An efficient synthesis of enantiomerically pure unnatural aryl glycinols and aryl glycines
SCIE
SCOPUS
- Title
- An efficient synthesis of enantiomerically pure unnatural aryl glycinols and aryl glycines
- Authors
- Ku, HY; Jung, J; Kim, SH; Kim, HY; Ahn, KH; Kim, SG
- Date Issued
- 2006-04-03
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Abstract
- A quick route to enantiomerically pure unnatural aryl glycinols and aryl glycines has been established based on an asymmetric azidation reaction using a chiral benzosultam auxiliary. The synthesis of aryl glycinols involves three steps starting from arylacetic acids, and the chiral auxiliary can be readily recovered. (c) 2006 Elsevier Ltd. All rights reserved.
- Keywords
- ALPHA-AMINO-ACIDS; METABOTROPIC GLUTAMATE RECEPTORS; CHIRAL MOLECULAR RECOGNITION; ASYMMETRIC-SYNTHESIS; PHENYLGLYCINE DERIVATIVES; ARTIFICIAL RECEPTORS; ORGANOAMMONIUM IONS; ARYLGLYCINES; AUXILIARIES; ENVIRONMENT
- URI
- https://oasis.postech.ac.kr/handle/2014.oak/23980
- DOI
- 10.1016/j.tetasy.2006.03.031
- ISSN
- 0957-4166
- Article Type
- Article
- Citation
- TETRAHEDRON-ASYMMETRY, vol. 17, no. 7, page. 1111 - 1115, 2006-04-03
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- There are no files associated with this item.
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