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Volumn 7, Issue 7, 2005, Pages 1219-1222

Iron-catalyzed cross-coupling of alkenyl sulfides with grignard reagents

Author keywords

[No Author keywords available]

Indexed keywords

ALKENYL GROUP; IRON; SULFIDE;

EID: 17444380857     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol047504c     Document Type: Article
Times cited : (93)

References (79)
  • 2
    • 0010831076 scopus 로고    scopus 로고
    • Cross-Coupling Reactions
    • Springer: New York
    • (b) Cross-Coupling Reactions; Miyaura, N., Ed.; Topics in Current Chemistry Vol. 219; Springer: New York, 2002.
    • (2002) Topics in Current Chemistry , vol.219
    • Miyaura, N.1
  • 12
    • 0000957922 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 5449
    • Molander, G.A.1    Rahn, B.J.2    Shubert, D.C.3    Bonde, S.E.4
  • 13
    • 0031871453 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1998) Synthesis , pp. 1199
    • Cahiez, G.1    Avedissian, H.2
  • 14
    • 0035212248 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (2001) Synlett , pp. 1901
    • Dohle, W.1    Kopp, F.2    Cahiez, G.3    Knochel, P.4
  • 15
    • 0001046481 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (2001) J. Organomet. Chem. , vol.624 , pp. 131
    • Fakhfakh, M.A.1    Franck, X.2    Hocquemiller, R.3    Figadère, B.4
  • 16
    • 0037459416 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (2003) Chem. Commun. , pp. 732
    • Hölzer, B.1    Hoffmann, R.W.2
  • 17
    • 0011771857 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1981) J. Org. Chem. , vol.46 , pp. 5074
    • Walborsky, H.M.1    Banks, R.B.2
  • 18
    • 0029970234 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 1773
    • Cahiez, G.1    Marquais, S.2
  • 19
    • 0001978151 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1996) Pure Appl. Chem. , vol.68 , pp. 53
    • Cahiez, G.1    Marquais, S.2
  • 20
    • 0030599259 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7009
    • Fürstner, A.1    Brunner, H.2
  • 21
    • 0001287532 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 2469
    • Fabre, J.L.1    Julia, M.2    Verpeaux, J.N.3
  • 22
    • 0011706413 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1988) Tetrahedron , vol.44 , pp. 111
    • Alvarez, E.1    Cuvigny, T.2    Du Penhoat, C.H.3    Julia, M.4
  • 23
    • 45549120361 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1988) Tetrahedron , vol.44 , pp. 119
    • Alvarez, E.1    Cuvigny, T.2    Du Penhoat, C.H.3    Julia, M.4
  • 24
    • 0001806567 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1953) J. Am. Chem. Soc. , vol.75 , pp. 3731
    • Percival, W.C.1    Wagner, R.B.2    Cook, N.C.3
  • 25
    • 0001425193 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 4805
    • Fiandanese, V.1    Marchese, G.2    Martina, V.3    Ronzini, L.4
  • 26
    • 0000591639 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 1285
    • Ritter, K.1    Hanack, M.2
  • 27
    • 0001648330 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 2053
    • Cardellicchio, C.1    Fiandanese, V.2    Marchese, G.3    Ronzini, L.4
  • 28
    • 0034613874 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (2000) J. Mol. Catal. A: Chem. , vol.161 , pp. 239
    • Dell'Anna, M.M.1    Mastrorilli, P.2    Nobile, C.F.3    Marchese, G.4    Taurino, M.R.5
  • 29
    • 0029745393 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 1700
    • Reddy, C.K.1    Knochel, P.2
  • 30
    • 0001140856 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 3595
    • Cardellicchio, C.1    Fiandanese, V.2    Marchese, G.3    Ronzini, L.4
