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Volumn , Issue 6, 1995, Pages 671-672

The first synthesis of (±)-cycloolivil: A highly stereoselective synthesis of 3-hydroxy-1-aryltetralin lignans based on the stereoselective hydroxylation of α,β-dibenzyl-γ-butyrolactones

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOOLIVIL; LACTONE DERIVATIVE; LIGNAN DERIVATIVE; TETRALIN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0028905675     PISSN: 00224936     EISSN: None     Source Type: Journal    
DOI: 10.1039/C39950000671     Document Type: Article
Times cited : (5)

References (14)
  • 12
    • 0027073264 scopus 로고
    • We previously reported that the acid-catalysed cyclisation of α'-hydroxydibenzyllactone afforded only one stereoisomer exclusively; the relative stereochemistry between the c-1 and c-2 carbon centres was trans
    • See, ref. 4 and
    • We previously reported that the acid-catalysed cyclisation of α'-hydroxydibenzyllactone afforded only one stereoisomer exclusively; the relative stereochemistry between the C-1 and C-2 carbon centres was trans. See, ref. 4 and T. Ogiku, S. Yoshida, T. Kuroda, M. Takahashi, H. Ohmizu and T. Iwasaki, Bull. Chem. Soc. Jpn., 1992, 65, 3495.
    • (1992) Bull. Chem. Soc. Jpn , vol.65 , pp. 3495
    • Ogiku, T.1    Yoshida, S.2    Kuroda, T.3    Takahashi, M.4    Ohmizu, H.5    Iwasaki, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.