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Dorian Didier - Publications

Affiliations: 
Ludwig-Maximilian University, München, Bayern, Germany 
Area:
Organic, Organometallic Chemistry
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39 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Baumann AN, Music A, Dechent J, Müller N, Jagau TC, Didier D. Electro-olefination - a Catalyst Free Stereoconvergent Strategy for the Functionalization of Alkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32203624 DOI: 10.1002/Chem.202001394  0.368
2020 Baumann AN, Reiners F, Mayer P, Siegle AF, Trapp O, Didier D. Thiete Dioxides as Templates towards Novel Twisted Scaffolds and Macrocyclic Structures. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32119146 DOI: 10.1002/Chem.201905751  0.379
2020 Music A, Baumann AN, Spieß P, Plantefol A, Jagau TC, Didier D. Electrochemical Synthesis of Biaryls via Oxidative Intramolecular Coupling of Tetra(hetero)arylborates. Journal of the American Chemical Society. PMID 32040918 DOI: 10.1021/Jacs.9B12300  0.369
2019 Music A, Baumann AN, Spieß P, Hilgert N, Köllen M, Didier D. Single-Pot Access to Bisorganoborinates: Applications in Zweifel Olefination. Organic Letters. PMID 30864807 DOI: 10.1021/Acs.Orglett.9B00493  0.432
2019 Music A, Hoarau C, Hilgert N, Zischka F, Didier D. Catalyst-Free Enantiospecific Olefination with In Situ Generated Organocerium Species. Angewandte Chemie (International Ed. in English). 58: 1188-1192. PMID 30468288 DOI: 10.1002/Anie.201810327  0.407
2019 Music A, Didier D. Organocerium: A New Contender for Halogen–Metal Exchanges Synlett. 30: 1843-1849. DOI: 10.1055/S-0037-1611843  0.405
2018 Baumann AN, Reiners F, Juli T, Didier D. Chemodivergent and Stereoselective Access to Fused Isoxazoline Azetidines and Thietanes through [3 + 2]-Cycloadditions. Organic Letters. 20: 6736-6740. PMID 30351958 DOI: 10.1021/Acs.Orglett.8B02848  0.431
2018 Eisold M, Müller-Deku A, Reiners F, Didier D. Parallel Approaches for the Functionalization of Thietes: α-Metalation versus C-H Activation. Organic Letters. 20: 4654-4658. PMID 30004710 DOI: 10.1021/Acs.Orglett.8B01961  0.313
2018 Baumann AN, Schüppel F, Eisold M, Kreppel A, de Vivie-Riedle R, Didier D. Oxidative Ring Contraction of Cyclobutenes: General Approach to Cyclopropylketones including Mechanistic Insights. The Journal of Organic Chemistry. 83: 4905-4921. PMID 29641195 DOI: 10.1021/Acs.Joc.8B00297  0.369
2018 Bruffaerts J, Vasseur A, Singh S, Masarwa A, Didier D, Oskar L, Perrin L, Eisenstein O, Marek I. Zirconocene-Mediated Selective C-C Bond Cleavage of Strained Carbocycles: Scope and Mechanism. The Journal of Organic Chemistry. PMID 29537856 DOI: 10.1021/Acs.Joc.7B03115  0.364
2018 Music A, Baumann AN, Eisold M, Didier D. Regiodivergent Stereoselective Access to Fused Alkylideneazetidines. The Journal of Organic Chemistry. 83: 783-792. PMID 29260549 DOI: 10.1021/Acs.Joc.7B02786  0.389
2018 Baumann AN, Eisold M, Music A, Didier D. One-Pot Preparation of Stable Organoboronate Reagents for the Functionalization of Unsaturated Four- and Five-Membered Carbo­- and Heterocycles Synthesis. 50: 3149-3160. DOI: 10.1055/S-0036-1592004  0.391
2018 Didier D, Baumann AN, Eisold M. Unsaturated four-membered N-heterocycles: From synthesis to applications Tetrahedron Letters. 59: 3975-3987. DOI: 10.1016/J.Tetlet.2018.09.055  0.31
