s-0034-1379603  0.308
2014 Aucktor J, Anselmi C, Brückner R, Keller M. Synthesis of tricyclic precursors of cyclitols Synlett. 25: 1312-1318. DOI: 10.1055/s-0033-1341266  0.336
2014 Walleser P, Brückner R. 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 protection of homoallylic alcohols European Journal of Organic Chemistry. 2014: 3210-3224. DOI: 10.1002/ejoc.201400145  0.734
2013 Arican D, Brückner R. Syntheses of 3,4-benzotropolones by ring-closing metatheses. Organic Letters. 15: 2582-5. PMID 23668533 DOI: 10.1021/ol400510j  0.355
2013 Walleser P, Brückner R. Enantioselective synthesis of (+)-obolactone based on a symmetry-breaking Wacker monooxidation of a diene. Organic Letters. 15: 1294-7. PMID 23451721 DOI: 10.1021/ol400232m  0.758
2013 Kamptmann SB, Brückner R. 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 European Journal of Organic Chemistry. 6584-6600. DOI: 10.1002/ejoc.201300183  0.362
2011 Mahlau M, Fernandes RA, Brückner R. First Synthesis of the Pyrano-Naphthoquinone Lactone (-)-Arizonin C1 (Eur. J. Org. Chem. 25/2011) European Journal of Organic Chemistry. 2011: n/a-n/a. DOI: 10.1002/Ejoc.201190066  0.537
2011 Mahlau M, Fernandes RA, Brückner R. First synthesis of the pyrano-naphthoquinone lactone (-)-arizonin C1 European Journal of Organic Chemistry. 4765-4772. DOI: 10.1002/Ejoc.201100599  0.584
2011 Burghart J, Brückner R. Sn/Li exchange reactions in 1,ω-distannylated conjugated trienes and tetraenes: An enabling step for polyene synthesis European Journal of Organic Chemistry. 150-165. DOI: 10.1002/ejoc.201001231  0.31
2010 Walleser P, Brückner R. Stereocontrolled synthesis of 1,3,5-triols by an iteration of asymmetric dihydroxylation and deoxygenation European Journal of Organic Chemistry. 4802-4822. DOI: 10.1002/Ejoc.201000280  0.725
2010 Bruckner R. ChemInform Abstract: The Synthesis of γ-Alkylidenebutenolides Cheminform. 32: no-no. DOI: 10.1002/chin.200146291  0.321
2010 Bruckner R. ChemInform Abstract: The Synthesis of γ-Alkylidenebutenolides Cheminform. 32: no-no. DOI: 10.1002/chin.200146291  0.321
2010 Bruckner R. ChemInform Abstract: The Synthesis of γ-Alkylidenebutenolides Cheminform. 32: no-no. DOI: 10.1002/chin.200146291  0.321
2010 Bruckner R. ChemInform Abstract: The Synthesis of γ-Alkylidenebutenolides Cheminform. 32: no-no. DOI: 10.1002/chin.200146291  0.321
2010 Bruckner R. ChemInform Abstract: The Synthesis of γ-Alkylidenebutenolides Cheminform. 32: no-no. DOI: 10.1002/chin.200146291  0.321
2009 Bernier D, Brückner R. Novel synthesis of naturally occurring pulvinones: A heck coupling, transesterification, and dieckmann condensation strategy (Synthesis (2007) (2249)) Synthesis. 1582. DOI: 10.1055/s-0028-1088054.pdf  0.339
2008 Burghart J, Brückner R. Total synthesis of naturally configured pyrrhoxanthin, a carotenoid butenolide from plankton. Angewandte Chemie (International Ed. in English). 47: 7664-8. PMID 18767089 DOI: 10.1002/anie.200801638  0.302
2007 Brückner R, Bernier D. Novel Synthesis of Naturally Occurring Pulvinones: A Heck Coupling, Transesterification­, and Dieckmann Condensation Strategy Synthesis. 2007: 2249-2272. DOI: 10.1055/s-2007-983803  0.303
2007 Brückner R, Bernier D. Novel Synthesis of Naturally Occurring Pulvinones: A Heck Coupling, Transesterification­, and Dieckmann Condensation Strategy Synthesis. 2007: 2249-2272. DOI: 10.1055/s-2007-983803  0.303
2007 Brückner R, Bernier D. Novel Synthesis of Naturally Occurring Pulvinones: A Heck Coupling, Transesterification­, and Dieckmann Condensation Strategy Synthesis. 2007: 2249-2272. DOI: 10.1055/s-2007-983803  0.303
2007 Bernier D, Moser F, Brückner R. Synthesis and cyclization of 3-aryl-2-(arylacetoxy)acrylates: A three-step access to pulvinones Synthesis. 2240-2248. DOI: 10.1055/s-2007-983800  0.388
