Enantioselective Synthesis of Aza Sugars from Amino Acids. 2. 1 The 3-Hydroxy-2-hydroxymethylpyrrolidines 2
β Scribed by Mascavage, Linda M.; Lu, Qing; Vey, Jessica; Dalton, David R.; Carroll, Patrick J.
- Book ID
- 125980691
- Publisher
- American Chemical Society
- Year
- 2001
- Tongue
- English
- Weight
- 79 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A highly stereoselective synthesis of 2-amino-l-hydroxy-3-phenylpropylphosphonic acid was achieved by simple addition of diethyl phosphite to enantiomeric N-blocked phenylalanlnals. These compouds exhibit sit, nificant herbicidal activity.
The Efficient, Enantioselective Synthesis of Aza Sugars from Amino Acids. Part 1. The Polyhydroxylated Pyrrolidines. -All eight stereoisomeric 2-hydroxymethyl-3,4-dihydroxypyrrolidines, e. g. (IX) and (X), are prepared from L-serine methylester (I) or D-serine methylester, respectively. Key step in