Visible light photoredox catalyzed one pot Stadler–Ziegler reaction of heteroaryl amines with heteroaryl thiols at room temperature: An efficient synthesis of diheteroaryl sulphides
By: Panja, Subir
.
Contributor(s): Sahu, Puneshwar.
Publisher: New Delhi CSIR 2019Edition: Vol.58(B), Feb.Description: 183-191p.Subject(s): GENERAL CHEMISTRYOnline resources: Click here
In:
Indian journal of chemistry (Section B)Summary: An efficient synthesis of diheteroaryl sulphides has been achieved by visible light photocatalyzed reaction of heteroaryl thiols and heteroaryl amines via in situ diazotization of heteroaryl amines with t-BuONO under LED light irradiation at room temperature. A library of functionalized diheteroaryl sulphides are obtained by using this protocol. This procedure is also effective for the synthesis of heteroaryl – aryl and heteroaryl – alkyl sulphides. The reaction avoids the use of transition metal catalysts, additives and strong acidic reaction medium.
| Item type | Current location | Call number | Status | Date due | Barcode | Item holds |
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Articles Abstract Database
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School of Pharmacy Archieval Section | Not for loan | 2022-0297 |
An efficient synthesis of diheteroaryl sulphides has been achieved by visible light photocatalyzed reaction of heteroaryl thiols and heteroaryl amines via in situ diazotization of heteroaryl amines with t-BuONO under LED light irradiation at room temperature. A library of functionalized diheteroaryl sulphides are obtained by using this protocol. This procedure is also effective for the synthesis of heteroaryl – aryl and heteroaryl – alkyl sulphides. The reaction avoids the use of transition metal catalysts, additives and strong acidic reaction medium.
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