Campus Units

Chemistry

Document Type

Article

Publication Version

Published Version

Publication Date

12-15-2017

Journal or Book Title

RSC Advances

Volume

7

Issue

89

First Page

56760

Last Page

56763

DOI

10.1039/C7RA12935A

Abstract

Methyl coumalate reacts with enol ethers to form stable adducts which can be converted into isophthalates in good to excellent yields. Alkyl vinyl ethers afford higher yields of isophthalates than enol silyl ethers. The adduct of the enol silyl ether of acetophenone with methyl coumalate reacted with PTSA to produce a styryl coumalate.

Comments

This article is published as Kraus, George A. and Shuai Wang. "Synthesis of isophthalates from methyl coumalate." RSC Advances 7, no. 89 (2017): 56760-56763. DOI: 10.1039/C7RA12935A. Posted with permission.

Creative Commons License

Creative Commons Attribution 3.0 License
This work is licensed under a Creative Commons Attribution 3.0 License.

Copyright Owner

The Royal Society of Chemistry

Language

en

File Format

application/pdf

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