  • 31
    • 33751014371 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1991) Synlett , pp. 513
    • Yanagisawa, A.1    Nomura, N.2    Yamamoto, H.3
  • 32
    • 0028233573 scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (1994) Tetrahedron , vol.50 , pp. 6017
    • Yanagisawa, A.1    Nomura, N.2    Yamamoto, H.3
  • 33
    • 0037083916 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 609
    • Fürstner, A.1    Leitner, A.2
  • 34
    • 0037146041 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 13856
    • Fürstner, A.1    Leitner, A.2    Méndez, M.3    Krause, H.4
  • 35
    • 0037029770 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 3547
    • Quintin, J.1    Franck, X.2    Hocquemiller, R.3    Figadère, B.4
  • 36
    • 0037455149 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M. Tetrahedron Lett. 1985, 26, 1285. (p) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1987, 28, 2053. (q) Dell'Anna, M. M.; Mastrorilli, P.; Nobile, C. F.; Marchese, G.; Taurino, M. R. J. Mol. Catal. A: Chem. 2000, 161, 239. (r) Reddy, C. K.; Knochel, P. Angew. Chem., Int. Ed. Engl. 1996, 35, 1700. Thioesters/Grignard reagents: (s) Cardellicchio, C.; Fiandanese, V.; Marchese, G.; Ronzini, L. Tetrahedron Lett. 1985, 26, 3595. Allylic phosphates/Grignard reagents: (t) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Synlett 1991, 513. (u) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017. Aryl halides (triflates)/Grignard reagents: (v) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2002, 41, 609. (w) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. J. Am. Chem. Soc. 2002, 124, 13856. (x) Quintin, J.; Franck, X.; Hocquemiller, R.; Figadère, B. Tetrahedron Lett. 2002, 43, 3547. (y) Fürstner, A.; Leitner, A. Angew. Chem., Int. Ed. 2003, 42, 308. (z) Hocek, M.; Hocková, D.; Dvřáková, H. Synthesis 2004, 889.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 308
    • Fürstner, A.1    Leitner, A.2
  • 37
    • 2342473773 scopus 로고    scopus 로고
    • Alkenyl halides/Grignard reagents: (a) Molander, G. A.; Rahn, B. J.; Shubert, D. C.; Bonde, S. E. Tetrahedron Lett. 1983, 24, 5449. (b) Cahiez, G.; Avedissian, H. Synthesis 1998, 1199. (c) Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. (d) Fakhfakh, M. A.; Franck, X.; Hocquemiller, R.; Figadère, B. J. Organomet. Chem. 2001, 624, 131. (e) Hölzer, B.; Hoffmann, R. W. Chem. Commun. 2003, 732. Alkenyl halides/organolithium reagents: (f) Walborsky, H. M.; Banks, R. B. J. Org. Chem. 1981, 46, 5074. Alkenyl halides/organomanganese reagents: (g) Cahiez, G.; Marquais, S. Tetrahedron Lett. 1996, 37, 1773. (h) Cahiez, G.; Marquais, S. Pure Appl. Chem. 1996, 68, 53. (i) Fürstner, A.; Brunner, H. Tetrahedron Lett. 1996, 37, 7009. Alkenyl sulfones/Grignard reagents: (j) Fabre, J. L.; Julia, M.; Verpeaux, J. N. Tetrahedron Lett. 1982, 23, 2469. (k) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 111. (l) Alvarez, E.; Cuvigny, T.; du Penhoat, C. H.; Julia, M. Tetrahedron 1988, 44, 119. Acyl halides/Grignard reagents: (m) Percival, W. C.; Wagner, R. B.; Cook, N. C. J. Am. Chem. Soc. 1953, 75, 3731. (n) Fiandanese, V.; Marchese, G.; Martina, V.; Ronzini, L. Tetrahedron Lett. 1984, 25, 4805. (o) Ritter, K.; Hanack, M.
    • (2004) Synthesis , pp. 889
    • Hocek, M.1    Hocková, D.2    Dvřáková, H.3
  • 41
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    • See also: (d) Brinker, U. H.; König, L. Chem. Ber. 1983, 116, 882. (e) Nishii, Y.; Wakasugi, K.; Tanabe, Y. Synlett 1998, 67. (f) Bedford, R. B.; Bruce, D. W.; Frost, R. M.; Goodby, J. W.; Hird, M. Chem. Commun. 2004, 2822.
