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Volumn 56, Issue 40, 2000, Pages 7859-7868

An unusual reversal of stereoselectivity in a boron mediated aldol reaction: Enantioselective synthesis of the C1-C6 segment of the epothilones

Author keywords

Aldol reaction; Enantioselectivity; Epothilones

Indexed keywords

2 (2,2 DIMETHYL 1,3 DIOXAN 4 YL) 2 METHYLPENTAN 3 ONE; 3 HYDROXY 4,4 DIMETHYL 5 OXOHEPTANOIC ACID; 7 [1,1 BIS(METHYLETHYL) 2 METHYL 1 SILAPROPOXY] 5 HYDROXY 4,4 DIMETHYLHEPTAN 3 ONE; EPOTHILONE A; EPOTHILONE B; HEPTANOIC ACID DERIVATIVE; MACROLIDE; UNCLASSIFIED DRUG;

EID: 0034730533     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00708-0     Document Type: Article
Times cited : (12)

References (33)
  • 25
    • 0007859655 scopus 로고    scopus 로고
    • 1H NMR spectra of the product mixture. The absolute stereochemistry of the aldol adducts were deduced by hydrolyzing the adducts to the corresponding hydroxy acids
  • 31
    • 0007817279 scopus 로고    scopus 로고
    • Structures of these isomers were determined by X-ray crystallography and by converting them to the compounds 16 and 17 by desulfurization with Raney Ni


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.