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Volumn 6, Issue 4, 2004, Pages 533-535

Catalytic C-H Functionalization Driven by CO as a Stoichiometric Reductant: Application to Carbazole Synthesis

Author keywords

[No Author keywords available]

Indexed keywords

CARBAZOLE DERIVATIVE; CARBON MONOXIDE; HYDROGEN; NITROGEN DERIVATIVE; PALLADIUM ACETATE; REDUCING AGENT;

EID: 1342332918     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol036294l     Document Type: Article
Times cited : (148)

References (36)
  • 7
    • 0000518357 scopus 로고
    • For a review of Pd(II)-catalyzed reactions, see: Hegedus, L. S. Tetrahedron 1984, 40, 2415-2434.
    • (1984) Tetrahedron , vol.40 , pp. 2415-2434
    • Hegedus, L.S.1
  • 17
    • 0028792613 scopus 로고
    • For applications in the syntheses of carbazole alkaloids, see: (a) Lowinger, T. B.; Chu, J.; Spence, P. L. Tetrahedron Lett. 1995, 36, 8383-8386. (b) Moody, J. C. Synlett 1994, 681-688. (c) Hughes, I.; Nolan, W. P.; Raphael, R. A. J. Chem. Soc., Perkin Trans. 1 1990, 2475-2477.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 8383-8386
    • Lowinger, T.B.1    Chu, J.2    Spence, P.L.3
  • 18
    • 0002551272 scopus 로고
    • For applications in the syntheses of carbazole alkaloids, see: (a) Lowinger, T. B.; Chu, J.; Spence, P. L. Tetrahedron Lett. 1995, 36, 8383-8386. (b) Moody, J. C. Synlett 1994, 681-688. (c) Hughes, I.; Nolan, W. P.; Raphael, R. A. J. Chem. Soc., Perkin Trans. 1 1990, 2475-2477.
    • (1994) Synlett , pp. 681-688
    • Moody, J.C.1
  • 19
    • 37049070960 scopus 로고
    • For applications in the syntheses of carbazole alkaloids, see: (a) Lowinger, T. B.; Chu, J.; Spence, P. L. Tetrahedron Lett. 1995, 36, 8383-8386. (b) Moody, J. C. Synlett 1994, 681-688. (c) Hughes, I.; Nolan, W. P.; Raphael, R. A. J. Chem. Soc., Perkin Trans. 1 1990, 2475-2477.
    • (1990) J. Chem. Soc., Perkin Trans. 1 , pp. 2475-2477
    • Hughes, I.1    Nolan, W.P.2    Raphael, R.A.3
  • 22
    • 0001641604 scopus 로고    scopus 로고
    • For palladium-catalyzed reductive cyclization to indoles, see: (a) Ragaini, F.; Sportiello, P.; Cenini, S. J. Organomet. Chem. 1999, 577, 283-291. (b) Tollari, S.; Cenini, S.; Crotti, C.; Gianella, E. J. Mol. Catal. 1994, 87, 203-214. (c) Scott, T. L.; Söderberg, B. C. G. Tetrahedron Lett. 2002, 43, 1621-1624. (d) Söderberg, B. C.; Rector, S. R.; O'Neil, S. N. Tetrahedron Lett. 1999, 40, 3657-3660. (e) Söderberg, B. C.; Shriver, J. A. J. Org. Chem. 1997, 62, 5838-5845.
    • (1999) J. Organomet. Chem. , vol.577 , pp. 283-291
    • Ragaini, F.1    Sportiello, P.2    Cenini, S.3
  • 23
    • 0028763695 scopus 로고
    • For palladium-catalyzed reductive cyclization to indoles, see: (a) Ragaini, F.; Sportiello, P.; Cenini, S. J. Organomet. Chem. 1999, 577, 283-291. (b) Tollari, S.; Cenini, S.; Crotti, C.; Gianella, E. J. Mol. Catal. 1994, 87, 203-214. (c) Scott, T. L.; Söderberg, B. C. G. Tetrahedron Lett. 2002, 43, 1621-1624. (d) Söderberg, B. C.; Rector, S. R.; O'Neil, S. N. Tetrahedron Lett. 1999, 40, 3657-3660. (e) Söderberg, B. C.; Shriver, J. A. J. Org. Chem. 1997, 62, 5838-5845.
    • (1994) J. Mol. Catal. , vol.87 , pp. 203-214
    • Tollari, S.1    Cenini, S.2    Crotti, C.3    Gianella, E.4
  • 24
    • 0037170155 scopus 로고    scopus 로고
    • For palladium-catalyzed reductive cyclization to indoles, see: (a) Ragaini, F.; Sportiello, P.; Cenini, S. J. Organomet. Chem. 1999, 577, 283-291. (b) Tollari, S.; Cenini, S.; Crotti, C.; Gianella, E. J. Mol. Catal. 1994, 87, 203-214. (c) Scott, T. L.; Söderberg, B. C. G. Tetrahedron Lett. 2002, 43, 1621-1624. (d) Söderberg, B. C.; Rector, S. R.; O'Neil, S. N. Tetrahedron Lett. 1999, 40, 3657-3660. (e) Söderberg, B. C.; Shriver, J. A. J. Org. Chem. 1997, 62, 5838-5845.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 1621-1624
    • Scott, T.L.1    Söderberg, B.C.G.2
  • 25
    • 0033531984 scopus 로고    scopus 로고
    • For palladium-catalyzed reductive cyclization to indoles, see: (a) Ragaini, F.; Sportiello, P.; Cenini, S. J. Organomet. Chem. 1999, 577, 283-291. (b) Tollari, S.; Cenini, S.; Crotti, C.; Gianella, E. J. Mol. Catal. 1994, 87, 203-214. (c) Scott, T. L.; Söderberg, B. C. G. Tetrahedron Lett. 2002, 43, 1621-1624. (d) Söderberg, B. C.; Rector, S. R.; O'Neil, S. N. Tetrahedron Lett. 1999, 40, 3657-3660. (e) Söderberg, B. C.; Shriver, J. A. J. Org. Chem. 1997, 62, 5838-5845.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 3657-3660
    • Söderberg, B.C.1    Rector, S.R.2    O'Neil, S.N.3
  • 26
    • 0038460609 scopus 로고    scopus 로고
    • For palladium-catalyzed reductive cyclization to indoles, see: (a) Ragaini, F.; Sportiello, P.; Cenini, S. J. Organomet. Chem. 1999, 577, 283-291. (b) Tollari, S.; Cenini, S.; Crotti, C.; Gianella, E. J. Mol. Catal. 1994, 87, 203-214. (c) Scott, T. L.; Söderberg, B. C. G. Tetrahedron Lett. 2002, 43, 1621-1624. (d) Söderberg, B. C.; Rector, S. R.; O'Neil, S. N. Tetrahedron Lett. 1999, 40, 3657-3660. (e) Söderberg, B. C.; Shriver, J. A. J. Org. Chem. 1997, 62, 5838-5845.
    • (1997) J. Org. Chem. , vol.62 , pp. 5838-5845
    • Söderberg, B.C.1    Shriver, J.A.2
  • 32
    • 1342306845 scopus 로고    scopus 로고
    • note
    • Optimization was accomplished by using a 6 x 8 module parallel pressure reactor system.
  • 35
  • 36
    • 1342328170 scopus 로고    scopus 로고
    • see ref 3
    • For counterion effects in Pd-catalyzed C-H functionalization reactions, see ref 3.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.