## Abstract **Amino sulfonamide catalyst**: A distal proton of the axially chiral amino sulfonamide (__S__)β**1** realized the opposite diastereoselectivity in Mannich and crossβaldol reactions compared with that observed in prolineβcatalyzed reactions. The reactions catalyzed by (__S__)β**1** proc
anti-Selective Direct Asymmetric Mannich Reactions Catalyzed by Axially Chiral Amino Sulfonamide as an Organocatalyst.
β Scribed by Taichi Kano; Yukako Yamaguchi; Osamu Tokuda; Keiji Maruoka
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 27 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract **The moderate nucleophilicity** of the axially chiral amino sulfonamide (__S__)β**1** suppresses the problematic side reactions, including aldol reactions, in the asymmetric Mannich reaction of NβBocβprotected imines with aldehydes. The corresponding adducts are obtained in good yield
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v