Issue 5, 2018

Reversible addition of terminal alkenes to digermynes

Abstract

Stable digermynes with sterically demanding Bbt (Bbt = 2,6-[CH(SiMe3)2]2-4-[C(SiMe3)3]-C6H2) or Tbb (Tbb = 4-tBu-2,6-[CH(SiMe3)2]2-C6H2) groups underwent [2+2] cycloadditions with terminal alkenes to give the corresponding 1,2-digermacyclobutenes. In the case of the Bbt-substituted digermyne, the reaction was reversible at room temperature, i.e., the 1,2-digermacyclobutene (Ge(II) species) is susceptible to a facile reductive elimination that affords the corresponding digermyne (Ge(I) species) and the alkene.

Graphical abstract: Reversible addition of terminal alkenes to digermynes

Supplementary files

Article information

Article type
Communication
Submitted
07 Nov 2017
Accepted
11 Dec 2017
First published
11 Dec 2017

Chem. Commun., 2018,54, 519-522

Reversible addition of terminal alkenes to digermynes

T. Sugahara, J. Guo, T. Sasamori, S. Nagase and N. Tokitoh, Chem. Commun., 2018, 54, 519 DOI: 10.1039/C7CC08555A

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