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Volumn 10, Issue 2, 2008, Pages 349-352

Stereospecific and stereoselective alkyl and silylcyclopropanation of α,β-unsaturated amides

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; CHLORIDE; CHROMIUM CHLORIDE; CHROMIUM DERIVATIVE; CYCLOPROPANE DERIVATIVE; SILANE DERIVATIVE;

EID: 38749097420     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702876r     Document Type: Article
Times cited : (14)

References (33)
  • 1
    • 0004258370 scopus 로고
    • Patai, S, Rappoport, Z, Eds, John Wiley and Sons, New York
    • Patai, S., Rappoport, Z., Eds. The Chemistry of the Cyclopropyl Group; John Wiley and Sons, New York, 1987.
    • (1987) The Chemistry of the Cyclopropyl Group
  • 8
    • 0000470204 scopus 로고
    • Biochemistry of the Cyclopropyl Group
    • Patai, S, Rappoport, Z, Eds, John Wiley and Sons: New York, Chapter 16, pp
    • (g) Liu, H. W.; Walsh, C. T. Biochemistry of the Cyclopropyl Group. In The Chemistry of the Cyclopropyl Group; Patai, S., Rappoport, Z., Eds.; John Wiley and Sons: New York, 1987; Chapter 16, pp 959-1025.
    • (1987) The Chemistry of the Cyclopropyl Group , pp. 959-1025
    • Liu, H.W.1    Walsh, C.T.2
  • 26
    • 0035898426 scopus 로고    scopus 로고
    • (E)-α,β-Unsaturated amides 1 were prepared following the methods described in: (a) Concellón, J. M.; Pérez-Andrés, J. A.; Rodríguez-Solla, H. Chem. Eur. J. 2001, 7, 3062-3068.
    • (E)-α,β-Unsaturated amides 1 were prepared following the methods described in: (a) Concellón, J. M.; Pérez-Andrés, J. A.; Rodríguez-Solla, H. Chem. Eur. J. 2001, 7, 3062-3068.
  • 28
    • 38749124293 scopus 로고    scopus 로고
    • In the case of compound 3b although dr, 95/5 the reaction was also completely stereoselective since the E/Z ratio of the starting α,β- unsaturated amide was 95/5
    • In the case of compound 3b although dr = 95/5 the reaction was also completely stereoselective since the E/Z ratio of the starting α,β- unsaturated amide was 95/5.
  • 29
    • 38749109926 scopus 로고    scopus 로고
    • CCDC 630875 contains the supplementary crystallographic data for compound 3e. These data can be obtained free of charge via: www.ccdc.cam.ac.uk/ conts/retrieving.html (or the Cambridge Data Center, 12 Union Road, Cambridge CB21EZ, UK; fax (+44)1223-336-033, or e-mail deposit@ccdc.cam.ac.uk).
    • CCDC 630875 contains the supplementary crystallographic data for compound 3e. These data can be obtained free of charge via: www.ccdc.cam.ac.uk/ conts/retrieving.html (or the Cambridge Data Center, 12 Union Road, Cambridge CB21EZ, UK; fax (+44)1223-336-033, or e-mail deposit@ccdc.cam.ac.uk).
  • 30
    • 38749128642 scopus 로고    scopus 로고
    • (Z)-N,N-Dimethyloct-2-enamide was obtained from the catalytic Lindlar's hydrogenation of N,N-dimethyloct-2-inamide.
    • (Z)-N,N-Dimethyloct-2-enamide was obtained from the catalytic Lindlar's hydrogenation of N,N-dimethyloct-2-inamide.
  • 31
    • 38749112470 scopus 로고    scopus 로고
    • The use of diamines, TMEDA or TEEDA, was necessary to carry out the silylcyclopropanation described in reference 6.
    • The use of diamines, TMEDA or TEEDA, was necessary to carry out the silylcyclopropanation described in reference 6.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.