2007 Kaczybura N, Brückner R. Tandem Claisen condensation/transesterification between arylacetate enolates and arylmethylene-substituted 2,2-dimethyl-1,3-dioxolan-4-ones: An improved synthesis of z-configured pulvinones Synthesis. 118-130. DOI: 10.1055/s-2006-950378  0.361
2006 Eckhardt M, Brückner R. The First Syntheses of 6-/10-Membered Ring Analogs and of a 6-/11-Membered Ring Analog of the Dienediyne Core of the Neocarzinostatin Chromophore by Ring-Closure According to the Nozaki-Hiyama Reaction Liebigs Annalen. 1996: 473-488. DOI: 10.1002/jlac.199619960407  0.318
2006 Eckhardt M, Brückner R. The First Syntheses of 6-/10-Membered Ring Analogs and of a 6-/11-Membered Ring Analog of the Dienediyne Core of the Neocarzinostatin Chromophore by Ring-Closure According to the Nozaki-Hiyama Reaction Liebigs Annalen. 1996: 473-488. DOI: 10.1002/jlac.199619960407  0.318
2006 Eckhardt M, Brückner R. The First Syntheses of 6-/10-Membered Ring Analogs and of a 6-/11-Membered Ring Analog of the Dienediyne Core of the Neocarzinostatin Chromophore by Ring-Closure According to the Nozaki-Hiyama Reaction Liebigs Annalen. 1996: 473-488. DOI: 10.1002/jlac.199619960407  0.318
2006 Eckhardt M, Brückner R. The First Syntheses of 6-/10-Membered Ring Analogs and of a 6-/11-Membered Ring Analog of the Dienediyne Core of the Neocarzinostatin Chromophore by Ring-Closure According to the Nozaki-Hiyama Reaction Liebigs Annalen. 1996: 473-488. DOI: 10.1002/jlac.199619960407  0.318
2006 Eckhardt M, Brückner R. The First Syntheses of 6-/10-Membered Ring Analogs and of a 6-/11-Membered Ring Analog of the Dienediyne Core of the Neocarzinostatin Chromophore by Ring-Closure According to the Nozaki-Hiyama Reaction Liebigs Annalen. 1996: 473-488. DOI: 10.1002/jlac.199619960407  0.318
2006 Suffert J, Abraham E, Raeppel S, Brückner R. Synthesis of 5-/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)-Mediated Ring-Closure Reaction Liebigs Annalen. 1996: 447-456. DOI: 10.1002/jlac.199619960405  0.661
2006 Suffert J, Abraham E, Raeppel S, Brückner R. Synthesis of 5-/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)-Mediated Ring-Closure Reaction Liebigs Annalen. 1996: 447-456. DOI: 10.1002/jlac.199619960405  0.376
2006 Suffert J, Abraham E, Raeppel S, Brückner R. Synthesis of 5-/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)-Mediated Ring-Closure Reaction Liebigs Annalen. 1996: 447-456. DOI: 10.1002/jlac.199619960405  0.376
2006 Suffert J, Abraham E, Raeppel S, Brückner R. Synthesis of 5-/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)-Mediated Ring-Closure Reaction Liebigs Annalen. 1996: 447-456. DOI: 10.1002/jlac.199619960405  0.376
2006 Suffert J, Abraham E, Raeppel S, Brückner R. Synthesis of 5-/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)-Mediated Ring-Closure Reaction Liebigs Annalen. 1996: 447-456. DOI: 10.1002/jlac.199619960405  0.376
2006 Braukmüller S, Brückner R. Enantioselective butenolide preparation for straightforward asymmetric syntheses of γ-lactones - Paraconic acids, avenaciolide, and hydroxylated eleutherol European Journal of Organic Chemistry. 2110-2118. DOI: 10.1002/ejoc.200500961  0.309
2005 Olpp T, Brückner R. Novel strategy for the synthesis of the butenolide moiety of peridinin. Angewandte Chemie (International Ed. in English). 44: 1553-7. PMID 15678429 DOI: 10.1002/anie.200460259  0.302
2005 Sorg A, Siegel K, Brückner R. Stereoselective syntheses of dihydroxerulin and xerulinic acid, anti-hypocholesterolemic dyes from the fungus Xerula melanotricha. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 1610-24. PMID 15669063 DOI: 10.1002/chem.200400913  0.306
2005 Körber K, Risch P, Brückner R. A novel strategy for the convergent synthesis of 1,3,5,...-polyols: Enone formation, asymmetric dihydroxylation, reductive cleavage, hydride addition Synlett. 2905-2910. DOI: 10.1055/s-2005-921915  0.343
