A NOVEL SYNTHETIC ROUTE TO OPEN-CHAINED A ND CYCLIC OLIGOETHERKETONES

Authors
Citation
D. Ozbilen et H. Meier, A NOVEL SYNTHETIC ROUTE TO OPEN-CHAINED A ND CYCLIC OLIGOETHERKETONES, Journal fur praktische Chemie, Chemiker-Zeitung, 340(2), 1998, pp. 135-139
Citations number
18
Categorie Soggetti
Chemistry,"Chemistry Applied
ISSN journal
09411216
Volume
340
Issue
2
Year of publication
1998
Pages
135 - 139
Database
ISI
SICI code
0941-1216(1998)340:2<135:ANSRTO>2.0.ZU;2-L
Abstract
Oligoetherketones of the structure 2a,b can be generated by repetitive insertion reactions of terminal biscarbenoids 4a,b into the O-H bends of diols like 5. The formation of the corresponding ring systems 7a a nd the involved carbene dimerization leading to 8b are processes which compete with the linear polyinsertion. A related one-component reacti on can be performed with omega-hydroxy-1-diazo-2-alkanones (13a-c --> 14a-c).