Tetrachlorocyclopentadienylidene and Thermal Rearrangements of Its Cyclopropyl Adducts1

ET McBee, JA Bosoms, CJ Morton

Index: McBee,E.T. et al. Journal of Organic Chemistry, 1966 , vol. 31, p. 768 - 772

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Citation Number: 20

Abstract

Tetrachlorocyclopentadienylidene, generated by the photolysis of tetrachlorodiazocyclopentadiene, has been shown to undergo carbon-hydrogen insertion in cyclohexane, carbon-chlorine insertion in carbon tetrachloride, and to add to olefins to give cyclopropyl compounds. The addition to cis-2-butene was nonstereospecific. The reaction with 2-methyl-2-butene gave 1, 2, 3, 4-tetrachloro-6, 6, 7-trimethylspiro [2.4] hepta-1, 3- ...

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NOTES BIBLIOGRAPHIQUES BIBLIOGRAFISCHE NOTA'S BIBLIOGRAPHICAL DATA

[Prins Recueil des Travaux Chimiques des Pays-Bas, 1953 , vol. 72, p. 253,256]

NOTES BIBLIOGRAPHIQUES BIBLIOGRAFISCHE NOTA'S BIBLIOGRAPHICAL DATA

[Prins Recueil des Travaux Chimiques des Pays-Bas, 1953 , vol. 72, p. 253,256]

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