2005 Fernandes RA, Brückner R. Efficient synthesis of (+)-kalafungin and (-)-nanaomycin D by asymmetric dihydroxylation, oxa-pictet-spengler cyclization, and H2SO 4-mediated isomerization Synlett. 1281-1285. DOI: 10.1055/S-2005-868505  0.609
2005 Schmidt-Leithoff J, Brückner R. 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 Helvetica Chimica Acta. 88: 1943-1959. DOI: 10.1002/hlca.200590149  0.308
2004 Brückner R, Siegel K, Sorg A. Chapter 14 Stereoselective synthesis of polyunsaturated γ-alkylidenebutenolides: The total synthesis of the xerulins Strategies and Tactics in Organic Synthesis. 5: 437-473. DOI: 10.1016/S1874-6004(04)80037-6  0.338
2004 Berkenbusch T, Laungani AC, Brückner R, Keller M. Serendipitous synthesis of a ditwistane: A one-step access! Tetrahedron Letters. 45: 9517-9520. DOI: 10.1016/j.tetlet.2004.10.124  0.327
2001 Harcken C, Brückner R. Elucidation of the stereostructure of the annonaceous acetogenin (+)-montecristin through total synthesis New Journal of Chemistry. 25: 40-54. DOI: 10.1039/B002905J  0.305
2001 Harcken C, Brückner R. Elucidation of the stereostructure of the annonaceous acetogenin (+)-montecristin through total synthesis New Journal of Chemistry. 25: 40-54. DOI: 10.1039/B002905J  0.305
2001 Harcken C, Brückner R. Elucidation of the stereostructure of the annonaceous acetogenin (+)-montecristin through total synthesis New Journal of Chemistry. 25: 40-54. DOI: 10.1039/B002905J  0.305
2000 von der Ohe F, Brückner R. Stereoselective synthesis of freelingyne and related γ-alkylidenebutenolides via vinylogous Mukaiyama aldol additions New Journal of Chemistry. 24: 659-669. DOI: 10.1039/B002903N  0.352
2000 von der Ohe F, Brückner R. Stereoselective synthesis of freelingyne and related γ-alkylidenebutenolides via vinylogous Mukaiyama aldol additions New Journal of Chemistry. 24: 659-669. DOI: 10.1039/B002903N  0.352
2000 von der Ohe F, Brückner R. Stereoselective synthesis of freelingyne and related γ-alkylidenebutenolides via vinylogous Mukaiyama aldol additions New Journal of Chemistry. 24: 659-669. DOI: 10.1039/B002903N  0.352
2000 von der Ohe F, Brückner R. Stereoselective synthesis of freelingyne and related γ-alkylidenebutenolides via vinylogous Mukaiyama aldol additions New Journal of Chemistry. 24: 659-669. DOI: 10.1039/B002903N  0.352
2000 von der Ohe F, Brückner R. Stereoselective synthesis of freelingyne and related γ-alkylidenebutenolides via vinylogous Mukaiyama aldol additions New Journal of Chemistry. 24: 659-669. DOI: 10.1039/B002903N  0.352
1999 Brückner R, Suffert J. The Bis(enol triflate) Route to Dienediyne Models of the Biradical Forming and DNA-Cleaving Natural Product Neocarzinostatin Chromophore Synlett. 1999: 657-679. DOI: 10.1055/s-1999-2699  0.555
1998 Ferri F, Brückner R, Herges R. Straightforward syntheses of biradical-producing bicyclic dienediynes—dienediyne ketones cycloaromatize ia the Saito–Myers and not ia the neocarzinostatin pathway New Journal of Chemistry. 22: 531-546. DOI: 10.1039/A709205I  0.342
1998 Berkenbusch T, Brückner R. Brief syntheses of (+)-blastmycinone and related γ-lactones from an asymmetrically dihydroxylated carboxylic ester Tetrahedron. 54: 11461-11470. DOI: 10.1016/S0040-4020(98)00687-5  0.33
1998 Berkenbusch T, Brückner R. Brief syntheses of (+)-blastmycinone and related γ-lactones from an asymmetrically dihydroxylated carboxylic ester Tetrahedron. 54: 11461-11470. DOI: 10.1016/S0040-4020(98)00687-5  0.33
1998 Berkenbusch T, Brückner R. Brief syntheses of (+)-blastmycinone and related γ-lactones from an asymmetrically dihydroxylated carboxylic ester Tetrahedron. 54: 11461-11470. DOI: 10.1016/S0040-4020(98)00687-5  0.33
1998 Berkenbusch T, Brückner R. Brief syntheses of (+)-blastmycinone and related γ-lactones from an asymmetrically dihydroxylated carboxylic ester Tetrahedron. 54: 11461-11470. DOI: 10.1016/S0040-4020(98)00687-5  0.33
