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Pd-catalyzed oxa-[4 + ] dipolar cycloaddition using 1,4-O/C dipole synthons for the synthesis of O-heterocycles. | LitMetric

Pd-catalyzed oxa-[4 + ] dipolar cycloaddition using 1,4-O/C dipole synthons for the synthesis of O-heterocycles.

Org Biomol Chem

Department of Chemistry (BK21 Four), Research Institute of Natural Science, Gyeongsang National University, Jinju 52828, Korea.

Published: December 2023


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Article Abstract

Transition metal-catalyzed dipolar cycloaddition is one of the most efficient and powerful synthetic strategies to produce diverse heterocycles. In particular, for the construction of oxygen-containing heterocycles, which are valuable structural motifs found in pharmaceuticals and natural compounds, transition metal-catalyzed oxa-dipolar cycloaddition using an oxygen-containing dipole has emerged as a promising method. In recent years, the 1,4-O/C dipole synthons 2-alkylidenetrimethylene carbonate and 2-hydroxymethylallyl carbonate have been developed and successfully applied to palladium-catalyzed oxa-[4 + ] dipolar cycloadditions with diverse dipolarophiles. In this review, we summarize recent advances in palladium-catalyzed oxa-[4 + ] dipolar cycloadditions using 1,4-O/C dipoles including asymmetric catalysis and divergent catalysis toward five- to nine-membered O-heterocycles.

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Source
http://dx.doi.org/10.1039/d3ob01619fDOI Listing

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