Abstract
The valence isomerization of the all-carbon and heteroelement analogues of cyclohepta-1,3,5-triene into the corresponding bicyclo[4.1.0]hepta-2,4-dienes is reviewed to show the impact of the heteroatom on the stability of both valence isomers. The focus is on the parent systems and their synthetic applications. © 2011 Jansen et al; licensee Beilstein-Institut.
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Jansen, H., Chris Slootweg, J., & Lammertsma, K. (2011). Valence isomerization of cyclohepta-1,3,5-triene and its heteroelement analogues. Beilstein Journal of Organic Chemistry, 7, 1713–1721. https://doi.org/10.3762/bjoc.7.201
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