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Royal Society of Chemistry, Chemical Communications, 40(55), p. 5732-5735, 2019

DOI: 10.1039/c9cc02418b

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Reduction of 1,3,5,7-cyclooctatetraene by a molecular calcium hydride: an even electron polarised insertion/deprotonation mechanism

Journal article published in 2019 by Michael S. Hill ORCID, Mary F. Mahon, Andrew S. S. Wilson ORCID, Chiara Dinoi, Laurent Maron ORCID, Emma Richards ORCID
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

The reductive aromatisation of 1,3,5,7-cyclooctatetraene by a dimeric calcium hydride occurs via two electron steps and does not necessitate the formation of radical intermediates.