Synthesis of novel polyamides starting from ferulic acid dimer derivative

Designed Monomers and Polymers

Volumn 7, Issue 6 SPEC. ISS., 2004, Pages 711-725

  Castillo, Erika A ^a   Miura, Hirohiko ^a   Hasegawa, Masaki ^a   Ogawa, Takeshi ^a,b  

^a UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^b CIBA Vision Corporation   (United States)

Author keywords

Anti oxidizer; Cyclobutane polymer; O Acetylferulic acid; Photo dimerization; Polyamides; Three dimensional network polymer; Topochemical 2 + 2 addition

Indexed keywords

AMINES; ANTIOXIDANTS; BUTANE; DIMERS; HEATING; INTERFACES (MATERIALS); PHENOLS; POLYCONDENSATION; POLYESTERS; SYNTHESIS (CHEMICAL); ACETIC ACID; AMIDES; CHLORINE COMPOUNDS; DIMERIZATION; FREE RADICALS; POLYAMIDES; POLYMERS; THREE DIMENSIONAL;

ANTI-OXIDIZERS; CYCLOBUTANE POLYMERS; O-ACETYLFERULIC ACID; PHOTO-DIMERIZATION; THREE-DIMENSIONALNETWORK POLYMERS; TOPOCHEMICAL [2 + 2] ADDITION;

POLYAMIDES; DIMERS;

ANTI-OXIDIZER; CYCLOBUTANE POLYMERS; O-ACETYLFERULIC ACID; PHOTODIMERIZATION; THREE-DIMENSIONAL NETWORKS; TOPOCHEMICAL [2 + 2] ADDITION;

EID: 11144288737     PISSN: 1385772X     EISSN: None     Source Type: Journal    
DOI: 10.1163/1568555042474185     Document Type: Article

References (23)

1. H. Takahashi, M. Sakuragi, M. Hasegawa and T. Takehashi, J. Polym. Sci. A-1 10, 1399 (1972).
2. F. Nakanishi, M. Hasegawa and H. Takahashi, Polymer 14, 440 (1973).
3. L. J. Markoski, K. A. Walker, G. A. Deeter, G. E. Spilman, D. C. Martin and J. S. Moor, Chem. Mater. 5, 248 (1993).
4. M. Hasegawa and K. Saigo, Photochem. Photophys. 2, 27 (1989).
5. K. Saigo, Y. Chen, N. Yonezawa, T. Kanoe, K. Tachibana and M. Hasegawa, Macromolecules 19, 1552 (1986).
6. M. Hasegawa, Chem. Rev. 83, 507 (1983)
7. M. Hasegawa, Adv. Phys. Org. Chem. 30, 117 (1995).
8. M. Hasegawa, C.-M. Cheng and K. Kinbara, J. Photochem. Sci. 4, 147 (1998).
9. M. Hasegawa, K. Kinbara, Y. Adegawa and K. Saigo, J. Am. Chem. Soc. 115, 3828 (1993).
10. H. Taniguchi, Japanese Patent 2095088 (1996).
11. H. Taniguchi, E. Nomura, T. Tsuno, S. Minami, K. Kato and C. Hayashi, US Patent 5, 288, 902 (1994).
12. H. Taniguchi, A. Hosoda, T. Tsuno, Y. Maruta and E. Nomura, Anticancer Res. 19, 3757 (1999).
13. F. Hashimoto, T. Yoshizawa, Symp. Natural Org. Compound, Oct. 14-16, 1996, Sendai, Japan, p. 43 (1996) (abstract).
14. C. W. Ford and R. D. Hartley, J. Chromatogr. 436, 484 (1998).
15. R. D. Hartley, F. R. Whatley and P. J. Harris, Phytochemistry 15, 1157 (1988).
16. C. W. Ford and R. D. Hartley, J. Sci. Food. Agric. 50, 29 (1990).
17. I. M. Morrison, G. W. Robertson, D. Stewart and F. Wightman, Phytochemistry 30, 2007 (1991).
18. M. Tsuchida, Mass Spectrosc. Rev. 17, 51 (1998).
19. M. Hasegawa, T. Katsumata, Y. Ito, K. Saigo and Y. Ichida, Macromolecules 21, 3134 (1988).
20. G. H. Schenk and D. J. Brown, Talanta 14, 257 (1967).
21. I. Shiihara, Bull. Chem. Soc. Jpn. 70, 3129 (1997).
22. E. Graf, Free Radic. Biol. Med. 13, 435 (1992).
23. J. Kanski, M. Aksenova, A. Stoyanova and D. A. Butterfield, J. Nutr. Biochem. 13, 273 (2002).