    • (1983) Chem. Ber. , vol.116 , pp. 882
    • Brinker, U.H.1    König, L.2
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    • See also: (d) Brinker, U. H.; König, L. Chem. Ber. 1983, 116, 882. (e) Nishii, Y.; Wakasugi, K.; Tanabe, Y. Synlett 1998, 67. (f) Bedford, R. B.; Bruce, D. W.; Frost, R. M.; Goodby, J. W.; Hird, M. Chem. Commun. 2004, 2822.
    • (1998) Synlett , pp. 67
    • Nishii, Y.1    Wakasugi, K.2    Tanabe, Y.3
  • 45
    • 0034614065 scopus 로고    scopus 로고
    • For our related works on multisubstituted olefin synthesis, see: (a) Itami, K.; Mitsudo, K.; Kamei, T.; Koike, T.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2000, 122, 12013. (b) Itami, K.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 5600. (c) Itami, K.; Nokami, T.; Ishimura, Y.; Mitsudo, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 11577. (d) Itami, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2003, 125, 14670. (e) Itami, K.; Ushiogi, Y.; Nokami, T.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 3695. (f) Itami, K.; Tonogaki, K.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 4093.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 12013
    • Itami, K.1    Mitsudo, K.2    Kamei, T.3    Koike, T.4    Nokami, T.5    Yoshida, J.6
  • 46
    • 0034820257 scopus 로고    scopus 로고
    • For our related works on multisubstituted olefin synthesis, see: (a) Itami, K.; Mitsudo, K.; Kamei, T.; Koike, T.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2000, 122, 12013. (b) Itami, K.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 5600. (c) Itami, K.; Nokami, T.; Ishimura, Y.; Mitsudo, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 11577. (d) Itami, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2003, 125, 14670. (e) Itami, K.; Ushiogi, Y.; Nokami, T.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 3695. (f) Itami, K.; Tonogaki, K.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 4093.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5600
    • Itami, K.1    Nokami, T.2    Yoshida, J.3
  • 47
    • 0035965684 scopus 로고    scopus 로고
    • For our related works on multisubstituted olefin synthesis, see: (a) Itami, K.; Mitsudo, K.; Kamei, T.; Koike, T.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2000, 122, 12013. (b) Itami, K.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 5600. (c) Itami, K.; Nokami, T.; Ishimura, Y.; Mitsudo, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 11577. (d) Itami, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2003, 125, 14670. (e) Itami, K.; Ushiogi, Y.; Nokami, T.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 3695. (f) Itami, K.; Tonogaki, K.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 4093.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 11577
    • Itami, K.1    Nokami, T.2    Ishimura, Y.3    Mitsudo, K.4    Kamei, T.5    Yoshida, J.6
  • 48
    • 0345293203 scopus 로고    scopus 로고
    • For our related works on multisubstituted olefin synthesis, see: (a) Itami, K.; Mitsudo, K.; Kamei, T.; Koike, T.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2000, 122, 12013. (b) Itami, K.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 5600. (c) Itami, K.; Nokami, T.; Ishimura, Y.; Mitsudo, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 11577. (d) Itami, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2003, 125, 14670. (e) Itami, K.; Ushiogi, Y.; Nokami, T.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 3695. (f) Itami, K.; Tonogaki, K.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 4093.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 14670
    • Itami, K.1    Kamei, T.2    Yoshida, J.3
  • 49
    • 7044284722 scopus 로고    scopus 로고
    • For our related works on multisubstituted olefin synthesis, see: (a) Itami, K.; Mitsudo, K.; Kamei, T.; Koike, T.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2000, 122, 12013. (b) Itami, K.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 5600. (c) Itami, K.; Nokami, T.; Ishimura, Y.; Mitsudo, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 11577. (d) Itami, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2003, 125, 14670. (e) Itami, K.; Ushiogi, Y.; Nokami, T.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 3695. (f) Itami, K.; Tonogaki, K.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 4093.
