1. Direct Access to Substituted 4-CF3 β-Lactams at the C-3 Position
- Author
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Monika Skibińska, Marcin Kaźmierczak, Thierry Milcent, Tomasz Cytlak, Henryk Koroniak, Benoit Crousse, Biomolécules : Conception, Isolement, Synthèse (BioCIS), Centre National de la Recherche Scientifique (CNRS)-Université Paris-Saclay-CY Cergy Paris Université (CY), Faculty of Chemistry [Poznań], Adam Mickiewicz University in Poznań (UAM), Institut de Chimie du CNRS (INC)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-CY Cergy Paris Université (CY), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Paris-Sud - Paris 11 (UP11)-Université de Cergy Pontoise (UCP), and Université Paris-Seine-Université Paris-Seine
- Subjects
Stereochemistry ,chemistry.chemical_element ,02 engineering and technology ,Alkylation ,010402 general chemistry ,01 natural sciences ,lcsh:Chemistry ,Deprotonation ,Position (vector) ,fluorine ,β lactams ,[CHIM]Chemical Sciences ,lactams ,alkylation ,ComputingMilieux_MISCELLANEOUS ,[CHIM.ORGA]Chemical Sciences/Organic chemistry ,General Chemistry ,021001 nanoscience & nanotechnology ,Triple bond ,0104 chemical sciences ,3. Good health ,lcsh:QD1-999 ,chemistry ,deprotonation ,Fluorine ,functionalization ,0210 nano-technology - Abstract
International audience; Mono- and disubstituted 4-CF3 β-lactams at the C-3 position have been obtained stereoselectively under basic conditions. A wide range of function such as alcohols, alkyls, aryls, esters, and double and triple bonds have been introduced.
- Published
- 2019