Issue 37, 2022

Asymmetric synthesis of (+)-teratosphaerone B, its non-natural analogue and (+)-xylarenone using an ene- and naphthol reductase cascade

Abstract

Herein, a one-pot bienzymatic cascade containing an ene and a naphthol reductase is developed. It is applied for the synthesis of (+)-(3R,4R)-teratosphaerone B, its non-natural regioisomer in both cis- and trans-forms and (+)-xylarenone by the reduction of chemically synthesized naphthoquinone precursors in high yields (76–92%) and excellent ee (>99%). This work implies similar biosynthetic steps in the formation of the synthesized natural products.

Graphical abstract: Asymmetric synthesis of (+)-teratosphaerone B, its non-natural analogue and (+)-xylarenone using an ene- and naphthol reductase cascade

Supplementary files

Article information

Article type
Communication
Submitted
15 Jul 2022
Accepted
01 Sep 2022
First published
12 Sep 2022

Org. Biomol. Chem., 2022,20, 7410-7414

Asymmetric synthesis of (+)-teratosphaerone B, its non-natural analogue and (+)-xylarenone using an ene- and naphthol reductase cascade

T. Manna, A. De, K. Nurjamal and S. M. Husain, Org. Biomol. Chem., 2022, 20, 7410 DOI: 10.1039/D2OB01262F

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