Synthesis of 2,3-Dihydro-1-benzofuran-2-ylmethyltellanes


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

Tellurium tetrabromide readily reacted with 2-allylphenol at room temperature in acetonitrile to give previously unknown tribromo(2,3-dihydro-1-benzofuran-2-ylmethyl)-λ4-tellane in quantitative yield. The reduction of the product afforded bis(2,3-dihydro-1-benzofuran-2-ylmethyl)ditellane and benzyl(2,3-dihydro-1-benzofuran-2-ylmethyl)tellane.

About the authors

M. V. Musalova

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

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

M. V. Musalov

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

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

S. I. Udalova

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

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

A. G. Khabibulina

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

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

V. A. Potapov

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

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

S. V. Amosova

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Author for correspondence.
Email: amosova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2018 Pleiades Publishing, Ltd.