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Volumn 53, Issue 32, 2014, Pages 8333-8337

Transition-metal-free tunable chemoselective nfunctionalization of indoles with ynamides

Author keywords

alkynes; density functional calculations; heterocycles; reaction mechanisms; synthetic methods

Indexed keywords

CHEMICAL REACTIONS; CHEMISTRY;

EID: 84905375007     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201402767     Document Type: Article
Times cited : (50)

References (51)
  • 3
    • 77950513362 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 2840-2859
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2840-2859
  • 6
    • 0000868359 scopus 로고
    • (Eds.: H. Kropf, E. Schaumann), Georg Thieme, Stuttgart
    • G. Himbert, in Methoden Der Organischen Chemie (Houben-Weyl) (Eds.:, H. Kropf, E. Schaumann,), Georg Thieme, Stuttgart, 1993, pp. 3267-3443
    • (1993) Methoden der Organischen Chemie (Houben-Weyl) , pp. 3267-3443
    • Himbert, G.1
  • 25
    • 33645291247 scopus 로고    scopus 로고
    • Y. Zhang, Tetrahedron 2006, 62, 3917-3927
    • (2006) Tetrahedron , vol.62 , pp. 3917-3927
    • Zhang, Y.1
  • 34
    • 84905367902 scopus 로고    scopus 로고
    • See the Supporting Information. CCDC979017 (4ga), 979018 (5a) and 979019 (10) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • See the Supporting Information. CCDC979017 (4ga), 979018 (5a) and 979019 (10) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 38
    • 84893845360 scopus 로고    scopus 로고
    • During finalization of this manuscript a related process involving the cleavage of one tosyl group of highly activated N,N-ditosylynamides has been reported
    • During finalization of this manuscript a related process involving the cleavage of one tosyl group of highly activated N,N-ditosylynamides has been reported:, Y. Kong, L. Yu, Y. Cui, J. Cao, Synthesis 2014, 183-188
    • (2014) Synthesis , pp. 183-188
    • Kong, Y.1    Yu, L.2    Cui, Y.3    Cao, J.4
  • 44
    • 0001686462 scopus 로고
    • Although a thorough base screening has not been carried out, sodium methoxide was also found to be suitable for this reaction when starting with the ynamide 1m.
    • I. Hasan, E. R. Marinelli, L.-C. Chang Lin, F. W. Fowler, A. B. Levy, J. Org. Chem. 1981, 46, 157-164. Although a thorough base screening has not been carried out, sodium methoxide was also found to be suitable for this reaction when starting with the ynamide 1m.
    • (1981) J. Org. Chem. , vol.46 , pp. 157-164
    • Hasan, I.1    Marinelli, E.R.2    Lin, L.-C.C.3    Fowler, F.W.4    Levy, A.B.5
  • 49
    • 84884570895 scopus 로고    scopus 로고
    • For a theoretical study aimed at rationalizing the reaction of two electrophiles together, see:, H. Gérard, I. Chataigner, J. Org. Chem. 2013, 78, 9233-9242.
    • (2013) J. Org. Chem. , vol.78 , pp. 9233-9242
    • Gérard, H.1    Chataigner, I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.