ChemInform Abstract: Vinyl Esters with an Epoxy Group. Part 17. Synthesis of Glycidyl Esters of N‐(2‐Vinyloxyethyl)‐ and N‐(2‐Methyl‐1,3‐oxazolidine)carbamic Acid.

Abstract

The reaction between equimolar quantities of the vinyloxyamine (I) and the cyclic carbonate (II) yields the polyfunctional adduct (III).

Chemistry of heterocyclic compounds at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, over 50 years (Review)

“…Various methods have been developed for synthesis of the various analogs of vinylox -the condensation of alkanediols and also of diethylene and triethylene glycols with epichlorohydrin [6][7][8][9][10], the selective addition of glycidol to the divinyl ethers of glycols [14][15][16][17], the successive treatment of 1,3-dioxolan-2-ones first with 2-(vinyloxy)ethylamine and then with an epichlorohydrin/base system [15,18] or with the base alone [15,19,20].…”

Synthesis and properties of polyhydroxyurethane bearing silicone backbone

“…Polyhydroxyurethane is a polyurethane derivative, bearing hydroxyl groups in the side chain . The most typical preparation method is the polyaddition of diamines and bifunctional five‐membered cyclic carbonates prepared from diepoxides and CO 2 (Scheme ).…”