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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
Low-probability matches (unlikely to be authored by this person)
2006 Kapferer T, Brückner R. Asymmetric dihydroxylation of β,γ-unsaturated carboxylic esters with trisubstituted C=C bonds - Enantioselective syntheses of trisubstituted γ-butyrolactones European Journal of Organic Chemistry. 2119-2133. DOI: 10.1002/ejoc.200500963  0.295
2011 Burghart J, Sorg A, Brückner R. Stereocomplementary syntheses of 1,ω-distannylated E,Z-isomeric conjugated trienes, tetraenes, and pentaenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 6469-83. PMID 21520302 DOI: 10.1002/chem.201001629  0.294
1991 Scheuplein SW, Brückner R. 1,3-Butadienyltributylphosphonium Bromide as a Conjunctive Reagent for the Synthesis of 1,3-Dienes from Carbonyl Compounds and Gilman Cuprates Chemische Berichte. 124: 1871-1874. DOI: 10.1002/cber.19911240827  0.292
1991 Scheuplein SW, Brückner R. 1,3-Butadienyltributylphosphonium Bromide as a Conjunctive Reagent for the Synthesis of 1,3-Dienes from Carbonyl Compounds and Gilman Cuprates Chemische Berichte. 124: 1871-1874. DOI: 10.1002/cber.19911240827  0.292
1991 Scheuplein SW, Brückner R. 1,3-Butadienyltributylphosphonium Bromide as a Conjunctive Reagent for the Synthesis of 1,3-Dienes from Carbonyl Compounds and Gilman Cuprates Chemische Berichte. 124: 1871-1874. DOI: 10.1002/cber.19911240827  0.292
1991 Scheuplein SW, Brückner R. 1,3-Butadienyltributylphosphonium Bromide as a Conjunctive Reagent for the Synthesis of 1,3-Dienes from Carbonyl Compounds and Gilman Cuprates Chemische Berichte. 124: 1871-1874. DOI: 10.1002/cber.19911240827  0.292
1991 Scheuplein SW, Brückner R. 1,3-Butadienyltributylphosphonium Bromide as a Conjunctive Reagent for the Synthesis of 1,3-Dienes from Carbonyl Compounds and Gilman Cuprates Chemische Berichte. 124: 1871-1874. DOI: 10.1002/cber.19911240827  0.292
1996 Weigand S, Brückner R. TiIV-BINOLate-Catalyzed Highly Enantioselective Additions of β-Substituted Allylstannanes to Aldehydes Chemistry - a European Journal. 2: 1077-1084. DOI: 10.1002/chem.19960020907  0.291
1996 Weigand S, Brückner R. TiIV-BINOLate-Catalyzed Highly Enantioselective Additions of β-Substituted Allylstannanes to Aldehydes Chemistry - a European Journal. 2: 1077-1084. DOI: 10.1002/chem.19960020907  0.291
1996 Weigand S, Brückner R. TiIV-BINOLate-Catalyzed Highly Enantioselective Additions of β-Substituted Allylstannanes to Aldehydes Chemistry - a European Journal. 2: 1077-1084. DOI: 10.1002/chem.19960020907  0.291
1996 Weigand S, Brückner R. TiIV-BINOLate-Catalyzed Highly Enantioselective Additions of β-Substituted Allylstannanes to Aldehydes Chemistry - a European Journal. 2: 1077-1084. DOI: 10.1002/chem.19960020907  0.291
1996 Weigand S, Brückner R. TiIV-BINOLate-Catalyzed Highly Enantioselective Additions of β-Substituted Allylstannanes to Aldehydes Chemistry - a European Journal. 2: 1077-1084. DOI: 10.1002/chem.19960020907  0.291
2011 Petrovi? D, Brückner R. Deslongchamps annulations with benzoquinone monoketals. Organic Letters. 13: 6524-7. PMID 22085275 DOI: 10.1021/ol202809y  0.288
2005 Sorg A, Blank F, Bruckner R. 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. 1286-1290. DOI: 10.1055/s-2005-868506  0.288
2005 Brückner R, Würthner F, Tschierske C, Krüger A, Herges R, Ditrich K, Pfau R, Priepke H, Beifuss U, Bräse S, Marx A, Kirschning A, Sewald N, Senge MO, Müller TJJ, et al. Organic chemistry 2004 | Organische chemie 2004 Nachrichten Aus Der Chemie. 53: 251-272.  0.287
2015 Weber F, Becker F, Keller M, Hillebrecht H, Brückner R. Aldol Additions of Titanium and Boron Enolates of Achiral and Chiral δ-Lactones to Achiral Model Aldehydes: Simple and Induced Diastereoselectivities European Journal of Organic Chemistry. 2015: 7892-7918. DOI: 10.1002/ejoc.201501128  0.287
2005 Vaz B, Alvarez R, Brückner R, de Lera AR. The Stille reaction in the synthesis of carotenoid butenolides: synthesis of 6'-epi-peridinin. Organic Letters. 7: 545-8. PMID 15704890 DOI: 10.1021/ol0478281  0.287
2005 Sorg A, Brückner R. Unexpected cis-selectivity in (Sylvestre) Julia Olefinations with Bu 3Sn-containing allyl benzothiazolyl sulfones: Stereoselective synthesis of 1,3-butadienyl- and 1,3,5-hexatrienylstannanes Synlett. 289-293. DOI: 10.1002/chin.200528050  0.286
2001 Harcken C, Brückner R. A Four-Step Route from Aldehydes to C2-Elongated Enantiomerically Pure α,β-Unsaturated γ-Hydroxy Esters Synlett. 2001: 0718-0721. DOI: 10.1055/s-2001-13372  0.285
2001 Harcken C, Brückner R. A Four-Step Route from Aldehydes to C2-Elongated Enantiomerically Pure α,β-Unsaturated γ-Hydroxy Esters Synlett. 2001: 0718-0721. DOI: 10.1055/s-2001-13372  0.285
2001 Harcken C, Brückner R. A Four-Step Route from Aldehydes to C2-Elongated Enantiomerically Pure α,β-Unsaturated γ-Hydroxy Esters Synlett. 2001: 0718-0721. DOI: 10.1055/s-2001-13372  0.285
2001 Harcken C, Brückner R. A Four-Step Route from Aldehydes to C2-Elongated Enantiomerically Pure α,β-Unsaturated γ-Hydroxy Esters Synlett. 2001: 0718-0721. DOI: 10.1055/s-2001-13372  0.285
2001 Harcken C, Brückner R. A Four-Step Route from Aldehydes to C2-Elongated Enantiomerically Pure α,β-Unsaturated γ-Hydroxy Esters Synlett. 2001: 0718-0721. DOI: 10.1055/s-2001-13372  0.285
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  0.285
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  0.285
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  0.285
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  0.285
1988 Brückner R, Peiseler B. Synthesis and reactions of [(allyloxy)methyl]sulfones - an equivalent for the [2,3]-wittig rearrangement of nonconjugated secondary carbanions Tetrahedron Letters. 29: 5233-5236. DOI: 10.1016/S0040-4039(00)80724-8  0.284
1988 Brückner R, Peiseler B. Synthesis and reactions of [(allyloxy)methyl]sulfones - an equivalent for the [2,3]-wittig rearrangement of nonconjugated secondary carbanions Tetrahedron Letters. 29: 5233-5236. DOI: 10.1016/S0040-4039(00)80724-8  0.284
1988 Brückner R, Peiseler B. Synthesis and reactions of [(allyloxy)methyl]sulfones - an equivalent for the [2,3]-wittig rearrangement of nonconjugated secondary carbanions Tetrahedron Letters. 29: 5233-5236. DOI: 10.1016/S0040-4039(00)80724-8  0.284
1988 Brückner R, Peiseler B. Synthesis and reactions of [(allyloxy)methyl]sulfones - an equivalent for the [2,3]-wittig rearrangement of nonconjugated secondary carbanions Tetrahedron Letters. 29: 5233-5236. DOI: 10.1016/S0040-4039(00)80724-8  0.284
1988 Brückner R, Peiseler B. Synthesis and reactions of [(allyloxy)methyl]sulfones - an equivalent for the [2,3]-wittig rearrangement of nonconjugated secondary carbanions Tetrahedron Letters. 29: 5233-5236. DOI: 10.1016/S0040-4039(00)80724-8  0.284
1994 Brickmann K, Hambloch F, Spolaore E, Brückner R. [2,3]-Thia-Wittig Rearrangements of α-Lithiated Sulfides Via De-aromatized Cyclohexadiene Intermediates Proceed with Inversion of Configuration at the Carbanionic Center Chemische Berichte. 127: 1949-1957. DOI: 10.1002/cber.19941271019  0.282
1994 Brickmann K, Hambloch F, Spolaore E, Brückner R. [2,3]-Thia-Wittig Rearrangements of α-Lithiated Sulfides Via De-aromatized Cyclohexadiene Intermediates Proceed with Inversion of Configuration at the Carbanionic Center Chemische Berichte. 127: 1949-1957. DOI: 10.1002/cber.19941271019  0.282
1994 Brickmann K, Hambloch F, Spolaore E, Brückner R. [2,3]-Thia-Wittig Rearrangements of α-Lithiated Sulfides Via De-aromatized Cyclohexadiene Intermediates Proceed with Inversion of Configuration at the Carbanionic Center Chemische Berichte. 127: 1949-1957. DOI: 10.1002/cber.19941271019  0.282
1994 Brickmann K, Hambloch F, Spolaore E, Brückner R. [2,3]-Thia-Wittig Rearrangements of α-Lithiated Sulfides Via De-aromatized Cyclohexadiene Intermediates Proceed with Inversion of Configuration at the Carbanionic Center Chemische Berichte. 127: 1949-1957. DOI: 10.1002/cber.19941271019  0.282
1994 Brickmann K, Hambloch F, Spolaore E, Brückner R. [2,3]-Thia-Wittig Rearrangements of α-Lithiated Sulfides Via De-aromatized Cyclohexadiene Intermediates Proceed with Inversion of Configuration at the Carbanionic Center Chemische Berichte. 127: 1949-1957. DOI: 10.1002/cber.19941271019  0.282
1997 Weigand S, Brückner R. Building Blocks for the Stereocontrolled Synthesis of 1,3-Diols of Various Configurations Synlett. 1997: 225-228. DOI: 10.1055/s-1997-732  0.282
1997 Weigand S, Brückner R. Building Blocks for the Stereocontrolled Synthesis of 1,3-Diols of Various Configurations Synlett. 1997: 225-228. DOI: 10.1055/s-1997-732  0.282
1997 Weigand S, Brückner R. Building Blocks for the Stereocontrolled Synthesis of 1,3-Diols of Various Configurations Synlett. 1997: 225-228. DOI: 10.1055/s-1997-732  0.282
1997 Weigand S, Brückner R. Building Blocks for the Stereocontrolled Synthesis of 1,3-Diols of Various Configurations Synlett. 1997: 225-228. DOI: 10.1055/s-1997-732  0.282
1997 Weigand S, Brückner R. Building Blocks for the Stereocontrolled Synthesis of 1,3-Diols of Various Configurations Synlett. 1997: 225-228. DOI: 10.1055/s-1997-732  0.282
2017 Engesser T, Brückner R. Synthesis of trans -Configured Enol Ethers by a Sequence of syn -Selective Glycolate Aldol Addition, Hydrolysis, and Grob Fragmentation European Journal of Organic Chemistry. 2017: 5789-5794. DOI: 10.1002/ejoc.201701197  0.282
2017 Engesser T, Brückner R. Synthesis of trans -Configured Enol Ethers by a Sequence of syn -Selective Glycolate Aldol Addition, Hydrolysis, and Grob Fragmentation European Journal of Organic Chemistry. 2017: 5789-5794. DOI: 10.1002/ejoc.201701197  0.282
