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Volumn 11, Issue 11, 2009, Pages 2425-2428

Hydroxyl group-directed organocatalytic asymmetric michael addition of α,β-unsaturated ketones with alkenylboronic acids

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; BORONIC ACID DERIVATIVE; KETONE; THIOUREA;

EID: 66149179009     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol9006053     Document Type: Article
Times cited : (63)

References (37)
  • 1
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    • For reviews, see: a
    • For reviews, see: (a) Miyaura, N. Bull. Chem. Soc. Jpn. 2008, 81, 1535.
    • (2008) Bull. Chem. Soc. Jpn , vol.81 , pp. 1535
    • Miyaura, N.1
  • 2
    • 0041738169 scopus 로고    scopus 로고
    • For recent examples, see
    • Hayashi, T.; Yamasaki, K. Chem. Rev. 2003, 103, 2829. For recent examples, see:
    • (2003) Chem. Rev , vol.103 , pp. 2829
    • Hayashi, T.1    Yamasaki, K.2
  • 12
    • 48649106016 scopus 로고    scopus 로고
    • For recent reviews of organocatalysts, see: a
    • For recent reviews of organocatalysts, see: (a) Yu, X.; Wang, W. Chem. Asian J. 2008, 3, 516.
    • (2008) Chem. Asian J , vol.3 , pp. 516
    • Yu, X.1    Wang, W.2
  • 21
    • 44449092080 scopus 로고    scopus 로고
    • Similar BINOL catalysts such as Chong's could be applied for the asymmetric 1,2-addition of organoboronic acids; see: (a) Lou, S.; Schaus, S. E. J. Am. Chem. Soc. 2008, 130, 6922.
    • Similar BINOL catalysts such as Chong's could be applied for the asymmetric 1,2-addition of organoboronic acids; see: (a) Lou, S.; Schaus, S. E. J. Am. Chem. Soc. 2008, 130, 6922.
  • 24
    • 50549097452 scopus 로고    scopus 로고
    • During the course of our investigation, a related report has appeared in the literature; see: a
    • During the course of our investigation, a related report has appeared in the literature; see: (a) Kim, S.-G. Tetrahedron Lett. 2008, 49, 6148.
    • (2008) Tetrahedron Lett , vol.49 , pp. 6148
    • Kim, S.-G.1
  • 32
    • 0037764897 scopus 로고    scopus 로고
    • When less reactive nucleophiles were used, 2-phenylfuran was produced as the byproduct, and the yield of the desired products had been decreased. For the reactions of ?-hydroxy enones, see: Greatrex, B. W.; Kimber, M. C.; Taylor, D. K.; Tiekink, T. K. J. Org. Chem. 2003, 68, 4239.
    • When less reactive nucleophiles were used, 2-phenylfuran was produced as the byproduct, and the yield of the desired products had been decreased. For the reactions of ?-hydroxy enones, see: Greatrex, B. W.; Kimber, M. C.; Taylor, D. K.; Tiekink, T. K. J. Org. Chem. 2003, 68, 4239.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.