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Published in 2025 at "Chemical science"
DOI: 10.1039/d5sc07853a
Abstract: A cationic Pd-catalysed multicomponent reaction enables the regio-reversed alkenyl–arylation of ynamides through a migratory difunctionalization strategy. A stereoselective 1,3-olefin shift of a keteniminium–alkenyl–Pd intermediate governs the carbopalladation pathway, generating a vinylic Pd species that subsequently…
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Keywords:
arylation ynamides;
reversed alkenyl;
alkenyl arylation;
olefin shift ... See more keywords