1998 Berkenbusch T, Brückner R. Brief syntheses of (+)-blastmycinone and related γ-lactones from an asymmetrically dihydroxylated carboxylic ester Tetrahedron. 54: 11461-11470. DOI: 10.1016/S0040-4020(98)00687-5  0.33
1997 Rucker M, Brückner R. First generation of the dienediyne portion of a dienediyne model of the neocarzinostatin chromophore by a McMurry reaction Tetrahedron Letters. 38: 7353-7356. DOI: 10.1016/S0040-4039(97)10010-7  0.34
1997 Allerheiligen S, Brückner R. Total Synthesis of theTolypothrix Pentaether via A Bis(γ-butyrolactone) → 1,3,7,9-Tetraol Route Liebigs Annalen. 1997: 1667-1676. DOI: 10.1002/jlac.199719970807  0.334
1997 Allerheiligen S, Brückner R. Total Synthesis of theTolypothrix Pentaether via A Bis(γ-butyrolactone) → 1,3,7,9-Tetraol Route Liebigs Annalen. 1997: 1667-1676. DOI: 10.1002/jlac.199719970807  0.334
1997 Allerheiligen S, Brückner R. Total Synthesis of theTolypothrix Pentaether via A Bis(γ-butyrolactone) → 1,3,7,9-Tetraol Route Liebigs Annalen. 1997: 1667-1676. DOI: 10.1002/jlac.199719970807  0.334
1997 Allerheiligen S, Brückner R. Total Synthesis of theTolypothrix Pentaether via A Bis(γ-butyrolactone) → 1,3,7,9-Tetraol Route Liebigs Annalen. 1997: 1667-1676. DOI: 10.1002/jlac.199719970807  0.334
1997 Allerheiligen S, Brückner R. Total Synthesis of theTolypothrix Pentaether via A Bis(γ-butyrolactone) → 1,3,7,9-Tetraol Route Liebigs Annalen. 1997: 1667-1676. DOI: 10.1002/jlac.199719970807  0.334
1997 Priepke H, Brückner R. A Butyrolactone → 1,3-diol Strategy for the Obtention ofTolypothrix Polyethers – Total Synthesis of theTolypothrix Pentaether from Enantiomerically EnrichedS-Glycidol Liebigs Annalen. 1997: 1645-1655. DOI: 10.1002/jlac.199719970805  0.3
1997 Priepke H, Brückner R. A Butyrolactone → 1,3-diol Strategy for the Obtention ofTolypothrix Polyethers – Total Synthesis of theTolypothrix Pentaether from Enantiomerically EnrichedS-Glycidol Liebigs Annalen. 1997: 1645-1655. DOI: 10.1002/jlac.199719970805  0.3
1997 Priepke H, Brückner R. A Butyrolactone → 1,3-diol Strategy for the Obtention ofTolypothrix Polyethers – Total Synthesis of theTolypothrix Pentaether from Enantiomerically EnrichedS-Glycidol Liebigs Annalen. 1997: 1645-1655. DOI: 10.1002/jlac.199719970805  0.3
1997 Priepke H, Brückner R. A Butyrolactone → 1,3-diol Strategy for the Obtention ofTolypothrix Polyethers – Total Synthesis of theTolypothrix Pentaether from Enantiomerically EnrichedS-Glycidol Liebigs Annalen. 1997: 1645-1655. DOI: 10.1002/jlac.199719970805  0.3
1997 Priepke H, Brückner R. A Butyrolactone → 1,3-diol Strategy for the Obtention ofTolypothrix Polyethers – Total Synthesis of theTolypothrix Pentaether from Enantiomerically EnrichedS-Glycidol Liebigs Annalen. 1997: 1645-1655. DOI: 10.1002/jlac.199719970805  0.3
1997 Priepke H, Weigand S, Brückner R. A Butyrolactone → 1,3-Diol Strategy for the Obtention ofTolypothrix Polyethers – Stereoselective Synthesis of a Key Lactone Precursor Liebigs Annalen. 1997: 1635-1644. DOI: 10.1002/jlac.199719970804  0.346
1997 Priepke H, Weigand S, Brückner R. A Butyrolactone → 1,3-Diol Strategy for the Obtention ofTolypothrix Polyethers – Stereoselective Synthesis of a Key Lactone Precursor Liebigs Annalen. 1997: 1635-1644. DOI: 10.1002/jlac.199719970804  0.346
1997 Priepke H, Weigand S, Brückner R. A Butyrolactone → 1,3-Diol Strategy for the Obtention ofTolypothrix Polyethers – Stereoselective Synthesis of a Key Lactone Precursor Liebigs Annalen. 1997: 1635-1644. DOI: 10.1002/jlac.199719970804  0.346
1997 Eckhardt M, Brückner R. Strategy for the Synthesis of Epoxide- and Carbonate-Containing Dienediyne Models of the Neocarzinostatin Chromophore – Application to the 6-Ring/11-Ring Case[1] Liebigs Annalen. 1997: 947-959. DOI: 10.1002/jlac.199719970526  0.301
1997 Eckhardt M, Brückner R. Strategy for the Synthesis of Epoxide- and Carbonate-Containing Dienediyne Models of the Neocarzinostatin Chromophore – Application to the 6-Ring/11-Ring Case[1] Liebigs Annalen. 1997: 947-959. DOI: 10.1002/jlac.199719970526  0.301
