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Understanding the competing pathways leading to hydropyrene and isoelisabethatriene.

Authors :
Zev S
Ringel M
Driller R
Loll B
Brück T
Major DT
Source :
Beilstein journal of organic chemistry [Beilstein J Org Chem] 2022 Aug 04; Vol. 18, pp. 972-978. Date of Electronic Publication: 2022 Aug 04 (Print Publication: 2022).
Publication Year :
2022

Abstract

Terpene synthases are responsible for the biosynthesis of terpenes, the largest family of natural products. Hydropyrene synthase generates hydropyrene and hydropyrenol as its main products along with two byproducts, isoelisabethatrienes A and B. Fascinatingly, a single active site mutation (M75L) diverts the product distribution towards isoelisabethatrienes A and B. In the current work, we study the competing pathways leading to these products using quantum chemical calculations in the gas phase. We show that there is a great thermodynamic preference for hydropyrene and hydropyrenol formation, and hence most likely in the synthesis of the isoelisabethatriene products kinetic control is at play.<br /> (Copyright © 2022, Zev et al.)

Details

Language :
English
ISSN :
1860-5397
Volume :
18
Database :
MEDLINE
Journal :
Beilstein journal of organic chemistry
Publication Type :
Academic Journal
Accession number :
35965858
Full Text :
https://doi.org/10.3762/bjoc.18.97