2017 Engesser T, Brückner R. Synthesis of trans -Configured Enol Ethers by a Sequence of syn -Selective Glycolate Aldol Addition, Hydrolysis, and Grob Fragmentation European Journal of Organic Chemistry. 2017: 5789-5794. DOI: 10.1002/ejoc.201701197  0.282
1998 Görth FC, Umland A, Brückner R. From Sugar Lactones to Stereodefined γ-Alkylidenebutenolides – Synthesis of Analogs of the γ-Alkylidenebutenolide Antibiotics Lissoclinolide and Tetrenolin European Journal of Organic Chemistry. 1998: 1055-1062. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1055::AID-EJOC1055>3.0.CO;2-M  0.279
1998 Görth FC, Umland A, Brückner R. From Sugar Lactones to Stereodefined γ-Alkylidenebutenolides – Synthesis of Analogs of the γ-Alkylidenebutenolide Antibiotics Lissoclinolide and Tetrenolin European Journal of Organic Chemistry. 1998: 1055-1062. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1055::AID-EJOC1055>3.0.CO;2-M  0.279
1998 Görth FC, Umland A, Brückner R. From Sugar Lactones to Stereodefined γ-Alkylidenebutenolides – Synthesis of Analogs of the γ-Alkylidenebutenolide Antibiotics Lissoclinolide and Tetrenolin European Journal of Organic Chemistry. 1998: 1055-1062. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1055::AID-EJOC1055>3.0.CO;2-M  0.279
1998 Görth FC, Umland A, Brückner R. From Sugar Lactones to Stereodefined γ-Alkylidenebutenolides – Synthesis of Analogs of the γ-Alkylidenebutenolide Antibiotics Lissoclinolide and Tetrenolin European Journal of Organic Chemistry. 1998: 1055-1062. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1055::AID-EJOC1055>3.0.CO;2-M  0.279
1998 Görth FC, Umland A, Brückner R. From Sugar Lactones to Stereodefined γ-Alkylidenebutenolides – Synthesis of Analogs of the γ-Alkylidenebutenolide Antibiotics Lissoclinolide and Tetrenolin European Journal of Organic Chemistry. 1998: 1055-1062. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1055::AID-EJOC1055>3.0.CO;2-M  0.279
1993 Menges M, Brückner R. Oxidative Degradation of γ-Butyrolactons into 1,3-Diols via a Criegee Rearrangement of Peroxosulfonates. An Enantioselective Synthesis of Compactin Lactone and its Diastereomer Synlett. 1993: 901-905. DOI: 10.1055/s-1993-22645  0.274
1993 Menges M, Brückner R. Oxidative Degradation of γ-Butyrolactons into 1,3-Diols via a Criegee Rearrangement of Peroxosulfonates. An Enantioselective Synthesis of Compactin Lactone and its Diastereomer Synlett. 1993: 901-905. DOI: 10.1055/s-1993-22645  0.274
1993 Menges M, Brückner R. Oxidative Degradation of γ-Butyrolactons into 1,3-Diols via a Criegee Rearrangement of Peroxosulfonates. An Enantioselective Synthesis of Compactin Lactone and its Diastereomer Synlett. 1993: 901-905. DOI: 10.1055/s-1993-22645  0.274
1993 Menges M, Brückner R. Oxidative Degradation of γ-Butyrolactons into 1,3-Diols via a Criegee Rearrangement of Peroxosulfonates. An Enantioselective Synthesis of Compactin Lactone and its Diastereomer Synlett. 1993: 901-905. DOI: 10.1055/s-1993-22645  0.274
1997 Harcken C, Brückner R. Synthesis of Optically Active Butenolides andγ-Lactones by the Sharpless Asymmetric Dihydroxylation ofβ,γ-Unsaturated Carboxylic Esters Angewandte Chemie International Edition in English. 36: 2750-2752. DOI: 10.1002/anie.199727501  0.274
1997 Harcken C, Brückner R. Synthesis of Optically Active Butenolides andγ-Lactones by the Sharpless Asymmetric Dihydroxylation ofβ,γ-Unsaturated Carboxylic Esters Angewandte Chemie International Edition in English. 36: 2750-2752. DOI: 10.1002/anie.199727501  0.274
1997 Harcken C, Brückner R. Synthesis of Optically Active Butenolides andγ-Lactones by the Sharpless Asymmetric Dihydroxylation ofβ,γ-Unsaturated Carboxylic Esters Angewandte Chemie International Edition in English. 36: 2750-2752. DOI: 10.1002/anie.199727501  0.274
1997 Goeppel D, Brückner R. 1,3-ASYMMETRIC INDUCTION IN RETRO-[1,4]-BROOK REARRANGEMENTS OF LITHIATED ALLYL METHYL ETHERS AND LITHIATED ALLYL MOM ETHERS Tetrahedron Letters. 38: 2937-2938. DOI: 10.1016/S0040-4039(97)00517-0  0.271
1997 Goeppel D, Brückner R. 1,3-ASYMMETRIC INDUCTION IN RETRO-[1,4]-BROOK REARRANGEMENTS OF LITHIATED ALLYL METHYL ETHERS AND LITHIATED ALLYL MOM ETHERS Tetrahedron Letters. 38: 2937-2938. DOI: 10.1016/S0040-4039(97)00517-0  0.271
1997 Goeppel D, Brückner R. 1,3-ASYMMETRIC INDUCTION IN RETRO-[1,4]-BROOK REARRANGEMENTS OF LITHIATED ALLYL METHYL ETHERS AND LITHIATED ALLYL MOM ETHERS Tetrahedron Letters. 38: 2937-2938. DOI: 10.1016/S0040-4039(97)00517-0  0.271
1997 Goeppel D, Brückner R. 1,3-ASYMMETRIC INDUCTION IN RETRO-[1,4]-BROOK REARRANGEMENTS OF LITHIATED ALLYL METHYL ETHERS AND LITHIATED ALLYL MOM ETHERS Tetrahedron Letters. 38: 2937-2938. DOI: 10.1016/S0040-4039(97)00517-0  0.271
1997 Goeppel D, Brückner R. 1,3-ASYMMETRIC INDUCTION IN RETRO-[1,4]-BROOK REARRANGEMENTS OF LITHIATED ALLYL METHYL ETHERS AND LITHIATED ALLYL MOM ETHERS Tetrahedron Letters. 38: 2937-2938. DOI: 10.1016/S0040-4039(97)00517-0  0.271
2009 Hampel T, Brückner R. A novel cis-selective cyclohexanone annulation as the key step of a total synthesis of the sesquiterpene isoacanthodoral. Organic Letters. 11: 4842-5. PMID 19775115 DOI: 10.1021/ol9018979  0.27
1989 Brückner R. Asymmetric Induction in the [2,3] Wittig Rearrangement The Stereoselective Synthesis of Unsaturated Alcohols with Three Contiguous Stereogenic Centers Chemische Berichte. 122: 193-198. DOI: 10.1002/cber.19891220130  0.269
1989 Brückner R. Asymmetric Induction in the [2,3] Wittig Rearrangement The Stereoselective Synthesis of Unsaturated Alcohols with Three Contiguous Stereogenic Centers Chemische Berichte. 122: 193-198. DOI: 10.1002/cber.19891220130  0.269
1989 Brückner R. Asymmetric Induction in the [2,3] Wittig Rearrangement The Stereoselective Synthesis of Unsaturated Alcohols with Three Contiguous Stereogenic Centers Chemische Berichte. 122: 193-198. DOI: 10.1002/cber.19891220130  0.269
1989 Brückner R. Asymmetric Induction in the [2,3] Wittig Rearrangement The Stereoselective Synthesis of Unsaturated Alcohols with Three Contiguous Stereogenic Centers Chemische Berichte. 122: 193-198. DOI: 10.1002/cber.19891220130  0.269
1989 Brückner R. Asymmetric Induction in the [2,3] Wittig Rearrangement The Stereoselective Synthesis of Unsaturated Alcohols with Three Contiguous Stereogenic Centers Chemische Berichte. 122: 193-198. DOI: 10.1002/cber.19891220130  0.269
2018 Loesche A, Brückner R. Dienolates of Cycloalkenones and α,β-Unsaturated Esters Form Diels-Alder Adducts by a Michael/Michael-Tandem Reaction Rather Than in One Step European Journal of Organic Chemistry. 2019: 562-573. DOI: 10.1002/ejoc.201801193  0.268
2018 Loesche A, Brückner R. Dienolates of Cycloalkenones and α,β-Unsaturated Esters Form Diels-Alder Adducts by a Michael/Michael-Tandem Reaction Rather Than in One Step European Journal of Organic Chemistry. 2019: 562-573. DOI: 10.1002/ejoc.201801193  0.268
2018 Loesche A, Brückner R. Dienolates of Cycloalkenones and α,β-Unsaturated Esters Form Diels-Alder Adducts by a Michael/Michael-Tandem Reaction Rather Than in One Step European Journal of Organic Chemistry. 2019: 562-573. DOI: 10.1002/ejoc.201801193  0.268
2018 Loesche A, Brückner R. Dienolates of Cycloalkenones and α,β-Unsaturated Esters Form Diels-Alder Adducts by a Michael/Michael-Tandem Reaction Rather Than in One Step European Journal of Organic Chemistry. 2019: 562-573. DOI: 10.1002/ejoc.201801193  0.268
2018 Loesche A, Brückner R. Dienolates of Cycloalkenones and α,β-Unsaturated Esters Form Diels-Alder Adducts by a Michael/Michael-Tandem Reaction Rather Than in One Step European Journal of Organic Chemistry. 2019: 562-573. DOI: 10.1002/ejoc.201801193  0.268
1998 Menges M, Brückner R. Synthesis of a Butyrolactone Precursor of an Algae Nonaether from an Enantiopure Glycol Obtained by Hoppe's Chemistry European Journal of Organic Chemistry. 1998: 1023-1030. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1023::AID-EJOC1023>3.0.CO;2-3  0.268
1998 Menges M, Brückner R. Synthesis of a Butyrolactone Precursor of an Algae Nonaether from an Enantiopure Glycol Obtained by Hoppe's Chemistry European Journal of Organic Chemistry. 1998: 1023-1030. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1023::AID-EJOC1023>3.0.CO;2-3  0.268
1998 Menges M, Brückner R. Synthesis of a Butyrolactone Precursor of an Algae Nonaether from an Enantiopure Glycol Obtained by Hoppe's Chemistry European Journal of Organic Chemistry. 1998: 1023-1030. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1023::AID-EJOC1023>3.0.CO;2-3  0.268
1994 Menges M, Brückner R. 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. DOI: 10.1055/s-1994-23012  0.263
1994 Menges M, Brückner R. 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. DOI: 10.1055/s-1994-23012  0.263
1994 Menges M, Brückner R. 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. DOI: 10.1055/s-1994-23012  0.263
1994 Menges M, Brückner R. 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. DOI: 10.1055/s-1994-23012  0.263
2004 Berkenbusch T, Brückner R. Stereocontrolled synthesis of the C21-C38 fragment of the unnatural enantiomer of the antibiotic nystatin A1. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 1545-57. PMID 15034898 DOI: 10.1002/chem.200305540  0.262
2018 Hermann D, Brückner R. Silver-Catalyzed tert-Butyl 3-Oxopent-4-ynoate π-Cyclizations: Controlling the Ring Size-Hydroxypyrone or Pulvinone Formation-by Counterion and Additive Optimization. Organic Letters. PMID 30444629 DOI: 10.1021/acs.orglett.8b03214  0.258
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  0.257
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  0.257
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  0.257
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  0.257
