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{c}
{tag=Work by Mieczysław Mąkosza}
{tag=Work by Tomasz Glinka}
{title2=1983}

https://doi.org/10.1021/jo00169a067

Journal of Organic Chemistry 48, 3860–3861. Isotope/base-rate effects and <hydrogen>-versus-halogen substitution competitions support reversible sigma-H addition and base-induced elimination, excluding the proposed hydride-shift alternative.

Reaction of organic anions. Part 108. On the mechanism of the vicarious nucleophilic substitution of hydrogen in nitroarenes by Mieczysław Mąkosza and Tomasz Glinka

Past exam of the chemistry B course of the University of Cambridge / 2024 / Paper 1 / B2 / b / ii / Solution

Reaction of organic anions. Part 108. On the mechanism of the vicarious nucleophilic substitution of hydrogen in nitroarenes by Mieczysław Mąkosza and Tomasz Glinka (1983)

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Reaction of organic anions. Part 108. On the mechanism of the vicarious nucleophilic substitution of hydrogen in nitroarenes by Mieczysław Mąkosza and Tomasz Glinka (1983)

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