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Volumn 64, Issue 13, 1999, Pages 4830-4833

Regioselective synthesis of isoquino[1,2-b][3]benzazepines (homoprotoberberines) through 11-membered-ring stilbene lactams obtained by radical macrocyclization

Author keywords

[No Author keywords available]

Indexed keywords

BENZAZEPINE DERIVATIVE; BERBERINE DERIVATIVE; HOMOPROTOBERBERINE; ISOQUINO[1,2 B][3]BENZAZEPINE; LACTAM; STILBENE; UNCLASSIFIED DRUG;

EID: 0345189471     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9901900     Document Type: Article
Times cited : (23)

References (24)
  • 13
    • 0008160297 scopus 로고
    • 2-Iodophenylacetic acid was prepared by a modification of the published procedure: Dippy, F. J.; Lewis, R. H. J. Chem. Soc. 1936, 644-649.
    • (1936) J. Chem. Soc. , pp. 644-649
    • Dippy, F.J.1    Lewis, R.H.2
  • 15
    • 0345675927 scopus 로고    scopus 로고
    • note
    • The assignment of the geometry of the silylated stilbene lactams is based on NOE studies.
  • 16
    • 0344813098 scopus 로고    scopus 로고
    • note
    • The formation of desilylated product is rationalized by invoking the amidate and further iminosilyl ether formation due to the singular spatial disposition of both groups. Final hydrolytic workup recovers the amide functionality.
  • 18


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.