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Volumn 2, Issue 6, 2000, Pages 855-857

Addition of metallo enolates to chiral 1-acylpyridinium salts: Total synthesis of (+)-cannabisativine

Author keywords

[No Author keywords available]

Indexed keywords

CANNABINOID; CANNABISATIVINE; ORGANOMETALLIC COMPOUND; PYRIDINIUM DERIVATIVE;

EID: 0034704647     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0056271     Document Type: Article
Times cited : (66)

References (19)
  • 8
    • 0042330530 scopus 로고    scopus 로고
    • The yield is of diastereomerically pure 4 isolated by radial preparative layer chromatography. The reaction proceeded in >95% de; see ref 4
    • The yield is of diastereomerically pure 4 isolated by radial preparative layer chromatography. The reaction proceeded in >95% de; see ref 4.
  • 11
    • 0041328988 scopus 로고    scopus 로고
    • This highly stereoselective reduction is likely a result of a chelation-controlled addition mechanism
    • This highly stereoselective reduction is likely a result of a chelation-controlled addition mechanism.
  • 16
    • 84970550124 scopus 로고
    • The 1-methoxy-1-trimethylsiloxyethene (13) was prepared by a literature procedure: Collins, D. J.; Cullen, J. D. Aust. J. Chem. 1988, 41, 735.
    • (1988) Aust. J. Chem. , vol.41 , pp. 735
    • Collins, D.J.1    Cullen, J.D.2
  • 18
    • 0041829528 scopus 로고    scopus 로고
    • The corresponding secondary amide suffers significant hydrolysis under these conditions
    • The corresponding secondary amide suffers significant hydrolysis under these conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.