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Volumn 14, Issue 21, 2012, Pages 5590-5593

Direct catalytic enantioselective vinylogous aldol reaction of α-branched enals with isatins

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EID: 84868352757     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol302711w     Document Type: Article
Times cited : (101)

References (31)
  • 27
    • 33749527371 scopus 로고    scopus 로고
    • An analog of catalyst C (the 3,5-trifluoromethyl aryl substituted derivative) has been used to promote the asymmetric γ-amination of linear unsubstituted enals via dienamine activation; see: Bertelsen, S.; Marigo, M.; Brandes, S.; Dinér, P.; Jørgensen, K. A. J. Am. Chem. Soc. 2006, 128, 12973
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 12973
    • Bertelsen, S.1    Marigo, M.2    Brandes, S.3    Dinér, P.4    Jørgensen, K.A.5
  • 31
    • 84943701775 scopus 로고
    • The presence of a phenyl substituent raises the HOMO energy of electron-rich dienes; see: Sustmann, R. Pure Appl. Chem. 1974, 40, 569
    • (1974) Pure Appl. Chem. , vol.40 , pp. 569
    • Sustmann, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.