98%
921
2 minutes
20
Vinyl sulfones are valued for their unique chemical properties and bioactivity, but creating a wide range of different analogs remains a challenge. To address this limitation, we have developed a novel approach that facilitates the synthesis of polysubstituted vinyl sulfones. This method utilizes the dual functionality of NIS as a promoter that enables sulfonation and elimination in the synthesis of vinyl sulfones. We used the broad applicability, efficiency, selectivity, and functional group tolerance of this approach to synthesize more than 70 examples. Additionally, competition experiments have provided insights into the reactivity and selectivity of the transient sulfonyl radical towards various C-C multiple bonds. Herein, we describe using this mild protocol in the late-stage vinyl sulfonation of complex molecules to simplify the synthesis of specific targets and enable the modification of complex natural products and advanced materials.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/chem.202403947 | DOI Listing |
Int J Biol Macromol
September 2025
Departamento de Biocatálisis, Instituto de Catálisis-CSIC, Campus UAM-CSIC, Madrid, Spain. Electronic address:
Lipase B from Candida antarctica immobilized on octyl (via interfacial activation) and octyl-vinyl sulfone (covalently attached) agarose beads via different immobilization protocols was submitted to amination and/or glutaraldehyde modifications. The catalytic performance of the resulting biocatalysts significantly varied across different substrates: using octyl-CALB with the double modification, activity increased 3.5 fold versus triacetin and decreased by 5 % using R-methyl mandelate, while using the covalent biocatalyst, activity increase by 2.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Department of Chemistry, Birla Institute of Technology and Science, Pilani (BITS Pilani), Hyderabad Campus, Jawahar Nagar, Telangana 500078, India.
Herein, we report the design and green synthesis of stereodefined tetrasubstituted alkenes (TPA-V-S, TPA-V-SO, and TPA-V-SO2) bearing a triphenyl amine (TPA) and a sulfenyl or sulfoxide, or sulfone functional group situated in the anti-orientation and two phenyl rings anti to each other. Notably, TPA-V-S exhibited reversible vis-to-NIR electrochromism with a high optical contrast of 70.6%, suitable for transparent-to-black (TTB) smart window applications.
View Article and Find Full Text PDFOrg Biomol Chem
September 2025
State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, Key Laboratory of Medicinal for Natural Resource, Ministry of Education and Yunnan Province, School of Pharmacy, School of Chemical Science and Technology, Yunnan University, Kunming 650091, China.
Herein, a visible-light-driven synthesis of 1,4-dicarbonyl vinyl sulfones sulfoxonium ylide homocoupling forming CC bonds, followed by sulfonyl hydrazide alkenylation is disclosed. Mechanistic studies support a sequential single-electron transfer (SET) and radical addition pathway. The method offers a sustainable alternative to conventional alkyne functionalization strategies.
View Article and Find Full Text PDFGels
August 2025
Departamento de Polímeros, Facultad de Ciencias Químicas, Universidad de Concepción, Edmundo Larenas 129, Concepcion 4070371, Chile.
Functional hydrogels have significant potential for applications in the pharmaceutical, agricultural, and environmental sectors. This study focuses on the synthesis of polyampholytic hydrogels through free radical polymerization using functionalized chitosans. The chitosan was modified with mono and disulfonic groups at different temperatures (25 °C and 60 °C) and reaction times (1, 8, 24 h), followed by further modification with glycidyl methacrylate to introduce vinyl groups into the polymers structure.
View Article and Find Full Text PDFJ Org Chem
August 2025
Department of Chemistry, SRM University-AP, Amaravati, Andhra Pradesh 522240, India.
An efficient nickel-photoredox dual-catalyzed intermolecular reductive coupling reaction of alkynes with vinyl phosphonates is described. The reaction is highly regio- and stereoselective, affording the homoallylic phosphonates in good to high yields. The present protocol is also successfully applied to other activated alkenes such as enones, acrylates, and vinyl sulfone.
View Article and Find Full Text PDF