Synthesis and Transformation of Bis(silyl)-Substituted Conjugated Vinylallene Compounds

We develop a copper-catalyzed disilylation of polysubstituted pent-1-en-4-yn-3-yl acetate derivatives, which in one pot furnishes the bis­(silyl)-substituted vinylallenes in moderate yields under mild reaction conditions. The reaction shows broad substrate scope and single stereoselectivity. Besides...

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Veröffentlicht in:Organic letters 2023-10, Vol.25 (40), p.7332-7337
Hauptverfasser: Qian, Yi-Sen, Zhao, Jin-Bo, Xu, Yun-He
Format: Artikel
Sprache:eng
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Zusammenfassung:We develop a copper-catalyzed disilylation of polysubstituted pent-1-en-4-yn-3-yl acetate derivatives, which in one pot furnishes the bis­(silyl)-substituted vinylallenes in moderate yields under mild reaction conditions. The reaction shows broad substrate scope and single stereoselectivity. Besides, we develop a method to decrease the electrocyclization temperature of vinylallenes for the synthesis of methylenecyclobutenes by installing bis­(silyl) substituents. And the effect of a silyl substituent on electrocyclization of vinylallenes was studied via DFT computation. The synthetic method features broad substrate scope and excellent stereoselectivity.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.3c02738