We developed an acridine-catalyzed, metal- and base-free decarboxylative allylation of carboxylic acids with allylic acetates under mild conditions. The reaction proceeds via a proton-coupled electron transfer (PCET) process, enabling efficient conversion of readily available feedstocks with broad functional group compatibility. This operationally simple and versatile method demonstrates significant potential for synthetic applications, particularly in late-stage modification of bioactive carboxylic acids.
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C. Ju
Nanjing Tech University
Xiaoyu Liu
Chinese Academy of Tropical Agricultural Sciences
Yanzhe Shi
Nanjing Tech University
Organic Letters
Nanyang Technological University
Nanjing Tech University
Division of Chemistry
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Ju et al. (Thu,) studied this question.
synapsesocial.com/papers/68d909fc41e1c178a14f5d4d — DOI: https://doi.org/10.1021/acs.orglett.5c03690