1997 Eckhardt M, Brückner R. Strategy for the Synthesis of Epoxide- and Carbonate-Containing Dienediyne Models of the Neocarzinostatin Chromophore – Application to the 6-Ring/11-Ring Case[1] Liebigs Annalen. 1997: 947-959. DOI: 10.1002/jlac.199719970526  0.301
1997 Eckhardt M, Brückner R. Strategy for the Synthesis of Epoxide- and Carbonate-Containing Dienediyne Models of the Neocarzinostatin Chromophore – Application to the 6-Ring/11-Ring Case[1] Liebigs Annalen. 1997: 947-959. DOI: 10.1002/jlac.199719970526  0.301
1997 Eckhardt M, Brückner R. Strategy for the Synthesis of Epoxide- and Carbonate-Containing Dienediyne Models of the Neocarzinostatin Chromophore – Application to the 6-Ring/11-Ring Case[1] Liebigs Annalen. 1997: 947-959. DOI: 10.1002/jlac.199719970526  0.301
1996 Weigand S, Brückner R. Direct Preparation of Allylstannanes from Allyl Alcohols: Convenient Synthesis of β-Substituted Allylstannanes and of Stereodefined γ-Substituted Allylstannanes Synthesis. 1996: 475-482. DOI: 10.1055/s-1996-4237  0.306
1996 Weigand S, Brückner R. Direct Preparation of Allylstannanes from Allyl Alcohols: Convenient Synthesis of β-Substituted Allylstannanes and of Stereodefined γ-Substituted Allylstannanes Synthesis. 1996: 475-482. DOI: 10.1055/s-1996-4237  0.306
1996 Weigand S, Brückner R. Direct Preparation of Allylstannanes from Allyl Alcohols: Convenient Synthesis of β-Substituted Allylstannanes and of Stereodefined γ-Substituted Allylstannanes Synthesis. 1996: 475-482. DOI: 10.1055/s-1996-4237  0.306
1995 Eckhardt M, Brückner R, Suffert J. The first 6-membered/10-membered ring analogues of the dienediyne core of neocarzinostatin chromophore Tetrahedron Letters. 36: 5167-5170. DOI: 10.1016/0040-4039(95)01025-D  0.602
1995 Eckhardt M, Brückner R, Suffert J. The first 6-membered/10-membered ring analogues of the dienediyne core of neocarzinostatin chromophore Tetrahedron Letters. 36: 5167-5170. DOI: 10.1016/0040-4039(95)01025-D  0.602
1995 Menges M, Brückner R. Enantioselective synthesis of bis(γ-butyrolactones). Their oxidative degradation to tetraols as a key step in stereoselective syntheses of 1,3,5,7,9-pentaol synthons for polyhydroxylated natural products Liebigs Annalen. 1995: 365-384. DOI: 10.1002/jlac.199519950246  0.322
1995 Menges M, Brückner R. Enantioselective synthesis of bis(γ-butyrolactones). Their oxidative degradation to tetraols as a key step in stereoselective syntheses of 1,3,5,7,9-pentaol synthons for polyhydroxylated natural products Liebigs Annalen. 1995: 365-384. DOI: 10.1002/jlac.199519950246  0.322
1995 Menges M, Brückner R. Enantioselective synthesis of bis(γ-butyrolactones). Their oxidative degradation to tetraols as a key step in stereoselective syntheses of 1,3,5,7,9-pentaol synthons for polyhydroxylated natural products Liebigs Annalen. 1995: 365-384. DOI: 10.1002/jlac.199519950246  0.322
1995 Menges M, Brückner R. Enantioselective synthesis of bis(γ-butyrolactones). Their oxidative degradation to tetraols as a key step in stereoselective syntheses of 1,3,5,7,9-pentaol synthons for polyhydroxylated natural products Liebigs Annalen. 1995: 365-384. DOI: 10.1002/jlac.199519950246  0.322
1995 Menges M, Brückner R. Enantioselective synthesis of bis(γ-butyrolactones). Their oxidative degradation to tetraols as a key step in stereoselective syntheses of 1,3,5,7,9-pentaol synthons for polyhydroxylated natural products Liebigs Annalen. 1995: 365-384. DOI: 10.1002/jlac.199519950246  0.322
1994 Winter E, Brückner R. High 1,3-Asymmetric Induction in Retro-[1,4]-Brook Rearrangements: Stereocontrolled Synthesis of Chiral Allyl Silanes Synlett. 1994: 1049-1053. DOI: 10.1055/s-1994-23082  0.349
1994 Winter E, Brückner R. High 1,3-Asymmetric Induction in Retro-[1,4]-Brook Rearrangements: Stereocontrolled Synthesis of Chiral Allyl Silanes Synlett. 1994: 1049-1053. DOI: 10.1055/s-1994-23082  0.349