2017 Baumann AN, Eisold M, Music A, Haas G, Kiw YM, Didier D. Correction to Methods for the Synthesis of Substituted Azetines. Organic Letters. 19: 6763. PMID 29166024 DOI: 10.1021/Acs.Orglett.7B03520  0.391
2017 Baumann AN, Eisold M, Music A, Haas G, Kiw YM, Didier D. Methods for the Synthesis of Substituted Azetines. Organic Letters. 19: 5681-5684. PMID 28976769 DOI: 10.1021/Acs.Orglett.7B02847  0.399
2017 Eisold M, Didier D. Stereoselective Access to Alkylidenecyclobutanes through γ-Selective Cross-Coupling Strategies. Organic Letters. 19: 4046-4049. PMID 28726420 DOI: 10.1021/Acs.Orglett.7B01803  0.411
2017 Baumann AN, Eisold M, Didier D. Stereoselective Sequence toward Biologically Active Fused Alkylidenecyclobutanes. Organic Letters. 19: 2114-2117. PMID 28374585 DOI: 10.1021/Acs.Orglett.7B00724  0.426
2017 Eisold M, Baumann AN, Kiefl GM, Emmerling ST, Didier D. Unsaturated Four-Membered Rings: Efficient Strategies for the Construction of Cyclobutenes and Alkylidenecyclobutanes. Chemistry (Weinheim An Der Bergstrasse, Germany). 23: 1634-1644. PMID 27862444 DOI: 10.1002/Chem.201604585  0.422
2016 Roy SR, Didier D, Kleiner A, Marek I. Diastereodivergent combined carbometalation/zinc homologation/C-C fragmentation reaction as an efficient tool to prepare acyclic allylic quaternary carbon stereocenters. Chemical Science. 7: 5989-5994. PMID 30034740 DOI: 10.1039/C6Sc02191C  0.434
2016 Eisold M, Kiefl GM, Didier D. Single-Pot Asymmetric Approach toward Enantioenriched Quaternary Stereocenter-Containing Alkylidenecyclobutanes. Organic Letters. 18: 3022-5. PMID 27281109 DOI: 10.1021/Acs.Orglett.6B01432  0.426
2016 Baumann AN, Music A, Karaghiosoff K, Didier D. Highly diastereoselective approach to methylenecyclopropanes via boron-homologation/allylboration sequences. Chemical Communications (Cambridge, England). 52: 2529-32. PMID 26741566 DOI: 10.1039/C5Cc09904H  0.404
2016 Roy SR, Didier D, Kleiner A, Marek I. Diastereodivergent combined carbometalation/zinc homologation/C-C fragmentation reaction as an efficient tool to prepare acyclic allylic quaternary carbon stereocenters Chemical Science. 7: 5989-5994. DOI: 10.1039/c6sc02191c  0.343
2015 Eisold M, Didier D. Highly Diastereoselective Synthesis of Methylenecyclobutanes by Merging Boron-Homologation and Boron-Allylation Strategies. Angewandte Chemie (International Ed. in English). 54: 15884-7. PMID 26563627 DOI: 10.1002/Anie.201507444  0.464
2015 Klatt T, Werner V, Maximova MG, Didier D, Apeloig Y, Knochel P. Preparation and Regioselective Magnesiation or Lithiation of Bis(trimethylsilyl)methyl-Substituted Heteroaryls for the Generation of Highly Functionalized Heterocycles. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 7830-4. PMID 25864885 DOI: 10.1002/Chem.201500627  0.472
2015 Moriya K, Didier D, Simon M, Hammann JM, Berionni G, Karaghiosoff K, Zipse H, Mayr H, Knochel P. Stereoselective synthesis and reactions of secondary alkyllithium reagents functionalized at the 3-position. Angewandte Chemie (International Ed. in English). 54: 2754-7. PMID 25640227 DOI: 10.1002/Anie.201409165  0.656
2015 Eisold M, Didier D. Diastereoselektive Synthese von Methylencyclobutanen durch Vereinigung von Bor‐Homologisierungs‐ und ‐Allylierungsstrategie Angewandte Chemie. 127: 16112-16115. DOI: 10.1002/Ange.201507444  0.339
