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Volumn 11, Issue 14, 2009, Pages 3160-3162

A chemoenzymatic total synthesis of (+)-amabiline

Author keywords

[No Author keywords available]

Indexed keywords

AMABILINE; AMARYLLIDACEAE ALKALOID; CRININE;

EID: 67650296165     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901230w     Document Type: Article
Times cited : (37)

References (18)
  • 1
    • 77957033352 scopus 로고
    • For reviews on the crinine alkaloids see: a, Brossi, A, Ed, Academic Press: San Diego
    • For reviews on the crinine alkaloids see: (a) Martin, S. F. In The Alkaloids; Brossi, A., Ed.; Academic Press: San Diego, 1987; Vol. 30, p 251.
    • (1987) The Alkaloids , vol.30 , pp. 251
    • Martin, S.F.1
  • 2
    • 77956708370 scopus 로고    scopus 로고
    • Cordell, G. A, Ed, Academic Press: San Diego
    • (b) Hoshino, O. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: San Diego, 1998; Vol. 51, p 323.
    • (1998) The Alkaloids , vol.51 , pp. 323
    • Hoshino, O.1
  • 7
    • 84984088671 scopus 로고
    • Muxfeldt and co-workers employed this reaction in developing the first total synthesis of (±)-crinine
    • (a) Wick, A. E.; Felix, D.; Steen, K.; Eschenmoser, A. Helv. Chim. Acta 1964, 47, 2425. Muxfeldt and co-workers employed this reaction in developing the first total synthesis of (±)-crinine:
    • (1964) Helv. Chim. Acta , vol.47 , pp. 2425
    • Wick, A.E.1    Felix, D.2    Steen, K.3    Eschenmoser, A.4
  • 9
    • 0001846314 scopus 로고    scopus 로고
    • Compound 3 can be obtained from the Aldrich Chemical Co. (Catalogue Number 489492) or from Questor, Queen's University of Belfast, Northern Ireland (http://questor.qub.ac.uk/newsite/contact.htm). For reviews on methods for generating cis-l,2-dihydrocatechols by microbial dihydroxylation of the corresponding aromatics, as well as the synthetic applications of these metabolites, see: (a) Hudlicky, T.; Gonzalez, D.; Gibson, D. T. Aldrichim. Acta 1999, 32, 35.
    • Compound 3 can be obtained from the Aldrich Chemical Co. (Catalogue Number 489492) or from Questor, Queen's University of Belfast, Northern Ireland (http://questor.qub.ac.uk/newsite/contact.htm). For reviews on methods for generating cis-l,2-dihydrocatechols by microbial dihydroxylation of the corresponding aromatics, as well as the synthetic applications of these metabolites, see: (a) Hudlicky, T.; Gonzalez, D.; Gibson, D. T. Aldrichim. Acta 1999, 32, 35.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.