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Volumn 349, Issue 17-18, 2007, Pages 2537-2548

Density functional theory study of the Cinchona thiourea-catalyzed Henry reaction: Mechanism and enantioselectivity

Author keywords

Cinchona alkaloids; Density functional theory; Enantioselectivity; Nitroaldol reaction; Organocatalysis

Indexed keywords


EID: 37349098707     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200700367     Document Type: Article
Times cited : (98)

References (55)
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    • For recent reviews on the asymmetric Henry reaction, see: a
    • For recent reviews on the asymmetric Henry reaction, see: a) C. Palomo, M. Oiarbide, A. Laso. Eur. J. Org. Chem. 2007, 2561-2574;
    • (2007) Eur. J. Org. Chem , pp. 2561-2574
    • Palomo, C.1    Oiarbide, M.2    Laso, A.3
  • 8
    • 0028129271 scopus 로고    scopus 로고
    • For early studies (with enantiomeric excesses not exceeding 52%), see: a) R. Chinchilla, C. Najera, P. Sanchez-Agullo, Tetrahedron: Asymmetry 1994, 5, 1393-1402;
    • For early studies (with enantiomeric excesses not exceeding 52%), see: a) R. Chinchilla, C. Najera, P. Sanchez-Agullo, Tetrahedron: Asymmetry 1994, 5, 1393-1402;
  • 13
    • 33746277515 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: a) S. J. Connon, Chem. Eur. J. 2006, 12, 5418-5427;
    • (2006) Chem. Eur. J , vol.12 , pp. 5418-5427
    • Connon, S.J.1
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    • 6044269452 scopus 로고    scopus 로고
    • For general reviews, see: a
    • For general reviews, see: a) P. I. Dalko, L. Moisan, Angew. Chem. Int. Ed. 2004, 43, 5138-5175;
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 5138-5175
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    • special issue of Acc. Chem. Res. 2004, 37, issue 8;
    • d) special issue of Acc. Chem. Res. 2004, 37, issue 8;
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    • Ed, P. I. Dalko, Wiley-VCH, Weinheim
    • f) Enantioselective Organocatalysis, (Ed.: P. I. Dalko), Wiley-VCH, Weinheim, 2007.
    • (2007) Enantioselective Organocatalysis
  • 28
    • 0345868508 scopus 로고    scopus 로고
    • Computational analyses of asymmetric heterogenous hydrogenation employing Cinchona alkaloids as surface modifiers are, on the other hand, more abundant. For recent examples, see: a J. Vayner, K. N. Houk, Y. K. Sun, J. Am. Chem. Soc. 2004, 126, 199-203;
    • Computational analyses of asymmetric heterogenous hydrogenation employing Cinchona alkaloids as surface modifiers are, on the other hand, more abundant. For recent examples, see: a) J. Vayner, K. N. Houk, Y. K. Sun, J. Am. Chem. Soc. 2004, 126, 199-203;
  • 31
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    • a values in DMSO, see: http://www.chem.wisc.edu/areas/reich/pKatable/index.htm, and cited references therein.
    • a values in DMSO, see: http://www.chem.wisc.edu/areas/reich/pKatable/index.htm, and cited references therein.
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    • and references cited therein
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    • Gutmann, V.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.