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Volumn , Issue 34, 2007, Pages 5740-5748

One-step addition of sulfonic acids to acetylene derivatives: An alternative and stereoselective approach to vinyl triflates and fluorosulfonates

Author keywords

Alkynes; Carbocations; Sulfones; Superacidic systems; Vinyl triflates

Indexed keywords


EID: 36849087880     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200700650     Document Type: Article
Times cited : (33)

References (42)
  • 2
    • 36849073000 scopus 로고    scopus 로고
    • U. Halbes-Letinois, P. Pale, P., Palladium Catalyzed Synthesis of Enynes in Leading Edge Organometallic Chemistry Research, (Ed.: M. A. Cato), Nova Publishers, New York, 2006, pp. 93-131;
    • a) U. Halbes-Letinois, P. Pale, P., "Palladium Catalyzed Synthesis of Enynes" in Leading Edge Organometallic Chemistry Research, (Ed.: M. A. Cato), Nova Publishers, New York, 2006, pp. 93-131;
  • 5
    • 0001058604 scopus 로고
    • Eds, E. W. Abel, F. G. A. Stone, G. Wilkinson, Pergamon, Oxford
    • d) V. Farina in Comprehensive Organometallic Chemistry II, (Eds.: E. W. Abel, F. G. A. Stone, G. Wilkinson), Pergamon, Oxford, 1995, vol. 12, pp. 222-225;
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 222-225
    • Farina, V.1
  • 6
    • 0000509322 scopus 로고
    • Eds, I. Fleming, B. M. Trost, Pergamon, Oxford
    • e) K. Sonogashira, in Comprehensive Organic Chemistry (Eds.: I. Fleming, B. M. Trost), Pergamon, Oxford, 1991, vol. 3, pp. 521-549.
    • (1991) Comprehensive Organic Chemistry , vol.3 , pp. 521-549
    • Sonogashira, K.1
  • 9
    • 0002268850 scopus 로고
    • They can also be obtained from amides, see
    • They can also be obtained from amides, see: T. Okita, M. Isobe, Synlett 1994, 589-591;
    • (1994) Synlett , pp. 589-591
    • Okita, T.1    Isobe, M.2
  • 10
    • 0029014202 scopus 로고
    • or from conjugated enones
    • C. J. Foti, D. L. Comins, J. Org. Chem. 1995, 60, 2656-2657 or from conjugated enones,
    • (1995) J. Org. Chem , vol.60 , pp. 2656-2657
    • Foti, C.J.1    Comins, D.L.2
  • 12
    • 36849003291 scopus 로고    scopus 로고
    • Chem. Abstr. 2004, 140, 339090;
    • Chem. Abstr. 2004, 140, 339090;
  • 29
    • 14944367862 scopus 로고    scopus 로고
    • Similar processes of O,C diprotonation of enone systems were previously investigated, see: a
    • Similar processes of O,C diprotonation of enone systems were previously investigated, see: a) S. Walspurger, A. Vasilyev, J. Sommer, P. Pale, Tetrahedron 2005, 61, 3559-3564;
    • (2005) Tetrahedron , vol.61 , pp. 3559-3564
    • Walspurger, S.1    Vasilyev, A.2    Sommer, J.3    Pale, P.4
  • 41
    • 36849036688 scopus 로고    scopus 로고
    • Performed with CAChe and Hyperchem softwares
    • Performed with CAChe and Hyperchem softwares.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.