2015 Moriya K, Didier D, Simon M, Hammann JM, Berionni G, Karaghiosoff K, Zipse H, Mayr H, Knochel P. Stereoselektive Synthese und Reaktionen von in Position 3 funktionalisierten sekundären Alkyllithiumverbindungen Angewandte Chemie. 127: 2793-2796. DOI: 10.1002/Ange.201409165  0.593
2014 Didier D, Delaye PO, Simaan M, Island B, Eppe G, Eijsberg H, Kleiner A, Knochel P, Marek I. Modulable and highly diastereoselective carbometalations of cyclopropenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 1038-48. PMID 24338953 DOI: 10.1002/Chem.201303569  0.481
2014 Masarwa A, Didier D, Zabrodski T, Schinkel M, Ackermann L, Marek I. Merging allylic carbon-hydrogen and selective carbon-carbon bond activation. Nature. 505: 199-203. PMID 24317692 DOI: 10.1038/Nature12761  0.387
2014 Knochel P, Haas D, Masarwa A, Didier D, Zabrodski T, Schinkel M, Ackermann L, Marek I. Zirconium-Promoted Combined C–H and C–C Bond Activation Synfacts. 10: 417-417. DOI: 10.1055/S-0033-1340933  0.324
2014 Nasrallah H, Pagnoux A, Didier D, Magnier C, Toupet L, Guillot R, Crévisy C, Mauduit M, Schulz E. Immobilization of an Anthracene-Tagged Ruthenium Complex on a 2,4,7-Trinitrofluoren-9-one-Grafted Silica: Efficiency and Recyclability in Olefin Metathesis Reactions European Journal of Organic Chemistry. 2014: 7781-7787. DOI: 10.1002/Ejoc.201403194  0.332
2014 Didier D, Delaye P, Simaan M, Island B, Eppe G, Eijsberg H, Kleiner A, Knochel P, Marek I. Cover Picture: Modulable and Highly Diastereoselective Carbometalations of Cyclopropenes (Chem. Eur. J. 4/2014) Chemistry - a European Journal. 20: 909-909. DOI: 10.1002/Chem.201490010  0.341
2013 Delaye PO, Didier D, Marek I. Diastereodivergent carbometalation/oxidation/selective ring opening: formation of all-carbon quaternary stereogenic centers in acyclic systems. Angewandte Chemie (International Ed. in English). 52: 5333-7. PMID 23589464 DOI: 10.1002/Anie.201300664  0.327
2013 Didier D, Schulz E. π-Stacking interactions at the service of [Cu]-bis(oxazoline) recycling Tetrahedron: Asymmetry. 24: 769-775. DOI: 10.1016/J.Tetasy.2013.05.008  0.381
2012 Schulz E, Didier D. A Reusable TNF-Tagged Chiral Bis(oxazoline)-Copper Catalyst for Diels- Alder Transformations Synlett. 23: 1309-1314. DOI: 10.1055/S-0031-1290918  0.39
2011 Didier D, Meddour A, Bezzenine-Lafollée S, Collin J. Samarium Iodobinaphtholate: An Efficient Catalyst for Enantioselective Aza-Michael Additions of O-Benzylhydroxylamine to N-Alkenoyloxazolidinones European Journal of Organic Chemistry. 2011: 2678-2684. DOI: 10.1002/Ejoc.201100041  0.353
2011 Didier D, Schulz E. Recycling Chiral Copper Bis(oxazoline) Complexes in an Original Multireaction Procedure Chemcatchem. 3: 1880-1884. DOI: 10.1002/Cctc.201100250  0.3
2011 Didier D, Magnier-Bouvier C, Schulz E. Charge-Transfer Interactions: An Efficient Tool for Recycling Bis(oxazoline)-Copper Complexes in Asymmetric Henry Reactions Advanced Synthesis & Catalysis. 353: 1087-1095. DOI: 10.1002/Adsc.201000934  0.396
2010 Chollet G, Didier D, Schulz E. Reusable chiral bis(oxazoline)–copper complexes immobilized by donor–acceptor interactions on insoluble organic supports Catalysis Communications. 11: 351-355. DOI: 10.1016/J.Catcom.2009.10.029  0.368
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