1994 Winter E, Brückner R. High 1,3-Asymmetric Induction in Retro-[1,4]-Brook Rearrangements: Stereocontrolled Synthesis of Chiral Allyl Silanes Synlett. 1994: 1049-1053. DOI: 10.1055/s-1994-23082  0.349
1994 Winter E, Brückner R. High 1,3-Asymmetric Induction in Retro-[1,4]-Brook Rearrangements: Stereocontrolled Synthesis of Chiral Allyl Silanes Synlett. 1994: 1049-1053. DOI: 10.1055/s-1994-23082  0.349
1994 von der Emde H, Langels A, Noltemeyer M, Brückner R. 1,2-asymmetric induction in the [2,3]-thia-wittig rearrangement applied to a synthesis of the C17–C22 subunit of ionomycin Tetrahedron Letters. 35: 7609-7612. DOI: 10.1016/S0040-4039(00)78355-9  0.305
1994 von der Emde H, Langels A, Noltemeyer M, Brückner R. 1,2-asymmetric induction in the [2,3]-thia-wittig rearrangement applied to a synthesis of the C17–C22 subunit of ionomycin Tetrahedron Letters. 35: 7609-7612. DOI: 10.1016/S0040-4039(00)78355-9  0.305
1994 von der Emde H, Langels A, Noltemeyer M, Brückner R. 1,2-asymmetric induction in the [2,3]-thia-wittig rearrangement applied to a synthesis of the C17–C22 subunit of ionomycin Tetrahedron Letters. 35: 7609-7612. DOI: 10.1016/S0040-4039(00)78355-9  0.305
1994 von der Emde H, Langels A, Noltemeyer M, Brückner R. 1,2-asymmetric induction in the [2,3]-thia-wittig rearrangement applied to a synthesis of the C17–C22 subunit of ionomycin Tetrahedron Letters. 35: 7609-7612. DOI: 10.1016/S0040-4039(00)78355-9  0.305
1994 von der Emde H, Langels A, Noltemeyer M, Brückner R. 1,2-asymmetric induction in the [2,3]-thia-wittig rearrangement applied to a synthesis of the C17–C22 subunit of ionomycin Tetrahedron Letters. 35: 7609-7612. DOI: 10.1016/S0040-4039(00)78355-9  0.305
1994 Brückner R, Huisgen R. Diels-alder reactions with 2,2-bis(trifluoromethyl)-ethylene-1,1-dicarbonitrile as dienophile Tetrahedron Letters. 35: 3285-3288. DOI: 10.1016/S0040-4039(00)76886-9  0.452
1994 Brückner R, Huisgen R. Homoallyl cyanide and N-allylketene imine; a [3,3]sigmatropic equilibrium Tetrahedron Letters. 35: 3281-3284. DOI: 10.1016/S0040-4039(00)76885-7  0.374
1994 Brückner R, Huisgen R. Homoallyl cyanide and N-allylketene imine; a [3,3]sigmatropic equilibrium Tetrahedron Letters. 35: 3281-3284. DOI: 10.1016/S0040-4039(00)76885-7  0.374
1994 Moniatte M, Eckhardt M, Brickmann K, Brückner R, Suffert J. Study of the regioselectivity of palladium-catalyzed monocouplings between conjugated bis(enoltriflates) and trimethylsilylacetylene Tetrahedron Letters. 35: 1965-1968. DOI: 10.1016/S0040-4039(00)73023-1  0.665
1994 Moniatte M, Eckhardt M, Brickmann K, Brückner R, Suffert J. Study of the regioselectivity of palladium-catalyzed monocouplings between conjugated bis(enoltriflates) and trimethylsilylacetylene Tetrahedron Letters. 35: 1965-1968. DOI: 10.1016/S0040-4039(00)73023-1  0.665
1993 Suffert J, Eggers A, Scheuplein SW, Brückner R. Contrasteric regioselectivity of palladium(O) catalyzed couplings of alkynes with a bis(enoltriflate). Novel syntheses of E-configurated dienediynes Tetrahedron Letters. 34: 4177-4180. DOI: 10.1016/S0040-4039(00)60521-X  0.609
1993 Scheuplein SW, Machinek R, Suffert J, Brückner R. Activation of a dienediyne model of neocarzinostatin chromophore through an acid mediated solvolysis. Evidence for a new cyclization mode of enyne[3]cumulenes Tetrahedron Letters. 34: 6549-6552. DOI: 10.1016/0040-4039(93)88101-N  0.553
1993 Scheuplein SW, Machinek R, Suffert J, Brückner R. Activation of a dienediyne model of neocarzinostatin chromophore through an acid mediated solvolysis. Evidence for a new cyclization mode of enyne[3]cumulenes Tetrahedron Letters. 34: 6549-6552. DOI: 10.1016/0040-4039(93)88101-N  0.553
1992 Scheuplein SW, Harms K, Brückner R, Suffert J. Regiocontrol in Pd(0)-Mediated Couplings of a Bis(enol triflate) with Alkynes — Stereoselective Syntheses of Monocyclic Dienediynes Related to the Neocarzinostatin Chromophore Chemische Berichte. 125: 271-278. DOI: 10.1002/cber.19921250143  0.586
