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 |
---|---|---|---|---|---|---|
Articles Abstract Database | 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.
There are no comments for this item.