2012 Nachbauer L, Brückner R. Converting a birch reduction product into a polyketide: Application to the synthesis of a C1-C11 building block of rimocidin European Journal of Organic Chemistry. 6904-6923. DOI: 10.1002/ejoc.201201112  0.251
1997 Rucker M, Brückner R. Practical Synthesis of the Trisubstituted Naphthalene Carboxylic Acid from Neocarzinostatin Chromophore Synlett. 1997: 1187-1189. DOI: 10.1055/s-1997-983  0.247
1997 Rucker M, Brückner R. Practical Synthesis of the Trisubstituted Naphthalene Carboxylic Acid from Neocarzinostatin Chromophore Synlett. 1997: 1187-1189. DOI: 10.1055/s-1997-983  0.247
1997 Rucker M, Brückner R. Practical Synthesis of the Trisubstituted Naphthalene Carboxylic Acid from Neocarzinostatin Chromophore Synlett. 1997: 1187-1189. DOI: 10.1055/s-1997-983  0.247
1997 Rucker M, Brückner R. Practical Synthesis of the Trisubstituted Naphthalene Carboxylic Acid from Neocarzinostatin Chromophore Synlett. 1997: 1187-1189. DOI: 10.1055/s-1997-983  0.247
1997 Rucker M, Brückner R. Practical Synthesis of the Trisubstituted Naphthalene Carboxylic Acid from Neocarzinostatin Chromophore Synlett. 1997: 1187-1189. DOI: 10.1055/s-1997-983  0.247
1988 Brückner R. Stereocontrolled synthesis of A C14-C20 building block for amphotericin B using a novel [2,3] wittig rearrangement Tetrahedron Letters. 29: 5747-5750. DOI: 10.1016/S0040-4039(00)82180-2  0.247
1988 Brückner R. Stereocontrolled synthesis of A C14-C20 building block for amphotericin B using a novel [2,3] wittig rearrangement Tetrahedron Letters. 29: 5747-5750. DOI: 10.1016/S0040-4039(00)82180-2  0.247
1988 Brückner R. Stereocontrolled synthesis of A C14-C20 building block for amphotericin B using a novel [2,3] wittig rearrangement Tetrahedron Letters. 29: 5747-5750. DOI: 10.1016/S0040-4039(00)82180-2  0.247
1988 Brückner R. Stereocontrolled synthesis of A C14-C20 building block for amphotericin B using a novel [2,3] wittig rearrangement Tetrahedron Letters. 29: 5747-5750. DOI: 10.1016/S0040-4039(00)82180-2  0.247
1988 Brückner R. Stereocontrolled synthesis of A C14-C20 building block for amphotericin B using a novel [2,3] wittig rearrangement Tetrahedron Letters. 29: 5747-5750. DOI: 10.1016/S0040-4039(00)82180-2  0.247
1992 Hoffmann R, Brückner R. Asymmetric induction in reductively initiated [2,3]-Wittig and retro [1,4]-brook rearrangements of secondary carbanions Chemische Berichte. 125: 1471-1484. DOI: 10.1002/cber.19921250625  0.243
1992 Hoffmann R, Brückner R. Asymmetric induction in reductively initiated [2,3]-Wittig and retro [1,4]-brook rearrangements of secondary carbanions Chemische Berichte. 125: 1471-1484. DOI: 10.1002/cber.19921250625  0.243
1992 Hoffmann R, Brückner R. Asymmetric induction in reductively initiated [2,3]-Wittig and retro [1,4]-brook rearrangements of secondary carbanions Chemische Berichte. 125: 1471-1484. DOI: 10.1002/cber.19921250625  0.243
1992 Hoffmann R, Brückner R. Asymmetric induction in reductively initiated [2,3]-Wittig and retro [1,4]-brook rearrangements of secondary carbanions Chemische Berichte. 125: 1471-1484. DOI: 10.1002/cber.19921250625  0.243
1992 Hoffmann R, Brückner R. Asymmetric induction in reductively initiated [2,3]-Wittig and retro [1,4]-brook rearrangements of secondary carbanions Chemische Berichte. 125: 1471-1484. DOI: 10.1002/cber.19921250625  0.243
1997 Ferri F, Brückner R. Synthesis of an Epoxide- and Carbonate-Containing 6-/10-Membered Bicyclodienediyne Analogue of the Neocarzinostaitin Chromophore Liebigs Annalen. 1997: 961-965. DOI: 10.1002/jlac.199719970527  0.242
1997 Ferri F, Brückner R. Synthesis of an Epoxide- and Carbonate-Containing 6-/10-Membered Bicyclodienediyne Analogue of the Neocarzinostaitin Chromophore Liebigs Annalen. 1997: 961-965. DOI: 10.1002/jlac.199719970527  0.242
1997 Ferri F, Brückner R. Synthesis of an Epoxide- and Carbonate-Containing 6-/10-Membered Bicyclodienediyne Analogue of the Neocarzinostaitin Chromophore Liebigs Annalen. 1997: 961-965. DOI: 10.1002/jlac.199719970527  0.242
1997 Ferri F, Brückner R. Synthesis of an Epoxide- and Carbonate-Containing 6-/10-Membered Bicyclodienediyne Analogue of the Neocarzinostaitin Chromophore Liebigs Annalen. 1997: 961-965. DOI: 10.1002/jlac.199719970527  0.242
2015 Ruppenthal S, Brückner R. Symmetric diarylsulfoxides as asymmetric sulfinylating reagents for dialkylmagnesium compounds. The Journal of Organic Chemistry. 80: 897-910. PMID 25553340 DOI: 10.1021/jo502417j  0.242
2004 Sorg A, Brückner R. Total synthesis of xerulinic acid. Angewandte Chemie (International Ed. in English). 43: 4523-6. PMID 15340960 DOI: 10.1002/anie.200453729  0.24
1998 Muñoz-Torrero D, Brückner R. Synthesis of a Key Building Block for a Butyrolactone → 1,3-Diol Approach to the Polyol Part of Roflamycoin European Journal of Organic Chemistry. 1998: 1031-1043. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1031::AID-EJOC1031>3.0.CO;2-D  0.24
1998 Muñoz-Torrero D, Brückner R. Synthesis of a Key Building Block for a Butyrolactone → 1,3-Diol Approach to the Polyol Part of Roflamycoin European Journal of Organic Chemistry. 1998: 1031-1043. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1031::AID-EJOC1031>3.0.CO;2-D  0.24
1998 Muñoz-Torrero D, Brückner R. Synthesis of a Key Building Block for a Butyrolactone → 1,3-Diol Approach to the Polyol Part of Roflamycoin European Journal of Organic Chemistry. 1998: 1031-1043. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1031::AID-EJOC1031>3.0.CO;2-D  0.24
1998 Muñoz-Torrero D, Brückner R. Synthesis of a Key Building Block for a Butyrolactone → 1,3-Diol Approach to the Polyol Part of Roflamycoin European Journal of Organic Chemistry. 1998: 1031-1043. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1031::AID-EJOC1031>3.0.CO;2-D  0.24
1998 Muñoz-Torrero D, Brückner R. Synthesis of a Key Building Block for a Butyrolactone → 1,3-Diol Approach to the Polyol Part of Roflamycoin European Journal of Organic Chemistry. 1998: 1031-1043. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1031::AID-EJOC1031>3.0.CO;2-D  0.24
2012 Stock C, Brückner R. Mild and high-yielding molybdenum(VI) dichloride dioxide-catalyzed formation of Mono-, Di-, Tri-, and tetracarbamates from alcohols and aromatic or aliphatic isocyanates Advanced Synthesis and Catalysis. 354: 2309-2330. DOI: 10.1002/adsc.201200303  0.239
1992 Hoffmann R, Brückner R. Retro [1,4]-Brook Rearrangements of Nonconjugated Secondary α-Lithio Ethers: Proof of Stereospecificity and of Retention of Configuration at the Carbanion Center Chemische Berichte. 125: 2731-2739. DOI: 10.1002/cber.19921251219  0.237
1992 Hoffmann R, Brückner R. Retro [1,4]-Brook Rearrangements of Nonconjugated Secondary α-Lithio Ethers: Proof of Stereospecificity and of Retention of Configuration at the Carbanion Center Chemische Berichte. 125: 2731-2739. DOI: 10.1002/cber.19921251219  0.237
1992 Hoffmann R, Brückner R. Retro [1,4]-Brook Rearrangements of Nonconjugated Secondary α-Lithio Ethers: Proof of Stereospecificity and of Retention of Configuration at the Carbanion Center Chemische Berichte. 125: 2731-2739. DOI: 10.1002/cber.19921251219  0.237
2007 Tricotet T, Brückner R. Enantio- and diastereomerically pure decalins by deslongchamps-type annulation of dienolates containing a chiral lactone substituent European Journal of Organic Chemistry. 1069-1074. DOI: 10.1002/ejoc.200601047  0.236
1995 Behrens K, Kneisel BO, Noltemeyer M, Brückner R. Preparation of α‐chiral crotylsilanes by retro‐[1,4]‐brook rearrangements. A stereochemical study Liebigs Annalen. 1995: 385-400. DOI: 10.1002/jlac.199519950247  0.236
2017 Neumeyer M, Brückner R. Establishing Consensus Stereostructures for the Naphthoquinonopyrano-γ-lactone Natural Products (-)-Arizonin B1 and (-)-Arizonin C1 by Total Syntheses. Diastereocontrol of Oxa-Pictet-Spengler Cyclizations by Protective-Group Optimization European Journal of Organic Chemistry. 2017: 2512-2539. DOI: 10.1002/ejoc.201700013  0.236
2017 Neumeyer M, Brückner R. Establishing Consensus Stereostructures for the Naphthoquinonopyrano-γ-lactone Natural Products (-)-Arizonin B1 and (-)-Arizonin C1 by Total Syntheses. Diastereocontrol of Oxa-Pictet-Spengler Cyclizations by Protective-Group Optimization European Journal of Organic Chemistry. 2017: 2512-2539. DOI: 10.1002/ejoc.201700013  0.236
2017 Brückner R, Peter D. A New Approach to Models of the 4,5-Dihydroxycyclopentenone Core of the Kodaistatins A-D. Elucidation of the Diol Configuration in Kodaistatin A. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28421637 DOI: 10.1002/chem.201701185  0.236
2021 Drescher C, Brückner R. Stereostructure Clarifying Total Synthesis of the (Polyenoyl)tetramic Acid Militarinone B. A Highly Acid-Labile -Protecting Group for Amides†. Organic Letters. PMID 34324347 DOI: 10.1021/acs.orglett.1c01652  0.232
1989 Kruse B, Brückner R. Reductive lithiation of sulfides and sulfones — A novel entry into [2,3] wittig rearrangements Chemische Berichte. 122: 2023-2025. DOI: 10.1002/cber.19891221033  0.23
1989 Kruse B, Brückner R. Reductive lithiation of sulfides and sulfones — A novel entry into [2,3] wittig rearrangements Chemische Berichte. 122: 2023-2025. DOI: 10.1002/cber.19891221033  0.23
1989 Kruse B, Brückner R. Reductive lithiation of sulfides and sulfones — A novel entry into [2,3] wittig rearrangements Chemische Berichte. 122: 2023-2025. DOI: 10.1002/cber.19891221033  0.23
1989 Kruse B, Brückner R. Reductive lithiation of sulfides and sulfones — A novel entry into [2,3] wittig rearrangements Chemische Berichte. 122: 2023-2025. DOI: 10.1002/cber.19891221033  0.23
1989 Kruse B, Brückner R. Reductive lithiation of sulfides and sulfones — A novel entry into [2,3] wittig rearrangements Chemische Berichte. 122: 2023-2025. DOI: 10.1002/cber.19891221033  0.23
