Chemistry Reference
In-Depth Information
63. For reviews of transition metal-catalyzed cross-couplings with poly-
halogenated substrates, see: (a) S. Schr ยจ ter, C. Stock and T. Bach, Tet-
rahedron, 2005, 61, 2245; (b) I. J. S. Fairlamb, Chem. Soc. Rev., 2007,
36, 1036; (c) J.-R. Wang and K. Manabe, Synthesis, 2009, 9, 1405;
(d) G. Chelucci, Chem. Rev., 2012, 112, 1344.
64. D. A. Evans and J. T. Starr, Angew. Chem. Int. Ed., 2002, 41, 1787.
65. For selected total syntheses utilizing polyhalogented substrates in
cross-coupling, see: (a) T. Bach and S. Heuser, Angew. Chem. Int. Ed.,
2001, 40, 3184; (b) L. S.-M. Wong, L. A. Sharp, N. M. C. Xavier, P. Turner
and M. S. Sherburn, Org. Lett., 2002, 4, 1955; (c) N. F. Langille and
J. S. Panek, Org. Lett., 2004, 6, 3203; (d) E. Roulland, Angew. Chem. Int.
Ed., 2008, 47, 3762.
66. S. T. Handy, T. Wilson and A. Muth, J. Org. Chem., 2007, 72, 8496.
67. S. T. Handy and Y. Zhang, Chem. Commun., 2006, 299.
68. (a) C. Y. Legault, Y. Garcia, C. A. Merlic and K. N. Houk, J. Am. Chem.
Soc., 2007, 129, 12664; (b) Y. Garcia, F. Schoenebeck, C. Y. Legault,
C. A. Merlic and K. N. Houk, J. Am. Chem. Soc., 2009, 131, 6632.
69. H. Nakamura, D. Takeuchi and A. Murai, Synlett, 1995, 1227.
70. (a) D. A. Colby, R. G. Bergman and J. A. Ellman, Chem. Rev., 2010,
110, 624; (b) L. Ackerman, Chem. Commun., 2010, 46, 4866;
(c) P. B. Arockiam, C. Bruneau and P. H. Dixneuf, Chem. Rev., 2010,
112, 5879; (d) G. Song, F. Wang and X. Li, Chem. Soc. Rev., 2012,
41, 3651; (e) K. M. Engle, T.-S. Mei, M. Wasa and J.-Q. Yu, Acc. Chem.
Res., 2012, 45, 788; (f) D. A. Colby, A. S. Tsai, R. G. Bergman and
J. A. Ellman, Acc. Chem. Res., 2012, 45, 814.
71. For a recent review of cascade Pd- and Cu-catalyzed heterocycle syn-
thesis, see: C. J. Ball and M. C. Willis, Eur. J. Org. Chem., 2013, 425.
72. M. C. Willis, G. N. Brace, T. J. K. Findlay and I. P. Holmes, Adv. Synth.
Catal., 2006, 348, 851.
73. J. A. Joule and K. Mills, Heterocyclic Chemistry, Wiley-Blackwell, Chi-
chester, 5th edn, 2010.
74. F. Ramirez, N. B. Desai and N. McKelvie, J. Am. Chem. Soc., 1962, 84, 1745.
75. Y.-Q. Fang and M. Lautens, Org. Lett., 2005, 7, 3549.
76. (a) Y.-Q. Fang and M. Lautens, J. Org. Chem., 2008, 73, 538;
(b) mechanistic studies conducted for a related gem-dibromoolefin
system suggest that E to Z isomerization of a vinylpalladium(II) halide
intermediate is a plausible pathway, which would lead to a formal
Z-selective oxidative addition product: R. Y. Huang, P. T. Franke,
N. Nicolaus and M. Lautens, Tetrahedron, 2013, 69, 4395
77. M. Nagamochi, Y.-Q. Fang and M. Lautens, Org. Lett., 2007, 9, 2955.
78. A. Fayol, Y.-Q. Fang and M. Lautens, Org. Lett., 2006, 8, 4203.
79. J. Yuen, Y.-Q. Fang and M. Lautens, Org. Lett., 2006, 8, 653.
80. C. S. Bryan and M. Lautens, Org. Lett., 2008, 10, 4633.
81. Y.-Q. Fang, J. Yuen and M. Lautens, J. Org. Chem., 2007, 72, 5152.
82. T. Kosjek and E. Heath, Top. Heterocycl. Chem., 2012, 27, 219.
Search WWH ::




Custom Search