1991 Brückner R, Huisgen R. Substitutions and dehydrogenations by 2,2-bis(trifluoromethyl)-ethylene-1,1-dicarbonitrile via hydride abstraction Tetrahedron Letters. 32: 1875-1878. DOI: 10.1016/S0040-4039(00)85985-7  0.418
1991 Brückner R, Huisgen R. Substitutions and dehydrogenations by 2,2-bis(trifluoromethyl)-ethylene-1,1-dicarbonitrile via hydride abstraction Tetrahedron Letters. 32: 1875-1878. DOI: 10.1016/S0040-4039(00)85985-7  0.418
1991 Brückner R, Huisgen R. Electrophilic substitutions by 2,2-bis(trifluoromethyl)ethylene-1,1-dicarbonitrile via addition Tetrahedron Letters. 32: 1871-1874. DOI: 10.1016/S0040-4039(00)85984-5  0.442
1991 Suffert J, Brückner R. Palladium catalyzed couplings of enol triflates with alkynes under very mild conditions - the stereoselective synthesis of dienediynes from bis(enoltriflates) Tetrahedron Letters. 32: 1453-1456. DOI: 10.1016/0040-4039(91)80356-B  0.671
1991 Suffert J, Brückner R. Palladium catalyzed couplings of enol triflates with alkynes under very mild conditions - the stereoselective synthesis of dienediynes from bis(enoltriflates) Tetrahedron Letters. 32: 1453-1456. DOI: 10.1016/0040-4039(91)80356-B  0.671
1991 Suffert J, Brückner R. Palladium catalyzed couplings of enol triflates with alkynes under very mild conditions - the stereoselective synthesis of dienediynes from bis(enoltriflates) Tetrahedron Letters. 32: 1453-1456. DOI: 10.1016/0040-4039(91)80356-B  0.671
1991 Suffert J, Brückner R. Palladium catalyzed couplings of enol triflates with alkynes under very mild conditions - the stereoselective synthesis of dienediynes from bis(enoltriflates) Tetrahedron Letters. 32: 1453-1456. DOI: 10.1016/0040-4039(91)80356-B  0.671
1991 Brückner R, Scheuplein SW, Suffert J. Rapid and stereoselective construction of dienediynes related to the neocarzinostatin chromophore Tetrahedron Letters. 32: 1449-1452. DOI: 10.1016/0040-4039(91)80355-A  0.552
1990 Brückner R, Huisgen R. 2,2-bis(trifluoromethyl)ethylene-1,1-dicarbonitrile and styrenes the concertedness of the [2 + 4] cycloaddition Tetrahedron Letters. 31: 7133-7136. DOI: 10.1016/S0040-4039(00)97260-5  0.415
1990 Brückner R, Huisgen R, Schmid J. 2,2-bis(trifluoromethyl)ethylene-1,1-dicarbonitrile and styrenes a dichotomy of cycloaddition pathways Tetrahedron Letters. 31: 7129-7132. DOI: 10.1016/S0040-4039(00)97259-9  0.443
1990 Brückner R, Huisgen R, Schmid J. 2,2-bis(trifluoromethyl)ethylene-1,1-dicarbonitrile and styrenes a dichotomy of cycloaddition pathways Tetrahedron Letters. 31: 7129-7132. DOI: 10.1016/S0040-4039(00)97259-9  0.443
1990 Brückner R, Huisgen R. [2 + 2] cycloadditions of 2,2-bis(trifluoromethyl)ethylene-1,1-dicarbonitrile with vinyl sulfides and ketene S,S-acetals Tetrahedron Letters. 31: 2561-2564. DOI: 10.1016/0040-4039(90)80125-6  0.452
1990 Brückner R, Huisgen R. Kinetics of [2+2] cycloadditions of 2,2-bis(trifluoromethylethylene-1,1-dicarbonitrile with enol ethers, 1,1-dimethylbutadiene, and allyltrimethylsilane Tetrahedron Letters. 31: 2557-2560. DOI: 10.1016/0040-4039(90)80124-5  0.483
1990 Brückner R, Huisgen R. Kinetics of [2+2] cycloadditions of 2,2-bis(trifluoromethylethylene-1,1-dicarbonitrile with enol ethers, 1,1-dimethylbutadiene, and allyltrimethylsilane Tetrahedron Letters. 31: 2557-2560. DOI: 10.1016/0040-4039(90)80124-5  0.483
1990 Scheuplein SW, Kusche A, Brückner R, Harms K. Asymmetric Induction in the [2,3] Witting Rearrangement by Chiral Substituents in the Allyl Moiety: 1,3-Asymmetric Induction Chemische Berichte. 123: 917-925. DOI: 10.1002/cber.19901230443  0.317
1990 Scheuplein SW, Kusche A, Brückner R, Harms K. Asymmetric Induction in the [2,3] Witting Rearrangement by Chiral Substituents in the Allyl Moiety: 1,3-Asymmetric Induction Chemische Berichte. 123: 917-925. DOI: 10.1002/cber.19901230443  0.317
