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Volumn 54, Issue 5, 2015, Pages 1608-1611

Catalytic asymmetric intramolecular homologation of ketones with α-diazoesters: Synthesis of cyclic α-Aryl/Alkyl β-ketoesters

Author keywords

Asymmetric catalysis; Homologation; Scandium; diazoesters; ketoesters

Indexed keywords

CHEMICAL REACTIONS; SCANDIUM;

EID: 85027953035     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201409572     Document Type: Article
Times cited : (56)

References (78)
  • 1
    • 0000356602 scopus 로고
    • For reviews, see: a)
    • For reviews, see: a) C. D. Gutsche, Org. React. 1954, 8, 364-429
    • (1954) Org. React. , vol.8 , pp. 364-429
    • Gutsche, C.D.1
  • 9
    • 0001743806 scopus 로고
    • For recent examples of the Roskamp reaction with aldehydes and diazo compounds, see: a)
    • For recent examples of the Roskamp reaction with aldehydes and diazo compounds, see: a) C. R. Holmquist, E. J. Roskamp, J. Org. Chem. 1989, 54, 3258-3260
    • (1989) J. Org. Chem. , vol.54 , pp. 3258-3260
    • Holmquist, C.R.1    Roskamp, E.J.2
  • 12
    • 84861488028 scopus 로고    scopus 로고
    • Angew. Chem. 2011, 123, 9251-9254
    • (2011) Angew. Chem. , vol.123 , pp. 9251-9254
  • 14
    • 84895116163 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 2603-2606
    • (2013) Angew. Chem. , vol.125 , pp. 2603-2606
  • 17
    • 67849092152 scopus 로고    scopus 로고
    • For recent examples of ketone homologation reactions with diazo compounds, see: a)
    • For recent examples of ketone homologation reactions with diazo compounds, see: a) D. C. Moebius, J. S. Kingsbury, J. Am. Chem. Soc. 2009, 131, 878-879
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 878-879
    • Moebius, D.C.1    Kingsbury, J.S.2
  • 23
    • 33846796155 scopus 로고    scopus 로고
    • For recent examples of the Roskamp reaction in natural product synthesis, see: a)
    • For recent examples of the Roskamp reaction in natural product synthesis, see: a) D. A. Evans, D. J. Adams, J. Am. Chem. Soc. 2007, 129, 1048-1049
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 1048-1049
    • Evans, D.A.1    Adams, D.J.2
  • 27
    • 79951992541 scopus 로고    scopus 로고
    • Angew. Chem. 2009, 121, 2382-2386
    • (2009) Angew. Chem. , vol.121 , pp. 2382-2386
  • 33
    • 84873928048 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 7906-7909
    • (2012) Angew. Chem. , vol.124 , pp. 7906-7909
  • 38
  • 43
    • 84874272208 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 8447-8450
    • (2012) Angew. Chem. , vol.124 , pp. 8447-8450
  • 44
    • 39749121974 scopus 로고    scopus 로고
    • for related regiose-lective examples, see: e)
    • for related regiose-lective examples, see: e) T Hashimoto, Y Naganawa, K. Maruoka, J. Am. Chem. Soc. 2008, 130, 2434-2435
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 2434-2435
    • Hashimoto, T.1    Naganawa, Y.2    Maruoka, K.3
  • 49
    • 84874269530 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 8772-8775
    • (2012) Angew. Chem. , vol.124 , pp. 8772-8775
  • 51
    • 84891770889 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 11083-11086
    • (2013) Angew. Chem. , vol.125 , pp. 11083-11086
  • 53
    • 0042379988 scopus 로고    scopus 로고
    • For selected reviews, see: a)
    • For selected reviews, see: a) B. M. Trost, M. L. Crawley, Chem. Rev. 2003, 103, 2921-2943
    • (2003) Chem. Rev. , vol.103 , pp. 2921-2943
    • Trost, B.M.1    Crawley, M.L.2
  • 55
    • 84883024744 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 4408-4445
    • (2013) Angew. Chem. , vol.125 , pp. 4408-4445
  • 63
    • 67650573135 scopus 로고    scopus 로고
    • Angew. Chem. 2007, 119, 5611-5615.
    • (2007) Angew. Chem. , vol.119 , pp. 5611-5615
  • 64
    • 0001521888 scopus 로고
    • For selected reviews on the construction of all-carbon quaternary stereocenters, see: a)
    • For selected reviews on the construction of all-carbon quaternary stereocenters, see: a) K. Fuji, Chem. Rev. 1993, 93, 2037-2066
    • (1993) Chem. Rev. , vol.93 , pp. 2037-2066
    • Fuji, K.1
  • 66
    • 0000084915 scopus 로고    scopus 로고
    • Angew. Chem. 1998, 110, 402-415
    • (1998) Angew. Chem. , vol.110 , pp. 402-415
  • 70
    • 84901586222 scopus 로고    scopus 로고
    • For reviews of chiral N, N'-dioxide-scandium(III), see: a)
    • For reviews of chiral N, N'-dioxide-scandium(III), see: a) X. H. Liu, L. L. Lin, X. M. Feng, Org. Chem. Front. 2014, 1, 298-302
    • (2014) Org. Chem. Front. , vol.1 , pp. 298-302
    • Liu, X.H.1    Lin, L.L.2    Feng, X.M.3
  • 72
    • 84863280512 scopus 로고    scopus 로고
    • Chiral scandium complexes in catalytic asymmetric reactions
    • (Ed.: V. A. Greene), Nova Science, New York
    • c) "Chiral Scandium Complexes in Catalytic Asymmetric Reactions": X. M. Feng, X. H. Liu, Scandium: Compounds, Productions and Applications (Ed.: V. A. Greene), Nova Science, New York, 2011, pp. 1-48.
    • (2011) Scandium: Compounds, Productions and Applications , pp. 1-48
    • Feng, X.M.1    Liu, X.H.2
  • 75
    • 84921450307 scopus 로고    scopus 로고
    • For recent examples, see: a)
    • For recent examples, see: a) A. Vasas, J. Hohmann, Chem. Rev. 2014, 114, 8579-8612
    • (2014) Chem. Rev. , vol.114 , pp. 8579-8612
    • Vasas, A.1    Hohmann, J.2
  • 77
    • 84921475485 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 2590-2628
    • (2014) Angew. Chem. , vol.126 , pp. 2590-2628


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.