Year |
Citation |
Score |
2023 |
Kastrati A, Jaquier V, Garbo M, Besnard C, Mazet C. Pd-Catalyzed Regioselective Cyclopropanation of 2-Substituted 1,3-Dienes. Acs Organic & Inorganic Au. 3: 291-298. PMID 37810406 DOI: 10.1021/acsorginorgau.3c00024 |
0.361 |
|
2023 |
Duhamel T, Scaringi S, Leforestier B, Poblador-Bahamonde AI, Mazet C. Assisted Tandem Pd Catalysis Enables Regiodivergent Heck Arylation of Transiently Generated Substituted Enol Ethers. Jacs Au. 3: 261-274. PMID 36711081 DOI: 10.1021/jacsau.2c00645 |
0.417 |
|
2022 |
Garbo M, Mazet C. Stereoselective Access to Conjugated and Cross-Conjugated Dienoates by Rh- and Ru-Catalyzed Isomerizations of Vinylcyclopropanes. Organic Letters. PMID 34978828 DOI: 10.1021/acs.orglett.1c04223 |
0.395 |
|
2020 |
Shao W, Besnard C, Guénée L, Mazet C. Ni-Catalyzed Regiodivergent and Stereoselective Hydroalkylation of Acyclic Branched Dienes with Unstabilized C(sp) Nucleophiles. Journal of the American Chemical Society. 142: 16486-16492. PMID 32869987 DOI: 10.1021/jacs.0c08319 |
0.667 |
|
2020 |
Desfeux C, Besnard C, Mazet C. []Dendralenes as a Platform for Selective Catalysis: Ligand-Controlled Cu-Catalyzed Chemo-, Regio-, and Enantioselective Borylations. Organic Letters. 22: 8181-8187. PMID 32559086 DOI: 10.1021/acs.orglett.0c01892 |
0.351 |
|
2020 |
Liu Y, Mazet C. A Catalytic Dual Isomerization/Allylboration Sequence for the Stereoselective Construction of Congested Secondary Homoallylic Alcohols. The Journal of Organic Chemistry. 85: 5638-5650. PMID 32212727 DOI: 10.1021/acs.joc.0c00565 |
0.359 |
|
2019 |
Fiorito D, Liu Y, Besnard C, Mazet C. Direct Access to Chiral Secondary Amides by Copper-Catalyzed Borylative Carboxamidation of Vinylarenes with Isocyanates. Journal of the American Chemical Society. PMID 31825212 DOI: 10.1021/jacs.9b12297 |
0.393 |
|
2019 |
Romano C, Fiorito D, Mazet C. Remote Functionalization of α,β-Unsaturated Carbonyls by Multimetallic Sequential Catalysis. Journal of the American Chemical Society. 141: 16983-16990. PMID 31587562 DOI: 10.1021/jacs.9b09373 |
0.323 |
|
2019 |
Tran G, Shao W, Mazet C. Ni-Catalyzed Enantioselective Intermolecular Hydroamination of Branched 1,3-Dienes Using Primary Aliphatic Amines. Journal of the American Chemical Society. PMID 31436415 DOI: 10.1021/jacs.9b07253 |
0.68 |
|
2018 |
Liu Y, Fiorito D, Mazet C. Copper-catalyzed enantioselective 1,2-borylation of 1,3-dienes. Chemical Science. 9: 5284-5288. PMID 29997884 DOI: 10.1039/c8sc01538d |
0.387 |
|
2018 |
Romano C, Mazet C. Multicatalytic Stereoselective Synthesis of Highly Substituted Alkenes by Sequential Isomerization/Cross-Coupling Reactions. Journal of the American Chemical Society. 140: 4743-4750. PMID 29561600 DOI: 10.1021/jacs.8b02134 |
0.344 |
|
2018 |
Fiorito D, Folliet S, Liu Y, Mazet C. A General Nickel-Catalyzed Kumada Vinylation for the Preparation of 2-Substituted 1,3-Dienes Acs Catalysis. 8: 1392-1398. DOI: 10.1021/ACSCATAL.7B04030 |
0.321 |
|
2017 |
Li H, Fiorito D, Mazet C. Exploring Site Selectivity of Iridium Hydride Insertion into Allylic Alcohols: Serendipitous Discovery and Comparative Study of Organic and Organometallic Catalysts for the Vinylogous Peterson Elimination Acs Catalysis. 7: 1554-1562. DOI: 10.1021/ACSCATAL.6B03376 |
0.651 |
|
2017 |
Borrajo-Calleja GM, Bizet V, Besnard C, Mazet C. Mechanistic Investigation of the Pd-Catalyzed Intermolecular Carboetherification and Carboamination of 2,3-Dihydrofuran: Similarities, Differences, and Evidence for Unusual Reaction Intermediates Organometallics. 36: 3553-3563. DOI: 10.1021/ACS.ORGANOMET.7B00483 |
0.686 |
|
2017 |
