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Volumn 67, Issue 11, 2002, Pages 1669-1680

Intramolecular Mannich reaction of 2-oxotryptamine and homologues with oxo reagents yielding spiro compounds. Part II

Author keywords

Alkaloids; Cyclizations; Indoles; Intramolecular Mannich reaction; Ketones; Oxindoles; Piperidines; Pyrrolidines; Spirocyclic compounds

Indexed keywords

1'' BENZYLDISPIRO(INDOLINE 3,3' PYRROLIDINE 2',4'' PIPERIDIN) 2 ONE; 1',2',2' TRIMETHYLSPIRO(INDOLINE 3,3' PIPERIDIN) 2 ONE; 2 ETHYL 2 METHYLSPIRO(INDOLINE 3,3' PIPERIDIN) 2 ONE; 2 OXOTRYPTAMINE; 2' ETHYL 2' METHYLSPIRO(INDOLINE 3,3' PYRROLIDIN) 2 ONE; 2' PHENYLSPIRO(INDOLINE 3,3' PIPERIDIN) 2 ONE; 2',2' DIMETHYLSPIRO(INDOLINE 3,3' PIPERIDIN) 2 ONE; ACETONE; INDOLE DERIVATIVE; KETONE DERIVATIVE; PYRROLIDINE DERIVATIVE; SPIRO COMPOUND; TRYPTAMINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0036881621     PISSN: 00100765     EISSN: None     Source Type: Journal    
DOI: 10.1135/cccc20021669     Document Type: Article
Times cited : (7)

References (18)
  • 6
    • 37049047869 scopus 로고
    • Intramolecular cyclization of 2-oxotryptamine with aldehydes resulting in a diastereomeric mixture of 2′-substituted spiro[indoline-3,3′-pyrrolidin]-2-ones via method A is widely used; the method was frequently utilized for the synthesis of various oxindole alkaloids (e.g. in the aspidosperma and strichnos series) published in the following references: a) Harley-Mason J., Ingleby R. F. J.: J. Chem. Soc. 1958, 3639;
    • (1958) J. Chem. Soc. , pp. 3639
    • Harley-Mason, J.1    Ingleby, R.F.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.