Cationic Ring-Opening Polymerization of Cyclic Monothiocarbonates:  Varying the Polymer Main Chain by Neighboring Group Participation

2001 ◽  
Vol 34 (22) ◽  
pp. 7642-7647 ◽  
Author(s):  
Nobukatsu Nemoto ◽  
Xiaoyu Xu ◽  
Fumio Sanda ◽  
Takeshi Endo



1993 ◽  
Vol 25 (1) ◽  
pp. 49-57 ◽  
Author(s):  
Kazukiyo Kobayashi ◽  
Takahiro Ishii ◽  
Masahiko Okada ◽  
Conrad Schuerch




1988 ◽  
Vol 179 ◽  
pp. 315-320 ◽  
Author(s):  
Haruo Ichikawa ◽  
Kazukiyo Kobayashi ◽  
Hiroshi Sumitomo ◽  
Conrad Schuerch




1982 ◽  
Vol 47 (11) ◽  
pp. 3062-3076 ◽  
Author(s):  
Václav Černý ◽  
Pavel Kočovský

Reactions of the title compounds (bearing an OH, OCH3 or OCOCH3 group at C(19)) involve 5(O)n, 7(O)π,n-participation by the 19-substituent or attack by an external nucleophile. The 6(O)π,n-participation does not occur. The behavior of 1,2-unsaturated (or epoxidated) compounds has been compared with the earlier described 2,3-unsaturated or epoxidated analogs. The 1,2-type is genarally less prone to participation. The reasons for this behavior are discussed.



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