trans-2-Phenyl-3-n-propyloxetan thermolysed at 250–300° to give trans-1-phenylpent-1-ene stereospecifically, whereas the cis-isomer decomposed more slowly (by a factor of ca. 2) to produce a mixture of cis- and trans-olefin.
N. Shimizu and S. Nishida, J. Chem. Soc., Chem. Commun., 1974, 734 DOI: 10.1039/C39740000734
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