Helical conformation of the copolymers of l-proline derivatives based propargylether and chiral N-propargylamide

Polymer

Volumn 48, Issue 19, 2007, Pages 5696-5701

  Dai, Jian ^a,b   Ha, Chengyong ^a   Chang, Dongliang ^a   Shen, Minmin ^a  

^a GUANGZHOU INSTITUTE OF CHEMISTRY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Copolymerization; Helical conformation; Propargylether

Indexed keywords

ALKYLATION; AMIDES; AMINO ACIDS; CHIRALITY; COPOLYMERIZATION; DERIVATIVES; ETHERS; HYDROGEN BONDS;

HELICAL CONFORMATION; PROPARGYL BROMIDE; PROPARGYLETHER;

COPOLYMERS;

AMINE; COPOLYMER; COPOLYMERIZATION; HOMOPOLYMER; MONOMER; SOLVENT; SYNTHETIC POLYAMIDE;

EID: 34548477921     PISSN: 00323861     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.polymer.2007.07.002     Document Type: Article

References (22)

1. Lockman J.W., Paul N.M., and Parquette J.R. Prog Polym Sci 30 (2005) 423-452
2. Tabei J., Shiotsuki M., Sato T., Sanda F., and Masuda T. Chem Eur J 11 (2005) 3591-3598
3. Ho R., Chiang Y., Tsai C., Lin C., Ko B., and Huang B. J Am Chem Soc 126 (2004) 2704-2705
4. Yorozuya S., Osaka I., Nakamura A., Inoue Y., and Akagi K. Synth Met 93 (2003) 135-136
5. Yue D., Shiotsuki M., Sanda F., and Masuda T. Polymer 48 (2007) 68-73
6. Green M.M., Peterson N.C., Sato T., Teramoto A., and Lifson S. Science 268 (1995) 1860-1866
7. Green M.M., Park J.W., Sato T., Teramoto A., Lifson S., Selinger R.L.B., et al. Angew Chem Int Ed 38 (1999) 3138-3154
8. Ciardelli F., Lanzillo S., and Pieroni O. Macromolecules 7 (1974) 174-179
9. Moore J.S., Gorman C.B., and Grubbs R.H. J Am Chem Soc 113 (1991) 1704-1712
10. Nakano T., and Okamoto Y. Chem Rev 101 (2001) 4013-4018
11. Yashima E., Maeda K., and Nishimura T. Chem Eur J 10 (2004) 42-51
12. Nomura R., Fukushima Y., Nakako H., and Masuda T. J Am Chem Soc 122 (2000) 8830-8836
13. Lam J.W.Y., and Tang B.Z. Acc Chem Res 38 (2005) 745-754
14. Gao G., Sanda F., and Masuda T. Macromolecules 36 (2003) 3938-3943
15. Zhao H., Sanda F., and Masuda T. Macromolecules 37 (2004) 8893-8896
16. Taylor C.M., Hardré R., and Edwards P.J.B. J Org Chem 70 (2005) 1306-1315
17. List B. Tetrahedron 58 (2002) 5573-5590
18. Dalko P.I., and Moisan L. Angew Chem Int Ed 43 (2004) 5138-5175
19. Schrock R.R., and Osborn J.A. Inorg Chem 9 (1970) 2339-2343
20. Gao G., Sanda F., and Masuda T. Macromolecules 36 (2003) 3932-3937
21. 3] (10.6 mg, 0.02 mmol), and the resulting mixture was vigorously stirred. It was kept in a water bath at 30 °C for 12 h. The resulting mixture was poured into n-hexane (200 mL) to precipitate a copolymer. It was separated by filtration, and dried under reduced pressure.
22. Kishimoto Y., Itou M., Miyatake T., Ikariya T., and Noyori R. Macromolecules 28 (1995) 6662-6666