Reactions of sodium 2-pyridylchalcogenolates with propargyl halides


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The nature of the chalcogen atom has a decisive effect on the direction of the nucleophilic substitution reaction between 2-pyridylchalcogenolate anions and propargyl halides. 2-Pyridylchalcogenolate anions react with sodium pyridyl tellurolate following 1,3-nucleophilic substitution mechanism to give selectively allenyl 2-pyridyl telluride. Under similar conditions, sodium 2-pyridyl selenolate and 2-pyridyl thiolate produce propargyl 2-pyridyl selenide and propargyl 2-pyridyl sulfide, respectively.

Sobre autores

M. Musalova

A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

Email: amosova@irioch.irk.ru
Rússia, 1 ul. Favorskogo, Irkutsk, 664033

V. Panov

A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

Email: amosova@irioch.irk.ru
Rússia, 1 ul. Favorskogo, Irkutsk, 664033

M. Musalov

A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

Email: amosova@irioch.irk.ru
Rússia, 1 ul. Favorskogo, Irkutsk, 664033

V. Potapov

A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

Email: amosova@irioch.irk.ru
Rússia, 1 ul. Favorskogo, Irkutsk, 664033

S. Amosova

A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

Autor responsável pela correspondência
Email: amosova@irioch.irk.ru
Rússia, 1 ul. Favorskogo, Irkutsk, 664033

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