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Volumn 47, Issue 42, 2006, Pages 7435-7438

Total synthesis of (-)-clavosolide A

Author keywords

2 Methyl 1,3 diol; Clavosolide A; Clavosolides; Diolide; Epoxide opening

Indexed keywords

CLAVOSOLIDE A; NATURAL PRODUCT; RADICAL; TETRAHYDROPYRAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33748434886     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.08.055     Document Type: Article
Times cited : (20)

References (30)
  • 3
    • 33344462675 scopus 로고    scopus 로고
    • For total syntheses of the first reported structure of clavosolide A see:
    • For total syntheses of the first reported structure of clavosolide A see:. Chakraborty T.K., and Reddy V.R. Tetrahedron Lett. 47 (2006) 2099-2102
    • (2006) Tetrahedron Lett. , vol.47 , pp. 2099-2102
    • Chakraborty, T.K.1    Reddy, V.R.2
  • 25
    • 33748425339 scopus 로고    scopus 로고
    • Under standard Yamaguchi reaction conditions (Ref. 14), in which DMAP was added to a solution of 14 and 2,4,6-trichlorobenzoyl chloride in toluene, the cyclic tetramer was formed as the major product.
  • 26
    • 33748418968 scopus 로고    scopus 로고
    • The hydroxy acid, obtained by selective deprotection of the C9-OTES of 11, under normal Yamaguchi reaction conditions gave a mixture of intramolecularly cyclized monomer, the diolide dimer and also the triolide.
  • 30
    • 33748418231 scopus 로고    scopus 로고
    • note
    • 16Na requires 879.4718.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.