ChemInform Abstract: γ-Amino-β-ketosulfones as Chiral Educts: A Facile Synthesis of Enantiopure α-Amino Ketones.
✍ Scribed by S. SENGUPTA; D. S. SARMA; S. MONDAL
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 42 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
1998 ketones ketones (acyclic compounds) P 0200
47 -080
γ-Amino-β-ketosulfones as Chiral Educts: A Facile Synthesis of Enantiopure α-Amino Ketones.
-A new method for the preparation of enantiopure α-amino ketones, precursors of synthetically and pharmaceutically important β-amino alcohols, is developed via mono-or dialkylation of γ-amino-β-ketosulfones and subsequent reductive removal of the sulfonyl group. This strategy is extended towards γ-hydroxy-β-ketosulfones. The starting sulfones are prepared from chiral-pool materials according to reported protocols.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v