Author:
Anderson James C.,James Daniel S.,Mathias John P.
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference10 articles.
1. (a) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, G. C.; Martin, C. J.; Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065–72. (b) Chelucci, G.; Cabras, M. A. Tetrahedron: Asymmetry 1996, 7, 965–6. (c) Morimoto, T.; Tachibana, K.; Achiwa, K. Synlett 1997, 783–5. (d) Chesney, A.; Bryce, M. R.; Chubb, R. W. J.; Batsanov, A. S.; Howard, J. A. K. Tetrahedron: Asymmetry 1997, 8, 2337–46.
2. Saitoh, A.; Morimoto, T.; Achiwa, K. Tetrahedron: Asymmetry 1997, 8, 3567–70.
3. These original assumptions have been supported by other workers. See Kang, J.; Kim, J. B.; Kim, J. W.; Lee, D. J. Chem. Soc., Perkin Trans. 2, 1997, 189–94.
4. Anderson, J. C.; Harding, M. Chem. Commun. 1998, 393–4.
5. R′=Ph, R″=H and R′=Ts, R″=H gave no product. R′=Ph, R″=Me gave only 10% yield of essentially racemic product under the reaction conditions described for 1.
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