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Volumn 46, Issue 36, 2010, Pages 6840-6842

Organocatalytic asymmetric Michael addition of α-aryl cyclopentanones to nitroolefins for construction of adjacent quaternary and tertiary stereocenters

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; CYCLOPENTANONE DERIVATIVE; ELECTROPHILE; NUCLEOPHILE;

EID: 77956301757     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0cc01987a     Document Type: Article
Times cited : (40)

References (53)
  • 11
    • 70349782136 scopus 로고    scopus 로고
    • For selected examples of catalytic asymmetric conjugate addition of α-substituted β-nitrocarbonyl pronucleophiles for the construction of adjacent quaternary and tertiary stereogenic centers, see:
    • Z. Yu X. Liu L. Zhou L. Lin X. Feng Angew. Chem., Int. Ed. 2009 48 5195
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 5195
    • Yu, Z.1    Liu, X.2    Zhou, L.3    Lin, L.4    Feng, X.5
  • 13
    • 50249092090 scopus 로고    scopus 로고
    • For review and selected examples of catalytic asymmetric conjugate addition of α-substituted β-cyanocarbonyl pronucleophiles for the construction of adjacent quaternary and tertiary stereogenic centers, see:
    • D. Uraguchi K. Koshimoto T. Ooi J. Am. Chem. Soc. 2008 130 10878
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 10878
    • Uraguchi, D.1    Koshimoto, K.2    Ooi, T.3
  • 48
    • 44349168328 scopus 로고    scopus 로고
    • 3 (12 h, 89% yield, ee: 73%); EtOAc (12 h, 85% yield, ee: 71%); THF (13 h, 80% yield, ee: 66%); MeCN (15 h, 92% yield, ee: 75%); acetone (16 h, 75% yield, ee: 76%); PhMe (19 h, 81% yield, ee: 78%); MeOH (16 h, 83% yield, ee: 2%)
    • S. J. Connon Chem. Commun. 2008 2499
    • (2008) Chem. Commun. , pp. 2499
    • Connon, S.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.