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Volumn 44, Issue 13, 1988, Pages 4073-4086

A highly efficient kinetic resolution of γ- and β- trimethylsilyl secondary allylic alcohols by the sharpless asymmetric epoxidation

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Indexed keywords


EID: 0000449963     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)86657-6     Document Type: Article
Times cited : (94)

References (36)
  • 15
    • 0000801515 scopus 로고
    • STEREOSPECIFIC REDUCTION OF PROPARGYL ALCOHOLS: (E)-3-TRIMETHYLSILYL-2-PROPEN-1-OL
    • (1986) Organic Syntheses , vol.64 , pp. 182
    • Jones1    Denmark2
  • 19
    • 84918148044 scopus 로고    scopus 로고
    • For determination of the absolute configuration of optically active 1; ref 9a for (R)-1a, ref 7 for (S)-1e, ref 14 for (S)-1f and (R)-1h, and ref 6 for (R)-1g and (S)-1i.
  • 21
    • 84918148043 scopus 로고    scopus 로고
    • In the case of entries 4 and 6, shorter reaction times must afford both the epoxy alcohol and the allylic alcohol with 〉62;99% e.e., respectively.
  • 24
    • 0006258302 scopus 로고
    • General method to transform chiral 2,3-epoxyalcohols into erythro or threo 1,2-epoxyalcohols with total stereochemical control
    • (1986) Tetrahedron Letters , vol.27 , pp. 4987
    • Palazón1    Martin2
  • 33
    • 84918148042 scopus 로고    scopus 로고
    • Since (R)-3b and 4b themselves were difficult to seperate effectively, they were converted into their acetates and separated by column chromatography on silica gel (see Experimental).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.