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Volumn 8, Issue 17, 2006, Pages 3689-3692

Total syntheses of (±)-β-erythroidine and (±)-8-oxo- β-erythroidine by an intramolecular Diels-Alder cycloaddition of a 2-amidoacrolein

Author keywords

[No Author keywords available]

Indexed keywords

2 AMIDOACROLEIN; 2-AMIDOACROLEIN; 8 OXO BETA ERYTHROIDINE; 8-OXO-BETA-ERYTHROIDINE; ACROLEIN; BETA ERYTHROIDINE; BETA-ERYTHROIDINE; DIHYDRO BETA ERYTHROIDINE; DRUG DERIVATIVE;

EID: 33748596356     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol061267r     Document Type: Article
Times cited : (25)

References (33)
  • 1
    • 77956830705 scopus 로고    scopus 로고
    • Cordell, G. A., Ed.; Academic Press: San Diego, CA
    • Tsuda, Y.; Sano, T. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: San Diego, CA, 1996; Vol. 48, p 249.
    • (1996) The Alkaloids , vol.48 , pp. 249
    • Tsuda, Y.1    Sano, T.2
  • 2
    • 33644780699 scopus 로고    scopus 로고
    • For very recent work, see: (a) Wang, Q.; Padwa, A. Org. Lett. 2006, 8, 601.
    • (2006) Org. Lett. , vol.8 , pp. 601
    • Wang, Q.1    Padwa, A.2
  • 10
    • 0002696069 scopus 로고
    • Rodrigo, R. G. A., Ed.; Academic Press: New York.
    • Dyke, S. F.; Quessy, S. N. In The Alkaloids; Rodrigo, R. G. A., Ed.; Academic Press: New York. 1981; Vol. 18, p 1.
    • (1981) The Alkaloids , vol.18 , pp. 1
    • Dyke, S.F.1    Quessy, S.N.2
  • 24
    • 85069766353 scopus 로고
    • Amine 10 was prepared in four steps and 56% overall yield from 3-butyn-1-ol, see: (a) Cousseau, J. Synthesis 1980, 805.
    • (1980) Synthesis , pp. 805
    • Cousseau, J.1
  • 29
    • 33748612826 scopus 로고    scopus 로고
    • note
    • In an initial investigation, we had found that the methoxy substituent could not be introduced at the outset of the total synthesis due, in part, to a competitive hetero Diels-Alder cycloaddition reaction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.