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Cited 17 time in webofscience Cited 21 time in scopus
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DIASTEREOSELECTIVE ALKYLATION REACTIONS EMPLOYING A CAMPHOR-BASED CHIRAL OXAZINONE AUXILIARY SCIE SCOPUS

Title
DIASTEREOSELECTIVE ALKYLATION REACTIONS EMPLOYING A CAMPHOR-BASED CHIRAL OXAZINONE AUXILIARY
Authors
AHN, KHLEE, SKLIM, AK
Date Issued
1993-12
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Abstract
An almost complete pi-face selectivity is obtained in asymmetric alkylation reactions of lithium enolates derived from imide 2 which contains a camphor-based chiral oxazinone auxiliary.
URI
https://oasis.postech.ac.kr/handle/2014.oak/22020
DOI
10.1016/S0957-4166(00)82218-1
ISSN
0957-4166
Article Type
Article
Citation
TETRAHEDRON-ASYMMETRY, vol. 4, no. 12, page. 2435 - 2436, 1993-12
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안교한AHN, KYO HAN
Dept of Chemistry
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