𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselective thio-Michael addition to chalcones in water catalyzed by bovine serum albumin

✍ Scribed by Nicoletta Gaggero; Domenico Carlo Maria Albanese; Giuseppe Celentano; Stefano Banfi; Alice Aresi


Book ID
113929499
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
262 KB
Volume
22
Category
Article
ISSN
0957-4166

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Stereoselective Thi
✍ Nicoletta Gaggero; Domenico Carlo Maria Albanese; Giuseppe Celentano; Stefano Ba πŸ“‚ Article πŸ“… 2012 πŸ› John Wiley and Sons βš– 50 KB

## Abstract The title non‐enzymic protein catalyzes the addition of aromatic or aliphatic thiols to Ξ±,β‐unsaturated ketones in a stereoselective fashion to give enantioenriched β‐sulfanyl ketones.

Asymmetric Michael addition of trisubsti
✍ Fu-Xin Chen; Cheng Shao; Qian Liu; Pin Gong; Chun-Liang Liu; Rui Wang πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 137 KB

## Abstract A mild method for the asymmetric synthesis of quaternary and tertiary carbon centers has been developed through Michael addition of trisubstituted carbon nucleophile to nitroalkenes catalyzed by low loading sodium demethylquinine salt in water. Chirality, 2008. Β© 2009 Wiley‐Liss, Inc.