A stereo-and enantio-specific synthesis of the natural1 occurring cis-%hydroxy-(L)-pipecolic acid (3) is described, starting from Z-(L -glutamic the key step involves c chsation of a Y, to trans-%hydroxy-(L -pipecolic acl 3 3 rotected chlorohydrin, and also gives access acid, .
Chirospecific synthesis of (+)-PS-5 from L-glutamic acid
✍ Scribed by Tomihisa Ohta; Nobuaki Sato; Toshihiko Kimura; Shigeo Nozoe; Kunisuke Izawa
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 229 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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