Add time:07/27/2019         Source:sciencedirect.com

Diels–Alder cycloaddition of 8,8-dimethylnaphthalene-1,4,5(8H)-trione with diastereomeric hydroxysulfinyldienes proceeded with high yields and good π-facial and regioselectivities. The hydroxysulfoxide moiety controls the regio- and stereoselectivities, through hydrogen bonds in the suggested transition state.

We also recommend Trading Suppliers and Manufacturers of N-Sulfinyl-o-toluidine (cas 15182-74-8). Pls Click Website Link as below: cas 15182-74-8 suppliers