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Volumn 44, Issue 14, 2003, Pages 2827-2830

Pauson-Khand reactions catalyzed by entrapped rhodium complexes

Author keywords

[No Author keywords available]

Indexed keywords

RHODIUM COMPLEX;

EID: 0037474641     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)00434-9     Document Type: Article
Times cited : (29)

References (23)
  • 1
    • 0034686072 scopus 로고    scopus 로고
    • 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.
    • (2000) Tetrahedron , vol.56 , pp. 3263
    • Brummond, K.M.1    Kent, J.L.2
  • 2
    • 0000939078 scopus 로고    scopus 로고
    • 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.
    • (1999) Coord. Chem. Rev. , vol.188 , pp. 297
    • Chung, Y.K.1
  • 3
    • 0000213863 scopus 로고    scopus 로고
    • Beller, M.; Bolm, C., Eds.; Wiley-VCH: Weinheim
    • 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.
    • (1998) Transition Metals in Organic Synthesis , vol.1 , pp. 560
    • Jeong, N.1
  • 19
    • 0012456998 scopus 로고    scopus 로고
    • 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.
    • (2002) Organometallics , vol.21 , pp. 3344
    • Bunten, K.A.1    Farrar, D.H.2    Poë, A.J.3    Lough, A.4
  • 20
    • 85031198638 scopus 로고    scopus 로고
    • 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
    • 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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