Application of N,N′-Diiodo-N,N′-1,2-ethandiylbis(p-toluene sulfonamide) as a New Reagent for Synthesis of 2-Arylbenzimidazoles and 2-Arylbenzothiazoles under Solvent-free Conditions
✍ Scribed by Hojat Veisi; Ramin Ghorbani-Vaghei; Alireza Faraji; Turan Ozturk
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 92 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0256-7660
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✦ Synopsis
Abstract
N,N′‐Diiodo‐N,N′‐1,2‐ethandiylbis(p‐toluene sulfonamide) (NIBTS) is a good and new reagent for synthesis of 2‐arylbenzimidazoles and 2‐arylbenzothiazoles at room temperature under solvent‐free condition with good to high yield. Absence of solvent, short reaction times, non‐corrosive, operational simplicity and environmentally friendliness are the main advantages of this procedure.
📜 SIMILAR VOLUMES
Several pyrrolidinofullerenes were N-arylated by phase-nitro groups on the N-phenyl ring have a strong influence on the reduction potential values. Theoretical calculations at the transfer catalysis in the absence of solvent. The electrochemical behaviour of the novel C 60 -acceptor dyads semiempiri