메뉴 건너뛰기




Volumn , Issue 1, 2013, Pages 105-110

Direct access to fully substituted 3-formyl-4-iodofurans through iodocyclization of α-alkynyl β-alkoxy enones

Author keywords

Alkynes; Cross coupling; Cyclization; Homogeneous catalysis; Oxygen heterocycles; Synthetic methods

Indexed keywords


EID: 84871256052     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201201203     Document Type: Article
Times cited : (17)

References (49)
  • 1
    • 1942504521 scopus 로고    scopus 로고
    • Gribble G.W., Gilchrist T.L. in: (Eds.:, Pergamon, Oxford, UK
    • X. L. Hou, Z. Yang, H. N. C. Wong, in: Progress in Heterocyclic Chemistry (Eds.:, G. W. Gribble, T. L. Gilchrist), Pergamon, Oxford, UK, 2003, vol. 15, pp. 167-205.
    • (2003) Progress in Heterocyclic Chemistry , vol.15 , pp. 167-205
    • Hou, X.L.1    Yang, Z.2    Wong, H.N.C.3
  • 2
    • 0001176061 scopus 로고    scopus 로고
    • Katritzky A.R., Rees C.W., Scriven E.F.V. in: (Eds.:, Elsevier, Oxford, UK
    • B. A. Keay, P. W. Dibble, in: Comprehensive Heterocyclic Chemistry II (Eds.:, A. R. Katritzky, C. W. Rees, E. F. V. Scriven), Elsevier, Oxford, UK, 1997, vol. 2, pp. 395-436.
    • (1997) Comprehensive Heterocyclic Chemistry II , vol.2 , pp. 395-436
    • Keay, B.A.1    Dibble, P.W.2
  • 3
    • 84943380362 scopus 로고
    • Katritzky A.R., Rees C.W. 4 vol. in: (Eds.:, Pergamon, Oxford, UK
    • D. M. X. Donnelly, M. J. Meegan, in: Comprehensive Heterocyclic Chemistry (Eds.:, A. R. Katritzky, C. W. Rees), Pergamon, Oxford, UK, 1984, vol. 4, pp. 657-712.
    • (1984) Comprehensive Heterocyclic Chemistry , pp. 657-712
    • Donnelly, D.M.X.1    Meegan, M.J.2
  • 11
    • 84890980591 scopus 로고    scopus 로고
    • F. Diederich, P. J. Stang, R. R. Tykwinsky), Wiley-VCH, Weinheim, Germany
    • R. C. Larock, in: Acetylene Chemistry (Eds.:, F. Diederich, P. J. Stang, R. R. Tykwinsky), Wiley-VCH, Weinheim, Germany, 2005, pp. 51-99.
    • (2005) Acetylene Chemistry , pp. 51-99
    • Larock, R.C.1
  • 13
  • 18
    • 33748699338 scopus 로고    scopus 로고
    • for a general review dealing with the syntheses of β-halofurans, see:, Top. Heterocycl. Chem. 2012, 65-100
    • H. Togo, S. Iida, Synlett 2006, 2159-2175 for a general review dealing with the syntheses of β-halofurans, see:, R. Dembinski, Y. Li, D. Gundapuneni, A. Decker, Top. Heterocycl. Chem. 2012, 27, 65-100.
    • (2006) Synlett , vol.27 , pp. 2159-2175
    • Togo, H.1    Iida, S.2    Dembinski, R.3    Li, Y.4    Gundapuneni, D.5    Decker, A.6
  • 24
    • 41949130150 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 1903-1906.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 1903-1906
  • 40
    • 79951664053 scopus 로고    scopus 로고
    • During the course of our preliminary investigations, Li and co-workers reported the formation of 3-formylfurans through the Cu-catalyzed cyclization of α-alkynyl enaminones
    • During the course of our preliminary investigations, Li and co-workers reported the formation of 3-formylfurans through the Cu-catalyzed cyclization of α-alkynyl enaminones., J. Yang, C. Wang, X. Xie, H. Li, E. Li, Y. Li, Org. Biomol. Chem. 2011, 9, 1342-1346.
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 1342-1346
    • Yang, J.1    Wang, C.2    Xie, X.3    Li, H.4    Li, E.5    Li, Y.6
  • 45
    • 24944532984 scopus 로고    scopus 로고
    • For another example of the beneficial effect of added water in NIS-promoted iodocyclization reactions, see
    • For another example of the beneficial effect of added water in NIS-promoted iodocyclization reactions, see:, S. Ma, L. Lu, J. Org. Chem. 2005, 70, 7629-7633.
    • (2005) J. Org. Chem. , vol.70 , pp. 7629-7633
    • Ma, S.1    Lu, L.2
  • 49
    • 34548299144 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 6502-6504.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 6502-6504


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.