2016 Diehl J, Brückner R. Synthesis of Enantiomerically Pure β-Hydroxy Ketones via β-Keto Weinreb Amides by a Condensation/Asymmetric-Hydrogenation/Acylation Sequence European Journal of Organic Chemistry. 2017: 278-286. DOI: 10.1002/ejoc.201601202  0.228
2016 Diehl J, Brückner R. Synthesis of Enantiomerically Pure β-Hydroxy Ketones via β-Keto Weinreb Amides by a Condensation/Asymmetric-Hydrogenation/Acylation Sequence European Journal of Organic Chemistry. 2017: 278-286. DOI: 10.1002/ejoc.201601202  0.228
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  0.228
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  0.228
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  0.228
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  0.228
2001 Harcken C, Brückner R. Stereopure 1,3-butadiene-2-carboxylates and their conversion into non-racemic α-alkylidenebutyrolactone natural products by asymmetric dihydroxylation Tetrahedron Letters. 42: 3967-3971. DOI: 10.1016/S0040-4039(01)00598-6  0.227
2001 Harcken C, Brückner R. Stereopure 1,3-butadiene-2-carboxylates and their conversion into non-racemic α-alkylidenebutyrolactone natural products by asymmetric dihydroxylation Tetrahedron Letters. 42: 3967-3971. DOI: 10.1016/S0040-4039(01)00598-6  0.227
2001 Harcken C, Brückner R. Stereopure 1,3-butadiene-2-carboxylates and their conversion into non-racemic α-alkylidenebutyrolactone natural products by asymmetric dihydroxylation Tetrahedron Letters. 42: 3967-3971. DOI: 10.1016/S0040-4039(01)00598-6  0.227
2001 Harcken C, Brückner R. Stereopure 1,3-butadiene-2-carboxylates and their conversion into non-racemic α-alkylidenebutyrolactone natural products by asymmetric dihydroxylation Tetrahedron Letters. 42: 3967-3971. DOI: 10.1016/S0040-4039(01)00598-6  0.227
2001 Harcken C, Brückner R. Stereopure 1,3-butadiene-2-carboxylates and their conversion into non-racemic α-alkylidenebutyrolactone natural products by asymmetric dihydroxylation Tetrahedron Letters. 42: 3967-3971. DOI: 10.1016/S0040-4039(01)00598-6  0.227
2016 Neumeyer M, Brückner R. Nonracemic γ-Lactones from the Sharpless Asymmetric Dihydroxylation of β,γ-Unsaturated Carboxylic Esters European Journal of Organic Chemistry. 2016: 5060-5087. DOI: 10.1002/ejoc.201600520  0.226
2016 Neumeyer M, Brückner R. Nonracemic γ-Lactones from the Sharpless Asymmetric Dihydroxylation of β,γ-Unsaturated Carboxylic Esters European Journal of Organic Chemistry. 2016: 5060-5087. DOI: 10.1002/ejoc.201600520  0.226
2016 Neumeyer M, Brückner R. Nonracemic γ-Lactones from the Sharpless Asymmetric Dihydroxylation of β,γ-Unsaturated Carboxylic Esters European Journal of Organic Chemistry. 2016: 5060-5087. DOI: 10.1002/ejoc.201600520  0.226
2016 Neumeyer M, Brückner R. Nonracemic γ-Lactones from the Sharpless Asymmetric Dihydroxylation of β,γ-Unsaturated Carboxylic Esters European Journal of Organic Chemistry. 2016: 5060-5087. DOI: 10.1002/ejoc.201600520  0.226
2016 Neumeyer M, Brückner R. Nonracemic γ-Lactones from the Sharpless Asymmetric Dihydroxylation of β,γ-Unsaturated Carboxylic Esters European Journal of Organic Chemistry. 2016: 5060-5087. DOI: 10.1002/ejoc.201600520  0.226
1994 Goeppel D, Münster I, Brückner R. The geometry of the carbanionic moiety influences the non-induced diastereoselectivity of the [2,3]-Wittig rearrangement of lithiated diallyl ethers Tetrahedron. 50: 3687-3708. DOI: 10.1016/S0040-4020(01)90391-6  0.224
1994 Goeppel D, Münster I, Brückner R. The geometry of the carbanionic moiety influences the non-induced diastereoselectivity of the [2,3]-Wittig rearrangement of lithiated diallyl ethers Tetrahedron. 50: 3687-3708. DOI: 10.1016/S0040-4020(01)90391-6  0.224
1994 Goeppel D, Münster I, Brückner R. The geometry of the carbanionic moiety influences the non-induced diastereoselectivity of the [2,3]-Wittig rearrangement of lithiated diallyl ethers Tetrahedron. 50: 3687-3708. DOI: 10.1016/S0040-4020(01)90391-6  0.224
1994 Goeppel D, Münster I, Brückner R. The geometry of the carbanionic moiety influences the non-induced diastereoselectivity of the [2,3]-Wittig rearrangement of lithiated diallyl ethers Tetrahedron. 50: 3687-3708. DOI: 10.1016/S0040-4020(01)90391-6  0.224
1994 Goeppel D, Münster I, Brückner R. The geometry of the carbanionic moiety influences the non-induced diastereoselectivity of the [2,3]-Wittig rearrangement of lithiated diallyl ethers Tetrahedron. 50: 3687-3708. DOI: 10.1016/S0040-4020(01)90391-6  0.224
2013 Weber F, Brückner R. Conformational analysis of δ-lactones by DFT calculations: the parent compound and its monomethyl and selected dimethyl derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 1288-302. PMID 23296596 DOI: 10.1002/chem.201202988  0.223
2013 Nachbauer L, Brückner R. Synthesis of a Cn-Cn+6 building block common to important polyol,polyene antibiotics from a divinylcarbinol by a desymmetrizing sharpless epoxidation European Journal of Organic Chemistry. 6545-6562. DOI: 10.1002/ejoc.201300181  0.22
2006 Schmidt-Leithoff J, Brückner R. Regioselective cis,vic-dihydroxylation of α,β,γ,δ- unsaturated carboxylic esters: Enhanced γ,δ-selectivity by employing trifluoroethyl or hexafluoroisopropyl esters Synlett. 2641-2645. DOI: 10.1055/s-2006-951473  0.218
2009 Bruckner RC, Jorns MS. Spectral and kinetic characterization of intermediates in the aromatization reaction catalyzed by NikD, an unusual amino acid oxidase. Biochemistry. 48: 4455-65. PMID 19354202 DOI: 10.1021/bi900179j  0.218
2013 Kramer R, Brückner R. Stereocontrolled synthesis of a Cn-Cn+6 building block for the unnatural enantiomers of important polyol,polyene antibiotics from an epoxy alcohol by a reduction/conjugate addition/hydroxylation sequence European Journal of Organic Chemistry. 6563-6583. DOI: 10.1002/ejoc.201300182  0.217
2009 Sälinger D, Brückner R. The first asymmetric halogen/metal-exchange reaction: desymmetrization of alcohols with enantiotopic bromoarene substituents. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 6688-703. PMID 19492368 DOI: 10.1002/chem.200802488  0.216
2010 Zörb A, Brückner R. Conversion of conjugated enones into enantiomerically pure β-hydroxy ketones or 1,3-diols - Samarium(II) bromide reductions of protected α,β-dihydroxy ketones European Journal of Organic Chemistry. 4785-4801. DOI: 10.1002/ejoc.201000279  0.215
1997 Weigand S, Brückner R. Total Synthesis of theTolypothrix Pentaether from Enantiomerically Pure Homoallyl Alcohols by A Butyrolactone → 1,3-Diol Strategy Liebigs Annalen. 1997: 1657-1666. DOI: 10.1002/jlac.199719970806  0.215
1997 Weigand S, Brückner R. Total Synthesis of theTolypothrix Pentaether from Enantiomerically Pure Homoallyl Alcohols by A Butyrolactone → 1,3-Diol Strategy Liebigs Annalen. 1997: 1657-1666. DOI: 10.1002/jlac.199719970806  0.215
1997 Weigand S, Brückner R. Total Synthesis of theTolypothrix Pentaether from Enantiomerically Pure Homoallyl Alcohols by A Butyrolactone → 1,3-Diol Strategy Liebigs Annalen. 1997: 1657-1666. DOI: 10.1002/jlac.199719970806  0.215
1997 Weigand S, Brückner R. Total Synthesis of theTolypothrix Pentaether from Enantiomerically Pure Homoallyl Alcohols by A Butyrolactone → 1,3-Diol Strategy Liebigs Annalen. 1997: 1657-1666. DOI: 10.1002/jlac.199719970806  0.215
1997 Weigand S, Brückner R. Total Synthesis of theTolypothrix Pentaether from Enantiomerically Pure Homoallyl Alcohols by A Butyrolactone → 1,3-Diol Strategy Liebigs Annalen. 1997: 1657-1666. DOI: 10.1002/jlac.199719970806  0.215
2015 Weber F, Brückner R. Asymmetric dihydroxylation of esters and amides of methacrylic, tiglic, and angelic acid: No exception to the sharpless mnemonic! European Journal of Organic Chemistry. 2015: 2428-2449. DOI: 10.1002/ejoc.201403622  0.21
2009 Sälinger D, Brückner R. High-yielding large-scale syntheses of enantiomerically pure NOBIN and a NOBIN-based enantiomerically pure NHC precursor Synlett. 109-111. DOI: 10.1055/s-0028-1087390  0.209
1991 Kusche A, Hoffmann R, Münster I, Keiner P, Brückner R. A direct synthesis of O,S-acetals from aldehydes Tetrahedron Letters. 32: 467-470. DOI: 10.1016/S0040-4039(00)79470-6  0.209
1991 Kusche A, Hoffmann R, Münster I, Keiner P, Brückner R. A direct synthesis of O,S-acetals from aldehydes Tetrahedron Letters. 32: 467-470. DOI: 10.1016/S0040-4039(00)79470-6  0.209
1991 Kusche A, Hoffmann R, Münster I, Keiner P, Brückner R. A direct synthesis of O,S-acetals from aldehydes Tetrahedron Letters. 32: 467-470. DOI: 10.1016/S0040-4039(00)79470-6  0.209
1991 Kusche A, Hoffmann R, Münster I, Keiner P, Brückner R. A direct synthesis of O,S-acetals from aldehydes Tetrahedron Letters. 32: 467-470. DOI: 10.1016/S0040-4039(00)79470-6  0.209
2004 Sorg A, Siegel K, Brückner R. A Novel Access to γ-Alkylidenebutenolides: Sequential Stille Couplings of Dibromomethylenebutenolides Synlett. 321-325.  0.208
2000 Görth F, Rucker M, Eckhardt M, Brückner R. Decagram-Scale Synthesis of the Neocarzinostatin Carboxylic Acid European Journal of Organic Chemistry. 2000: 2605-2611. DOI: 10.1002/1099-0690(200007)2000:14<2605::AID-EJOC2605>3.0.CO;2-Y  0.207
2000 Görth F, Rucker M, Eckhardt M, Brückner R. Decagram-Scale Synthesis of the Neocarzinostatin Carboxylic Acid European Journal of Organic Chemistry. 2000: 2605-2611. DOI: 10.1002/1099-0690(200007)2000:14<2605::AID-EJOC2605>3.0.CO;2-Y  0.207
2002 Zhang CS, Stratmann A, Block O, Brückner R, Podeschwa M, Altenbach HJ, Wehmeier UF, Piepersberg W. Biosynthesis of the C(7)-cyclitol moiety of acarbose in Actinoplanes species SE50/110. 7-O-phosphorylation of the initial cyclitol precursor leads to proposal of a new biosynthetic pathway. The Journal of Biological Chemistry. 277: 22853-62. PMID 11937512 DOI: 10.1074/Jbc.M202375200  0.206
1990 Bruckner R. [2, 3]-Wittig-Umlagerung Nachrichten Aus Chemie, Technik Und Laboratorium. 38: 1506-1510. DOI: 10.1002/nadc.19900381207  0.206