Huang H, Humbert N, Bizet V, Patra M, Chao H, Mazet C, Gasser G. Influence of the dissolution solvent on the cytotoxicity of octahedral cationic Ir(III) hydride complexes Journal of Organometallic Chemistry. 839: 15-18. DOI: 10.1016/J.Jorganchem.2016.12.010 |
0.624 |
|
2016 |
Li H, Mazet C. Iridium-Catalyzed Selective Isomerization of Primary Allylic Alcohols. Accounts of Chemical Research. PMID 27159335 DOI: 10.1021/acs.accounts.6b00144 |
0.714 |
|
2016 |
Borrajo-Calleja GM, Bizet V, Mazet C. Palladium-Catalyzed Enantioselective Intermolecular Carboetherification of Dihydrofurans. Journal of the American Chemical Society. 138: 4014-7. PMID 26978243 DOI: 10.1021/jacs.6b02158 |
0.724 |
|
2016 |
Bizet V, Borrajo-Calleja GM, Besnard C, Mazet C. Direct Access to Furoindolines by Palladium-Catalyzed Intermolecular Carboamination Acs Catalysis. 6: 7183-7187. DOI: 10.1021/ACSCATAL.6B02238 |
0.694 |
|
2015 |
Borrajo-Calleja GM, Bizet V, Bürgi T, Mazet C. Access to enantioenriched 2,3- and 2,5-dihydrofurans with a fully substituted C2 stereocenter by Pd-catalyzed asymmetric intermolecular Heck reaction. Chemical Science. 6: 4807-4811. PMID 29142715 DOI: 10.1039/C5Sc01460C |
0.732 |
|
2015 |
Zhang B, Kaziz S, Li H, Wodka D, Malola S, Safonova O, Nachtegaal M, Mazet C, Dolamic I, Llorca J, Kalenius E, Lawson Daku LM, Hakkinen H, Bürgi T, Barrabés N. Pd2Au36(SR)24 cluster: structure studies. Nanoscale. PMID 26415984 DOI: 10.1039/C5Nr04324G |
0.61 |
|
2015 |
Li H, Mazet C. Catalyst-Directed Diastereoselective Isomerization of Allylic Alcohols for the Stereoselective Construction of C(20) in Steroid Side Chains: Scope and Topological Diversification. Journal of the American Chemical Society. 137: 10720-7. PMID 26237282 DOI: 10.1021/jacs.5b06281 |
0.704 |
|
2015 |
Zhang B, Kaziz S, Li H, Hevia MG, Wodka D, Mazet C, Bürgi T, Barrabés N. Modulation of active sites in supported Au<inf>38</inf>(SC<inf>2</inf>H<inf>4</inf>Ph)<inf>24</inf> cluster catalysts: Effect of atmosphere and support material Journal of Physical Chemistry C. 119: 11193-11199. DOI: 10.1021/Jp512022V |
0.636 |
|
2014 |
Larionov E, Lin L, Guénée L, Mazet C. Scope and mechanism in palladium-catalyzed isomerizations of highly substituted allylic, homoallylic, and alkenyl alcohols. Journal of the American Chemical Society. 136: 16882-94. PMID 25397681 DOI: 10.1021/ja508736u |
0.36 |
|
2014 |
Larionov E, Li H, Mazet C. Well-defined transition metal hydrides in catalytic isomerizations. Chemical Communications (Cambridge, England). 50: 9816-26. PMID 24901411 DOI: 10.1039/c4cc02399d |
0.614 |
|
2014 |
Humbert N, Larionov E, Mantilli L, Nareddy P, Besnard C, Guénée L, Mazet C. Highly modular C(1) -symmetric chiral (P,N) ligands with a stereolabile P center: experimental and theoretical studies. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 745-51. PMID 24318387 DOI: 10.1002/chem.201303146 |
0.357 |
|
2013 |
Mazet C. Complementary catalytic strategies to access alpha-chiral aldehydes. Chimia. 67: 658-62. PMID 24388344 DOI: 10.2533/chimia.2013.658 |
0.392 |
|
2013 |
Li H, Mazet C. Steric parameters in the Ir-catalyzed regio- and diastereoselective isomerization of primary allylic alcohols. Organic Letters. 15: 6170-3. PMID 24219058 DOI: 10.1021/ol403023x |
0.679 |
|
2013 |
Vyas DJ, Larionov E, Besnard C, Guénée L, Mazet C. Isomerization of terminal epoxides by a [Pd-H] catalyst: a combined experimental and theoretical mechanistic study. Journal of the American Chemical Society. 135: 6177-83. PMID 23528226 DOI: 10.1021/ja400325w |
0.422 |
|
2012 |
Nareddy P, Mantilli L, Guénée L, Mazet C. Atropoisomeric (P,N) ligands for the highly enantioselective Pd-catalyzed intramolecular asymmetric α-arylation of α-branched aldehydes. Angewandte Chemie (International Ed. in English). 51: 3826-31. PMID 22389114 DOI: 10.1002/anie.201108061 |
