CrossRef enabled

PAC Archives

Contents index →

Adobe Acrobat Reader

Our PDF files are best viewed with Adobe Acrobat Reader 6 or higher.

Get Adobe Reader!

Pure Appl. Chem., 2008, Vol. 80, No. 5, pp. 1071-1077

doi:10.1351/pac200880051071

Asymmetric epoxidation of olefins catalyzed by Ti(salan) complexes using aqueous hydrogen peroxide as the oxidant

Kazuhiro Matsumoto, Yuji Sawada, and Tsutomu Katsuki

Department of Chemistry, Faculty of Science, Graduate School, Kyushu University, Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan

References:

  • 1. A. K. Yudin (Ed.). Aziridines and Epoxides in Organic Synthesis, Wiley-VCH, Weinheim (2006).
  • 2. (a) A. Berkessel, H. Groger (Eds.). Asymmetric Organocatalysis, Wiley-VCH, Weinheim (2005);
  • 2. (b) T. Katsuki. In Comprehensive Coordination Chemistry II, Vol. 9, J. A. McCleverty, T. J. Meyer (Eds.), Elsevier Science, Oxford (2003);
  • 2. (c) T. Katsuki. In Catalytic Asymmetric Synthesis, 2nd ed., I. Ojima (Ed.), Wiley-VCH, New York (2000);
  • 2. (d) E. N. Jacobsen, M. N. Wu. In Comprehensive Asymmetric Catalysis, Vol. 2, E. N. Jacobsen, A. Pfaltz, H. Yamamoto (Eds.), Springer, Berlin (1999).
  • 3. (a) S. Julia, J. Masana, J. C. Vega. Angew. Chem., Int. Ed. 19, 929 (1980); (doi:10.1002/anie.198009291)
  • 3. (b) S. Colonna, H. Molinari, S. Banfi, S. Julia, J. Masana, A. Alvalez. Tetrahedron 39, 1635 (1983); (doi:10.1016/S0040-4020(01)88574-4)
  • 3. (c) P. Pietikainen. Tetrahedron Lett. 50, 941 (1994); (doi:10.1016/S0040-4039(00)76006-0)
  • 3. (d) A. Berkessel, M. Frauenkron, T. Schwekreis, A. Steinmetz, G. Baum, D. Fenske. J. Mol. Catal. A 113, 321 (1996); (doi:10.1016/S1381-1169(96)00116-1)
  • 3. (e) P. Pietikainen. Tetrahedron 54, 4319 (1998); (doi:10.1016/S0040-4020(98)00145-8)
  • 3. (f) S. Arai, H. Tsuge, T. Shioiri. Tetrahedron Lett. 39, 7563 (1998); (doi:10.1016/S0040-4039(98)01646-3)
  • 3. (g) L. Shu, Y. Shi. Tetrahedron 57, 5213 (2001); (doi:10.1016/S0040-4020(01)00362-3)
  • 3. (h) R. I. Kureshy, N. H. Kahn, S. H. R. Abdi, S. Singh, I. Ahmed, R. S. Shunkla, R. V. Jasra. J. Catal. 219, 1 (2003); (doi:10.1016/S0021-9517(03)00163-5)
  • 3. (i) M. K. Tse, C. Dobler, S. Bhor, M. Klawonn, W. Magerlein, H. Hugl, M. Beller. Angew. Chem., Int. Ed. 43, 5255 (2004); (doi:10.1002/anie.200460528)
  • 3. (j) M. Marigo, J. Franzen, T. B. Poulsen, W. Zhuang, K. A. Jorgensen. J. Am. Chem. Soc. 127, 6964 (2005); (doi:10.1021/ja051808s)
  • 3. (k) M. Colladon, A. Scarso, P. Sgarbossa, R. A. Michelin, G. Strukul. J. Am. Chem. Soc. 128, 14006 (2006); (doi:10.1021/ja0647607)
  • 3. (l) C. P. Burke, L. Shu, Y. Shi. J. Org. Chem. 72, 6320 (2007); (doi:10.1021/jo0708644)
  • 3. (m) F. G. Gelalcha, B. Bitterlich, G. Anilkumar, M. K. Tse, M. Beller. Angew. Chem., Int. Ed. 46, 7293 (2007). (doi:10.1002/anie.200701235)
  • 4. (a) B. Saito, T. Katsuki. Tetrahedron Lett. 42, 3873 (2001); (doi:10.1016/S0040-4039(01)00590-1)
  • 4. (b) B. Saito, T. Katsuki. Tetrahedron Lett. 42, 8333 (2001). (doi:10.1016/S0040-4039(01)01789-0)
  • 5. (a) T. Tanaka, B. Saito, T. Katsuki. Tetrahedron Lett. 43, 3259 (2002); (doi:10.1016/S0040-4039(02)00535-X)
  • 5. (b) B. Saito, T. Katsuki. Chirality 15, 24 (2003). (doi:10.1002/chir.10149)
  • 6. K. Matsumoto, Y. Sawada, B. Saito, K. Sakai, T. Katsuki. Angew. Chem., Int. Ed. 44, 4935 (2005). (doi:10.1002/anie.200501318)
  • 7. Y. Sawada, K. Matsumoto, T. Katsuki. Angew. Chem., Int. Ed. 46, 4559 (2007). (doi:10.1002/anie.200700949)
  • 8. Y. Sawada, K. Matsumoto, S. Kondo, H. Watanabe, T. Ozawa, K. Suzuki, B. Saito, T. Katsuki. Angew. Chem., Int. Ed. 45, 3478 (2006). (doi:10.1002/anie.200600636)
  • 9. K. Matsumoto, Y. Sawada, T. Katsuki. Synlett 3545 (2006).
  • 10. Y. Shimada, S. Kondo, Y. Ohara, K. Matsumoto, T. Katsuki. Synlett 2445 (2007).
  • 11. The study on asymmetric epoxidation under buffered conditions was carried out in collaboration with a group of Nissan Chemical Industries, Ltd.