1990 Bruckner R. [2, 3]-Wittig-Umlagerung Nachrichten Aus Chemie, Technik Und Laboratorium. 38: 1506-1510. DOI: 10.1002/nadc.19900381207  0.206
1990 Bruckner R. [2, 3]-Wittig-Umlagerung Nachrichten Aus Chemie, Technik Und Laboratorium. 38: 1506-1510. DOI: 10.1002/nadc.19900381207  0.206
1990 Bruckner R. [2, 3]-Wittig-Umlagerung Nachrichten Aus Chemie, Technik Und Laboratorium. 38: 1506-1510. DOI: 10.1002/nadc.19900381207  0.206
1990 Bruckner R. [2, 3]-Wittig-Umlagerung Nachrichten Aus Chemie, Technik Und Laboratorium. 38: 1506-1510. DOI: 10.1002/nadc.19900381207  0.206
1996 Eckhardt M, Brückner R. The First Model of the Neocarzinostatin Chromophore with an Epoxide Ring and a Carbonate Moiety Angewandte Chemie International Edition in English. 35: 1093-1096. DOI: 10.1002/anie.199610931  0.206
1996 Eckhardt M, Brückner R. The First Model of the Neocarzinostatin Chromophore with an Epoxide Ring and a Carbonate Moiety Angewandte Chemie International Edition in English. 35: 1093-1096. DOI: 10.1002/anie.199610931  0.206
1996 Eckhardt M, Brückner R. The First Model of the Neocarzinostatin Chromophore with an Epoxide Ring and a Carbonate Moiety Angewandte Chemie International Edition in English. 35: 1093-1096. DOI: 10.1002/anie.199610931  0.206
1996 Eckhardt M, Brückner R. The First Model of the Neocarzinostatin Chromophore with an Epoxide Ring and a Carbonate Moiety Angewandte Chemie International Edition in English. 35: 1093-1096. DOI: 10.1002/anie.199610931  0.206
1996 Eckhardt M, Brückner R. The First Model of the Neocarzinostatin Chromophore with an Epoxide Ring and a Carbonate Moiety Angewandte Chemie International Edition in English. 35: 1093-1096. DOI: 10.1002/anie.199610931  0.206
2009 Kommoju PR, Bruckner RC, Ferreira P, Carrell CJ, Mathews FS, Jorns MS. Factors that affect oxygen activation and coupling of the two redox cycles in the aromatization reaction catalyzed by NikD, an unusual amino acid oxidase. Biochemistry. 48: 9542-55. PMID 19702312 DOI: 10.1021/bi901056a  0.205
2014 Hofferberth ML, Brückner R. α- and β-Lipomycin: total syntheses by sequential stille couplings and assignment of the absolute configuration of all stereogenic centers. Angewandte Chemie (International Ed. in English). 53: 7328-34. PMID 24895187 DOI: 10.1002/anie.201402255  0.201
2014 Weber F, Brückner R. 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. Organic Letters. 16: 6428-31. PMID 25483968 DOI: 10.1021/ol5032602  0.2
1998 Berkenbusch T, Brückner R. Synthesis of (+)-ginnol, a type Rlong-CH(OH)-R′long alcohol, by an asymmetric β,γ-unsaturated ester → γ-butyrolactone conversion Tetrahedron. 54: 11471-11480. DOI: 10.1016/S0040-4020(98)00688-7  0.2
1998 Berkenbusch T, Brückner R. Synthesis of (+)-ginnol, a type Rlong-CH(OH)-R′long alcohol, by an asymmetric β,γ-unsaturated ester → γ-butyrolactone conversion Tetrahedron. 54: 11471-11480. DOI: 10.1016/S0040-4020(98)00688-7  0.2
1998 Berkenbusch T, Brückner R. Synthesis of (+)-ginnol, a type Rlong-CH(OH)-R′long alcohol, by an asymmetric β,γ-unsaturated ester → γ-butyrolactone conversion Tetrahedron. 54: 11471-11480. DOI: 10.1016/S0040-4020(98)00688-7  0.2
1998 Berkenbusch T, Brückner R. Synthesis of (+)-ginnol, a type Rlong-CH(OH)-R′long alcohol, by an asymmetric β,γ-unsaturated ester → γ-butyrolactone conversion Tetrahedron. 54: 11471-11480. DOI: 10.1016/S0040-4020(98)00688-7  0.2
1998 Berkenbusch T, Brückner R. Synthesis of (+)-ginnol, a type Rlong-CH(OH)-R′long alcohol, by an asymmetric β,γ-unsaturated ester → γ-butyrolactone conversion Tetrahedron. 54: 11471-11480. DOI: 10.1016/S0040-4020(98)00688-7  0.2
2004 Olpp T, Brückner R. Stereoselective preparation of (E)-α-bromoacrylates from mixtures of brominated ando phosphonates Synthesis. 2135-2152. DOI: 10.1055/s-2004-831166  0.198
2000 Gebauer O, Brückner R. β-Alkoxycarbonyl Enol Triflates as Precursors of Stereopure 3-Ene-1,5-diyne Building Blocks for the Chromophores of Neocarzinostatin, C-1027, Kedarcidin, Maduropeptin, and N1999A2 Synthesis. 2000: 588-602. DOI: 10.1055/s-2000-6366  0.189
2000 Gebauer O, Brückner R. β-Alkoxycarbonyl Enol Triflates as Precursors of Stereopure 3-Ene-1,5-diyne Building Blocks for the Chromophores of Neocarzinostatin, C-1027, Kedarcidin, Maduropeptin, and N1999A2 Synthesis. 2000: 588-602. DOI: 10.1055/s-2000-6366  0.189
2000 Gebauer O, Brückner R. β-Alkoxycarbonyl Enol Triflates as Precursors of Stereopure 3-Ene-1,5-diyne Building Blocks for the Chromophores of Neocarzinostatin, C-1027, Kedarcidin, Maduropeptin, and N1999A2 Synthesis. 2000: 588-602. DOI: 10.1055/s-2000-6366  0.189
2000 Gebauer O, Brückner R. β-Alkoxycarbonyl Enol Triflates as Precursors of Stereopure 3-Ene-1,5-diyne Building Blocks for the Chromophores of Neocarzinostatin, C-1027, Kedarcidin, Maduropeptin, and N1999A2 Synthesis. 2000: 588-602. DOI: 10.1055/s-2000-6366  0.189
2000 Gebauer O, Brückner R. β-Alkoxycarbonyl Enol Triflates as Precursors of Stereopure 3-Ene-1,5-diyne Building Blocks for the Chromophores of Neocarzinostatin, C-1027, Kedarcidin, Maduropeptin, and N1999A2 Synthesis. 2000: 588-602. DOI: 10.1055/s-2000-6366  0.189
2017 Kreibich M, Petrović D, Brückner R. Mechanistic Studies of the Deslongchamps Annulation. The Journal of Organic Chemistry. PMID 29131961 DOI: 10.1021/acs.joc.7b02341  0.187
2017 Kreibich M, Petrović D, Brückner R. Mechanistic Studies of the Deslongchamps Annulation. The Journal of Organic Chemistry. PMID 29131961 DOI: 10.1021/acs.joc.7b02341  0.187
2017 Kreibich M, Petrović D, Brückner R. Mechanistic Studies of the Deslongchamps Annulation. The Journal of Organic Chemistry. PMID 29131961 DOI: 10.1021/acs.joc.7b02341  0.187
2017 Kreibich M, Petrović D, Brückner R. Mechanistic Studies of the Deslongchamps Annulation. The Journal of Organic Chemistry. PMID 29131961 DOI: 10.1021/acs.joc.7b02341  0.187
2006 Kramer R, Brückner R. Desymmetrizing asymmetric epoxidations of bis(cis-configured) divinylcarbinols: Unusual syn-selectivity combined with ee-enhancement through kinetic resolution Synlett. 33-38. DOI: 10.1055/s-2005-922778  0.187
1998 von der Ohe F, Brückner R. Z- or E-configurated γ-alkylidenebutenolides from a 2-(trimethylsiloxy)furan and iodomethacrolein - stereoselective synthesis of Z- and E-freelingyne Tetrahedron Letters. 39: 1909-1910. DOI: 10.1016/S0040-4039(98)00240-8  0.187
1998 von der Ohe F, Brückner R. Z- or E-configurated γ-alkylidenebutenolides from a 2-(trimethylsiloxy)furan and iodomethacrolein - stereoselective synthesis of Z- and E-freelingyne Tetrahedron Letters. 39: 1909-1910. DOI: 10.1016/S0040-4039(98)00240-8  0.187
1998 von der Ohe F, Brückner R. Z- or E-configurated γ-alkylidenebutenolides from a 2-(trimethylsiloxy)furan and iodomethacrolein - stereoselective synthesis of Z- and E-freelingyne Tetrahedron Letters. 39: 1909-1910. DOI: 10.1016/S0040-4039(98)00240-8  0.187
1998 von der Ohe F, Brückner R. Z- or E-configurated γ-alkylidenebutenolides from a 2-(trimethylsiloxy)furan and iodomethacrolein - stereoselective synthesis of Z- and E-freelingyne Tetrahedron Letters. 39: 1909-1910. DOI: 10.1016/S0040-4039(98)00240-8  0.187
1998 von der Ohe F, Brückner R. Z- or E-configurated γ-alkylidenebutenolides from a 2-(trimethylsiloxy)furan and iodomethacrolein - stereoselective synthesis of Z- and E-freelingyne Tetrahedron Letters. 39: 1909-1910. DOI: 10.1016/S0040-4039(98)00240-8  0.187
2008 Knobloch E, Brückner R. Selective cleavage and decarboxylation of β-keto esters derived from (trimethylsilyl)ethanol in the presence of β-keto esters derived from other alcohols Synlett. 1865-1869. DOI: 10.1055/s-2008-1078568  0.186
1994 Keiner P, Brückner R. The [2,3]-Wittig rearrangements of lithioalkyl allyl ethers exhibit different cis,trans-selectivities than [2,3] shifts in their lithiomethyl analogues Tetrahedron. 50: 13417-13424. DOI: 10.1016/S0040-4020(01)89348-0  0.183
1994 Keiner P, Brückner R. The [2,3]-Wittig rearrangements of lithioalkyl allyl ethers exhibit different cis,trans-selectivities than [2,3] shifts in their lithiomethyl analogues Tetrahedron. 50: 13417-13424. DOI: 10.1016/S0040-4020(01)89348-0  0.183
1994 Keiner P, Brückner R. The [2,3]-Wittig rearrangements of lithioalkyl allyl ethers exhibit different cis,trans-selectivities than [2,3] shifts in their lithiomethyl analogues Tetrahedron. 50: 13417-13424. DOI: 10.1016/S0040-4020(01)89348-0  0.183
1994 Keiner P, Brückner R. The [2,3]-Wittig rearrangements of lithioalkyl allyl ethers exhibit different cis,trans-selectivities than [2,3] shifts in their lithiomethyl analogues Tetrahedron. 50: 13417-13424. DOI: 10.1016/S0040-4020(01)89348-0  0.183
1994 Keiner P, Brückner R. The [2,3]-Wittig rearrangements of lithioalkyl allyl ethers exhibit different cis,trans-selectivities than [2,3] shifts in their lithiomethyl analogues Tetrahedron. 50: 13417-13424. DOI: 10.1016/S0040-4020(01)89348-0  0.183
2014 Diehl J, Brückner R. Unexpected rearrangements of rhodium carbenoids containing a pyrrolidin-1-yl group Tetrahedron Letters. 55: 2629-2632. DOI: 10.1016/j.tetlet.2014.02.132  0.177
1996 Gebauer O, Brückner R. A Practical Synthesis of Enantiopure (R)-4-Hydroxy-2-cyclohexen-1-one Liebigs Annalen. 1996: 1559-1563. DOI: 10.1002/jlac.199619961010  0.177
1996 Gebauer O, Brückner R. A Practical Synthesis of Enantiopure (R)-4-Hydroxy-2-cyclohexen-1-one Liebigs Annalen. 1996: 1559-1563. DOI: 10.1002/jlac.199619961010  0.177
1996 Gebauer O, Brückner R. A Practical Synthesis of Enantiopure (R)-4-Hydroxy-2-cyclohexen-1-one Liebigs Annalen. 1996: 1559-1563. DOI: 10.1002/jlac.199619961010  0.177
1996 Gebauer O, Brückner R. A Practical Synthesis of Enantiopure (R)-4-Hydroxy-2-cyclohexen-1-one Liebigs Annalen. 1996: 1559-1563. DOI: 10.1002/jlac.199619961010  0.177
