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ChemInform Abstract: A Catalytic Michael Addition of Thiols to α,β-Unsaturated Carbonyl Compounds: Asymmetric Michael Additions and Asymmetric Protonations.
✍ Scribed by E. EMORI; T. ARAI; H. SASAI; M. SHIBASAKI
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 38 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
1998 stereochemistry stereochemistry (general, optical resolution) O 0030
33 -051
A Catalytic Michael Addition of Thiols to α,β-Unsaturated Carbonyl Compounds: Asymmetric Michael Additions and Asymmetric Protonations.
-The heterobimetallic asymmetric lanthanum and samarium complexes are useful catalysts for the title reactions. In particular, the asymmetric protonation in Michael additions of thiols to carbonyl compounds (IV) and (VI) offers a very efficient route to a variety of biologically significant compounds. -(EMORI, E.;
📜 SIMILAR VOLUMES
Catalytic Enantioselective Conjugate Addition of Grignard Reagents to Cyclic α,β-Unsaturated Carbonyl Compounds. -The outcome of the title reaction is influenced by many factors such as amount and structure of the chiral phosphine, copper salt, Grignard reagent, as well as the solvent used.