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Asymmetric synthesis of furo[3,2-i]indolizines from L-malic acid

Authors
Lee, YS; Lee, JY; Kim, DW; Park, HK
Issue Date
1999-04
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
TETRAHEDRON, v.55, no.15, pp.4631 - 4636
Abstract
A chiral enamide 6, derived from L-malic acid, was converted to furo-indolizine 2 via N-acyliminium ion cyclization. Furo-indolizine 2 was transformed to indolizine derivatives 8 and 9 which have a substituent at angular position. (C) 1999 Elsevier Science Ltd. All rights reserved.
Keywords
ACYLIMINIUM ION CYCLIZATION; DERIVATIVES; EFFICIENT; ERYTHRINA; ALKALOIDS; PYRROLIDINONES; HETEROCYCLES; ENANTIOMERS; ROUTE; furoindole; L-malic acid; N-acyliminium ion
ISSN
0040-4020
URI
https://pubs.kist.re.kr/handle/201004/142254
DOI
10.1016/S0040-4020(99)00158-1
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KIST Article > Others
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