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Volumn 72, Issue 24, 2007, Pages 9181-9189

Diastereoselective Michael initiated ring closure on vinyl sulfone-modified carbohydrates: A stereospecific and general route to α-substituted cyclopropanes

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANATED CARBOHYDRATES; DIASTEREOSELECTIVE MICHAEL; RING CLOSURE;

EID: 36649028269     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo701378d     Document Type: Article
Times cited : (26)

References (28)
  • 7
    • 36649025175 scopus 로고    scopus 로고
    • This type of reaction using 3-halo-1-alkenylsulfones was rarely studied, see: (a) Ogura, K, Iihama, T, Takahashi, K, Iida, H. Bull. Chem. Soc. Jpn. 1984, 57, 3347
    • This type of reaction using 3-halo-1-alkenylsulfones was rarely studied, see: (a) Ogura, K.; Iihama, T.; Takahashi, K.; Iida, H. Bull. Chem. Soc. Jpn. 1984, 57, 3347.
  • 28
    • 36649014401 scopus 로고    scopus 로고
    • Schemes 8 and 9 represent a non-Michael addition approach to the synthesis of cyclopropanated carbohydrates containing an electron withdrawing group at C-3 of pentofuranosides, at is less efficient through Michael addition to vinyl sulfone-modified carbohydrates
    • Schemes 8 and 9 represent a non-Michael addition approach to the synthesis of cyclopropanated carbohydrates containing an electron withdrawing group at C-3 of pentofuranosides. This strategy may be explored when the introduction of a group at C-2 is less efficient through Michael addition to vinyl sulfone-modified carbohydrates.
    • This strategy may be explored when the introduction of a group


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.