Enantioselective [5 + 1] cycloaddition of sulfur ylides and vinylethylene carbonates via synergistic palladium/chiral phosphonic acid catalysis

Abstract

An effective method for the synthesis of dihydropyrans through synergistic palladium and chiral phosphonic acid catalysis was reported. This protocol proceeded under mild reactions and provided dihydropyrans in up to 87% yield and up to 97% ee. Meanwhile, various derivations such as oxidation, Wittig-reaction, reductions, nucleophilic substitution, and Baeyer–Villiger were accomplished to furnish interesting compounds. To gain insight into the reaction mechanism, nonlinear relationship experiments and Hammett plot experiments were carried out. In addition, a range of products (3i, 4b, 4f, 4g, and 4j) accessible from this method exhibit various anti-inflammatory activities on NO and ROS inhibition.

Graphical abstract: Enantioselective [5 + 1] cycloaddition of sulfur ylides and vinylethylene carbonates via synergistic palladium/chiral phosphonic acid catalysis

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Article information

Article type
Edge Article
Submitted
10 Feb 2025
Accepted
24 Mar 2025
First published
08 Apr 2025
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2025, Advance Article

Enantioselective [5 + 1] cycloaddition of sulfur ylides and vinylethylene carbonates via synergistic palladium/chiral phosphonic acid catalysis

M. Ke, J. Zheng, J. Zong, K. Tang, J. Wang, G. Zheng, B. Zhang, D. Cheng, Z. Ju and F. Chen, Chem. Sci., 2025, Advance Article , DOI: 10.1039/D5SC01050K

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