Reactions of 1, 2-dihaloethanes with chalcogenide anions

NV Russavskaya, VA Grabel'nykh…

Index: Russavskaya; Grabel'nykh; Levanova; Sukhomazova; Klyba; Zhanchipova; Tatarinova; Elaev; Deryagina; Korchevin; Trofimov Russian Journal of Organic Chemistry, 2006 , vol. 42, # 5 p. 652 - 658

Full Text: HTML

Citation Number: 9

Abstract

Abstract Reactions of 1, 2-dihaloethanes with chalcogenide anions generated from elemental chalcogens and dimethylchalcogens were performed in the hydrazine hydrate- KOH system. The use of anions Se x 2− and Te x 2−(x= 1− 4) resulted in ethylene evolution and chalcogen regeneration (or in increased x value in an anion). Oligomers of Thiokol type formed only in the reaction of the 1, 2-dichloroethane with a mixture of potassium disulfide ...

Related Articles:

Electrophilic addition of diselenides to alkenes: New synthesis of 1, 2-bis (selenides).

[Hermans, Bernard; Colard, Nicole; Hevesi, Laszlo Tetrahedron Letters, 1992 , vol. 33, # 32 p. 4629 - 4632]

More Articles...