Synthesis of novel selenium and tellurium-containing tetrazoles: a class of chalcogen compounds with antifungal activity
摘要:
We describe herein the synthesis and antifungal activity of new 5-arylchalcogenoalkyl-1H-tetrazoles 4. Arylchalcogenoalkyl-1H-tetrazoles 4 have been synthesized in high yields by reaction of arylchalcogenolate anions with chloronitriles 2, and subsequent [2+3] cycloaddition of resulting arylchalcogenoalkylnitriles 3 with sodium azide by zinc catalysis in aqueous solution. The obtained compound 4a was screened for antifungal activity and presented inhibitory property against seven fungal strains. This protocol is an efficient method to produce new selenium-nitrogen compounds with antifungal activity. (C) 2012 Published by Elsevier Ltd.
An Effective Synthesis of β- Selenium and β- Tellurium Carbonyl Compounds Via Reaction of Diaryldiselenides Or Diarylditellurides with α,β- Unsaturated Carbonyl Compounds Induced by Low-Valent Titanium
作者:Long-Hu Zhou、Yong-Min Zhang
DOI:10.1080/00397919908085796
日期:1999.2
Abstract P-Selenium and β-tellurium carbonylcompounds have been prepared in good yield by reaction of diaryldiselenides or diarylditelluride with α,β-unsaturated carbonylcompoundsinduced by TiC14 / Sm /THF system under mild reaction conditions.
Direct Michael addition to electron-deficient alkenes using diorganyl dichalcogenides (Te/S) and NaBH4/PEG-400
作者:Gelson Perin、Elton L. Borges、Thiago J. Peglow、Eder J. Lenardão
DOI:10.1016/j.tetlet.2014.08.101
日期:2014.10
Nucleophilic species of tellurium and sulfur were generated in situ from the reaction of the respective diorganyl dichalcogenides with NaBH4 in PEG-400 as solvent and selectively added to electron-deficient alkenes. Chalcogenolate anions were directly added at mild conditions by this simple procedure and in all cases furnished the respective Michael adducts in short reaction times and good yields. (C) 2014 Elsevier Ltd. All rights reserved.
Li, Xue; Zhang, Songlin; Wang, Yulu, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2003, vol. 42, # 7, p. 1771 - 1773