Issue 11, 2024

Palladium-catalysed fragmentary esterification-induced allylic alkylation of allyl carbonates and cyclic vinylogous anhydrides

Abstract

An unprecedented palladium-catalysed fragmentary esterification-induced allylic alkylation (FEAA) of cyclic vinylogous anhydrides (CVAs) and allyl carbonates has been disclosed. The protocol features broad sp3-rich scaffold tolerance, rendering highly functionalized 1,6 and 1,7-dicarbonyls in up to high yields and diastereoselectivities. Three-component FEAA is also well tolerant to generate 1,6-dicarbonyls through the addition of extra O/N-nucleophiles. Furthermore, cyclic allyl carbonate-involved FEAA provides an efficient approach for the synthesis of structurally complex medium-sized rings.

Graphical abstract: Palladium-catalysed fragmentary esterification-induced allylic alkylation of allyl carbonates and cyclic vinylogous anhydrides

Supplementary files

Article information

Article type
Communication
Submitted
24 Nov 2023
Accepted
03 Jan 2024
First published
04 Jan 2024

Chem. Commun., 2024,60, 1416-1419

Palladium-catalysed fragmentary esterification-induced allylic alkylation of allyl carbonates and cyclic vinylogous anhydrides

S. Wu, Y. Li, P. Shen, X. Yang and G. Ran, Chem. Commun., 2024, 60, 1416 DOI: 10.1039/D3CC05758E

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