    • (2004) Org. Lett. , vol.6 , pp. 3695
    • Itami, K.1    Ushiogi, Y.2    Nokami, T.3    Ohashi, Y.4    Yoshida, J.5
  • 50
    • 8744315897 scopus 로고    scopus 로고
    • For our related works on multisubstituted olefin synthesis, see: (a) Itami, K.; Mitsudo, K.; Kamei, T.; Koike, T.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2000, 122, 12013. (b) Itami, K.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 5600. (c) Itami, K.; Nokami, T.; Ishimura, Y.; Mitsudo, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2001, 123, 11577. (d) Itami, K.; Kamei, T.; Yoshida, J. J. Am. Chem. Soc. 2003, 125, 14670. (e) Itami, K.; Ushiogi, Y.; Nokami, T.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 3695. (f) Itami, K.; Tonogaki, K.; Ohashi, Y.; Yoshida, J. Org. Lett. 2004, 6, 4093.
    • (2004) Org. Lett. , vol.6 , pp. 4093
    • Itami, K.1    Tonogaki, K.2    Ohashi, Y.3    Yoshida, J.4
  • 51
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    • note
    • 4w
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    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (1979) Tetrahedron Lett. , pp. 43
    • Okamura, H.1    Miura, M.2    Takei, H.3
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    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (1979) J. Chem. Soc., Chem. Commun. , pp. 637
    • Wenkert, E.1    Ferreira, T.W.2    Michelotti3
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    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (1979) Tetrahedron Lett. , pp. 1447
    • Takei, H.1    Miura, M.2    Sugimura, H.3    Okamura, H.4
  • 55
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    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (1979) Tetrahedron Lett. , pp. 3425
    • Okamura, H.1    Takei, H.2
  • 56
    • 84992259765 scopus 로고
    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (1990) Synthesis , pp. 89
    • Luh, T.-Y.1    Ni, Z.-J.2
  • 57
    • 0032516391 scopus 로고    scopus 로고
    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 3189
    • Tokuyama, H.1    Yokoshima, S.2    Yamashita, T.3    Fukuyama, T.4
  • 58
    • 0033552293 scopus 로고    scopus 로고
    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 9449
    • Srogl, J.1    Liu, W.2    Marshall, D.3    Liebeskind, L.S.4
  • 59
    • 0034669524 scopus 로고    scopus 로고
    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 11260
    • Liebeskind, L.S.1    Srogl, J.2
  • 60
    • 0034609680 scopus 로고    scopus 로고
    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (2000) Org. Lett. , vol.2 , pp. 3229
    • Savarin, C.1    Srogl, J.2    Liebeskind, L.S.3
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    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (2000) Synlett , pp. 905
    • Angiolelli, M.E.1    Casalnuovo, A.L.2    Selby, T.P.3
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    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 1039
    • Shimizu, T.1    Seki, M.2
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    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (2002) Org. Lett. , vol.4 , pp. 979
    • Liebeskind, L.S.1    Srogl, J.2
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    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
    • (2002) Synlett , pp. 447
    • Alphonse, F.-A.1    Suzenet, F.2    Keromnes, A.3    Lebret, B.4    Guillaumet, G.5
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    • 17444375952 scopus 로고    scopus 로고
    • Reference 6
    • There are many reports on nickel- or palladium-catalyzed cross-coupling reaction using sulfides. For early works, see: (a) Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 43. (b) Wenkert, E.; Ferreira, T. W.; Michelotti, J. Chem. Soc., Chem. Commun. 1979, 637. (c) Takei, H.; Miura, M.; Sugimura, H.; Okamura, H. Tetrahedron Lett. 1979, 1447. (d) Okamura, H.; Takei, H. Tetrahedron Lett. 1979, 3425. For a review, see: (e) Luh, T.-Y.; Ni, Z.-J. Synthesis 1990, 89. For recent examples, see: (f) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Fukuyama, T. Tetrahedron Lett. 1998, 39, 3189. (g) Srogl, J.; Liu, W.; Marshall, D.; Liebeskind, L. S. J. Am. Chem. Soc. 1999, 121, 9449. (h) Liebeskind, L. S.; Srogl, J. J. Am. Chem. Soc. 2000, 122, 11260. (i) Savarin, C.; Srogl, J. Liebeskind, L. S. Org. Lett. 2000, 2, 3229. (j) Angiolelli, M. E.; Casalnuovo, A. L.; Selby, T. P. Synlett 2000, 905. (k) Shimizu, T.; Seki, M. Tetrahedron Lett. 2002, 43, 1039. (l) Liebeskind, L. S.; Srogl, J. Org. Lett. 2002, 4, 979. (m) Alphonse, F.-A.; Suzenet, F.; Keromnes, A.; Lebret, B.; Guillaumet, G. Synlett 2002, 447. (n) Reference 6.
