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0034686072
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For reviews, see: (a) Brummond, K. M.; Kent, J. L. Tetrahedron 2000, 56, 3263; (b) Chung, Y. K. Coord. Chem. Rev. 1999, 188, 297; (c) Jeong, N. In Transition Metals in Organic Synthesis; Beller, M.; Bolm, C., Eds.; Wiley-VCH: Weinheim, 1998; Vol. 1, p. 560.
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Tetrahedron
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, pp. 3263
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Brummond, K.M.1
Kent, J.L.2
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0000939078
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For reviews, see: (a) Brummond, K. M.; Kent, J. L. Tetrahedron 2000, 56, 3263; (b) Chung, Y. K. Coord. Chem. Rev. 1999, 188, 297; (c) Jeong, N. In Transition Metals in Organic Synthesis; Beller, M.; Bolm, C., Eds.; Wiley-VCH: Weinheim, 1998; Vol. 1, p. 560.
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(1999)
Coord. Chem. Rev.
, vol.188
, pp. 297
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Chung, Y.K.1
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3
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0000213863
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Beller, M.; Bolm, C., Eds.; Wiley-VCH: Weinheim
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For reviews, see: (a) Brummond, K. M.; Kent, J. L. Tetrahedron 2000, 56, 3263; (b) Chung, Y. K. Coord. Chem. Rev. 1999, 188, 297; (c) Jeong, N. In Transition Metals in Organic Synthesis; Beller, M.; Bolm, C., Eds.; Wiley-VCH: Weinheim, 1998; Vol. 1, p. 560.
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Transition Metals in Organic Synthesis
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Jeong, N.1
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0343114422
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Kim S.-W., Son S.U., Lee S.-I., Hyeon T., Chung Y.K. J. Am. Chem. Soc. 122:2000;1550.
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J. Am. Chem. Soc.
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Kim, S.-W.1
Son, S.U.2
Lee, S.-I.3
Hyeon, T.4
Chung, Y.K.5
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0037061055
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Köckritz A., Bischoff S., Morawsky V., Prusse U., Vorlop K.-D. J. Mol. Catal. A: Chem. 180:2002;231.
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J. Mol. Catal. A: Chem.
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Köckritz, A.1
Bischoff, S.2
Morawsky, V.3
Prusse, U.4
Vorlop, K.-D.5
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Abu-Rezig R., Avnir D., Miloslavski I., Schumann H., Blum J. J. Mol. Catal. A: Chem. 185:2002;179;
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Avnir, D.2
Miloslavski, I.3
Schumann, H.4
Blum, J.5
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19
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0012456998
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Rh-P=171.3 Hz), 41.7 (s) ppm; see the paper by Bunten, K. A.; Farrar, D. H.; Poë, A. J.; Lough, A. Organometallics 2002, 21, 3344. During the sol-gel process, one of the phosphines was oxidized to phosphine oxide.
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Bunten, K.A.1
Farrar, D.H.2
Poë, A.J.3
Lough, A.4
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85031198638
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General procedure for catalytic Pauson-Khand reactions: To a solution of 1,6-enyne (0.20 g, 1.2 mmol; entry 1 in Table 1) in 5 mL of THF was added entrapped Rh (12.5 mg, 0.12 mmol, 10 mol%). The reactor was charged with 5 atm of CO and heated at 100°C for 12 h. After the reactor was cooled to rt, the solution was filtered, concentrated, and chromatographed on a silica gel column eluting with hexane and diethyl ether (v/v, 5:1). When the catalyst was recycled, the catalyst was filtered, dried in vacuum, and reused for the further catalytic reaction
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General procedure for catalytic Pauson-Khand reactions: To a solution of 1,6-enyne (0.20 g, 1.2 mmol; entry 1 in Table 1) in 5 mL of THF was added entrapped Rh (12.5 mg, 0.12 mmol, 10 mol%). The reactor was charged with 5 atm of CO and heated at 100°C for 12 h. After the reactor was cooled to rt, the solution was filtered, concentrated, and chromatographed on a silica gel column eluting with hexane and diethyl ether (v/v, 5:1). When the catalyst was recycled, the catalyst was filtered, dried in vacuum, and reused for the further catalytic reaction.
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23
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0037458972
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Lipshutz B.H., Tasler S., Chrisman W., Spliethoff B., Tesche B. J. Org. Chem. 68:2003;1177.
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J. Org. Chem.
, vol.68
, pp. 1177
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Lipshutz, B.H.1
Tasler, S.2
Chrisman, W.3
Spliethoff, B.4
Tesche, B.5
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