1996 Gebauer O, Brückner R. A Practical Synthesis of Enantiopure (R)-4-Hydroxy-2-cyclohexen-1-one Liebigs Annalen. 1996: 1559-1563. DOI: 10.1002/jlac.199619961010  0.177
1988 Brückner R, Priepke H. Asymmetrische Induktion bei der [2,3]-Wittig-Umlagerung durch chirale Substituenten im Allylteil Angewandte Chemie. 100: 285-286. DOI: 10.1002/ange.19881000219  0.176
1988 Brückner R, Priepke H. Asymmetrische Induktion bei der [2,3]-Wittig-Umlagerung durch chirale Substituenten im Allylteil Angewandte Chemie. 100: 285-286. DOI: 10.1002/ange.19881000219  0.176
1988 Brückner R, Priepke H. Asymmetrische Induktion bei der [2,3]-Wittig-Umlagerung durch chirale Substituenten im Allylteil Angewandte Chemie. 100: 285-286. DOI: 10.1002/ange.19881000219  0.176
1988 Brückner R, Priepke H. Asymmetrische Induktion bei der [2,3]-Wittig-Umlagerung durch chirale Substituenten im Allylteil Angewandte Chemie. 100: 285-286. DOI: 10.1002/ange.19881000219  0.176
1988 Brückner R, Priepke H. Asymmetrische Induktion bei der [2,3]-Wittig-Umlagerung durch chirale Substituenten im Allylteil Angewandte Chemie. 100: 285-286. DOI: 10.1002/ange.19881000219  0.176
1997 Harcken C, Brückner R. Synthese optisch aktiver Butenolide und γ-Lactone aus β,γ-ungesättigten Carbonsäureestern mit der asymmetrischen Dihydroxylierung nach Sharpless Angewandte Chemie. 109: 2866-2868. DOI: 10.1002/ange.19971092410  0.172
1997 Harcken C, Brückner R. Synthese optisch aktiver Butenolide und γ-Lactone aus β,γ-ungesättigten Carbonsäureestern mit der asymmetrischen Dihydroxylierung nach Sharpless Angewandte Chemie. 109: 2866-2868. DOI: 10.1002/ange.19971092410  0.172
1997 Harcken C, Brückner R. Synthese optisch aktiver Butenolide und γ-Lactone aus β,γ-ungesättigten Carbonsäureestern mit der asymmetrischen Dihydroxylierung nach Sharpless Angewandte Chemie. 109: 2866-2868. DOI: 10.1002/ange.19971092410  0.172
1997 Harcken C, Brückner R. Synthese optisch aktiver Butenolide und γ-Lactone aus β,γ-ungesättigten Carbonsäureestern mit der asymmetrischen Dihydroxylierung nach Sharpless Angewandte Chemie. 109: 2866-2868. DOI: 10.1002/ange.19971092410  0.172
1997 Harcken C, Brückner R. Synthese optisch aktiver Butenolide und γ-Lactone aus β,γ-ungesättigten Carbonsäureestern mit der asymmetrischen Dihydroxylierung nach Sharpless Angewandte Chemie. 109: 2866-2868. DOI: 10.1002/ange.19971092410  0.172
2009 Kommoju PR, Bruckner RC, Ferreira P, Jorns MS. Probing the role of active site residues in NikD, an unusual amino acid oxidase that catalyzes an aromatization reaction important in nikkomycin biosynthesis. Biochemistry. 48: 6951-62. PMID 19530706 DOI: 10.1021/bi9006918  0.169
2014 Hampel T, Bruns M, Bayer M, Handgretinger R, Bruchelt G, Brückner R. Synthesis and biological effects of new hybrid compounds composed of benzylguanidines and the alkylating group of busulfan on neuroblastoma cells. Bioorganic & Medicinal Chemistry Letters. 24: 2728-33. PMID 24814532 DOI: 10.1016/j.bmcl.2014.04.030  0.169
2005 Kapferer T, Brückner R, Herzig A, König WA. Enantioselective syntheses and configuration assignments of gamma-chiral butenolides from Plagiomnium undulatum: butenolide synthesis from tetronic acids. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 2154-62. PMID 15714528 DOI: 10.1002/chem.200401135  0.168
1998 Schön U, Antel J, Brückner R, Messinger J, Franke R, Gruska A. Synthesis, pharmacological characterization, and quantitative structure-activity relationship analyses of 3,7,9,9-tetraalkylbispidines: derivatives with specific bradycardic activity. Journal of Medicinal Chemistry. 41: 318-31. PMID 9464363 DOI: 10.1021/jm970120q  0.167
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  0.167
1998 Gibson C, Buck T, Walker M, Brückner R. Approaching the C33-C38 Fragments of Amphotericin B and Nystatin by a Retro-[1,4]-Brook Rearrangement and the Stereoselective Manipulation of the Resulting Allylsilane Synlett. 1998: 201-205. DOI: 10.1055/s-1998-1599  0.166
1998 Siegel K, Brückner R. First Total Synthesis of Dihydroxerulin, a Potent Inhibitor of the Biosynthesis of Cholesterol Chemistry - a European Journal. 4: 1116-1122. DOI: 10.1002/(SICI)1521-3765(19980615)4:6<1116::AID-CHEM1116>3.0.CO;2-5  0.164
1998 Siegel K, Brückner R. First Total Synthesis of Dihydroxerulin, a Potent Inhibitor of the Biosynthesis of Cholesterol Chemistry - a European Journal. 4: 1116-1122. DOI: 10.1002/(SICI)1521-3765(19980615)4:6<1116::AID-CHEM1116>3.0.CO;2-5  0.164
2012 Hampel T, Ruppenthal S, Sälinger D, Brückner R. Desymmetrization of prochiral diaryl sulfoxides by an asymmetric sulfoxide-magnesium exchange. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 3136-40. PMID 22354614 DOI: 10.1002/chem.201103928  0.164
2010 Haug-Schifferdecker E, Arican D, Brückner R, Heide L. A new group of aromatic prenyltransferases in fungi, catalyzing a 2,7-dihydroxynaphthalene 3-dimethylallyl-transferase reaction. The Journal of Biological Chemistry. 285: 16487-94. PMID 20351110 DOI: 10.1074/jbc.M110.113720  0.164
1999 Siegel K, Brückner R. First Synthesis of Xerulin, an Inhibitor of the Biosynthesis of Cholesterol Synlett. 1999: 1227-1230. DOI: 10.1055/s-1999-3162  0.162
1999 Siegel K, Brückner R. First Synthesis of Xerulin, an Inhibitor of the Biosynthesis of Cholesterol Synlett. 1999: 1227-1230. DOI: 10.1055/s-1999-3162  0.162
1999 Siegel K, Brückner R. First Synthesis of Xerulin, an Inhibitor of the Biosynthesis of Cholesterol Synlett. 1999: 1227-1230. DOI: 10.1055/s-1999-3162  0.162
1999 Siegel K, Brückner R. First Synthesis of Xerulin, an Inhibitor of the Biosynthesis of Cholesterol Synlett. 1999: 1227-1230. DOI: 10.1055/s-1999-3162  0.162
1999 Siegel K, Brückner R. First Synthesis of Xerulin, an Inhibitor of the Biosynthesis of Cholesterol Synlett. 1999: 1227-1230. DOI: 10.1055/s-1999-3162  0.162
2013 Wüster T, Kaczybura N, Brückner R, Keller M. 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. 69: 7785-7809. DOI: 10.1016/j.tet.2013.05.091  0.162
2008 Knobloch E, Brückner R. β-Keto esters derived from 2-(trimethylsilyl)ethanol: An orthogonal protective group for β-keto esters Synthesis. 2229-2246. DOI: 10.1055/s-2008-1067157  0.161
2000 Bringmann G, Feineis D, Brückner R, Blank M, Peters K, Peters EM, Reichmann H, Janetzky B, Grote C, Clement HW, Wesemann W. Bromal-derived tetrahydro-beta-carbolines as neurotoxic agents: chemistry, impairment of the dopamine metabolism, and inhibitory effects on mitochondrial respiration. Bioorganic & Medicinal Chemistry. 8: 1467-78. PMID 10896123 DOI: 10.1016/S0968-0896(00)00073-0  0.16
2008 Kramer R, Berkenbusch T, Brückner R. Stereocomplementary desymmetrizations of divinylcarbinols by zirconium(IV)- vs. titanium(IV)-mediated asymmetric epoxidations Advanced Synthesis and Catalysis. 350: 1131-1148. DOI: 10.1002/adsc.200700608  0.159
2019 Brückner R, Baumann T. Atropselective Dibrominations of a 1,1'-Disubstituted 2,2'-Biindolyl With Diverging Point-to-Axial Asymmetric Inductions. Deriving Diphosphane Ligands for Asymmetric Catalysis. Angewandte Chemie (International Ed. in English). PMID 30648782 DOI: 10.1002/anie.201806294  0.157
2006 Olpp T, Brückner R. Total synthesis of the light-harvesting carotenoid peridinin. Angewandte Chemie (International Ed. in English). 45: 4023-7. PMID 16683293 DOI: 10.1002/anie.200600502  0.157
2007 Dormann KL, Brückner R. Variable synthesis of the optically active thiotetronic acid antibiotics thiolactomycin, thiotetromycin, and 834-B1. Angewandte Chemie (International Ed. in English). 46: 1160-3. PMID 17183501 DOI: 10.1002/anie.200603562  0.156
1997 Sammtleben F, Noltemeyer M, Brückner R. 1,3-Asymmetric induction in retro-[1,4]-brook rearrangements of propargyllithium compounds to propargylsilanes Tetrahedron Letters. 38: 3893-3896. DOI: 10.1016/S0040-4039(97)00762-4  0.156
1997 Sammtleben F, Noltemeyer M, Brückner R. 1,3-Asymmetric induction in retro-[1,4]-brook rearrangements of propargyllithium compounds to propargylsilanes Tetrahedron Letters. 38: 3893-3896. DOI: 10.1016/S0040-4039(97)00762-4  0.156
1997 Sammtleben F, Noltemeyer M, Brückner R. 1,3-Asymmetric induction in retro-[1,4]-brook rearrangements of propargyllithium compounds to propargylsilanes Tetrahedron Letters. 38: 3893-3896. DOI: 10.1016/S0040-4039(97)00762-4  0.156
1997 Sammtleben F, Noltemeyer M, Brückner R. 1,3-Asymmetric induction in retro-[1,4]-brook rearrangements of propargyllithium compounds to propargylsilanes Tetrahedron Letters. 38: 3893-3896. DOI: 10.1016/S0040-4039(97)00762-4  0.156
1993 Brickmann K, Brückner R. [2,3]1-Thia-Wittig Rearrangements Proceeding with Complete Inversion or with Partial Loss of Configuration at the Carbanionic Center Chemische Berichte. 126: 1227-1239. DOI: 10.1002/cber.19931260524  0.153
1993 Brickmann K, Brückner R. [2,3]1-Thia-Wittig Rearrangements Proceeding with Complete Inversion or with Partial Loss of Configuration at the Carbanionic Center Chemische Berichte. 126: 1227-1239. DOI: 10.1002/cber.19931260524  0.153
1993 Brickmann K, Brückner R. [2,3]1-Thia-Wittig Rearrangements Proceeding with Complete Inversion or with Partial Loss of Configuration at the Carbanionic Center Chemische Berichte. 126: 1227-1239. DOI: 10.1002/cber.19931260524  0.153
1993 Brickmann K, Brückner R. [2,3]1-Thia-Wittig Rearrangements Proceeding with Complete Inversion or with Partial Loss of Configuration at the Carbanionic Center Chemische Berichte. 126: 1227-1239. DOI: 10.1002/cber.19931260524  0.153
1993 Brickmann K, Brückner R. [2,3]1-Thia-Wittig Rearrangements Proceeding with Complete Inversion or with Partial Loss of Configuration at the Carbanionic Center Chemische Berichte. 126: 1227-1239. DOI: 10.1002/cber.19931260524  0.153
