The diels-alder reaction of a 2,2-dimethoxyethyl ester via a cationic intermediate-Science-Chemical Encyclopedia-lookchem

The diels-alder reaction of a 2,2-dimethoxyethyl ester via a cationic intermediate
Add time:09/07/2019 Source:sciencedirect.com

2,2-Dimethoxyethyl acrylate, which is easily prepared by the Mitsunobu reaction, reacts with dienes at −78 °C in the presence of a Lewis acid such as titanium(IV) chloride to afford the corresponding DielsAlder adducts in high yields.

We also recommend Trading Suppliers and Manufacturers of 4-(2,2-DIMETHOXYETHYL)-5-PHENYL-4H-1,2,4-TRIAZOLE-3-THIOL (cas 136745-20-5). Pls Click Website Link as below: cas 136745-20-5 suppliers

Prev:Regioselective synthesis of 1-(2,2-dimethoxyethyl)-1,2,3-triazoles by copper(I)-catalyzed [3+2] cyclization of 2-azido-1,1-dimethoxyethane with alkynes
Next: Crosslinked poly[acryloylN,N,-bis(2,2-dimethoxyethyl) amine] and crosslinked poly[acryloylmorpholine/acryloyl N,N,-bis(2,2-dimethoxyethyl) amine] gel networks and their application to the immobilization of β-d-glucosidase)

Encyclopedia