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Volumn 45, Issue 34, 2004, Pages 6509-6512

Synthesis of the diazatricyclic core of the marine alkaloids madangamines

Author keywords

Alkaloid; Cyclization; Madangamine; Michael reaction; N,O acetalization

Indexed keywords

ALKALOID DERIVATIVE; AMINE; ANTINEOPLASTIC AGENT;

EID: 4143116649     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.06.103     Document Type: Article
Times cited : (30)

References (16)
  • 11
    • 4143138136 scopus 로고    scopus 로고
    • note
    • The cis stereochemistry of the major adduct 11 was established by X-ray crystallographic analysis of ii derived from 13 as shown below
  • 12
    • 4143063101 scopus 로고    scopus 로고
    • note
    • 4 couplig constant (J = 10.0 Hz) for both diastereomers
  • 13
    • 4143123879 scopus 로고    scopus 로고
    • note
    • Preliminary studies using the ketal-protected amino ketone iii lacking the o-hydroxybenzyl substitution at nitrogen indicated that deprotection followed by exposure to reductive amination conditions did not result in cyclization to the expected azabicyclo skeleton iv, but instead gave a complex mixture
  • 16
    • 4143086509 scopus 로고    scopus 로고
    • note
    • 2), 127.3 (CH), 127.4 (CH), 127.6 (2 carbons, CH), 127.7 (2 carbons, CH), 127.8 (2 carbons, CH), 127.9 (2 carbons, CH), 128.3 (2 carbons, CH), 128.4 (3 carbons, CH), 136.8 (C), 136.9 (C), 138.1 (C), 156.2 (2 carbons, C)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.