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Synlett
DOI: 10.1055/a-2500-7798
DOI: 10.1055/a-2500-7798
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Enzymatic Peroxidation in the Chemoenzymatic Synthesis of 13-Oxoverruculogen
Financial support for this work was provided by the National Science Foundation in the form of a CAREER award to C.P.T. (CHE-2338495). B.S. is supported by the National Institute of General Medical Sciences (T32 GM135126). We gratefully acknowledge a grant from the National Institutes of Health (NIH) Shared Instrumentation Program (1S10OD034395).
Abstract
Verruculogens are fumitremorgin alkaloids that contain an eight-membered endoperoxide ring. Due to their unusual structure and bioactivity, there has been much interest in these natural products since their discovery over forty years ago. Similarly, interest in their biosynthesis resulted in the discovery of verruculogen synthase (FtmOx1) that catalyzes endoperoxide formation in these natural products. Herein, we describe our work in this area through the chemoenzymatic synthesis of 13-oxoverruculogen by endoperoxidation of a substrate analogue using FtmOx1.
1 Introduction
2 Pentacyclic Ring Formation
3 Promiscuous Enzymatic Peroxidation
4 Conclusion
Publication History
Received: 21 October 2024
Accepted after revision: 11 December 2024
Accepted Manuscript online:
11 December 2024
Article published online:
20 January 2025
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