Reactivity of boryl- and silyl-substituted carbenoids toward alkynes: insertion and cycloaddition chemistry

Andrey V Protchenko, Matthew P Blake, Andrew D Schwarz, Cameron Jones, Philip Mountford, Simon Aldridge

Research output: Contribution to journalArticleResearchpeer-review

32 Citations (Scopus)

Abstract

Three modes of reactivity of phenyl-substituted alkynes toward acyclic tetrelenes are reported, with reaction pathways found to be dependent not only on the nature of the group 14 element but also on the supporting ligand set. Systems featuring Sn–B or Ge–B bonds undergo insertion chemistry, forming borane-appended (vinyl)SnII and GeII species. With a bis(amido)stannylene, phenylacetylene acts as a protic acid, generating a SnII acetylide with a unique bridged structure. Reactivity toward a more strongly reducing SiII system is dominated by the possibility of accessing SiIV via [2 + 1] cycloaddition chemistry.
Original languageEnglish
Pages (from-to)2126-2129
Number of pages4
JournalOrganometallics
Volume34
Issue number11
DOIs
Publication statusPublished - 2015

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