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Volumn 26, Issue 5-6, 2015, Pages 262-270

Highly enantioselective catalytic asymmetric Mukaiyama-Michael reactions of cyclic α-alkylidene β-oxo imides

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EID: 84939933919     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2015.01.012     Document Type: Article
Times cited : (11)

References (73)
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    • For the catalytic asymmetric Diels-Alder reaction of quinones with an ester group, see: D.A. Evans, and J. Wu J. Am. Chem. Soc. 125 2003 10162
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 10162
    • Evans, D.A.1    Wu, J.2
  • 15
    • 0030566793 scopus 로고    scopus 로고
    • For the catalytic asymmetric Mukaiyama-Michael reactions of a cyclic α-alkylidene β-keto ester, see: A. Bernardi, G. Colombo, and C. Scolastico Tetrahedron Lett. 37 1996 8921 In this paper, the authors described only one example affording the product in 65% yield with 63% ee.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 8921
    • Bernardi, A.1    Colombo, G.2    Scolastico, C.3
  • 21
    • 84859593626 scopus 로고    scopus 로고
    • For the recent use of α-alkylidene β-keto esters in asymmetric catalysis, see: C. Schotes, and A. Mezzetti ACS Catal. 2 2012 528
    • (2012) ACS Catal. , vol.2 , pp. 528
    • Schotes, C.1    Mezzetti, A.2
  • 22
    • 0342740235 scopus 로고
    • Strictly speaking, the bisoxazoline-Cu(II) complex may have a distorted square-planar geometry. See: D.A. Evans, S.J. Miller, and T. Lectka J. Am. Chem. Soc. 115 1993 6460
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 6460
    • Evans, D.A.1    Miller, S.J.2    Lectka, T.3
  • 32
    • 0032540703 scopus 로고    scopus 로고
    • Selected references for the utility of N-acryloyl oxazolidin-2-one and its congeners. For 1,3-dipolar additions, see: S. Kobayashi, and M. Kawamura J. Am. Chem. Soc. 120 1998 5840
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5840
    • Kobayashi, S.1    Kawamura, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.