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Volumn 51, Issue 13, 2012, Pages 3236-3239

Lewis base catalyzed enantioselective additions of an N-silyl vinylketene imine

Author keywords

allylic compounds; asymmetric catalysis; enantioselectivity; ketenes; Lewis bases

Indexed keywords

ALLYLIC COMPOUNDS; ASYMMETRIC CATALYSIS; CURRENT LIMITATION; DOUBLE BONDS; ENANTIOSELECTIVE ADDITION; HIGH YIELD; KETENES; LEWIS BASE; LEWIS BASIS; LITHIUM DIISOPROPYLAMIDE; SITE SELECTIVITY; SYNTHETIC EQUIVALENTS; UNSATURATED NITRILES;

EID: 84858754652     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201108795     Document Type: Article
Times cited : (28)

References (31)
  • 6
    • 24044453210 scopus 로고    scopus 로고
    • We are aware of a single example where aliphatic aldehydes are utilized in the copper-catalyzed addition of acetonitrile. Syringe pump addition was used to avoid self-condensation; see
    • We are aware of a single example where aliphatic aldehydes are utilized in the copper-catalyzed addition of acetonitrile. Syringe pump addition was used to avoid self-condensation; see:, Y. Suto, T. Riichiro, M. Kanai, M. Shibasaki, Org. Lett. 2005, 7, 3757-3760.
    • (2005) Org. Lett. , vol.7 , pp. 3757-3760
    • Suto, Y.1    Riichiro, T.2    Kanai, M.3    Shibasaki, M.4
  • 11
    • 23044486219 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4682-4698
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4682-4698
  • 25
    • 50249134990 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 1560-1638.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 1560-1638
  • 27
    • 15744387149 scopus 로고    scopus 로고
    • In the presense of silicon tetrachloride and Lewis base, aliphatic aldehydes form trichlorosilyl chlorohydrins that do not react with enoxysilane nucleophiles, see
    • In the presense of silicon tetrachloride and Lewis base, aliphatic aldehydes form trichlorosilyl chlorohydrins that do not react with enoxysilane nucleophiles, see:, S. E. Denmark, G. L. Beutner, T. Wynn, M. D. Eastgate, J. Am. Chem. Soc. 2005, 127, 3774-3789.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 3774-3789
    • Denmark, S.E.1    Beutner, G.L.2    Wynn, T.3    Eastgate, M.D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.