Photolysis of alkylthiodihydroxybenzenes and related thiols and disulfides under argon proceeds with partial desulfurization to give the parent hydroxybenzenes in 13-36% yield. Under the same conditions, benzenethiol decomps. slowly to give low amts. of benzene. Irradn. of sulfides I (R = H, Me) results in the selective cleavage of the C-S bond on the hydroxy- or methoxy-substituted ring to yield the desulfurized products in more than 60% yield.

Photochemical desulfurization of phenolic thioethers, thiols and disulfides / D'Ischia, Marco; Testa, G.; Mascagna, D.; Napolitano, Alessandra. - In: GAZZETTA CHIMICA ITALIANA. - ISSN 0016-5603. - STAMPA. - 125:(1995), pp. 315-318.

Photochemical desulfurization of phenolic thioethers, thiols and disulfides

D'ISCHIA, MARCO;NAPOLITANO, ALESSANDRA
1995

Abstract

Photolysis of alkylthiodihydroxybenzenes and related thiols and disulfides under argon proceeds with partial desulfurization to give the parent hydroxybenzenes in 13-36% yield. Under the same conditions, benzenethiol decomps. slowly to give low amts. of benzene. Irradn. of sulfides I (R = H, Me) results in the selective cleavage of the C-S bond on the hydroxy- or methoxy-substituted ring to yield the desulfurized products in more than 60% yield.
1995
Photochemical desulfurization of phenolic thioethers, thiols and disulfides / D'Ischia, Marco; Testa, G.; Mascagna, D.; Napolitano, Alessandra. - In: GAZZETTA CHIMICA ITALIANA. - ISSN 0016-5603. - STAMPA. - 125:(1995), pp. 315-318.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/458065
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