Ring expansion route to cyclopentenes via regiospecific 1,2-vinyl migration
Abstract
Cyclobut-2-enylmethyl cations undergo regiospecific and highly stereoselective ring expansions via 1,2-vinyl shifts to produce 4-chlorocyclopentenes.
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- Paper
J. Chem. Soc., Chem. Commun., 1982, 874-875
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Ring expansion route to cyclopentenes via regiospecific 1,2-vinyl migration
J. A. Miller and M. Ullah, J. Chem. Soc., Chem. Commun., 1982, 874 DOI: 10.1039/C39820000874
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