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Volumn 65, Issue 7, 2000, Pages 2253-2256

Double isomerization of oxetane amides to azetidine esters with ring expansion and contraction

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; AZETIDINE DERIVATIVE; ESTER DERIVATIVE; OXETANE DERIVATIVE;

EID: 0034616139     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo991888g     Document Type: Note
Times cited : (22)

References (22)
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    • Reviews on the cationic ring-opening polymerization of oxetane: (a) Dreyfuss, M. P.; Dreyfuss, P. In Encyclopedia of Polymer Science and Engineering, 2nd ed.; Mark, H. F., Bikales, N. M., Overberger, C. G., Menges, G., Eds.; John Wiley and Sons: New York, 1987; Vol. 10, pp 653-670. (b) Penczek, S.; Kubisa, P. In Comprehensive Polymer Science; Allen, G., Ed.; Pergamon Press: Oxford, 1989; Vol. 3, pp 751-786. (c) Desai, H. In Polymeric Materials Encyclopedia; Salamone, J. C., Ed.; CRC Press: New York, 1996; Vol. 11, pp 8268-8279.
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    • Our previous works on the cationic ring-opening polymerization of substituted oxetanes: (a) Ogawa, H.; Kodera, Y.; Kanoh, S.; Ueyama, A.; Motoi, M. Bull. Chem. Soc. Jpn. 1998, 71, 433-442. (b) Hiruma, T.; Kanoh, K.; Yamamoto, T.; Kanoh, S.; Motoi, M. Polym. J. 1995, 27, 78-89. (c) Motoi, M.; Saito, E.; Kyoda, S.; Takahata, N.; Nagai, S.; Arano, A. Polym. J. 1991, 23, 1225-1241. (d) Motoi, M.; Nagahara, S.; Akiyama, H.; Horiuchi, M.; Kanoh, S. Polym. J. 1989, 21, 987- 1001.
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    • Our previous works on the cationic ring-opening polymerization of substituted oxetanes: (a) Ogawa, H.; Kodera, Y.; Kanoh, S.; Ueyama, A.; Motoi, M. Bull. Chem. Soc. Jpn. 1998, 71, 433-442. (b) Hiruma, T.; Kanoh, K.; Yamamoto, T.; Kanoh, S.; Motoi, M. Polym. J. 1995, 27, 78-89. (c) Motoi, M.; Saito, E.; Kyoda, S.; Takahata, N.; Nagai, S.; Arano, A. Polym. J. 1991, 23, 1225-1241. (d) Motoi, M.; Nagahara, S.; Akiyama, H.; Horiuchi, M.; Kanoh, S. Polym. J. 1989, 21, 987-1001.
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    • note
    • 2, m/e 233.1417).
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    • note
    • 2, m/e 233.1417).
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    • BnTA was prepared by Endo's method and recrystallized from 2-propanol: 60% yield, mp 112-113 0C (lit. mp 121.5-122°C): Endo, T.; Uno, H. J. Polym. Sci., Polym. Lett. Ed. 1985, 23, 359-363.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.