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Volumn 52, Issue 11, 1996, Pages 3905-3920

Chiral bipyrindine and biquinoline ligands: Their asymmetric synthesis and application to the synthesis of trans-whisky lactone

Author keywords

[No Author keywords available]

Indexed keywords

2,2' BIPYRIDINE DERIVATIVE; FURANONE DERIVATIVE; LACTONE DERIVATIVE; UNCLASSIFIED DRUG; WHISKEY LACTONE;

EID: 0030012272     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(96)00058-0     Document Type: Article
Times cited : (89)

References (38)
  • 30
    • 0001001461 scopus 로고
    • Syntheses using catalytic asymmetric epoxidation or kinetic resolution with esterase as a step for the introduction of chirality, have been reported: a) Bloch, R.; Gilbert, L. J. Org. Chem. 1987, 52, 4603-4605.
    • (1987) J. Org. Chem. , vol.52 , pp. 4603-4605
    • Bloch, R.1    Gilbert, L.2
  • 37
    • 85030196077 scopus 로고    scopus 로고
    • note
    • Differing from the original Lemieux-Johnson method, potassium osmate and periodic acid were used instead of osmium tetroxide and sodium periodate (see experimental section).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.