1992 Hoffmann R, Brückner R. [2,3]-Wittig-Umlagerungen von nichtkonjugierten sekundären α-Lithioethern: Nachweis von Stereospezifität und Umkehr der Konfiguration am Carbanion-C-Atom Angewandte Chemie. 104: 646-648. DOI: 10.1002/ange.19921040533  0.151
1992 Hoffmann R, Brückner R. [2,3]-Wittig-Umlagerungen von nichtkonjugierten sekundären α-Lithioethern: Nachweis von Stereospezifität und Umkehr der Konfiguration am Carbanion-C-Atom Angewandte Chemie. 104: 646-648. DOI: 10.1002/ange.19921040533  0.151
1992 Hoffmann R, Brückner R. [2,3]-Wittig-Umlagerungen von nichtkonjugierten sekundären α-Lithioethern: Nachweis von Stereospezifität und Umkehr der Konfiguration am Carbanion-C-Atom Angewandte Chemie. 104: 646-648. DOI: 10.1002/ange.19921040533  0.151
1992 Hoffmann R, Brückner R. [2,3]-Wittig-Umlagerungen von nichtkonjugierten sekundären α-Lithioethern: Nachweis von Stereospezifität und Umkehr der Konfiguration am Carbanion-C-Atom Angewandte Chemie. 104: 646-648. DOI: 10.1002/ange.19921040533  0.151
1992 Hoffmann R, Brückner R. [2,3]-Wittig-Umlagerungen von nichtkonjugierten sekundären α-Lithioethern: Nachweis von Stereospezifität und Umkehr der Konfiguration am Carbanion-C-Atom Angewandte Chemie. 104: 646-648. DOI: 10.1002/ange.19921040533  0.151
1992 Hoffmann R, Brückner R. [2,3] Wittig Rearrangements of Nonconjugated Secondaryα-Lithioethers: Proof of Stereospecificity and Inversion of the Configuration of the Carbanion C Atom Angewandte Chemie International Edition in English. 31: 647-649. DOI: 10.1002/anie.199206471  0.147
1992 Hoffmann R, Brückner R. [2,3] Wittig Rearrangements of Nonconjugated Secondaryα-Lithioethers: Proof of Stereospecificity and Inversion of the Configuration of the Carbanion C Atom Angewandte Chemie International Edition in English. 31: 647-649. DOI: 10.1002/anie.199206471  0.147
1992 Hoffmann R, Brückner R. [2,3] Wittig Rearrangements of Nonconjugated Secondaryα-Lithioethers: Proof of Stereospecificity and Inversion of the Configuration of the Carbanion C Atom Angewandte Chemie International Edition in English. 31: 647-649. DOI: 10.1002/anie.199206471  0.147
1992 Hoffmann R, Brückner R. [2,3] Wittig Rearrangements of Nonconjugated Secondaryα-Lithioethers: Proof of Stereospecificity and Inversion of the Configuration of the Carbanion C Atom Angewandte Chemie International Edition in English. 31: 647-649. DOI: 10.1002/anie.199206471  0.147
1992 Hoffmann R, Brückner R. [2,3] Wittig Rearrangements of Nonconjugated Secondaryα-Lithioethers: Proof of Stereospecificity and Inversion of the Configuration of the Carbanion C Atom Angewandte Chemie International Edition in English. 31: 647-649. DOI: 10.1002/anie.199206471  0.147
2011 Burghart-Stoll H, Kapferer T, Brückner R. Asymmetric dihydroxylations of enynes with a trisubstituted C═C bond. An unprecedented route to γ-lactone building blocks with a quaternary stereocenter. Organic Letters. 13: 1016-9. PMID 21271731 DOI: 10.1021/ol103061g  0.142
2006 Bringmann G, Feineis D, Brückner R, God R, Grote C, Wesemann W. Synthesis of radiolabelled 1-trichloromethyl-1,2,3,4-tetrahydro-beta-carboline (TaClo), a neurotoxic chloral-derived mammalian alkaloid, and its biodistribution in rats. European Journal of Pharmaceutical Sciences : Official Journal of the European Federation For Pharmaceutical Sciences. 28: 412-22. PMID 16713202 DOI: 10.1016/J.Ejps.2006.03.009  0.141
2005 Olpp T, Brückner R. Eine neue Strategie für die Synthese des Butenolid-Teils von Peridinin Angewandte Chemie. 117: 1577-1581. DOI: 10.1002/ange.200460259  0.134
2005 Olpp T, Brückner R. Eine neue Strategie für die Synthese des Butenolid-Teils von Peridinin Angewandte Chemie. 117: 1577-1581. DOI: 10.1002/ange.200460259  0.134
2005 Olpp T, Brückner R. Eine neue Strategie für die Synthese des Butenolid-Teils von Peridinin Angewandte Chemie. 117: 1577-1581. DOI: 10.1002/ange.200460259  0.134
2018 Peter D, Brückner R. Syntheses of a Pair of Simplified Model Compounds of the Dihydroxycyclopentenone Core of the Kodaistatins A-D European Journal of Organic Chemistry. 2018: 6256-6273. DOI: 10.1002/ejoc.201801117  0.133
2018 Peter D, Brückner R. Syntheses of a Pair of Simplified Model Compounds of the Dihydroxycyclopentenone Core of the Kodaistatins A-D European Journal of Organic Chemistry. 2018: 6256-6273. DOI: 10.1002/ejoc.201801117  0.133
2018 Peter D, Brückner R. Syntheses of a Pair of Simplified Model Compounds of the Dihydroxycyclopentenone Core of the Kodaistatins A-D European Journal of Organic Chemistry. 2018: 6256-6273. DOI: 10.1002/ejoc.201801117  0.133
2018 Peter D, Brückner R. Syntheses of a Pair of Simplified Model Compounds of the Dihydroxycyclopentenone Core of the Kodaistatins A-D European Journal of Organic Chemistry. 2018: 6256-6273. DOI: 10.1002/ejoc.201801117  0.133
2018 Peter D, Brückner R. Syntheses of a Pair of Simplified Model Compounds of the Dihydroxycyclopentenone Core of the Kodaistatins A-D European Journal of Organic Chemistry. 2018: 6256-6273. DOI: 10.1002/ejoc.201801117  0.133
2012 Denapaite D, Brückner R, Hakenbeck R, Vollmer W. Biosynthesis of teichoic acids in Streptococcus pneumoniae and closely related species: lessons from genomes. Microbial Drug Resistance (Larchmont, N.Y.). 18: 344-58. PMID 22432701 DOI: 10.1089/mdr.2012.0026  0.132
2018 Ruppenthal S, Brückner R. Prochiral Diheteroaryl Sulfoxides and Their Reactions with (S)-Li2-BINOLate-Activated Diisobutylmagnesium European Journal of Organic Chemistry. 2018: 89-98. DOI: 10.1002/ejoc.201701309  0.13
2018 Ruppenthal S, Brückner R. Prochiral Diheteroaryl Sulfoxides and Their Reactions with (S)-Li2-BINOLate-Activated Diisobutylmagnesium European Journal of Organic Chemistry. 2018: 89-98. DOI: 10.1002/ejoc.201701309  0.13
2018 Ruppenthal S, Brückner R. Prochiral Diheteroaryl Sulfoxides and Their Reactions with (S)-Li2-BINOLate-Activated Diisobutylmagnesium European Journal of Organic Chemistry. 2018: 89-98. DOI: 10.1002/ejoc.201701309  0.13
2018 Ruppenthal S, Brückner R. Prochiral Diheteroaryl Sulfoxides and Their Reactions with (S)-Li2-BINOLate-Activated Diisobutylmagnesium European Journal of Organic Chemistry. 2018: 89-98. DOI: 10.1002/ejoc.201701309  0.13
2018 Ruppenthal S, Brückner R. Prochiral Diheteroaryl Sulfoxides and Their Reactions with (S)-Li2-BINOLate-Activated Diisobutylmagnesium European Journal of Organic Chemistry. 2018: 89-98. DOI: 10.1002/ejoc.201701309  0.13
2011 Burghart-Stoll H, Böhnke O, Brückner R. Asymmetric dihydroxylations of 1-substituted (E)- and (Z)-3-methylpent-2-en-4-ynes: full compliance with the Sharpless mnemonic re-established and embellished. Organic Letters. 13: 1020-3. PMID 21271732 DOI: 10.1021/ol103063t  0.129
1992 von der Emde H, Brückner R. [2,3]-Thia-Wittig rearrangements with A marked starting material dependence of stereoselectivity Tetrahedron Letters. 33: 7323-7326. DOI: 10.1016/S0040-4039(00)60177-6  0.127
1992 von der Emde H, Brückner R. [2,3]-Thia-Wittig rearrangements with A marked starting material dependence of stereoselectivity Tetrahedron Letters. 33: 7323-7326. DOI: 10.1016/S0040-4039(00)60177-6  0.127
1992 von der Emde H, Brückner R. [2,3]-Thia-Wittig rearrangements with A marked starting material dependence of stereoselectivity Tetrahedron Letters. 33: 7323-7326. DOI: 10.1016/S0040-4039(00)60177-6  0.127
1992 von der Emde H, Brückner R. [2,3]-Thia-Wittig rearrangements with A marked starting material dependence of stereoselectivity Tetrahedron Letters. 33: 7323-7326. DOI: 10.1016/S0040-4039(00)60177-6  0.127
1992 von der Emde H, Brückner R. [2,3]-Thia-Wittig rearrangements with A marked starting material dependence of stereoselectivity Tetrahedron Letters. 33: 7323-7326. DOI: 10.1016/S0040-4039(00)60177-6  0.127
2018 Ruppenthal S, Brückner R. Asymmetric Sulfinylations of N -Methylephedrine-Modified Tri- or Tetraalkyl Zincates by Symmetric Diaryl Sulfoxides European Journal of Organic Chemistry. 2018: 2518-2530. DOI: 10.1002/ejoc.201701603  0.124
2018 Ruppenthal S, Brückner R. Asymmetric Sulfinylations of N -Methylephedrine-Modified Tri- or Tetraalkyl Zincates by Symmetric Diaryl Sulfoxides European Journal of Organic Chemistry. 2018: 2518-2530. DOI: 10.1002/ejoc.201701603  0.124
2018 Ruppenthal S, Brückner R. Asymmetric Sulfinylations of N -Methylephedrine-Modified Tri- or Tetraalkyl Zincates by Symmetric Diaryl Sulfoxides European Journal of Organic Chemistry. 2018: 2518-2530. DOI: 10.1002/ejoc.201701603  0.124
2018 Ruppenthal S, Brückner R. Asymmetric Sulfinylations of N -Methylephedrine-Modified Tri- or Tetraalkyl Zincates by Symmetric Diaryl Sulfoxides European Journal of Organic Chemistry. 2018: 2518-2530. DOI: 10.1002/ejoc.201701603  0.124
2018 Ruppenthal S, Brückner R. Asymmetric Sulfinylations of N -Methylephedrine-Modified Tri- or Tetraalkyl Zincates by Symmetric Diaryl Sulfoxides European Journal of Organic Chemistry. 2018: 2518-2530. DOI: 10.1002/ejoc.201701603  0.124
2017 Neumeyer M, Brückner R. Die erste stereoselektive Totalsynthese eines dimeren γ-Lacton- anellierten Pyranonaphthochinons: (+)-γ-Actinorhodin Angewandte Chemie. 129: 3432-3437. DOI: 10.1002/ange.201611183  0.124
2006 Tricotet T, Brückner R. [4+2]-Annulations leading to configurationally homogeneous bicyclo[4.4.0]decanediones with five new stereocenters Tetrahedron Letters. 47: 8499-8502. DOI: 10.1016/j.tetlet.2006.09.144  0.122
2002 Riederer P, Foley P, Bringmann G, Feineis D, Brückner R, Gerlach M. Biochemical and pharmacological characterization of 1-trichloromethyl-1,2,3,4-tetrahydro-beta-carboline: a biologically relevant neurotoxin? European Journal of Pharmacology. 442: 1-16. PMID 12020676 DOI: 10.1016/S0014-2999(02)01308-0  0.121
