Base catalyzed isomerizations of allyl ethers to 1-propenyl ethers using mixed alkali systems

Journal of Macromolecular Science - Pure and Applied Chemistry

Volumn 35, Issue 3, 1998, Pages 411-426

  Crivello, J V ^a   Kaur, Sarjit ^a,b  

^a Rensselaer Polytechnic Institute   (United States)

^b VASSAR COLLEGE   (United States)

Author keywords

1 Propenyl Ethers; Allyl Ethers; Isomerization; Mixed Alkali Catalysts

Indexed keywords

EID: 0004460126     PISSN: 10601325     EISSN: None     Source Type: Journal    
DOI: 10.1080/10601329808001986     Document Type: Article

References (29)

1. J. V. Crivello, Die Angew. Makromol. Chemie, Appl. Macromol. Chem. Phys., 240, 83 (1996).
2. J. V. Crivello, in: Ultraviolet Curing Science and Technology, Chapter 2, S. P. Pappas, Editor, Technology Marketing Corp., Stamford, Conn., 1978.
3. J. V. Crivello, in: Ring-Opening Polymerization, D. J. Brunelle, Editor, Hanser Pub., Munich, 1993, p. 157.
4. C. E. Schildknecht, Vinyl and Related Polymers, John Wiley & Sons, New York, 1952, p. 600.
5. J. V. Crivello and D. A. Conlon, J. Polym. Sci., Polym. Chem. Ed., 22, 2105 (1984).
6. J. V. Crivello and K. D. Jo, J. Polym. Sci., Polym. Chem. Ed., 31(6), 1473 (1993).
7. J. V. Crivello, S. Bratslavsky, and B. Yang, Polymer Mat. Sci. and Eng. Preprints, 72, 473 (1995).
8. J. V. Crivello and B. Yang, J. Polym. Sci., Polym. Chem. Ed., 33(8), 1381 (1995).
9. J. V. Crivello and S. A. Bratslavski, J. Macromol. Sci., Pure and Chem., A31(12), 1927 (1994).
10. E. Taskinen, Tetrahedron, 48, 11389 (1993).
11. T. J. Prosser, J. Am. Chem. Soc., 83, 1701 (1961).
12. C. C. Price and W. H. Snyder, J. Am. Chem. Soc., 83, 1773 (1961).
13. P. Caubere and M.-F. Hochu, Bull. Soc. Chim. Fr., 459 (1968).
14. A. J. Jubert, A. Georis, R. Warin, and P. Teyssié, J. Chem. Soc., Perkin Trans. II, 366 (1972).
15. A. Loupy, B. B. Singh, A. S. Radharkrisha, B. N. Hiep, L. D. Hanh, and L. N. Thach, Synth. Commun., 23 (10), 1379 (1193).
16. Y. Ogata, Japanese Patent 5331 ('51) Sept. 15, 1952; Chem. Abstr., 47, 9360c (1953).
17. T. Baba, T. Endo, H. Handa, and Y. Ono, J. Applied Catalysis A: General, 97, L19-L23 (1993).
18. R. Wilhelm, M. Vogl, M Ger. Offen. DE 3,514,451, 23, Oct. 1986; Chem. Abstr., 106, 18827s (1987).
19. G. Gati and G. Resofszki, J. Molecular Cat., 51, 295 (1989);
20. (b) K. Arata, S. Kobayashi, and M. Hino, Bull. Chem. Soc. Jpn., 61, 565 (1988).
21. E. Ruckenstein and A. Z. Khan, J. Catal., 143, 1 (1993).
22. Ibid, J. Catal., 143, 628 (1993).
23. E. Ruckenstein and A. Khan, J. Chem. Soc., Chem. Commun., 1290 (1993).
24. (a) R. Gigg and C. D. Warren, J. Chem. Soc. (C), 1903 (1968);
25. (b) R. J. Gigg, J. Chem. Soc., 2968 (1965);
26. (c) Chem. Abstr., 61:11915;
27. (d) Chem. Abstr., 67, 90349f (1967).
28. G. Kesslin and C. M. Orlando, Jr., J. Org. Chem., 31, 2682 (1966).
29. S. Torii, H. Tanaka, and M. Akada, US Patent 4588835, 1986; Chem. Abstr., 106, 18095b (1987).