Molecular orbital theory : an introductory lecture note and by C J Ballhausen

By C J Ballhausen

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Lawrence, and T. Gallagher, Org. , 2003, 5, 811. S. Frere, V. Thiery, and T. Besson, Synth. , 2003, 33, 3795. U. Rinner, D. R. Adams, M. L. dos Santos, K. A. Abboud, and T. Hudlicky, Synlett, 2003, 1247. M. Reggelin, H. Weinberger, and V. Spohr, Adv. Synth. , 2004, 346, 1295. A. Avenoza, J. H. Busto, F. Corzana, G. Jimenez-Oses, and J. M. Peregrina, J. Chem. , Chem. , 2004, 980. K. C. Nicolaou, S. A. Snyder, D. A. Longbottom, A. Z. Nalbandian, and X. Huang, Chem. Eur. , 2004, 10, 5581. L. Beer, J.

B. Aguilera, A. Fernandez-Mayoralas, and C. Jaramillo, Tetrahedron, 1997, 53, 5863. T. M. Barclay, A. W. Cordes, R. T. Oakley, K. E. Preuss, and R. W. Reed, J. Chem. , Chem. , 1998, 1039. C. W. -Y. Yue, J. Chem. , Chem. , 1998, 1207. T. M. Barclay, I. J. Burgess, A. W. Cordes, R. T. Oakley, and R. W. Reed, J. Chem. , Chem. , 1998, 1939. V. Thiery, C. W. Rees, T. Besson, G. -M. Pons, Eur. J. Med. , 1998, 33, 149. D. Clarke, K. Emayan, and C. W. Rees, J. Chem. , Perkin Trans. 1, 1998, 77. T. Besson, J.

The structure of all of them was proved by X-ray analysis. One of these, 1,2,3-dithiazole 49, can be obtained by spontaneous transformation of phosphinimine 161 (Equation 46). ð46Þ Reaction of N-sulfinyl derivative 162 with oxiranes in the presence of a catalyst such as Et4NBr and LiCl or LiBr gave the cyclocondensation products – 1,2,3-oxathiazolidines 163 (Equation 47) <1996JFC49>. 1,2-Oxa/thia-3-azoles ð47Þ Reaction of 2-dialkylaminoazirines 164 with N-sulfonylalkylamines 165, prepared in situ from sulfamoylchlorides and triethylamine, gave 1,2,3-oxathiazoles 166 (Scheme 31) <1996J(P1)1629>.

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