The reaction of bis(trimethylstannyl) sulphide and sodium with toluene, m-xylene, p-xylene and thioanisole gives stannylation at the methyl group whereas anisole was stannylated at the aromatic nucleus with very high ortho selectivity.

G., C., S., M., A., R., Taddei, M. (1990). Direct Stannylation of Aromatic Derivatives Using Bis(trimethylstannyl)sulphide and Sodium. GAZZETTA CHIMICA ITALIANA, 120, 721-722.

Direct Stannylation of Aromatic Derivatives Using Bis(trimethylstannyl)sulphide and Sodium

TADDEI, MAURIZIO
1990-01-01

Abstract

The reaction of bis(trimethylstannyl) sulphide and sodium with toluene, m-xylene, p-xylene and thioanisole gives stannylation at the methyl group whereas anisole was stannylated at the aromatic nucleus with very high ortho selectivity.
1990
G., C., S., M., A., R., Taddei, M. (1990). Direct Stannylation of Aromatic Derivatives Using Bis(trimethylstannyl)sulphide and Sodium. GAZZETTA CHIMICA ITALIANA, 120, 721-722.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/30872
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