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Volumn 49, Issue 20, 2008, Pages 3335-3340

An expeditious and environmentally benign methodology for the synthesis of substituted indoles from cyclic enol ethers and enol lactones

Author keywords

Aryl hydrazine; Cyclic enol ether; Indole; Montmorillonite K 10

Indexed keywords

3 (1H INDOL 3 YL)PROPAN 1 OL; CYCLIC ACYL HYDRAZONE; ETHER DERIVATIVE; HYDRAZINE DERIVATIVE; INDOLE DERIVATIVE; LACTONE DERIVATIVE; MONTMORILLONITE; N BENZYL 2 METHYLINDOLE ACETIC ACID; UNCLASSIFIED DRUG;

EID: 42149187557     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.02.107     Document Type: Article
Times cited : (13)

References (26)
  • 23
    • 0034940147 scopus 로고    scopus 로고
    • This is a commonly observed intermediate when the N-acylhydrazone forms a six-membered heterocycle:
    • This is a commonly observed intermediate when the N-acylhydrazone forms a six-membered heterocycle:. Gouault N., Cupif J.F., Picard S., Lecat A., and David M. J. Pharm. Pharmacol. 53 (2001) 981
    • (2001) J. Pharm. Pharmacol. , vol.53 , pp. 981
    • Gouault, N.1    Cupif, J.F.2    Picard, S.3    Lecat, A.4    David, M.5
  • 25
    • 0004180734 scopus 로고
    • Wiley, New York p 470 Collect
    • Woods G.F. Organic Syntheses vol. 3 (1955), Wiley, New York p 470 Collect
    • (1955) Organic Syntheses , vol.3
    • Woods, G.F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.