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Recent reviews of the Pauson-Khand(-type) reaction: (a) Jeong, N. In Transition Metals In Organic Synthesis, Vol. 1; Beller, M.; Bolm, C., Eds.; Wiley-VCH: Weinheim, 1998, 560. (b) Chung, Y. K. Coord. Chem. Rev. 1999, 188, 297. (c) Hanson, B. E. Comments on Inorg. Chem. 2002, 23, 289.
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Recent reviews of the Pauson-Khand(-type) reaction: (a) Jeong, N. In Transition Metals In Organic Synthesis, Vol. 1; Beller, M.; Bolm, C., Eds.; Wiley-VCH: Weinheim, 1998, 560. (b) Chung, Y. K. Coord. Chem. Rev. 1999, 188, 297. (c) Hanson, B. E. Comments on Inorg. Chem. 2002, 23, 289.
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Recent reviews of the Pauson-Khand(-type) reaction: (a) Jeong, N. In Transition Metals In Organic Synthesis, Vol. 1; Beller, M.; Bolm, C., Eds.; Wiley-VCH: Weinheim, 1998, 560. (b) Chung, Y. K. Coord. Chem. Rev. 1999, 188, 297. (c) Hanson, B. E. Comments on Inorg. Chem. 2002, 23, 289.
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Recent examples of Co catalysts: (a) Jeong, N.; Hwang, S. H. Angew. Chem. Int. Ed. 2000, 39, 636. (b) Kim, S.-W.; Son, S. U.; Lee, S. I.; Hyeon, T.; Chung, Y. K. J. Am. Chem. Soc. 2000, 122, 1550. (c) Comely, A. C.; Gibson, S. F.; Stevenazzi, A.; Hales, N. J. Tetrahedron Lett. 2001, 42, 1183. (d) Sugihara, T.; Yamaguchi, M.; Nishizawa, M. Chem.-Eur. J. 2001, 7, 1589. (e) Krafft, M. E.; Boñaga, L. V. R.; Hirosawa, J. J. Org. Chem. 2001, 66, 3004.
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Recent examples of Co catalysts: (a) Jeong, N.; Hwang, S. H. Angew. Chem. Int. Ed. 2000, 39, 636. (b) Kim, S.-W.; Son, S. U.; Lee, S. I.; Hyeon, T.; Chung, Y. K. J. Am. Chem. Soc. 2000, 122, 1550. (c) Comely, A. C.; Gibson, S. F.; Stevenazzi, A.; Hales, N. J. Tetrahedron Lett. 2001, 42, 1183. (d) Sugihara, T.; Yamaguchi, M.; Nishizawa, M. Chem.-Eur. J. 2001, 7, 1589. (e) Krafft, M. E.; Boñaga, L. V. R.; Hirosawa, J. J. Org. Chem. 2001, 66, 3004.
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Recent examples of Co catalysts: (a) Jeong, N.; Hwang, S. H. Angew. Chem. Int. Ed. 2000, 39, 636. (b) Kim, S.-W.; Son, S. U.; Lee, S. I.; Hyeon, T.; Chung, Y. K. J. Am. Chem. Soc. 2000, 122, 1550. (c) Comely, A. C.; Gibson, S. F.; Stevenazzi, A.; Hales, N. J. Tetrahedron Lett. 2001, 42, 1183. (d) Sugihara, T.; Yamaguchi, M.; Nishizawa, M. Chem.-Eur. J. 2001, 7, 1589. (e) Krafft, M. E.; Boñaga, L. V. R.; Hirosawa, J. J. Org. Chem. 2001, 66, 3004.
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Recent examples of Co catalysts: (a) Jeong, N.; Hwang, S. H. Angew. Chem. Int. Ed. 2000, 39, 636. (b) Kim, S.-W.; Son, S. U.; Lee, S. I.; Hyeon, T.; Chung, Y. K. J. Am. Chem. Soc. 2000, 122, 1550. (c) Comely, A. C.; Gibson, S. F.; Stevenazzi, A.; Hales, N. J. Tetrahedron Lett. 2001, 42, 1183. (d) Sugihara, T.; Yamaguchi, M.; Nishizawa, M. Chem.-Eur. J. 2001, 7, 1589. (e) Krafft, M. E.; Boñaga, L. V. R.; Hirosawa, J. J. Org. Chem. 2001, 66, 3004.
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Recent examples of Co catalysts: (a) Jeong, N.; Hwang, S. H. Angew. Chem. Int. Ed. 2000, 39, 636. (b) Kim, S.-W.; Son, S. U.; Lee, S. I.; Hyeon, T.; Chung, Y. K. J. Am. Chem. Soc. 2000, 122, 1550. (c) Comely, A. C.; Gibson, S. F.; Stevenazzi, A.; Hales, N. J. Tetrahedron Lett. 2001, 42, 1183. (d) Sugihara, T.; Yamaguchi, M.; Nishizawa, M. Chem.-Eur. J. 2001, 7, 1589. (e) Krafft, M. E.; Boñaga, L. V. R.; Hirosawa, J. J. Org. Chem. 2001, 66, 3004.