0.34 |
|
2011 |
Mazet C. New catalytic asymmetric strategies to access chiral aldehydes. Chimia. 65: 802-5. PMID 22054135 DOI: 10.2533/chimia.2011.802 |
0.375 |
|
2011 |
Quintard A, Alexakis A, Mazet C. Access to high levels of molecular complexity by one-pot iridium/enamine asymmetric catalysis. Angewandte Chemie (International Ed. in English). 50: 2354-8. PMID 21351353 DOI: 10.1002/Anie.201007001 |
0.407 |
|
2011 |
Mazet C, Gérard D. Highly regio- and enantioselective catalytic asymmetric hydroboration of α-substituted styrenyl derivatives. Chemical Communications (Cambridge, England). 47: 298-300. PMID 20697639 DOI: 10.1039/c0cc01547d |
0.363 |
|
2011 |
Quintard A, Alexakis A, Mazet C. One-Pot Iridium and Enamine Catalysis Synfacts. 2011: 519-519. DOI: 10.1055/S-0030-1259834 |
0.393 |
|
2011 |
Mazet C. Privileged Chiral Ligands and Catalysts. Edited by Qi-Lin Zhou. Angewandte Chemie International Edition. 51: 305-305. DOI: 10.1002/ANIE.201106819 |
0.327 |
|
2011 |
Quintard A, Alexakis A, Mazet C. Access to high levels of molecular complexity by one-pot iridium/enamine asymmetric catalysis Angewandte Chemie - International Edition. 50: 2354-2358. DOI: 10.1002/anie.201007001 |
0.393 |
|
2011 |
Mazet C. Privileged Chiral Ligands and Catalysts. Herausgegeben von Qi-Lin Zhou. Angewandte Chemie. 124: 311-311. DOI: 10.1002/ANGE.201106819 |
0.325 |
|
2010 |
Mantilli L, Gérard D, Torche S, Besnard C, Mazet C. Improved catalysts for the iridium-catalyzed asymmetric isomerization of primary allylic alcohols based on Charton analysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 12736-45. PMID 20845413 DOI: 10.1002/chem.201001311 |
0.399 |
|
2010 |
Mantilli L, Mazet C. Expanded scope for the iridium-catalyzed asymmetric isomerization of primary allylic alcohols using readily accessible second-generation catalysts. Chemical Communications (Cambridge, England). 46: 445-7. PMID 20066320 DOI: 10.1039/b920342g |
0.362 |
|
2010 |
Mantilli L, Gérard D, Torche S, Besnard C, Mazet C. Highly enantioselective isomerization of primary allylic alcohols catalyzed by (P,N)-iridium complexes Pure and Applied Chemistry. 82: 1461-1469. DOI: 10.1351/PAC-CON-09-09-10 |
0.44 |
|
2010 |
Mazet C, Gade LH. ChemInform Abstract: A Bis(oxazolinyl)pyrrole as a New Monoanionic Tridentate Supporting Ligand: Synthesis of a Highly Active Palladium Catalyst for Suzuki-Type C-C Coupling. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200202074 |
0.345 |
|
2009 |
Mantilli L, Gérard D, Torche S, Besnard C, Mazet C. Iridium-catalyzed asymmetric isomerization of primary allylic alcohols. Angewandte Chemie (International Ed. in English). 48: 5143-7. PMID 19526480 DOI: 10.1002/anie.200901863 |
0.391 |
|
2009 |
Mantilli L, Mazet C. Iridium-catalyzed isomerization of primary allylic alcohols under mild reaction conditions Tetrahedron Letters. 50: 4141-4144. DOI: 10.1016/J.TETLET.2009.04.130 |
0.337 |
|
2009 |
Mantilli L, Mazet C. ChemInform Abstract: Iridium-Catalyzed Isomerization of Primary Allylic Alcohols under Mild Reaction Conditions. Cheminform. 40. DOI: 10.1002/CHIN.200943076 |
0.345 |
|
2008 |
Köhler V, Mazet C, Toussaint A, Kulicke K, Häussinger D, Neuburger M, Schaffner S, Kaiser S, Pfaltz A. Chiral boron-bridged bisoxazoline (borabox) ligands: structures and reactivities of Pd and Cu complexes. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 8530-9. PMID 18688831 DOI: 10.1002/Chem.200800822 |
0.57 |
|
2008 |
