Synthesis of pyrrolidine or piperidine ring-fused azepino[5,4,3-cd]indole derivatives

Authors
Lee, YSMin, BJPark, YKLee, JYLee, SJPark, H
Issue Date
1999-07
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
TETRAHEDRON LETTERS, v.40, no.30, pp.5569 - 5572
Abstract
The synthesis of pyrrolidine or piperidine ring-fused 2-phenylazepino[5,4,3-cd]indole derivatives (2) has been accomplished through the N-acyliminium ion cyclization of hydroxy- or alkoxylactams (5) derived from cyclic anhydrides or chiral hydroxy acids. (C) 1999 Elsevier Science Ltd. All rights reserved.
Keywords
ACYLIMINIUM ION CYCLIZATION; ASYMMETRIC-SYNTHESIS; CLAVICIPITIC ACID; METHYL-ESTER; RECEPTOR; ENANTIOMERS; INDOLES; pyrrolidine; Synthesis of pyrrolidine or piperidine ring-fused
ISSN
0040-4039
URI
https://pubs.kist.re.kr/handle/201004/142046
DOI
10.1016/S0040-4039(99)01076-X
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KIST Article > Others
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