Synthesis of pyrrolidine or piperidine ring-fused azepino[5,4,3-cd]indole derivatives
- Authors
- Lee, YS; Min, BJ; Park, YK; Lee, JY; Lee, SJ; Park, 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
- Appears in Collections:
- KIST Article > Others
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