The Diorgano Dichalcogenides Addition to Benzyne under Mild Conditions

Fabiano Toledo; Henrique Marques; João Comasseto; Cristiano Raminelli

doi:10.3390/ecsoc-11-01344

x Selected file doesn't exist!

Previous Article in event

Catalyst-controlled Asymmetric Syntheses of Organoselenium Compounds. β-Hydroxyselenides by Desymmetrization of meso Epoxides

Next Article in event

Thermodynamically controlled Reactions of Selenenylphosphonium Ion Me3PSeMe+ toward Electrophiles and Nucleophiles

The Diorgano Dichalcogenides Addition to Benzyne under Mild Conditions

Fabiano T. Toledo

Henrique Marques

João V. Comasseto

Cristiano Raminelli

¹ Instituto de Química, Universidade de São Paulo, Av. Prof. Lineu Prestes, 748, 05508-000, São Paulo, SP, Brazil

Published: 30 November 2007 by MDPI in The 11th International Electronic Conference on Synthetic Organic Chemistry session Symposium on Selenium and Tellurium Chemistry

https://doi.org/10.3390/ecsoc-11-01344

Abstract: The reaction between diorgano dichalcogenides and o-(trimethylsilyl)phenyl triflate in the presence of CsF at room temperature produced o-bis(organochalcogenide)benzenes in moderate to good yields.

Keywords: n/a

View paper

37 Reads
0 Recommendations

Fabiano Toledo

Henrique Marques

João Comasseto

Cristiano Raminelli