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Volumn 127, Issue 39, 2005, Pages 13496-13497

Total synthesis of (+)-lithospermic acid by asymmetric intramolecular alkylation via catalytic C-H bond activation

Author keywords

[No Author keywords available]

Indexed keywords

ACID; ALCOHOL; ALDEHYDE; CARBON; CINNAMIC ACID; DIHYDROBENZOFURAN DERIVATIVE; ESTER; FORMIC ACID DERIVATIVE; HYDROGEN; IMINE; INTEGRASE INHIBITOR; ISOVANILLIN; LITHOSPERMIC ACID; METHANOL; METHYL GROUP; METHYLCHLOROFORMATE; PYRIDINE; RHODIUM; ROSMARINIC ACID; SOLVENT; UNCLASSIFIED DRUG;

EID: 25844469333     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja052680h     Document Type: Article
Times cited : (192)

References (21)
  • 11
    • 25844446321 scopus 로고    scopus 로고
    • note
    • For use of our method to the synthesis of a drug candidate, see 3b.
  • 12
    • 0037418795 scopus 로고    scopus 로고
    • For other examples of total syntheses using C-H activation, see: (a) Davies, H. M. L.; Jin, Q. Tetrahedron: Asymmetry 2003, 14, 941-949.
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 941-949
    • Davies, H.M.L.1    Jin, Q.2
  • 19
    • 25844439772 scopus 로고    scopus 로고
    • note
    • Cyclization of (E)-9, though capable of directly establishing the desired anti relationship in 3, was not thoroughly investigated because it was the minor isomer produced and was found to cyclize less efficiently.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.