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Krafft, M.E.1
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Recent examples of Rh catalysts: (a) Kobayashi, T.; Koga, Y.; Narasaka, K. J. Orgmet. Chem. 2001, 624, 73. (b) Jeong, N.; Sung, B. K.; Choi, Y. K. J. Am. Chem. Soc. 2000, 122, 6771. (c) Evans, P. A.; Robinson, J. E. J. Am. Chem. Soc. 2001, 123, 4609. (d) Morimoto, T.; Fuji, K.; Tsutsumi, K.; Kakiuchi, K. J. Am. Chem. Soc. 2002, 124, 3806. (e) Shibata, T.; Toshida, N.; Takagi, K. Org. Lett. 2002, 4, 1619.
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Recent examples of Rh catalysts: (a) Kobayashi, T.; Koga, Y.; Narasaka, K. J. Orgmet. Chem. 2001, 624, 73. (b) Jeong, N.; Sung, B. K.; Choi, Y. K. J. Am. Chem. Soc. 2000, 122, 6771. (c) Evans, P. A.; Robinson, J. E. J. Am. Chem. Soc. 2001, 123, 4609. (d) Morimoto, T.; Fuji, K.; Tsutsumi, K.; Kakiuchi, K. J. Am. Chem. Soc. 2002, 124, 3806. (e) Shibata, T.; Toshida, N.; Takagi, K. Org. Lett. 2002, 4, 1619.
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Recent examples of Rh catalysts: (a) Kobayashi, T.; Koga, Y.; Narasaka, K. J. Orgmet. Chem. 2001, 624, 73. (b) Jeong, N.; Sung, B. K.; Choi, Y. K. J. Am. Chem. Soc. 2000, 122, 6771. (c) Evans, P. A.; Robinson, J. E. J. Am. Chem. Soc. 2001, 123, 4609. (d) Morimoto, T.; Fuji, K.; Tsutsumi, K.; Kakiuchi, K. J. Am. Chem. Soc. 2002, 124, 3806. (e) Shibata, T.; Toshida, N.; Takagi, K. Org. Lett. 2002, 4, 1619.
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Recent examples of Rh catalysts: (a) Kobayashi, T.; Koga, Y.; Narasaka, K. J. Orgmet. Chem. 2001, 624, 73. (b) Jeong, N.; Sung, B. K.; Choi, Y. K. J. Am. Chem. Soc. 2000, 122, 6771. (c) Evans, P. A.; Robinson, J. E. J. Am. Chem. Soc. 2001, 123, 4609. (d) Morimoto, T.; Fuji, K.; Tsutsumi, K.; Kakiuchi, K. J. Am. Chem. Soc. 2002, 124, 3806. (e) Shibata, T.; Toshida, N.; Takagi, K. Org. Lett. 2002, 4, 1619.
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Recent examples of Rh catalysts: (a) Kobayashi, T.; Koga, Y.; Narasaka, K. J. Orgmet. Chem. 2001, 624, 73. (b) Jeong, N.; Sung, B. K.; Choi, Y. K. J. Am. Chem. Soc. 2000, 122, 6771. (c) Evans, P. A.; Robinson, J. E. J. Am. Chem. Soc. 2001, 123, 4609. (d) Morimoto, T.; Fuji, K.; Tsutsumi, K.; Kakiuchi, K. J. Am. Chem. Soc. 2002, 124, 3806. (e) Shibata, T.; Toshida, N.; Takagi, K. Org. Lett. 2002, 4, 1619.
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We already reported that iridium-chiral phosphine complex is an efficient catalyst for highly enantioselective Pauson-Khand type reaction of enynes: Shibata, T.; Takagi, K. J. Am. Chem. Soc. 2000, 122, 9852.
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note
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2: 240.1150.
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31
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0037176294
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Under CO-free conditions, Rh-catalyzed ene-type reaction proceeds to give cross-conjugated trienes: (a) Brummond, K. M.; Chen, H.; Sill, P.; You, L. J. Am. Chem. Soc. 2002, 124, 15186. (b) Shibata, T.; Takesue, Y.; Kadowaki, S.; Takagi, K. Synlett 2003, 268.
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Brummond, K.M.1
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Sill, P.3
You, L.4
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32
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0037287106
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Under CO-free conditions, Rh-catalyzed ene-type reaction proceeds to give cross-conjugated trienes: (a) Brummond, K. M.; Chen, H.; Sill, P.; You, L. J. Am. Chem. Soc. 2002, 124, 15186. (b) Shibata, T.; Takesue, Y.; Kadowaki, S.; Takagi, K. Synlett 2003, 268.
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Synlett
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Shibata, T.1
Takesue, Y.2
Kadowaki, S.3
Takagi, K.4
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