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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, HYJung, JKim, SHKim, HYAhn, KHKim, 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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안교한AHN, KYO HAN
Dept of Chemistry
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