2007 Carrell CJ, Bruckner RC, Venci D, Zhao G, Jorns MS, Mathews FS. NikD, an unusual amino acid oxidase essential for nikkomycin biosynthesis: structures of closed and open forms at 1.15 and 1.90 A resolution. Structure (London, England : 1993). 15: 928-41. PMID 17697998 DOI: 10.1016/j.str.2007.06.010  0.119
2011 Burghart-Stoll H, Brückner R. A serendipitous synthesis of (+)-gregatin B, second structure revisions of the aspertetronins, gregatins, and graminin A, structure revision of the penicilliols. Organic Letters. 13: 2730-3. PMID 21526752 DOI: 10.1021/ol2008318  0.119
1998 Harcken C, Brückner R, Rank E. Total Syntheses of (−)-Grandinolide and (−)-Sapranthin by the Sharpless Asymmetric Dihydroxylation of Methyltrans-3-Pentenoate: Elucidation of the Stereostructure of (−)-Sapranthin Chemistry - a European Journal. 4: 2342-2352. DOI: 10.1002/(SICI)1521-3765(19981102)4:11<2342::AID-CHEM2342>3.0.CO;2-Q  0.117
1998 Harcken C, Brückner R, Rank E. Total Syntheses of (−)-Grandinolide and (−)-Sapranthin by the Sharpless Asymmetric Dihydroxylation of Methyltrans-3-Pentenoate: Elucidation of the Stereostructure of (−)-Sapranthin Chemistry - a European Journal. 4: 2342-2352. DOI: 10.1002/(SICI)1521-3765(19981102)4:11<2342::AID-CHEM2342>3.0.CO;2-Q  0.117
1998 Harcken C, Brückner R, Rank E. Total Syntheses of (−)-Grandinolide and (−)-Sapranthin by the Sharpless Asymmetric Dihydroxylation of Methyltrans-3-Pentenoate: Elucidation of the Stereostructure of (−)-Sapranthin Chemistry - a European Journal. 4: 2342-2352. DOI: 10.1002/(SICI)1521-3765(19981102)4:11<2342::AID-CHEM2342>3.0.CO;2-Q  0.117
1998 Harcken C, Brückner R, Rank E. Total Syntheses of (−)-Grandinolide and (−)-Sapranthin by the Sharpless Asymmetric Dihydroxylation of Methyltrans-3-Pentenoate: Elucidation of the Stereostructure of (−)-Sapranthin Chemistry - a European Journal. 4: 2342-2352. DOI: 10.1002/(SICI)1521-3765(19981102)4:11<2342::AID-CHEM2342>3.0.CO;2-Q  0.117
1998 Harcken C, Brückner R, Rank E. Total Syntheses of (−)-Grandinolide and (−)-Sapranthin by the Sharpless Asymmetric Dihydroxylation of Methyltrans-3-Pentenoate: Elucidation of the Stereostructure of (−)-Sapranthin Chemistry - a European Journal. 4: 2342-2352. DOI: 10.1002/(SICI)1521-3765(19981102)4:11<2342::AID-CHEM2342>3.0.CO;2-Q  0.117
1997 Gibson C, Buck T, Noltemeyer M, Brückner* R. METAL DEPENDENT 1,3-ASYMMETRIC INDUCTION IN THE RETRO-[1,4]-BROOK REARRANGEMENT OF A SILYLATED TIGLYL ALKALIMETAL COMPOUND Tetrahedron Letters. 38: 2933-2936. DOI: 10.1016/S0040-4039(97)00516-9  0.116
1997 Gibson C, Buck T, Noltemeyer M, Brückner* R. METAL DEPENDENT 1,3-ASYMMETRIC INDUCTION IN THE RETRO-[1,4]-BROOK REARRANGEMENT OF A SILYLATED TIGLYL ALKALIMETAL COMPOUND Tetrahedron Letters. 38: 2933-2936. DOI: 10.1016/S0040-4039(97)00516-9  0.116
1997 Gibson C, Buck T, Noltemeyer M, Brückner* R. METAL DEPENDENT 1,3-ASYMMETRIC INDUCTION IN THE RETRO-[1,4]-BROOK REARRANGEMENT OF A SILYLATED TIGLYL ALKALIMETAL COMPOUND Tetrahedron Letters. 38: 2933-2936. DOI: 10.1016/S0040-4039(97)00516-9  0.116
1997 Gibson C, Buck T, Noltemeyer M, Brückner* R. METAL DEPENDENT 1,3-ASYMMETRIC INDUCTION IN THE RETRO-[1,4]-BROOK REARRANGEMENT OF A SILYLATED TIGLYL ALKALIMETAL COMPOUND Tetrahedron Letters. 38: 2933-2936. DOI: 10.1016/S0040-4039(97)00516-9  0.116
1997 Gibson C, Buck T, Noltemeyer M, Brückner* R. METAL DEPENDENT 1,3-ASYMMETRIC INDUCTION IN THE RETRO-[1,4]-BROOK REARRANGEMENT OF A SILYLATED TIGLYL ALKALIMETAL COMPOUND Tetrahedron Letters. 38: 2933-2936. DOI: 10.1016/S0040-4039(97)00516-9  0.116
2010 Stock C, Brückner R. Exceptionally active catalysts for the formation of carbamates from alcohols and isocyanates: Molybdenum(VI) dichloride dioxide and its DMF complex Synlett. 2429-2434. DOI: 10.1055/s-0030-1258552  0.116
1992 Hoffmann R, Brückner R. Ein neuartiger Einstieg in Wittig-Umlagerungen – Eine stereoselektive [1,2]-Wittig-Umlagerung mit Konfigurationsumkehr am Carbanion-Zentrum Chemische Berichte. 125: 1957-1963. DOI: 10.1002/cber.19921250824  0.109
1992 Hoffmann R, Brückner R. Ein neuartiger Einstieg in Wittig-Umlagerungen – Eine stereoselektive [1,2]-Wittig-Umlagerung mit Konfigurationsumkehr am Carbanion-Zentrum Chemische Berichte. 125: 1957-1963. DOI: 10.1002/cber.19921250824  0.109
1992 Hoffmann R, Brückner R. Ein neuartiger Einstieg in Wittig-Umlagerungen – Eine stereoselektive [1,2]-Wittig-Umlagerung mit Konfigurationsumkehr am Carbanion-Zentrum Chemische Berichte. 125: 1957-1963. DOI: 10.1002/cber.19921250824  0.109
1992 Hoffmann R, Brückner R. Ein neuartiger Einstieg in Wittig-Umlagerungen – Eine stereoselektive [1,2]-Wittig-Umlagerung mit Konfigurationsumkehr am Carbanion-Zentrum Chemische Berichte. 125: 1957-1963. DOI: 10.1002/cber.19921250824  0.109
1992 Hoffmann R, Brückner R. Ein neuartiger Einstieg in Wittig-Umlagerungen – Eine stereoselektive [1,2]-Wittig-Umlagerung mit Konfigurationsumkehr am Carbanion-Zentrum Chemische Berichte. 125: 1957-1963. DOI: 10.1002/cber.19921250824  0.109
2003 Pruitt JR, Pinto DJ, Galemmo RA, Alexander RS, Rossi KA, Wells BL, Drummond S, Bostrom LL, Burdick D, Bruckner R, Chen H, Smallwood A, Wong PC, Wright MR, Bai S, et al. Discovery of 1-(2-aminomethylphenyl)-3-trifluoromethyl-N- [3-fluoro-2'-(aminosulfonyl)[1,1'-biphenyl)]-4-yl]-1H-pyrazole-5-carboxyamide (DPC602), a potent, selective, and orally bioavailable factor Xa inhibitor(1). Journal of Medicinal Chemistry. 46: 5298-315. PMID 14640539 DOI: 10.1021/jm030212h  0.107
1996 Eckhardt M, Brückner R. Erste Modellverbindung des Neocarzinostatin-Chromophors mit Epoxid-und Carbonatring Angewandte Chemie. 108: 1185-1188. DOI: 10.1002/ange.19961081016  0.106
1996 Eckhardt M, Brückner R. Erste Modellverbindung des Neocarzinostatin-Chromophors mit Epoxid-und Carbonatring Angewandte Chemie. 108: 1185-1188. DOI: 10.1002/ange.19961081016  0.106
1996 Eckhardt M, Brückner R. Erste Modellverbindung des Neocarzinostatin-Chromophors mit Epoxid-und Carbonatring Angewandte Chemie. 108: 1185-1188. DOI: 10.1002/ange.19961081016  0.106
1996 Eckhardt M, Brückner R. Erste Modellverbindung des Neocarzinostatin-Chromophors mit Epoxid-und Carbonatring Angewandte Chemie. 108: 1185-1188. DOI: 10.1002/ange.19961081016  0.106
1996 Eckhardt M, Brückner R. Erste Modellverbindung des Neocarzinostatin-Chromophors mit Epoxid-und Carbonatring Angewandte Chemie. 108: 1185-1188. DOI: 10.1002/ange.19961081016  0.106
2008 Zhao G, Bruckner RC, Jorns MS. Identification of the oxygen activation site in monomeric sarcosine oxidase: role of Lys265 in catalysis. Biochemistry. 47: 9124-35. PMID 18693755 DOI: 10.1021/bi8008642  0.105
1998 Rank E, Brückner R. A McMurry Route to the Dienediyne Portion of Models of the Neocarzinostatin Chromophore European Journal of Organic Chemistry. 1998: 1045-1053. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1045::AID-EJOC1045>3.0.CO;2-O  0.104
1998 Rank E, Brückner R. A McMurry Route to the Dienediyne Portion of Models of the Neocarzinostatin Chromophore European Journal of Organic Chemistry. 1998: 1045-1053. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1045::AID-EJOC1045>3.0.CO;2-O  0.104
1998 Rank E, Brückner R. A McMurry Route to the Dienediyne Portion of Models of the Neocarzinostatin Chromophore European Journal of Organic Chemistry. 1998: 1045-1053. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1045::AID-EJOC1045>3.0.CO;2-O  0.104
1998 Rank E, Brückner R. A McMurry Route to the Dienediyne Portion of Models of the Neocarzinostatin Chromophore European Journal of Organic Chemistry. 1998: 1045-1053. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1045::AID-EJOC1045>3.0.CO;2-O  0.104
1998 Rank E, Brückner R. A McMurry Route to the Dienediyne Portion of Models of the Neocarzinostatin Chromophore European Journal of Organic Chemistry. 1998: 1045-1053. DOI: 10.1002/(SICI)1099-0690(199806)1998:6<1045::AID-EJOC1045>3.0.CO;2-O  0.104
2018 Brückner R, Diehl Née Knobloch E. Turning the Nitrogen Atoms of an Ar2P-CH2-N-N-CH2-PAr2 Motif Into Uniquely Configured Stereocenters: A Novel Diphosphane Design for Asymmetric Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29292850 DOI: 10.1002/chem.201706160  0.104
2018 Brückner R, Diehl Née Knobloch E. Turning the Nitrogen Atoms of an Ar2P-CH2-N-N-CH2-PAr2 Motif Into Uniquely Configured Stereocenters: A Novel Diphosphane Design for Asymmetric Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29292850 DOI: 10.1002/chem.201706160  0.104
2007 Kramer R, Brückner R. Asymmetric hydrogenations one by one: differentiation of up to three beta-ketocarboxylic acid derivatives based on Ruthenium(II)-binap catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 9076-86. PMID 17694528 DOI: 10.1002/chem.200700527  0.102
2007 Dormann K, Brückner R. Variationsfähige Synthese der optisch aktiven Thiotetronsäure-Antibiotika Thiolactomycin, Thiotetromycin und 834-B1 Angewandte Chemie. 119: 1178-1182. DOI: 10.1002/ange.200603562  0.094
2007 Dormann K, Brückner R. Variationsfähige Synthese der optisch aktiven Thiotetronsäure-Antibiotika Thiolactomycin, Thiotetromycin und 834-B1 Angewandte Chemie. 119: 1178-1182. DOI: 10.1002/ange.200603562  0.094
2007 Dormann K, Brückner R. Variationsfähige Synthese der optisch aktiven Thiotetronsäure-Antibiotika Thiolactomycin, Thiotetromycin und 834-B1 Angewandte Chemie. 119: 1178-1182. DOI: 10.1002/ange.200603562  0.094
2007 Dormann K, Brückner R. Variationsfähige Synthese der optisch aktiven Thiotetronsäure-Antibiotika Thiolactomycin, Thiotetromycin und 834-B1 Angewandte Chemie. 119: 1178-1182. DOI: 10.1002/ange.200603562  0.094
2007 Dormann K, Brückner R. Variationsfähige Synthese der optisch aktiven Thiotetronsäure-Antibiotika Thiolactomycin, Thiotetromycin und 834-B1 Angewandte Chemie. 119: 1178-1182. DOI: 10.1002/ange.200603562  0.094
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