Solvolysis of t-butyl substituted cyclob
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Paul v.R. Schleyer; P. LePerchec; Douglas J. Raber
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Article
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1969
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Elsevier Science
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French
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received in lg for publication g!l Sapfaber 1969) Rigidly held cyclobutyl tosylates show a remarkable dependence of eolvolysis rates on the conformation of the leaving gr0up.a Thus, in both the bicyclo[2.l.l]pentyl and bicyclo[3.1.1]hexyl series, the equatorial isomers (A) are strongly accelerated a