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Volumn 134, Issue 44, 2012, Pages 18209-18212

Asymmetric approach toward chiral cyclohex-2-enones from anisoles via an enantioselective isomerization by a new chiral diamine catalyst

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC INDUCTION; ASYMMETRIC TRANSFORMATIONS; CHIRAL DIAMINE; ELECTRONICALLY TUNABLE; ENANTIOSELECTIVE; ENANTIOSELECTIVE TOTAL SYNTHESIS; OPTICALLY ACTIVE; ORGANIC CATALYSTS; SYNTHETIC UTILITY;

EID: 84868548661     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja308623n     Document Type: Article
Times cited : (50)

References (69)
  • 31
    • 0004290301 scopus 로고
    • Patai, S. Rappoport, Z. Johns Wiley and Sons; Chichester, Chapter 13
    • Pollack, R. M.; Bounds, P. L.; Bevins, C. L. In The Chemistry of Enones; Patai, S.; Rappoport, Z., Eds.; Johns Wiley and Sons; Chichester, 1989; Chapter 13.
    • (1989) The Chemistry of Enones
    • Pollack, R.M.1    Bounds, P.L.2    Bevins, C.L.3
  • 47
    • 0025318913 scopus 로고
    • a of the α proton of cyclohex-3-enone in water was determined to be 15.2
    • a of the α proton of cyclohex-3-enone in water was determined to be 15.2: Dzingeleski, G. D.; Blotny, G.; Pollack, R. M. J. Org. Chem. 1990, 55, 1019
    • (1990) J. Org. Chem. , vol.55 , pp. 1019
    • Dzingeleski, G.D.1    Blotny, G.2    Pollack, R.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.