Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/184703
Title: Recyclable g-C3N4 catalyzed decarboxylative alkenylation of N-aryl glycines with vinyl sulfones under visible-light irradiation
Authors: Guo, Chengjie
Zhao, Guozhi
Feng, Yabiao
Chen, Dong
Loh, Teck-Peng
Wang, Dongping
Jia, Zhenhua
Keywords: Chemistry
Issue Date: 2025
Source: Guo, C., Zhao, G., Feng, Y., Chen, D., Loh, T., Wang, D. & Jia, Z. (2025). Recyclable g-C3N4 catalyzed decarboxylative alkenylation of N-aryl glycines with vinyl sulfones under visible-light irradiation. Organic Chemistry Frontiers, 12(7), 2409-2414. https://dx.doi.org/10.1039/d5qo00100e
Project: M21K2c0114 
M22K9b0049 
Journal: Organic Chemistry Frontiers 
Abstract: Allylamines are a versatile class of compounds with significant applications in pharmaceuticals and as building blocks in organic synthesis. Herein we present a straightforward protocol for visible-light driven g-C3N4-catalyzed decarboxylative alkenylation of N-aryl glycines with vinyl sulfones to access allylamines in moderate to excellent yields (up to 91%), and it demonstrated broad substrate compatibility, including primary, secondary, and tertiary N-aryl glycines and diverse vinyl sulfones. Notably, the g-C3N4 catalyst is recyclable up to five times without obvious loss of catalytic performance. Preliminary mechanistic studies indicated that visible light is essential to achieve the desired transformation efficiently.
URI: https://hdl.handle.net/10356/184703
ISSN: 2052-4129
DOI: 10.1039/d5qo00100e
Schools: School of Physical and Mathematical Sciences 
Rights: © 2025 The Author(s). Published by Royal Society of Chemistry and Chinese Chemical Society. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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