Mazet C, Jacobsen EN. Dinuclear {(salen)Al} complexes display expanded scope in the conjugate cyanation of alpha,beta-unsaturated imides. Angewandte Chemie (International Ed. in English). 47: 1762-5. PMID 18219639 DOI: 10.1002/Anie.200704461 |
0.499 |
|
2008 |
Köhler V, Mazet C, Toussaint A, Kulicke K, Häussinger D, Neuburger M, Schaffner S, Kaiser S, Pfaltz A. Chiral boron-bridged bisoxazoline (borabox) ligands: Structures and reactivities of Pd and Cu complexes Chemistry - a European Journal. 14: 8530-8539. DOI: 10.1002/chem.200800822 |
0.536 |
|
2007 |
Mazet C, Kohler V, Roseblade S, Toussaint A, Pfaltz A. Synthesis of Boron-Bridged Anionic C2-Symmetric Bisoxazolines and Their Application in Asymmetric Catalysis Cheminform. 38. DOI: 10.1002/CHIN.200713249 |
0.493 |
|
2006 |
Mazet C, Roseblade S, Köhler V, Pfaltz A. Kinetic resolution of diols and pyridyl alcohols by Cu(II)(borabox)-catalyzed acylation. Organic Letters. 8: 1879-82. PMID 16623574 DOI: 10.1021/Ol060443T |
0.544 |
|
2006 |
Mazet C, Köhler V, Roseblade S, Toussaint A, Pfaltz A. Synthesis of boron-bridged anionic C2-symmetric bisoxazolines and their application in asymmetric catalysis Chimia. 60: 195-198. DOI: 10.2533/000942906777674958 |
0.607 |
|
2006 |
Mazet C, Roseblade S, Köhler V, Pfaltz A. Kinetic Resolution of Diols and Pyridyl Alcohols Synfacts. 2006: 694-694. DOI: 10.1055/S-2006-941919 |
0.463 |
|
2006 |
Mazet C, Roseblade S, Köhler V, Pfaltz A. Kinetic resolution of diols and pyridyl alcohols by cu(II)(borabox)- catalyzed acylation Organic Letters. 8: 1879-1882. DOI: 10.1021/ol060443t |
0.48 |
|
2005 |
Mazet C, Köhler V, Pfaltz A. Chiral boron-bridged bisoxazolines: readily available anionic ligands for asymmetric catalysis. Angewandte Chemie (International Ed. in English). 44: 4888-91. PMID 16007719 DOI: 10.1002/Anie.200501111 |
0.599 |
|
2005 |
Mazet C, Köhler V, Pfaltz A. Boron-Bridged Bisoxazolines (Borabox): Anionic Ligands for Asymmetric Catalysis Synfacts. 2005: 232-232. DOI: 10.1055/S-2005-916102 |
0.523 |
|
2004 |
Mazet C, Smidt SP, Meuwly M, Pfaltz A. A combined experimental and computational study of dihydrido(phosphinooxazoline)iridium complexes. Journal of the American Chemical Society. 126: 14176-81. PMID 15506783 DOI: 10.1021/Ja046318Z |
0.547 |
|
2003 |
Mazet C, Gade LH. Double bonds in motion: bis(oxazolinylmethyl)pyrroles and their metal-induced planarization to a new class of rigid chiral C2-symmetric complexes. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 1759-67. PMID 12698433 DOI: 10.1002/Chem.200390202 |
0.567 |
|
2003 |
Mazet C, Gade LH. Synthesis and coordination chemistry of the first C2-chiral bisoxazine ligand. Inorganic Chemistry. 42: 210-5. PMID 12513097 DOI: 10.1021/Ic025947B |
0.594 |
|
2003 |
Mazet C, Gade L. [Bis(oxazolinyl)pyrrole]palladium Complexes as Catalysts in Heck- and Suzuki-Type C−C Coupling Reactions European Journal of Inorganic Chemistry. 2003: 1161-1168. DOI: 10.1002/Ejic.200390148 |
0.602 |
|
2003 |
Mazet C, Gade LH. [Bis(oxazolinyl)pyrrole]palladium Complexes as Catalysts in Heck- and Suzuki-Type C—C Coupling Reactions. Cheminform. 34. DOI: 10.1002/chin.200328105 |
0.567 |
|
2002 |
Mazet C, Gade LH. Charging and deforming the pybox ligand: enantiomerically pure double helices and their interconversion. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 4308-18. PMID 12298023 DOI: 10.1002/1521-3765(20020916)8:18<4308::Aid-Chem4308>3.0.Co;2-T |
0.457 |
|
2001 |
Mazet C, Gade LH. A Bis(oxazolinyl)pyrrole as a New Monoanionic Tridentate Supporting Ligand: Synthesis of a Highly Active Palladium Catalyst for Suzuki-Type C−C Coupling Organometallics. 20: 4144-4146. DOI: 10.1021/Om010586D |
0.582 |
|
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