A new approach to the synthesis of benzylidene derivatives of 1-(α-aminobenzyl)-2-naphthols (Betti bases), promising chiral inductors

Mendeleev Communications

Volumn 17, Issue 4, 2007, Pages 239-240

  Zheltukhin, Victor F ^a   Metlushka, Kirill E ^a   Sadkova, Dilyara N ^a   McKenna, Charles E ^b   Kashemirov, Boris A ^b   Alfonsov, Vladimir A ^a  

^a A E ARBUZOV INSTITUTE OF ORGANIC AND PHYSICAL CHEMISTRY   (Russian Federation)

^b UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 34447289179     PISSN: 09599436     EISSN: 1364551X     Source Type: Journal    
DOI: 10.1016/j.mencom.2007.06.020     Document Type: Article

References (34)

1. Stinson S.C. Chem. Eng. News 79 40 (2001) 79
2. Szatmári I., and Fülöp F. Curr. Org. Synth. 1 (2004) 155
3. Cardellicchio C., Ciccarella G., Naso F., Perna F., and Tortorella P. Tetrahedron 55 (1999) 14685
4. Palmieri G. Tetrahedron: Asymmetry 11 (2000) 3361
5. Cimareli C., Mazzanti A., Palmieri G., and Volpini E. J. Org. Chem. 66 (2001) 4759
6. Liu D.-X., Zhang L.-C., Wang Q., Da C.-S., Xin Z.-Q., Wang R., Choi M.C.K., and Chan A.S.C. Org. Lett. 3 (2001) 2733
7. Wang Y., Li X., and Ding K. Tetrahedron: Asymmetry 13 (2002) 1291
8. Lu J., Xu X., Wang C., He J., Hu Y., and Hu H. Tetrahedron Lett. 43 (2002) 8367
9. Zhang Y., Zhang L., Guo Z., and Zhu L. J. Coord. Chem. 55 (2002) 1393
10. Li K., Zhou Z., Wang L., Zhou Q., and Tang C. Main Group Met. Chem. 25 (2002) 663
11. Saidi M.R., and Azizi N. Tetrahedron: Asymmetry 14 (2003) 389
12. Ji J.-X., Qiu L.-Q., Yip C.W., and Chan A.S.C. J. Org. Chem. 68 (2003) 1589
13. Xu X., Lu J., Dong Y., Li R., Ge Z., and Hu Y. Tetrahedron: Asymmetry 15 (2004) 475
14. Dong Y., Sun J., Wang X., Xu X., Cao L., and Hu Y. Tetrahedron: Asymmetry 15 (2004) 1667
15. Szatmári I., Martinek T.A., Lázár L., Koch A., Kleinpeter E., Neuvonen K., and Fülöp F. J. Org. Chem. 69 (2004) 3645
16. Xu X., Lu J., Li R., Ge Z., Dong Y., and Hu Y. Synlett. (2004) 122
17. Szatmári I., Hetényi A., Lázár L., and Fülöp F. J. Heterocycl. Chem. 41 (2004) 367
18. Wang X., Dong Y., Sun J., Xu X., Li R., and Hu Y. J. Org. Chem. 70 (2005) 1897
19. Dahmen S., and Lormann M. Org. Lett. 7 (2005) 4597
20. Ji J.-X., Wu J., Au-Yeung T.T.-L., Yip C.-W., Haynes R.K., and Chan A.S.C. J. Org. Chem. 70 (2005) 1093
21. Betti M. Gazz. Chim. Ital. 30 II (1900) 310
22. Betti M. Org. Synth. Coll. Vol. I (1941) 381
23. Smith H.E., and Cooper N.E. J. Org. Chem. 35 (1970) 2212
24. Mohrle H., Miller C., and Wendisch D. Chem. Ber. 107 (1974) 2675
25. Szatmári I., Martinek T.A., Lázár L., and Fülöp F. Tetrahedron 59 (2003) 2877
26. Mamaev V.P., and Ignat'ev V.M. Izv. Akad. Nauk SSSR, Ser. Khim. (1965) 1107 (Bull. Acad. Sci. USSR, Div. Chem. Sci., 1965, 14, 1074)
27. Betti M., and Torichelli A. Gazz. Chim. Ital. 33 (1903) 1
28. Saidi M.R., Azizi N., and Naimi-Jamal M.R. Tetrahedron Lett. 42 (2001) 8111
29. Betti M. Gazz. Chim. Ital. 31 II (1901) 176
30. Gong Y., and Kato K. Tetrahedron: Asymmetry 12 (2001) 2121
31. Brode W.R., and Littman J.B. J. Am. Chem. Soc. 52 (1930) 1655
32. Sachs F., and Steinert P.S. Ber. Dtsch. Chem. Ges. 37 (1904) 1736
33. Hunter D.H., and Sim S.K. Can. J. Chem. 50 (1972) 669
34. Lozinskaya N.A., Tsybezova V.V., Proskurnina M.V., and Zefirov N.S. Izv. Akad. Nauk, Ser. Khim. (2003) 646 (Russ. Chem. Bull., Int. Ed., 2003, 52, 674)