Michael Parmentier

Novartis Pharma AG, Basel, Basel, Basel-Stadt, Switzerland 
organic chemistry, R&D, catalysis
"Michael Parmentier"
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Debrauwer V, Leito I, Lõkov M, et al. (2021) Synthesis and Physicochemical Properties of 2-SF-(Aza)Indoles, a New Family of SF Heterocycles. Acs Organic & Inorganic Au. 1: 43-50
Antien K, Geraci A, Parmentier M, et al. (2021) A New Dioxazolone for the Synthesis of 1,2-Aminoalcohols via Iridium(III)-Catalyzed C(sp )-H Amidation. Angewandte Chemie (International Ed. in English)
Cortes-Clerget M, Akporji N, Zhou J, et al. (2019) Bridging the gap between transition metal- and bio-catalysis via aqueous micellar catalysis. Nature Communications. 10: 2169
Guo P, Zhang H, Zhou J, et al. (2018) Micelle-Enabled Suzuki-Miyaura Cross-coupling of Heteroaryl Boronate Esters. The Journal of Organic Chemistry
Gabriel CM, Lee NR, Bigorne F, et al. (2016) Effects of Co-solvents on Reactions Run under Micellar Catalysis Conditions. Organic Letters
Parmentier M, Hartung T, Pfaltz A, et al. (2014) Iridium-catalyzed H/D exchange: ligand complexes with improved efficiency and scope. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 11496-504
Lebel H, Spitz C, Leogane O, et al. (2011) Stereoselective rhodium-catalyzed amination of alkenes. Organic Letters. 13: 5460-3
Lebel H, Lectard S, Parmentier M. (2007) Copper-catalyzed alkene aziridination with N-tosyloxycarbamates. Organic Letters. 9: 4797-800
Lebel H, Parmentier M. (2007) Copper-catalyzed methylenation reaction: total synthesis of (+)-desoxygaliellalactone. Organic Letters. 9: 3563-6
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