Diastereoselective Synthesis of Heteroaromatic Glycine Derivatives
β Scribed by Trygve Andreassen; Lars-Kristian Hansen; Odd R. Gautun
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 170 KB
- Volume
- 2008
- Category
- Article
- ISSN
- 1434-193X
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β¦ Synopsis
Abstract
A TMSOTf promoted addition of an Nβtertβbutanesulfinyl Ξ±βimino ester to fiveβmembered aromatic heterocycles furnishes optically active heteroaromatic glycine derivatives with moderateβtoβgood yield in diastereomeric ratios up to 99β%. The absolute configuration of two of the addition products were solved by Xβray analysis. (Β© WileyβVCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
π SIMILAR VOLUMES
## N-benzyloxycarbonyl[14C] -glycine, a lipophilic derivative of glycine exhibiting anticonvulsant properties, was prepared in one step from [U-14C) glycine and benzyl chloroformate in alkali medium. A comparative study of biodistribution was carried on mice between this compound and the parent am