메뉴 건너뛰기




Volumn 8, Issue 5, 2002, Pages 632-634

Organocatalytic asymmetric vinylogous addition to quinones - Formation of optically active α-aryl ketones

Author keywords

[No Author keywords available]

Indexed keywords

1,4 DIKETONE; ALPHA KETONE DERIVATIVE; CINCHONA ALKALOID; KETONE DERIVATIVE; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 38349103457     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b716485h     Document Type: Article
Times cited : (12)

References (25)
  • 1
    • 0001644556 scopus 로고    scopus 로고
    • Angew. Chem., Int. Ed. 2001 40 3726
    • P. I. Dalko L. Moisan Angew. Chem. 2001 113 3840 Angew. Chem., Int. Ed. 2001 40 3726
    • (2001) Angew. Chem. , vol.113 , pp. 3840
    • Dalko, P.I.1    Moisan, L.2
  • 3
    • 11144263200 scopus 로고    scopus 로고
    • Angew. Chem., Int. Ed. 2004 43 5138
    • P. I. Dalko L. Moisan Angew. Chem. 2004 116 5248 Angew. Chem., Int. Ed. 2004 43 5138
    • (2004) Angew. Chem. , vol.116 , pp. 5248
    • Dalko, P.I.1    Moisan, L.2
  • 4
    • 33646558310 scopus 로고    scopus 로고
    • (8), special issue on organocatalysis;
    • Acc. Chem. Res., 2004, 37 (8)
    • (2004) Acc. Chem. Res.
  • 12
    • 0003829752 scopus 로고
    • S. Patai and Z. Rapoport, Wiley, New York,. For a review of quinone chemistry see:
    • The Chemistry of the Quinoid Compounds, ed., S. Patai, and, Z. Rapoport,, Wiley, New York, 1988
    • (1988) The Chemistry of the Quinoid Compounds, Ed.
  • 16
    • 36348935166 scopus 로고    scopus 로고
    • Different attempts with 3-pentanone and cyclohexanone have been carried out with the quinone 2a, however in different conditions and with different catalysts no reaction took place. See ESI Tables S1 and S2 Although highly successful direct asymmetric funtionalizations of ketones have been achieved using enamine catalysis, the corresponding functionalization of α-tetralone cannot be carried out
    • K. Bogle D. J. Hirst D. J. Dixon Org. Lett. 2007 9 4901
    • (2007) Org. Lett. , vol.9 , pp. 4901
    • Bogle, K.1    Hirst, D.J.2    Dixon, D.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.