메뉴 건너뛰기




Volumn 65, Issue 20, 2009, Pages 4007-4012

Total synthesis and confirmation of the absolute stereochemistry of semiviriditoxin, a naphthopyranone metabolite from the fungus Paecilomyces variotii

Author keywords

[No Author keywords available]

Indexed keywords

MYCOTOXIN; SEMIVIRIDITOXIN; UNCLASSIFIED DRUG;

EID: 64249126688     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.03.016     Document Type: Article
Times cited : (30)

References (21)
  • 18
    • 84981786018 scopus 로고
    • The addition of alcohols to α,β-acetylenic esters is known to lead predominantly to the Z-isomer:
    • The addition of alcohols to α,β-acetylenic esters is known to lead predominantly to the Z-isomer:. Winterfeldt E. Angew. Chem., Int. Ed. Engl. 6 (1967) 423-434
    • (1967) Angew. Chem., Int. Ed. Engl. , vol.6 , pp. 423-434
    • Winterfeldt, E.1
  • 21
    • 64249092849 scopus 로고    scopus 로고
    • note
    • Although 2 and 3 possess different descriptors, (S) and (R), respectively, they are stereochemically analogous and would therefore be expected to exhibit similar Cotton effects in their circular dichroism spectra.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.