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101. S. G. Newman, J. K. Howell, N. Nicolaus and M. Lautens, J. Am. Chem.
Soc., 2011, 133, 14916.
102. D. A. Petrone, H. A. Malik, A. Clemenceau and M. Lautens, Org. Lett.,
2012, 14, 4806.
103. For use of Lewis acids, see: H. L. van Lingen, W. Zhuang, T. Hansen,
F. P. J. T. Rutjes and K. A. Jørgensen, Org. Biomol. Chem, 2003, 1, 1953.
104. For use of organocatalysis, see: (a) Y. Lee, S. W. Seo and S.-G. Kim, Adv.
Synth. Catal., 2011, 353, 2671; (b) D.-F. Yu, Y. Wang and P. F. Xu, Adv.
Synth. Catal., 2011, 353, 2960; (c) D. Enders, G. Urbanietz, R. Hahn and
G. Raabe, Synthesis, 2012, 44, 773; (d) F. Hu, X. Guan and M. Shi, Tet-
rahedron, 2012, 68, 4782.
105. For use of Pd catalysis, see: (a) L. Yu, D.-H. Wang, K. M. Engle and
J.-Q. Yu, J. Am. Chem. Soc., 2010, 132, 5916; (b) M. Leibeling, B. Milde,
D. Kratzert, D. Stalke and D. B. Werz, Chem. Eur. J., 2011, 17, 9888;
(c) A. F. Ward, Y. Xu and J. P. Wolfe, Chem. Commun., 2012, 48, 609;
(d) J. S. Cannon, A. C. Olsen, L. E. Overman and N. S. Solomon, J. Org.
Chem., 2012, 77, 1961.
106. For other approaches, see: (a) M. R. Medeiros, R. S. Narayan,
N. T. McDougal, S. E. Schaus and J. A. Porco Jr, Org. Lett., 2010,
12, 3222; (b) N. Kern, A. Blanc, J. M. Weibel and P. Pale, Chem. Com-
mun., 2011, 47, 6665; (c) H. C. Shen, Tetrahedron, 2009, 65, 3931.
107. M. Leibeling, D. C. Koester, M. Pawliczek, S. V. Schild and D. B. Werz,
Nat. Chem. Biol., 2010, 6, 199.
108. X. Jia, D. A. Petrone and M. Lautens, Angew. Chem. Int. Ed., 2012,
51, 9870.
109. (a) M. Lautens and Y.-Q. Fang, Org. Lett., 2003, 5, 3679; (b) T. Saget,
D. Perez and N. Cramer, Org. Lett., 2013, 15, 1354.
110. D. A. Petrone, M. Lischka and M. Lautens, Angew. Chem. Int. Ed., 2013,
52, 10635.
111. (a) C. C. C. Johansson Seechurn, M. O. Kitching, T. J. Colacot and
V. Snieckus, Angew. Chem. Int. Ed., 2012, 51, 5062; (b) H. Li, C. C.
C. Johansson Seechurn and T. J. Colacot, ACS Catal., 2012, 2, 1147.
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