A highly stereoselective synthesis of stilbenes under solvent-free conditions

6Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

A highly stereoselective synthesis of stilbenes (trans-1,2-diarylethylenes) was achieved under solvent-free conditions from aryl-aldehydes and aromatic substances bearing an activated methyl group in the presence of anhydrous K 2CO3 and poly(ethylene glycol). This method avoided the need for completely anhydrous condition and use of a noxious organic solvent.

Cite

CITATION STYLE

APA

Li, X. B., Wang, L., Zhang, X. Q., Gu, H. M., Guo, J., & Li, B. L. (2010). A highly stereoselective synthesis of stilbenes under solvent-free conditions. Journal of Chemical Research, (9), 489–492. https://doi.org/10.3184/030823410X12814419570511

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free