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Volumn 64, Issue 27, 2008, Pages 6444-6451

Chemoenzymatic approaches to the montanine alkaloids: a total synthesis of (+)-nangustine

Author keywords

[No Author keywords available]

Indexed keywords

1,2 DIHYDROCATECHOL; ALKALOID DERIVATIVE; AMINOCYCLITOL; AROMATIC CARBOXYLIC ACID; CATECHOL DERIVATIVE; CHLOROBENZENE; DIOXYGENASE; MONTANINE ALKALOID DERIVATIVE; NANGUSTINE; PLANT EXTRACT; TOLUENE;

EID: 44349110050     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.04.070     Document Type: Article
Times cited : (32)

References (41)
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    • For reviews dealing with this class of alkaloid see:
    • For reviews dealing with this class of alkaloid see:
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    • Martin S.F. In: Brossi A. (Ed). The Alkaloids Vol. 30 (1987), Academic, San Diego, CA p 251
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    • Martin, S.F.1
  • 6
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    • Cordell G.A. (Ed), Academic, San Diego, CA p 323
    • Hoshino O. In: Cordell G.A. (Ed). The Alkaloids Vol. 51 (1998), Academic, San Diego, CA p 323
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    • Hoshino, O.1
  • 7
    • 0034141667 scopus 로고    scopus 로고
    • and previous reviews in the series
    • Lewis J.R. Nat. Prod. Rep. 17 (2000) 57 and previous reviews in the series
    • (2000) Nat. Prod. Rep. , vol.17 , pp. 57
    • Lewis, J.R.1
  • 18
    • 44349087630 scopus 로고    scopus 로고
    • note
    • Compound 3 can be obtained from the Aldrich Chemical Co. (Catalogue Number 489492) or from Questor, Queen's University of Belfast, Northern Ireland (see http://questor.qub.ac.uk/newsite/contact.htm).
  • 19
    • 44349160137 scopus 로고    scopus 로고
    • For reviews on methods for generating cis-1,2-dihydrocatechols by microbial dihydroxylation of the corresponding aromatics, as well as the synthetic applications of these metabolites, see:
    • For reviews on methods for generating cis-1,2-dihydrocatechols by microbial dihydroxylation of the corresponding aromatics, as well as the synthetic applications of these metabolites, see:
  • 24
    • 0034676584 scopus 로고    scopus 로고
    • For an example of a closely related cleavage process see:
    • For an example of a closely related cleavage process see:. Banwell M.G., and McRae K.J. Org. Lett. 2 (2000) 3583
    • (2000) Org. Lett. , vol.2 , pp. 3583
    • Banwell, M.G.1    McRae, K.J.2
  • 25
    • 44349158413 scopus 로고    scopus 로고
    • For examples of related cleavage processes see:
    • For examples of related cleavage processes see:
  • 26
    • 44349086444 scopus 로고    scopus 로고
    • Ref. 13;
    • Ref. 13;
  • 29
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    • Ref. 18.
    • Ref. 18.
  • 31
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    • For a useful point-of-entry into the literature on the Staudinger reaction see:, Elsevier Academic, Burlington, MA pp 428-429
    • For a useful point-of-entry into the literature on the Staudinger reaction see:. Kürti L., and Czakó B. Strategic Applications of Named Reactions in Organic Synthesis (2005), Elsevier Academic, Burlington, MA pp 428-429
    • (2005) Strategic Applications of Named Reactions in Organic Synthesis
    • Kürti, L.1    Czakó, B.2
  • 33
    • 44349129065 scopus 로고    scopus 로고
    • For related examples of this type of radical reaction see:
    • For related examples of this type of radical reaction see:
  • 39
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    • Processing of X-ray Diffraction Data Collected in Oscillation Mode
    • DENZO-SMN:. Methods in Enzymology. Carter Jr. C.W., and Sweet R.M. (Eds), Academic, New York, NY pp 307-326
    • DENZO-SMN:. Otwinowski Z., and Minor W. Processing of X-ray Diffraction Data Collected in Oscillation Mode. In: Carter Jr. C.W., and Sweet R.M. (Eds). Methods in Enzymology. Macromolecular Crystallography, Part A Vol. 276 (1997), Academic, New York, NY pp 307-326
    • (1997) Macromolecular Crystallography, Part A , vol.276
    • Otwinowski, Z.1    Minor, W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.