A NOVEL METHOD FOR THE PREPARATION OF VARIOUS 2-PYRIDYL SULFIDES FROM ALCOHOLS

5 November 1975

journal article
research article
Published by Oxford University Press (OUP) in Chemistry Letters

Vol. 4 (11), 1159-1162
https://doi.org/10.1246/cl.1975.1159

Abstract

1-Methyl-2-alkoxypyridinium salts, easily formed in situ from l-methyl-2-fluoropyridinium salt and alcohols, react with pyrid-2-thione in the presence of triethylamine to give the corresponding 2-pyridyl sulfides in good yields.

Keywords

SALT
NOVEL METHOD
PYRIDYL SULFIDES
THIONE
EASILY
REACT
GOOD

This publication has 1 reference indexed in Scilit:

SELECTIVE CARBON–CARBON BOND FORMING REACTION BY THE USE OF ALLYL 2-PYRIDYL SULFIDE DERIVATIVES—TOTAL SYNTHESIS OF α-cis-BERGAMOTENE
Chemistry Letters, 1972

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