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Volumn 62, Issue 3, 1997, Pages 578-583

Flow thermolysis rearrangements in the indole alkaloid series: Strictamine and akuammicine derivatives. The absolute configurations of ngouniensine and epi-ngouniensine

Author keywords

[No Author keywords available]

Indexed keywords

AKUAMMICINE; EPINGOUNIENSINE; INDOLE ALKALOID; NGOUNIENSINE; STRICTAMINE; UNCLASSIFIED DRUG;

EID: 0031029397     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo961816e     Document Type: Article
Times cited : (24)

References (31)
  • 18
    • 0016383518 scopus 로고
    • Scott, A. I.; Yeh, C. L. J. Am. Chem. Soc. 1974, 96, 2273-74. The authors postulated the ionic intermediate i, which seems more prone to cyclization to ii (ngouniensine skeleton) or to the anilinoacrylic ester iii than to reversal to the akuammicine skeleton. Most probably the reaction proceeds through the thermally produced nonionic intermediate iv. Chemical equation presented.
    • (1974) J. Am. Chem. Soc. , vol.96 , pp. 2273-2274
    • Scott, A.I.1    Yeh, C.L.2
  • 19
    • 8044259941 scopus 로고    scopus 로고
    • note
    • 2c
  • 29
    • 0345311216 scopus 로고
    • HMQC/HMBC: heteronuclear multiple quantum/multiple bond correlation
    • Bax, A.; Summers, M. F. J. Am. Chem. Soc. 1986, 108, 2093 (HMQC/HMBC: heteronuclear multiple quantum/multiple bond correlation).
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 2093
    • Bax, A.1    Summers, M.F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.