## Abstract For Abstract see ChemInform Abstract in Full Text.
Facile synthesis of both enantiomers of (pyrrolidin-2-yl)phosphonate from l-proline
✍ Scribed by Shigeo Hirata; Masami Kuriyama; Osamu Onomura
- Book ID
- 113928968
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- French
- Weight
- 599 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract A new enantioselective synthesis of furan‐2‐yl amines and amino acids is described, in which the key step is the oxazaborolidine‐catalyzed enantioselective reduction of __O__‐benzyl (__E__)__‐__ and (__Z__)‐furan‐2‐yl ketone oximes to the corresponding chiral amines. The chirality of th
Xiisriacrt Ai~eenyi-a-amliropiiospiio~ales are qciizeu'tiy 4ntramokculti amrnomercuration to grvepyrrolidin-and'prperrdin-&yi phosphonates whrch lead, after ondatron wrlh m-CPBA, ro the correspondtng stable /?-phosphotylated nwoxides