Toward the Valorization of Cotton Wastes: Application of a Gossypol‐Derived Ligand to an Asymmetric Diels–Alder Reaction

ABSTRACT Gossypol, a major metabolite of cotton plants, has been used for the first time as a source material for the preparation of derivatives employed in asymmetric catalysis. Specifically, the (R)‐enantiomer of the 6,6’,7,7’‐O‐tetramethyl derivative of apogossypol has been synthesized in five steps and 47% total yield from enantiopure (‒)‐(R)‐gossypol. This axially chiral diol was used as a ligand in the enantioselective boron‐catalyzed Diels–Alder reactions of 2’‐hydroxychalcones and dienes, achieving high yields and moderate enantioselectivities. Considering the potentially high amounts of gossypol isolable from agricultural wastes of cotton crops, these results open the way for the introduction of a promising new class of biomass‐derived asymmetric catalysts.

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Journal
ChemistrySelect
Published
2026-04-01
DOI
https://doi.org/10.1002/slct.202600041
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
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0.00

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article

Toward the Valorization of Cotton Wastes: Application of a Gossypol‐Derived Ligand to an Asymmetric Diels–Alder Reaction

Daniela Imperio, Irene Izzo, Francesco De Riccardis, Alberto Minassi et al.
ChemistrySelect
Axial and Atropisomeric Chirality Synthesis
article

Toward the Valorization of Cotton Wastes: Application of a Gossypol‐Derived Ligand to an Asymmetric Diels–Alder Reaction

Daniela Imperio, Irene Izzo, Francesco De Riccardis, Alberto Minassi, Federica Pollastro, Giorgio Della Sala, Gianluca Montella, Yassine Benhamidat
article en

Abstract

ABSTRACT Gossypol, a major metabolite of cotton plants, has been used for the first time as a source material for the preparation of derivatives employed in asymmetric catalysis. Specifically, the (R)‐enantiomer of the 6,6’,7,7’‐O‐tetramethyl derivative of apogossypol has been synthesized in five steps and 47% total yield from enantiopure (‒)‐(R)‐gossypol. This axially chiral diol was used as a ligand in the enantioselective boron‐catalyzed Diels–Alder reactions of 2’‐hydroxychalcones and dienes, achieving high yields and moderate enantioselectivities. Considering the potentially high amounts of gossypol isolable from agricultural wastes of cotton crops, these results open the way for the introduction of a promising new class of biomass‐derived asymmetric catalysts.

ChemistrySelectVol. 11(14)
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” (IT), University of Salerno (IT)
Università degli Studi di Salerno
Zero hunger
Openalex Percentile: Top 22%
Axial and Atropisomeric Chirality Synthesis
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Toward the Valorization of Cotton Wastes: Application of a Gossypol‐Derived Ligand to an Asymmetric Diels–Alder Reaction — Daniela Imperio, Irene Izzo, et al. · ChemistrySelect (2026) | TGRS Research Map | TGRS