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Volumn 65, Issue 21, 2009, Pages 4124-4129

Highly enantioselective conjugate addition of 1-bromonitroalkanes to α,β-unsaturated ketones catalyzed by 9-amino-9-deoxyepiquinine

Author keywords

, Unsaturated ketone; 1 Bromonitroalkane; 9 Amino 9 deoxyepiquinine; Conjugate addition; Organocatalysis

Indexed keywords

1 BROMONITROALKANE; 9 AMINO 9 DEOXYPIQUININE; ALPHA,BETA KETONE; AMINE; KETONE; NITROALKANE; UNCLASSIFIED DRUG;

EID: 64649093783     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.03.055     Document Type: Article
Times cited : (35)

References (51)
  • 1
    • 64649088796 scopus 로고    scopus 로고
    • For the general reviews on asymmetric organocatalysis, see
    • For the general reviews on asymmetric organocatalysis, see:
  • 5
    • 38349142750 scopus 로고    scopus 로고
    • The special issue devoted to:. List B. (Ed)
    • The special issue devoted to:. In: List B. (Ed). Asymmetric Organocatalysis. Chem. Rev. 107 (2007) 5413
    • (2007) Chem. Rev. , vol.107 , pp. 5413
  • 7
    • 64649086639 scopus 로고    scopus 로고
    • For the reviews on the activation of α,β-unsaturated aldehydes and ketones with chiral secondary amines, see
    • For the reviews on the activation of α,β-unsaturated aldehydes and ketones with chiral secondary amines, see:
  • 12
    • 64649091998 scopus 로고    scopus 로고
    • For the reviews of primary amine catalysts, see
    • For the reviews of primary amine catalysts, see:
  • 31
    • 64649095373 scopus 로고    scopus 로고
    • For the selected examples of asymmetric catalysis by primary amines derived from cinchona alkaloids, see
    • For the selected examples of asymmetric catalysis by primary amines derived from cinchona alkaloids, see:
  • 50
    • 64649102771 scopus 로고    scopus 로고
    • note
    • 13C NMR data were obtained by analyzing the NMR spectra of the mixtures. However, IR and MS spectroscopic data could not be assigned individually for them.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.