The Synthesis of Bicyclic Lactam Ether
- 1 July 1966
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 39 (7) , 1556-1559
- https://doi.org/10.1246/bcsj.39.1556
Abstract
The bicyclic lactam ether, 3-aza-10-oxabicyclic[4.3.1]decane-4-one has been attempted to synthesize by the Beckmann rearrangement of the oxime of 9-oxabicyclo[3.3.1]nonane-3-one; this rearrangement caused polymerization through the cleavage of the ether group in acidic media. Therefore, it may be presumed that the cationic polymerization of lactam ethers in the presence of Lewis acid proceeds through the opening of the ether linkage.This publication has 1 reference indexed in Scilit:
- Synthese des 9-oxa-bicyclo-[3.3.1]-nonanons-(3)Tetrahedron Letters, 1964