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    • note
    • 3) afforded p-methoxystyrene (88.2 mg, 66%) as a pale yellow oil. All products listed in Table 1 exhibited spectral data in agreement with literature values.
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    • Such an addition/elimination sequence has been proposed for the reaction of organocopper reagents with β-alkylthio-substituted α,β- unsaturated carbonyl compounds. (a) Coates, R. M.; Sowerby, R. L. J. Am. Chem. Soc. 1971, 93, 1027. (b) Posner, G. H.; Brunelle, D. J. J. Org. Chem. 1973, 38, 2747. (c) Posner, G. H.; Brunelle, D. J. J. Chem. Soc., Chem. Commun. 1973, 907. (d) Gammill, R. B.; Bryson, T. A. Tetrahedron Lett. 1975, 3793.
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    • Such an addition/elimination sequence has been proposed for the reaction of organocopper reagents with β-alkylthio-substituted α,β- unsaturated carbonyl compounds. (a) Coates, R. M.; Sowerby, R. L. J. Am. Chem. Soc. 1971, 93, 1027. (b) Posner, G. H.; Brunelle, D. J. J. Org. Chem. 1973, 38, 2747. (c) Posner, G. H.; Brunelle, D. J. J. Chem. Soc., Chem. Commun. 1973, 907. (d) Gammill, R. B.; Bryson, T. A. Tetrahedron Lett. 1975, 3793.
    • (1973) J. Org. Chem. , vol.38 , pp. 2747
    • Posner, G.H.1    Brunelle, D.J.2
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    • Such an addition/elimination sequence has been proposed for the reaction of organocopper reagents with β-alkylthio-substituted α,β- unsaturated carbonyl compounds. (a) Coates, R. M.; Sowerby, R. L. J. Am. Chem. Soc. 1971, 93, 1027. (b) Posner, G. H.; Brunelle, D. J. J. Org. Chem. 1973, 38, 2747. (c) Posner, G. H.; Brunelle, D. J. J. Chem. Soc., Chem. Commun. 1973, 907. (d) Gammill, R. B.; Bryson, T. A. Tetrahedron Lett. 1975, 3793.
    • (1973) J. Chem. Soc., Chem. Commun. , pp. 907
    • Posner, G.H.1    Brunelle, D.J.2
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    • Such an addition/elimination sequence has been proposed for the reaction of organocopper reagents with β-alkylthio-substituted α,β- unsaturated carbonyl compounds. (a) Coates, R. M.; Sowerby, R. L. J. Am. Chem. Soc. 1971, 93, 1027. (b) Posner, G. H.; Brunelle, D. J. J. Org. Chem. 1973, 38, 2747. (c) Posner, G. H.; Brunelle, D. J. J. Chem. Soc., Chem. Commun. 1973, 907. (d) Gammill, R. B.; Bryson, T. A. Tetrahedron Lett. 1975, 3793.
    • (1975) Tetrahedron Lett. , pp. 3793
    • Gammill, R.B.1    Bryson, T.A.2
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    • There are some reports on the iron-catalyzed addition reactions (carbometalation) of organometallic reagents across alkenes and alkynes. (a) Nakamura, M.; Hirai, A.; Nakamura, E. J. Am. Chem. Soc. 2000, 122, 978. (b) Nakamura, M.; Matsuo, K.; Inoue, T.; Nakamura, E. Org. Lett. 2003, 5, 1373. (c) Hojo, M.; Murakami, Y.; Aihara, H.; Sakuragi, R.; Baba, Y.; Hosomi, A. Angew. Chem., Int. Ed. 2001, 40, 621.
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