Upgrading malic acid to bio-based benzoates via a Diels–Alder-initiated sequence with the methyl coumalate platform-Reference-Cited by-同舟云学术

Upgrading malic acid to bio-based benzoates via a Diels–Alder-initiated sequence with the methyl coumalate platform

Published:2014 Issue:86 Volume:4 Page:45657-45664
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Lee Jennifer J.¹²³,Pollock III Gerald R.¹²³,Mitchell Donald¹²³,Kasuga Lindsay¹²³,Kraus George A.¹²³

Affiliation:

1. Department of Chemistry and NSF Engineering Research Center for Biorenewable Chemicals

2. Iowa State University

3. Ames, USA

Abstract

Malic acid dimerization was optimized to methyl coumalate from which a Diels–Alder strategy produced a variety of bio-based benzoates.

Funder

National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA07105K

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