Evidence for a 1,3-Dipolar Cyclo-addition Mechanism in the Decarboxylation of Phenylacrylic Acids Catalyzed by Ferulic Acid Decarboxylase
Author:
Affiliation:
1. Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States
2. Department of Biological Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States
Funder
Division of Chemistry
Division of Chemical, Bioengineering, Environmental, and Transport Systems
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.7b05060
Reference31 articles.
1. Catalysis in Enzymatic Decarboxylations: Comparison of Selected Cofactor-Dependent and Cofactor-Independent Examples.
2. Enzymatic Decarboxylation-An Emerging Reaction for Chemicals Production from Renewable Resources
3. Technoeconomic evaluation of bio-based styrene production by engineered Escherichia coli
4. Rational and combinatorial approaches to engineering styrene production by Saccharomyces cerevisiae
5. Isofunctional Enzymes PAD1 and UbiX Catalyze Formation of a Novel Cofactor Required by Ferulic Acid Decarboxylase and 4-Hydroxy-3-polyprenylbenzoic Acid Decarboxylase
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