Synthesis of 1,3-Dienes from Alkenes via Alkenyl Thianthrenium Salts
Sven Müller1,2, Nicolai Klask1,2, Aboubacar Daff1
1Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, Germany.
Abstract:
Herein, we show the conversion of alkenes into functionalized 1,3-dienes in two steps. First, C-H thianthrenation is used to access a wide pool of alkenyl electrophiles directly from alkenes. Second, the alkenyl thianthrenium salts undergo a Pd-catalyzed three-component coupling reaction with allene gas and nonorganometallic nucleophiles to afford 1,3-dienes. This method provides a robust and modular platform for accessing structurally complex 1,3-dienes that would be challenging to access otherwise.
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