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Volumn 62, Issue 49, 2006, Pages 11499-11505

A general organic catalyst for asymmetric addition of stabilized nucleophiles to acyl imines

Author keywords

Aza Henry reaction; Cinchona alkaloids; Imines; Mannich reaction; Organic catalysis; Thiourea

Indexed keywords

AMINE; CINCHONA ALKALOID; DIMETHYLMALONATE; ESTER DERIVATIVE; HYDROQUININE; IMINE; MALONIC ACID DERIVATIVE; NITROALKANE; THIOUREA; UNCLASSIFIED DRUG;

EID: 33750463431     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.07.071     Document Type: Article
Times cited : (99)

References (75)
  • 30
    • 33750475735 scopus 로고    scopus 로고
    • For catalytic Mannich, see:
  • 36
    • 0037438599 scopus 로고    scopus 로고
    • for organocatalytic Mannich, see:
    • Trost B.M., and Terrell L.M. J. Am. Chem. Soc. 125 (2003) 4712-4713 for organocatalytic Mannich, see:
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 4712-4713
    • Trost, B.M.1    Terrell, L.M.2
  • 38
    • 33750459520 scopus 로고    scopus 로고
    • For nitro-Mannich, see:
  • 53
    • 33750463883 scopus 로고    scopus 로고
    • See Ref. 7g;
  • 65
    • 33750486961 scopus 로고    scopus 로고
    • See Ref. 14c.
  • 67
    • 33750463554 scopus 로고    scopus 로고
    • note
    • 15 for absolute configuration determination. Comparison of optical rotation data assigns the absolute configuration of our β-nitroamine adducts as (1S,2R).{A figure is presented}
  • 68
    • 33750446482 scopus 로고    scopus 로고
    • Molecular Operating Environment 2004.03, MOE, Chemical Computing Group: Montreal, Quebec, Canada.
  • 70
    • 33750468802 scopus 로고    scopus 로고
    • Similar models have been proposed for diastereoselective β-keto ester additions to nitroolefins, see:
  • 73
    • 33750475009 scopus 로고    scopus 로고
    • For conformational studies of cinchona alkaloid catalyzed reactions, see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.