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Volumn 135, Issue 18, 2013, Pages 6802-6805

Catalytic asymmetric synthesis of pyrroloindolines via a rhodium(II)-catalyzed annulation of indoles

Author keywords

[No Author keywords available]

Indexed keywords

[3+2]-CYCLOADDITION; ASYMMETRIC SYNTHESIS; CARBENOIDS; ENANTIOSELECTIVE; SUBSTITUTED INDOLES;

EID: 84877279503     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja4025337     Document Type: Article
Times cited : (330)

References (65)
  • 2
    • 77957077902 scopus 로고    scopus 로고
    • Naturally Occurring Cyclotryptophans and Cyclotryptamines
    • Pelletier, S. W. Pergamon: Oxford
    • Anthoni, U.; Christophersen, C.; Nielsen, P. H. Naturally Occurring Cyclotryptophans and Cyclotryptamines. In Alkaloids: Chemical & Biological Perspectives; Pelletier, S. W., Ed.; Pergamon: Oxford, 1999; Vol. 13, pp 163-236.
    • (1999) Alkaloids: Chemical & Biological Perspectives , vol.13 , pp. 163-236
    • Anthoni, U.1    Christophersen, C.2    Nielsen, P.H.3
  • 56
    • 84875727243 scopus 로고    scopus 로고
    • Formal [3+2] reactivity was observed by the Fokin group in a reaction of the Rh(II)-bound carbenoid derived from 4-phenyl-1-(trifluoromethanesulfonyl)-1, 2,3-triazole(9e) and in a recent report by the Davies group in the synthesis of pyrroles from the reaction of 1-sulfonyl-1,2,3-triazoles with furans. - 4718
    • Formal [3+2] reactivity was observed by the Fokin group in a reaction of the Rh(II)-bound carbenoid derived from 4-phenyl-1-(trifluoromethanesulfonyl)-1, 2,3-triazole(9e) and in a recent report by the Davies group in the synthesis of pyrroles from the reaction of 1-sulfonyl-1,2,3-triazoles with furans. Parr, B. T.; Green, S. A.; Davies, H. M. L. J. Am. Chem. Soc. 2013, 135, 4716-4718
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 4716
    • Parr, B.T.1    Green, S.A.2    Davies, H.M.L.3
  • 65
    • 79951542336 scopus 로고    scopus 로고
    • We suspect that a concerted [3+2] cycloaddition would be disfavored due to steric repulsion. A related mechanism was proposed by Fox and co-workers. - 1653
    • We suspect that a concerted [3+2] cycloaddition would be disfavored due to steric repulsion. A related mechanism was proposed by Fox and co-workers. DeAngelis, A.; Shurtleff, V. W.; Dmitrenko, O.; Fox, J. M. J. Am. Chem. Soc. 2011, 133, 1650-1653
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 1650
    • Deangelis, A.1    Shurtleff, V.W.2    Dmitrenko, O.3    Fox, J.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.