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Volumn 10, Issue 41, 2012, Pages 8322-8325

Highly enantioselective and recyclable organocatalytic Michael addition of malonates to α,β-unsaturated aldehydes in aqueous media

Author keywords

[No Author keywords available]

Indexed keywords

AQUEOUS MEDIA; AQUEOUS SOLVENTS; ENANTIOSELECTIVE; MALONATES; MICHAEL ADDITION REACTIONS; MICHAEL ADDITIONS; ORGANOCATALYSTS; ORGANOCATALYTIC; UNSATURATED ALDEHYDES;

EID: 84867244518     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob26248g     Document Type: Article
Times cited : (28)

References (34)
  • 16
    • 33845788846 scopus 로고    scopus 로고
    • For some selected examples of Michael reactions in aqueous media through enamine mechanism, see
    • Y. Hayashi Angew. Chem., Int. Ed. 2006 45 8103
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 8103
    • Hayashi, Y.1
  • 25
    • 68149110229 scopus 로고    scopus 로고
    • For examples of Michael additions in aqueous media through iminium mechanism, see
    • J. Wu B. Ni A. D. Headley Org. Lett. 2009 11 3354
    • (2009) Org. Lett. , vol.11 , pp. 3354
    • Wu, J.1    Ni, B.2    Headley, A.D.3
  • 32
    • 79958104509 scopus 로고    scopus 로고
    • Other recyclable organocatalysts for the asymmetric Michael reaction of malonates to α,β-unsaturated aldehydes, see
    • D. Sarkar R. Bhattarai A. D. Headley B. Ni Synthesis 2011 1993
    • (2011) Synthesis , pp. 1993
    • Sarkar, D.1    Bhattarai, R.2    Headley, A.D.3    Ni, B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.