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Volumn 55, Issue 16, 2014, Pages 2571-2584

Catalytic asymmetric synthesis of 3,3-disubstituted oxindoles: Diazooxindole joins the field

Author keywords

3,3 Disubstituted oxindoles; Asymmetric catalysis; Diazooxindole; Privileged scaffold; Spirocyclic oxindoles

Indexed keywords

CYCLOPROPANE DERIVATIVE; DIAZOOXINDOLE DERIVATIVE; OXINDOLE; POLYCYCLIC HYDROCARBON; UNCLASSIFIED DRUG; ALKENE; CARBENOID; CARBON; COPPER; DIAZOOXINDOLE; GOLD; INDOLE DERIVATIVE; METAL; NATURAL PRODUCT; PALLADIUM; REAGENT; RHODIUM; SPIROCYCLIC OXINDOLE;

EID: 84898042143     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2014.01.084     Document Type: Review
Times cited : (138)

References (185)
  • 8
    • 84867379828 scopus 로고    scopus 로고
    • For reviews, please see
    • For reviews, please see: A. Kumar, and S.S. Chimni RSC Adv. 2 2012 9748 9762
    • (2012) RSC Adv. , vol.2 , pp. 9748-9762
    • Kumar, A.1    Chimni, S.S.2
  • 78
    • 70449382104 scopus 로고    scopus 로고
    • For reviews, please see
    • For reviews, please see: B.M. Trost, and M.K. Bernnan Synthesis 18 2009 3003 3025
    • (2009) Synthesis , vol.18 , pp. 3003-3025
    • Trost, B.M.1    Bernnan, M.K.2
  • 115
    • 0041878773 scopus 로고    scopus 로고
    • For the definition of donor/acceptor diazo reagents, see an excellent review
    • For the definition of donor/acceptor diazo reagents, see an excellent review: H.M.L. Davies, and R.E.J. Beckwith Chem. Rev. 103 2003 2861 2903
    • (2003) Chem. Rev. , vol.103 , pp. 2861-2903
    • Davies, H.M.L.1    Beckwith, R.E.J.2
  • 116
    • 84878771450 scopus 로고    scopus 로고
    • For selective asymmetric catalytic reactions using acyclic donor/acceptor diazo compounds, see
    • For selective asymmetric catalytic reactions using acyclic donor/acceptor diazo compounds, see: H.-B. Wang, D.M. Guptill, A. Varela-Alvarez, D.G. Musaev, and H.M.L. Davies Chem. Sci. 4 2013 2844 2850
    • (2013) Chem. Sci. , vol.4 , pp. 2844-2850
    • Wang, H.-B.1    Guptill, D.M.2    Varela-Alvarez, A.3    Musaev, D.G.4    Davies, H.M.L.5
  • 163
    • 84888623668 scopus 로고    scopus 로고
    • For an account, see
    • For an account, see: X. Guo, and W.-H. Hu Acc. Chem. Res. 46 2013 2427 2440
    • (2013) Acc. Chem. Res. , vol.46 , pp. 2427-2440
    • Guo, X.1    Hu, W.-H.2
  • 174
    • 79959788014 scopus 로고    scopus 로고
    • For one recent excellent review on C-H insertion, please see
    • For one recent excellent review on C-H insertion, please see: H.M.L. Davies, and D. Morton Chem. Soc. Rev. 40 2011 1857 1869
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 1857-1869
    • Davies, H.M.L.1    Morton, D.2
  • 175
    • 84865312995 scopus 로고    scopus 로고
    • For heteroatom-H insertion, Please see
    • For heteroatom-H insertion, Please see: S.-F. Zhu, and Q.-L. Zhou Acc. Chem. Res. 45 2012 1365 1377
    • (2012) Acc. Chem. Res. , vol.45 , pp. 1365-1377
    • Zhu, S.-F.1    Zhou, Q.-L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.