Total synthesis of maltepolide F

Herein, we present the total synthesis of the polyketide macrolide maltepolide F. D-Mannitol serves as the chiral pool material for constructing the tetrahydrofuran unit. Key steps in the synthesis include cyclo-etherification, Brown asymmetric allylation, the Evans aldol reaction, Yamaguchi esterification, and intramolecular Heck cyclization.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-12-03
DOI
https://doi.org/10.1039/d5ob01725d
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
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article

Total synthesis of maltepolide F

Bashweshawar S. Dhulshette, subhash ghosh
Organic & Biomolecular Chemistry
Synthetic Organic Chemistry Methods
article

Total synthesis of maltepolide F

Bashweshawar S. Dhulshette, subhash ghosh
article en

Abstract

Herein, we present the total synthesis of the polyketide macrolide maltepolide F. D-Mannitol serves as the chiral pool material for constructing the tetrahydrofuran unit. Key steps in the synthesis include cyclo-etherification, Brown asymmetric allylation, the Evans aldol reaction, Yamaguchi esterification, and intramolecular Heck cyclization.

Organic & Biomolecular ChemistryVol. 24(2)
Indian Institute of Chemical Technology (IN), Academy of Scientific and Innovative Research (IN)
Openalex Percentile: Top 71%
Synthetic Organic Chemistry Methods
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Total synthesis of maltepolide F — Bashweshawar S. Dhulshette, subhash ghosh · Organic & Biomolecular Chemistry (2025) | TGRS Research Map | TGRS