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Volumn 9, Issue 16, 2007, Pages 3153-3156

Double conjugate addition of a nitropropionate ester to a quinone monoketal: Synthesis of an advanced intermediate to (±)-gelsemine

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; BENZOQUINONE; BENZOQUINONE DERIVATIVE; ETHYL 3 NITROPROPIONATE; ETHYL 3-NITROPROPIONATE; GELSEMINE; LITHIUM; NITRO DERIVATIVE; PROPIONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34547958616     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol071174p     Document Type: Article
Times cited : (27)

References (20)
  • 17
    • 0002654419 scopus 로고    scopus 로고
    • Intramolecular Heck reactions in Natural Product Chemistry
    • For a review of Heck reactions in total synthesis, see:, Diederich, F, Stang, P, Eds, Wiley-VCH: New York
    • (a) For a review of Heck reactions in total synthesis, see: Link, J. T.; Overman, L. E. Intramolecular Heck reactions in Natural Product Chemistry. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F., Stang, P., Eds.; Wiley-VCH: New York, 1998; pp 231-269.
    • (1998) Metal-Catalyzed Cross-Coupling Reactions , pp. 231-269
    • Link, J.T.1    Overman, L.E.2
  • 20
    • 34547950035 scopus 로고    scopus 로고
    • The stereochemistry of the spirooxindoles was determined by NOE spectroscopy for each diastereomer. See the Supporting Information for details
    • The stereochemistry of the spirooxindoles was determined by NOE spectroscopy for each diastereomer. See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.