메뉴 건너뛰기




Volumn 28, Issue 12, 2007, Pages 2153-2161

Transition metal-catalyzed and -promoted reactions via carbene and vinylidene complexes generated from alkynes

Author keywords

Alkyne activation; Carbene complexes; Catalytic reactions; Transition metals; Vinylidene complexes

Indexed keywords

CHEMICAL ACTIVATION; FUNCTIONAL GROUPS; METAL COMPLEXES; NUCLEOPHILES; SUBSTITUTION REACTIONS; VINYL RESINS;

EID: 38049104037     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2007.28.12.2153     Document Type: Review
Times cited : (21)

References (110)
  • 6
    • 38049162146 scopus 로고    scopus 로고
    • Metal Carbenes in Organic Synthesis; Dötz, K. H., Ed.; Topics in Organometallic Chemistry, 13; Springer-Verlag: Berlin, 2004.
    • (f) Metal Carbenes in Organic Synthesis; Dötz, K. H., Ed.; Topics in Organometallic Chemistry, Vol. 13; Springer-Verlag: Berlin, 2004.
  • 8
    • 10944244244 scopus 로고    scopus 로고
    • For reviews on transition metal-catalyzed reactions via carbene, vinylidene, and allenylidene intermediates generated from alkynes, see: (a) Ohe, K.; Miki, K.; Uemura, S. J. Synth. Org. Chem. Jpn. 2004, 62, 978.
    • For reviews on transition metal-catalyzed reactions via carbene, vinylidene, and allenylidene intermediates generated from alkynes, see: (a) Ohe, K.; Miki, K.; Uemura, S. J. Synth. Org. Chem. Jpn. 2004, 62, 978.
  • 10
    • 34250824768 scopus 로고    scopus 로고
    • For other guides to the literature of this research field, see: a
    • For other guides to the literature of this research field, see: (a) Fürstner, A.; Davies, P. W. Angew. Chem. Int. Ed. 2007, 46, 3410.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 3410
    • Fürstner, A.1    Davies, P.W.2
  • 18
    • 0000874926 scopus 로고    scopus 로고
    • For selected papers on catalytic cycloisomerization of enynes via cyclopropylcarbene complexes, see: (a) Trost, B. M.; Tanoury, G. J. J. Am. Chem. Soc. 1988, 110, 1636.
    • For selected papers on catalytic cycloisomerization of enynes via cyclopropylcarbene complexes, see: (a) Trost, B. M.; Tanoury, G. J. J. Am. Chem. Soc. 1988, 110, 1636.
  • 27
    • 0037620537 scopus 로고    scopus 로고
    • For selected papers on catalytic cycloisomerization of α,ω-enynes via cyclopropylcarbene or vinylcarbene complex, see: a
    • For selected papers on catalytic cycloisomerization of α,ω-enynes via cyclopropylcarbene or vinylcarbene complex, see: (a) Martín-Matute, B.; Nevado, C.; Cárdenas, D. J.; Echavarren, A. M. J. Am. Chem. Soc. 2003, 125, 5757.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 5757
    • Martín-Matute, B.1    Nevado, C.2    Cárdenas, D.J.3    Echavarren, A.M.4
  • 40
    • 33846088547 scopus 로고    scopus 로고
    • and references therein
    • (c) Kusama, H.; Iwasawa, N. Chem. Lett. 2006, 35, 1082, and references therein.
    • (2006) Chem. Lett , vol.35 , pp. 1082
    • Kusama, H.1    Iwasawa, N.2
  • 45
    • 0000005509 scopus 로고
    • For ruthenium-promoted similar reaction, see: c
    • For ruthenium-promoted similar reaction, see: (c) Wang, Y.; Finn, M. G. J. Am. Chem. Soc. 1995, 117, 8045.
    • (1995) J. Am. Chem. Soc , vol.117 , pp. 8045
    • Wang, Y.1    Finn, M.G.2
  • 55
    • 0037474798 scopus 로고    scopus 로고
    • For transition metal-catalyzed olefination of aldehydes using diazoalkanes and phosphines, see: b, and references therein
    • For transition metal-catalyzed olefination of aldehydes using diazoalkanes and phosphines, see: (b) Cheng, G.; Mirafzal, G. A.; Woo, L. K. Organometallics 2003, 22, 1468, and references therein.
    • (2003) Organometallics , vol.22 , pp. 1468
    • Cheng, G.1    Mirafzal, G.A.2    Woo, L.K.3
  • 59
    • 0025338138 scopus 로고
    • For palladium-catalyzed oxidative rearrangement of propargylic esters, see: c
    • For palladium-catalyzed oxidative rearrangement of propargylic esters, see: (c) Kataoka, H.; Watanabe, K.; Goto, K. Tetrahedron Lett. 1990, 31, 4181.
    • (1990) Tetrahedron Lett , vol.31 , pp. 4181
    • Kataoka, H.1    Watanabe, K.2    Goto, K.3
  • 62
    • 4544333104 scopus 로고    scopus 로고
    • For recent advances in isomerization of propargyl esters into allenyl esters, see: a
    • For recent advances in isomerization of propargyl esters into allenyl esters, see: (a) Stomerk, A. W.; Kel'in, A. V.; Gevorgyan, V. Angew. Chem. Int. Ed. 2004, 43, 2280.
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 2280
    • Stomerk, A.W.1    Kel'in, A.V.2    Gevorgyan, V.3
  • 73
    • 21644450531 scopus 로고    scopus 로고
    • Most recent papers render a planar vinylcarbene complex as the actual intermediate improbable. See: a
    • Most recent papers render a planar vinylcarbene complex as the actual intermediate improbable. See: (a) Soriano, E.; Ballesteros, P.; Marco-Contelles, J. Organometallics 2005, 24, 3172.
    • (2005) Organometallics , vol.24 , pp. 3172
    • Soriano, E.1    Ballesteros, P.2    Marco-Contelles, J.3
  • 80
    • 17744400103 scopus 로고    scopus 로고
    • For Pt- or Au-catalyzed similar pentannulation reactions, see: a
    • For Pt- or Au-catalyzed similar pentannulation reactions, see: (a) Shi, X.; Gorin, D. J.; Toste, F. D. J. Am. Chem. Soc. 2005, 127, 5802.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 5802
    • Shi, X.1    Gorin, D.J.2    Toste, F.D.3
  • 96
    • 0141507090 scopus 로고    scopus 로고
    • A [1,1.5] shift for Re and Mn carbene complexes was defined as different metallotropic shifts. See: [Re]; (a) Casey, C. P.; Dzwiniel, T. L.; Kraft, S.; Guzei, I. A. Organometallics 2003, 22, 3915.
    • A [1,1.5] shift for Re and Mn carbene complexes was defined as different metallotropic shifts. See: [Re]; (a) Casey, C. P.; Dzwiniel, T. L.; Kraft, S.; Guzei, I. A. Organometallics 2003, 22, 3915.
  • 107
    • 33748789481 scopus 로고    scopus 로고
    • For recent advances in catalytic metallotropic shift, see: a
    • For recent advances in catalytic metallotropic shift, see: (a) Cho, E. J.; Kim, M.; Lee, D. Eur. J. Org. Chem. 2006, 3074.
    • (2006) Eur. J. Org. Chem , pp. 3074
    • Cho, E.J.1    Kim, M.2    Lee, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.