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Issue 20, 1994
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Mechanism of nucleophilic solvolysis of 1,2-dibromo-1,2-dihydrocyclobuta[b]pyridine; X-ray crystal structure analysis of 1,2-dihydro-1-methoxycyclobuta[b]pyridine methiodide

Abstract

trans-1,2-Dibromo-1,2-dihydrocyclobuta[b]pyridine 1a undergoes nucleophilic methanolysis with retention of configuration via 2-bromocyclobuta[b]pyridine 2; the crystal structure of 1,2-dihydro-1-methoxycyclobuta[b]pyridine methiodide is described.

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Article type: Paper
DOI: 10.1039/C39940002339
Citation: J. Chem. Soc., Chem. Commun., 1994,0, 2339-2340
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    Mechanism of nucleophilic solvolysis of 1,2-dibromo-1,2-dihydrocyclobuta[b]pyridine; X-ray crystal structure analysis of 1,2-dihydro-1-methoxycyclobuta[b]pyridine methiodide

    G. Conole and M. K. Shepherd, J. Chem. Soc., Chem. Commun., 1994, 0, 2339
    DOI: 10.1039/C39940002339

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