GAS PHASE ISOPROPYLATION OF AROMATIC HYDROCARBONS. FLUORINE AND METHYL SUBSTITUENT EFFECTS ON REACTIVITY AND ORIENTATION.

DOI: 10.1016/S0040-4039(00)87659-5

Source and publish data:

Tetrahedron Letters p. 3525 - 3528 (1982)

Update date:2022-08-03

Topics:

Authors:

Attina, Marina

Petris, Giulia de

Giacomello, Pierluigi

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Article abstract of DOI:10.1016/S0040-4039(00)87659-5

The isopropylation of substituted benzenes by s-C3H7⁺ cations is studied to evaluate the directive effects of fluorine, methyl group and their combinations as ring substituents in the gas-phase aromatic substitution.

Full text of DOI:10.1016/S0040-4039(00)87659-5

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