From the journal:

Chemical Communications

Readily available systems for the cycloaddition of CO2 to epoxides through a water-enhanced application of alkaloid organocatalysts

Yanisa Pongsupradit, ORCID logo a   Wuttichai Natongchaia  and  Valerio D’Elia ORCID logo *ab  

* Corresponding authors

a School of Molecular Science and Engineering, VISTEC Advanced Laboratory for Environment-Related Inorganic and Organic Syntheses (V.A.L.E.R.I.O.S.), Vidyasirimedhi Institute of Science and Technology, (VISTEC), Payupnai, Wangchan, Rayong 21210, Thailand
E-mail: valerio.delia@vistec.ac.th

b Department of Biological and Environmental Sciences and Technologies (DiSTeBA), University of Salento, Lecce, Italy
E-mail: valerio.delia@unisalento.it

Abstract

Biobased quinine forms active homogeneous and recyclable heterogeneous organocatalysts for cyclic carbonate synthesis by simple modifications, such as neutralization with HI or grafting on resin.

Graphical abstract: Readily available systems for the cycloaddition of CO2 to epoxides through a water-enhanced application of alkaloid organocatalysts

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Article information

DOI
https://doi.org/10.1039/D6CC00971A
Article type
Communication
Submitted
13 Feb 2026
Accepted
10 Mar 2026
First published
10 Mar 2026

Chem. Commun., 2026, Advance Article

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Readily available systems for the cycloaddition of CO2 to epoxides through a water-enhanced application of alkaloid organocatalysts

Y. Pongsupradit, W. Natongchai and V. D’Elia, Chem. Commun., 2026, Advance Article , DOI: 10.1039/D6CC00971A

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