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Volumn , Issue 47, 2008, Pages 6315-6317

Asymmetric organocatalytic Michael addition of ketones to vinyl sulfone

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; CINCHONA ALKALOID; CYCLAMATE SODIUM; KETONE DERIVATIVE; ORGANIC COMPOUND; SULFONE DERIVATIVE; VINYL DERIVATIVE;

EID: 57249104995     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b816307c     Document Type: Article
Times cited : (108)

References (37)
  • 2
    • 0000036801 scopus 로고
    • For examples of non-stereoselective Michael additions to vinyl sulfones, see:
    • N. S. Simpkins Tetrahedron 1990 46 6951
    • (1990) Tetrahedron , vol.46 , pp. 6951
    • Simpkins, N.S.1
  • 34
    • 57249089841 scopus 로고    scopus 로고
    • See supporting information for the details
    • See supporting information for the details
  • 35
    • 57249112982 scopus 로고    scopus 로고
    • When 3-pentanone was used as the donor, the yield of the reaction was below 30%. The Michael reaction of O-benzyl-hydroxyacetone with vinyl sulfone gave the adduct in 61% yield and with only 27% ee
    • When 3-pentanone was used as the donor, the yield of the reaction was below 30%. The Michael reaction of O-benzyl-hydroxyacetone with vinyl sulfone gave the adduct in 61% yield and with only 27% ee


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.