1990 Scheuplein SW, Kusche A, Brückner R, Harms K. Asymmetric Induction in the [2,3] Witting Rearrangement by Chiral Substituents in the Allyl Moiety: 1,3-Asymmetric Induction Chemische Berichte. 123: 917-925. DOI: 10.1002/cber.19901230443  0.317
1990 Scheuplein SW, Kusche A, Brückner R, Harms K. Asymmetric Induction in the [2,3] Witting Rearrangement by Chiral Substituents in the Allyl Moiety: 1,3-Asymmetric Induction Chemische Berichte. 123: 917-925. DOI: 10.1002/cber.19901230443  0.317
1990 Scheuplein SW, Kusche A, Brückner R, Harms K. Asymmetric Induction in the [2,3] Witting Rearrangement by Chiral Substituents in the Allyl Moiety: 1,3-Asymmetric Induction Chemische Berichte. 123: 917-925. DOI: 10.1002/cber.19901230443  0.317
1990 Priepke H, Brückner R, Harms K. Asymmetric Induction in the Wittig-Still Rearrangement of Ethers Containing an Allylic Stereocenter – Diastereocontrol by Allylic Nitrogen Chemische Berichte. 123: 555-563. DOI: 10.1002/cber.19901230323  0.339
1990 Priepke H, Brückner R, Harms K. Asymmetric Induction in the Wittig-Still Rearrangement of Ethers Containing an Allylic Stereocenter – Diastereocontrol by Allylic Nitrogen Chemische Berichte. 123: 555-563. DOI: 10.1002/cber.19901230323  0.339
1990 Priepke H, Brückner R, Harms K. Asymmetric Induction in the Wittig-Still Rearrangement of Ethers Containing an Allylic Stereocenter – Diastereocontrol by Allylic Nitrogen Chemische Berichte. 123: 555-563. DOI: 10.1002/cber.19901230323  0.339
1990 Priepke H, Brückner R, Harms K. Asymmetric Induction in the Wittig-Still Rearrangement of Ethers Containing an Allylic Stereocenter – Diastereocontrol by Allylic Nitrogen Chemische Berichte. 123: 555-563. DOI: 10.1002/cber.19901230323  0.339
1989 Brückner R. Asymmetric Induction and Simple Diastereoselectivity in the [2,3] Wittig Rearrangement of Ester Enolates Chemische Berichte. 122: 703-710. DOI: 10.1002/cber.19891220417  0.373
1989 Brückner R. Asymmetric Induction and Simple Diastereoselectivity in the [2,3] Wittig Rearrangement of Ester Enolates Chemische Berichte. 122: 703-710. DOI: 10.1002/cber.19891220417  0.373
1989 Brückner R. Asymmetric Induction and Simple Diastereoselectivity in the [2,3] Wittig Rearrangement of Ester Enolates Chemische Berichte. 122: 703-710. DOI: 10.1002/cber.19891220417  0.373
1989 Brückner R. Asymmetric Induction and Simple Diastereoselectivity in the [2,3] Wittig Rearrangement of Ester Enolates Chemische Berichte. 122: 703-710. DOI: 10.1002/cber.19891220417  0.373
1989 Brückner R. Asymmetric Induction and Simple Diastereoselectivity in the [2,3] Wittig Rearrangement of Ester Enolates Chemische Berichte. 122: 703-710. DOI: 10.1002/cber.19891220417  0.373
1988 Brückner R, Priepke H. Asymmetric Induction in the [2,3] Wittig Rearrangement by Chiral Substituents in the Allyl Moiety Angewandte Chemie International Edition in English. 27: 278-280. DOI: 10.1002/anie.198802781  0.33
1988 Brückner R, Priepke H. Asymmetric Induction in the [2,3] Wittig Rearrangement by Chiral Substituents in the Allyl Moiety Angewandte Chemie International Edition in English. 27: 278-280. DOI: 10.1002/anie.198802781  0.33
1988 Brückner R, Priepke H. Asymmetric Induction in the [2,3] Wittig Rearrangement by Chiral Substituents in the Allyl Moiety Angewandte Chemie International Edition in English. 27: 278-280. DOI: 10.1002/anie.198802781  0.33
1988 Brückner R, Priepke H. Asymmetric Induction in the [2,3] Wittig Rearrangement by Chiral Substituents in the Allyl Moiety Angewandte Chemie International Edition in English. 27: 278-280. DOI: 10.1002/anie.198802781  0.33
1988 Brückner R, Priepke H. Asymmetric Induction in the [2,3] Wittig Rearrangement by Chiral Substituents in the Allyl Moiety Angewandte Chemie International Edition in English. 27: 278-280. DOI: 10.1002/anie.198802781  0.33
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