Combinatorial synthesis of isoxazole library and their liquid crystalline properties

Tetrahedron

Volumn 63, Issue 3, 2007, Pages 652-665

  Tanaka, Masahiro ^a   Haino, Takeharu ^a   Ideta, Keiko ^b   Kubo, Kanji ^b   Mori, Akira ^b   Fukazawa, Yoshimasa ^a  

^a HIROSHIMA UNIVERSITY   (Japan)

^b KYUSHU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ISOXAZOLE DERIVATIVE; NITRILE OXIDE;

ARTICLE; BILAYER MEMBRANE; CALCULATION; CHEMICAL ANALYSIS; COMPARATIVE STUDY; CRYSTAL STRUCTURE; CYCLOADDITION; LIQUID CRYSTAL; MOLECULAR MECHANICS; PRIORITY JOURNAL; SYNTHESIS; X RAY DIFFRACTION;

EID: 33845417941     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.11.005     Document Type: Article

References (41)

1. Demus D., Goodby J., Gray G.W., Spiess H.-W., and Vill V. Handbook of Liquid Crystals (1998), VCH, Weinheim
2. Lagerwall S., Dahlgren A., Jägemalm P., Rudquist P., D'havé K., Pauwels H., Dabrowski R., and Drzewinski W. Adv. Funct. Mater. 11 (2001) 87-94
3. Kirsch P., and Bremer M. Angew. Chem., Int. Ed. 39 (2000) 4216-4235
4. Hudson S.A., and Maitlis P.M. Chem. Rev. 93 (1993) 861-885
5. Bruce D.W. Acc. Chem. Res. 33 (2000) 831-840
6. Tschierske C. J. Mater. Chem. 8 (1998) 1485-1508
7. Pelzl G., Diele S., and Weissflog W. Adv. Mater. 11 (2001) 87-94
8. Watanabe J., Niori T., Choi S.W., Takanishi Y., and Takezoe H. Jpn. J. Appl. Phys. 37 (1998) L401-L403
9. Brown D.H., and Styring P. Liq. Cryst. 30 (2003) 23-30
10. Gallardo H., Zucco C., and Da Silva L. Mol. Cryst. Liq. Cryst. 373 (2002) 181-190
11. Bartulin J., Martinez R., Gallardo H., Muller J., and Taylor T.R. Mol. Cryst. Liq. Cryst. 225 (1993) 175-182
12. Bartulin J., Martinez R., Müller H.J., Fan Z.X., and Haase W. Mol. Cryst. Liq. Cryst. 220 (1992) 67-75
13. Barbera J., Cativiela C., Serrano J.L., and Zurbano M.M. Liq. Cryst. 11 (1992) 887-897
14. Seguel C.G., Borchers B., Haase W., and Aguilera C. Liq. Cryst. 11 (1992) 899-903
15. Iglesias R., Serrano J.L., and Sierra T. Liq. Cryst. 22 (1997) 37-46
16. Barbera J., Gimenez R., Serrano J.L., Alcala R., Villacampa B., Villalba J., Ledoux I., and Zyss J. Liq. Cryst. 22 (1997) 265-273
17. Hashimoto M., Mori A., Inoue H., Nagamiya H., Doi T., and Takahashi T. Tetrahedron Lett. 44 (2003) 1251-1254
18. Mori A., Akahoshi I., Hashimoto M., Doi T., and Takahashi T. Tetrahedron Lett. 45 (2004) 813-815
19. Hioki H., Fukutaka M., Takahashi H., Kodama M., Kubo K., Ideta K., and Mori A. Tetrahedron Lett. 45 (2004) 7591-7594
20. Hioki H., Fukutaka M., Takahashi H., Kubo M., Matsushita K., Kodama M., Kubo K., Ideta K., and Mori A. Tetrahedron 61 (2005) 10643-10651
21. Haino T., Tanaka M., Ideta K., Kubo K., Mori A., and Fukazawa Y. Tetrahedron Lett. 45 (2004) 2277-2279
22. Fuchi N., Doi T., and Takahashi T. Chem. Lett. 34 (2005) 438-439
23. Fuchi N., Doi T., Cao B., Kahn M., and Takahashi T. Synlett (2002) 285-289
24. Bose D.S., and Jayalakshmi B. Synthesis (1999) 64-65
25. Kantorowski E.J., and Kurth M.J. Mol. Divers. 2 (1997) 207-216
26. Liu K.C., Shelton B.R., and Howe R.K. J. Org. Chem. 45 (1980) 3916-3918
27. Mohamadi F., Richards N.G.J., Guida W.C., Liskamp R., Lipton M., Caufield C., Chang G., Hendrickson T., and Still W.C. J. Comput. Chem. 11 (1990) 440-467
28. o |. The structure was solved by the direct method (Sir 97). Full-matrix least squares refinements converged to a conventional R factor of 0.093, wR=0.27, GOF=0.99. Supplementary crystallographic data have been deposited at the Cambridge Crystallographic Data Centre, UK as supplementary publication number CCDC no. 604935.
29. Katritzky A.R., Button M.A.C., and Denisenko S.N. J. Heterocycl. Chem. 37 (2000) 1505-1510
30. Wang H.J., Ling W., and Lu L. J. Fluorine Chem. 111 (2001) 241-246
31. Weissflog W., and Schubert H. J. Prakt. Chem. 318 (1976) 785-794
32. Peake C.J., and Strickland J.H. Synth. Commun. 16 (1986) 763-765
33. Miller C.P., and Kaufman D.H. Synlett (2000) 1169-1171
34. Malthete J., Canceill J., Gabard J., and Jacques J. Tetrahedron 37 (1981) 2815-2821
35. Nakai H., Konno M., Kosuge S., Sakuyama S., Toda M., Arai Y., Obata T., Katsube N., Miyamoto T., Okegawa T., and Kawasaki A. J. Med. Chem. 31 (1988) 84-91
36. Borisch K., Diele S., Goring P., Kresse H., and Tschierske C. J. Mater. Chem. 8 (1998) 529-543
37. Pickaert G., and Ziessel R. Synthesis 16 (2004) 2716-2726
38. Soerme P., Arnoux P., Kahl-Knutsson B., Leffler H., Rini J.M., and Nilsson U.J. J. Am. Chem. Soc. 127 (2005) 1737-1743
39. Mertesdorf C., and Ringsdorf H. Liq. Cryst. 5 (1989) 1757-1772
40. Ungar G., Abramic D., Percec V., and Heck J.A. Liq. Cryst. 21 (1996) 73-86
41. Terazzi E., Torelli S., Bernardinelli G., Rivera J.-P., Benech J.-M., Bourgogne C., Donnio B., Guillon D., Imbert D., Buenzli J.-C.G., Pinto A., Jeannerat D., and Piguet C. J. Am. Chem. Soc. 127 (2005) 888-903