| dc.contributor.author |
Sakhuja, Rajeev |
|
| dc.date.accessioned |
2021-11-11T10:59:10Z |
|
| dc.date.available |
2021-11-11T10:59:10Z |
|
| dc.date.issued |
2017-09-26 |
|
| dc.identifier.uri |
https://onlinelibrary.wiley.com/doi/10.1002/asia.201701274 |
|
| dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3356 |
|
| dc.description.abstract |
Two efficient iodine-mediated strategies, which are economical and one-pot, are described to access bis(imidazo[1,2-a]pyridin-3-yl)sulfanes and bis(imidazo[1,2-a]pyridin-3-yl)disulfanes in chloroform and acetic acid, respectively, by a direct oxidative homocoupling of imidazo-heterocycles using inexpensive sodium sulfide as a sulfur source. These strategies are scalable, and an array of substrates delivered their corresponding stable sulfur-bridged imidazo-heterocycles in excellent yields. |
en_US |
| dc.language.iso |
en |
en_US |
| dc.publisher |
Wiley |
en_US |
| dc.subject |
Chemistry |
en_US |
| dc.subject |
Solvent-Driven |
en_US |
| dc.subject |
Synthesis of Bis(imidazo[1,2-a]pyridin-3-yl) |
en_US |
| dc.subject |
Disulfanes |
en_US |
| dc.title |
Solvent-Driven Iodine-Mediated Oxidative Strategies for the Synthesis of Bis(imidazo[1,2-a]pyridin-3-yl)sulfanes and Disulfanes |
en_US |
| dc.type |
Article |
en_US |