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Volumn 39, Issue 3, 2000, Pages 631-633

Phosphane sulfide/octacarbonyldicobalt-catalyzed Pauson - Khand reaction under an atmospheric pressure of carbon monoxide

Author keywords

Cobalt; Cycloadditions; Homogeneous catalysis; Pauson Khand reactions; S ligands

Indexed keywords

CARBON MONOXIDE; COBALT DERIVATIVE; CYCLOPENTENONE DERIVATIVE; ORGANOPHOSPHORUS COMPOUND;

EID: 0034603010     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(20000204)39:3<631::AID-ANIE631>3.0.CO;2-B     Document Type: Article
Times cited : (79)

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  • 15
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    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 10782-10783
    • Sugihara, T.1    Yamaguchi, M.2
  • 16
    • 0000515507 scopus 로고    scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1998) Synlett , pp. 1384-1386
    • Sugihara, T.1    Yamaguchi, M.2
  • 17
    • 0032532517 scopus 로고    scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 7637-7640
    • Belanger, O.B.1    O'Mahony, D.J.R.2    Livinghouse, T.3
  • 18
    • 0032532236 scopus 로고    scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 7641-7644
    • Belanger, D.H.1    Livinghouse, T.2
  • 19
    • 0031936070 scopus 로고    scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1998) Synthesis , pp. 142-144
    • Kim, J.W.1    Chung, Y.K.2
  • 20
    • 0029952824 scopus 로고    scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 9450-9451
    • Hicks, F.A.1    Kablaoui, N.M.2    Buchwald, S.L.3
  • 21
    • 0029909515 scopus 로고    scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 11688-11689
    • Hicks, K.A.1    Buchawald, S.L.2
  • 22
    • 0000443422 scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 4912-4913
    • Berk, S.C.1    Grossman, R.B.2    Buchwald, S.L.3
  • 23
    • 0032360438 scopus 로고    scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1998) Chem. Lett. , pp. 249-250
    • Koga, Y.1    Kobayashi, T.2    Narasaka, K.3
  • 24
    • 0001171594 scopus 로고    scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1998) Organometallics , vol.17 , pp. 3642-3644
    • Jeong, N.1    Lee, S.2    Sung, B.K.3
  • 25
    • 0030746742 scopus 로고    scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187-6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 6187-6188
    • Kondo, T.1    Suzuki, N.2    Okada, T.3    Mitsudo, T.4
  • 26
    • 0000687565 scopus 로고    scopus 로고
    • For Co-catalyzed reactions, see: a) V. Rautenstrauch, P. Mégard, José Conesa, W. Küster, Angew. Chem. 1990, 102, 1441-1443; Angew. Chem. Int. Ed. Engl. 1990, 29, 1413-1416; b) N. Jeong, S. H. Hwang, Y. Lee, J. Am. Chem. Soc. 1994, 116, 3159-3160; c) B. Y. Lee, Y. K. Chung, J. Am. Chem. Soc. 1994, 116, 8793-8794; d) N. Y. Lee, Y. K. Chung, Tetrahedron Lett. 1996, 37, 3145-3148; e) B. L. Pagenkopf, T. Livinghouse, J. Am. Chem. Soc. 1996, 118, 2285-2286; f) N. Jeong, S. H. Hwang, Y. W. Lee, J. S. Lim, J. Am. Chem. Soc. 1997, 119, 10549-10550; g) T. Sugihara, M. Yamaguchi, J. Am. Chem. Soc. 1998, 120, 10782 10783; h) T. Sugihara, M. Yamaguchi, Synlett 1998, 1384-1386; i) O. B. Belanger, D. J. R. O'Mahony, T. Livinghouse, Tetrahedron Lett. 1998, 39, 7637-7640; j) D. H. Belanger, T. Livinghouse. Tetrahedron Lett. 1998, 39, 7641-7644; k) J. W. Kim, Y. K. Chung. Synthesis 1998, 142-144. For Ti-catalyzed reactions, see: l) F. A. Hicks, N.M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1996, 118, 9450 9451; m) K A. Hicks, S. L. Buchawald, J. Am. Chem. Soc. 1996, 118, 11 688- 11 689; n) S. C. Berk, R. B. Grossman, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 4912-4913. For Rh-catalyzed reactions, see; o) Y. Koga, T. Kobayashi, K. Narasaka, Chem. Lett. 1998, 249-250; p) N. Jeong, S. Lee, B. K. Sung, Organometallics 1998, 17, 3642-3644. For Ru-catalyzed reactions, see: q) T. Kondo, N. Suzuki, T. Okada, T. Mitsudo, J. Am. Chem. Soc. 1997, 119, 6187- 6188; r) T. Morimoto, N. Chatani, Y. Fukumoto, S. Murai, J. Org. Chem. 1997, 62, 3762-3765.
    • (1997) J. Org. Chem. , vol.62 , pp. 3762-3765
    • Morimoto, T.1    Chatani, N.2    Fukumoto, Y.3    Murai, S.4
  • 30
    • 85021282149 scopus 로고    scopus 로고
    • We used commercially available octacarhonyldicobalt (Fluka and Kanto Chemicals) without further purification. Both products gave comparable results; in many cases the difference in yield was less than 2%
    • We used commercially available octacarhonyldicobalt (Fluka and Kanto Chemicals) without further purification. Both products gave comparable results; in many cases the difference in yield was less than 2%.
  • 31
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    • A similar equilibrium was proposed to account for the acceleration arising from an internal sulfur ligand in an intramolecular Pauson-Khand reaction: M. E. Krafft, I. L. Scott, R. H. Romero, Tetrahedron Lett. 1992, 33, 3829-3832.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 3829-3832
    • Krafft, M.E.1    Scott, I.L.2    Romero, R.H.3
  • 32
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    • Cobalt-calalyzed Pauson-Khand reactions are usually performed in DME; see refs. [2b-c, 2h-j]
    • Cobalt-calalyzed Pauson-Khand reactions are usually performed in DME; see refs. [2b-c, 2h-j].
  • 33
    • 85021307100 scopus 로고    scopus 로고
    • In the case of entry 5, reaction with a catalyst to additive ratio of 1:4 gave a better result than with a ratio of 1:6, but the reason for this is unclear
    • In the case of entry 5, reaction with a catalyst to additive ratio of 1:4 gave a better result than with a ratio of 1:6, but the reason for this is unclear.
  • 35
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    • T. Sugihara, M. Yamada, H. Ban, M. Yamaguchi, C. Kaneko, Angew. Chem. 1997, 109, 2884-2886; Angew. Chem. Int. Ed. Engl. 1997, 36, 2801-2804.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 2801-2804


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