A diastereoselective phenylselenium-induced lactamization of olefinic amides. A possible route to alpha- and beta-amino acid derivatives
SCIE
SCOPUS
- Title
- A diastereoselective phenylselenium-induced lactamization of olefinic amides. A possible route to alpha- and beta-amino acid derivatives
- Authors
- Chung, SK; Jeong, TH; Kang, DH
- Date Issued
- 1997-01-09
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Abstract
- The organoselenium-induced cyclofunctionalization of (S)-N-(alpha,beta-unsaturated-acyl)prolinamides was found to produce with a high degree of chirality transfer, 7- and 6-membered bislactam derivatives depending on the substitution pattern of the starting material. (C) 1997 Published by Elsevier Science Ltd.
- Keywords
- STEREOSELECTIVE SYNTHESIS; CYCLIZATION; LACTAMS; OXIMES
- URI
- https://oasis.postech.ac.kr/handle/2014.oak/21395
- DOI
- 10.1016/S0957-4166(96)00496-X
- ISSN
- 0957-4166
- Article Type
- Article
- Citation
- TETRAHEDRON-ASYMMETRY, vol. 8, no. 1, page. 5 - 9, 1997-01-09
- Files in This Item:
- There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.