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Propargyl alcohols as alkyne sources: Synthesis of heterocyclic compounds under microwave irradiation
Published in Elsevier B.V.
2020
Volume: 922
   
Abstract
Fused heterocyclic compounds with alkyne substituent, have been achieved using a domino microwave-assisted [Pd]-catalysis. Interestingly, tert-propargyl alcohols underwent a selective degradative β-carbon cleavage and served as masked alkynyl equivalents, in water as the sole reaction medium. Dihydrobenzofurans, indolines, and oxindoles have been accomplished using this dual C–C bond-forming strategy. © 2020 Elsevier B.V.
About the journal
JournalData powered by TypesetJournal of Organometallic Chemistry
PublisherData powered by TypesetElsevier B.V.
ISSN0022328X