A divergent and metal free synthesis of sulfoximine tethered imidazoles, imidazopyridines, imidazothiazoles, imidazobenzothiazines, thiazoles and selenazoles
Author:
Affiliation:
1. Medicinal Chemistry
2. Jubilant Biosys Ltd
3. Bangalore
4. India
5. Department of Chemistry
6. Jawaharlal Nehru Technological University Ananthapur College of Engineering Pulivendula
7. Kadapa
8. Rayalaseema University
9. Kurnool 518002
Abstract
A divergent and metal free approach has been successfully developed for the synthesis of sulfoximine tethered heterocycles from a α-bromoalkanone building block.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB00601B
Reference68 articles.
1. Facile Synthesis of Polysubstituted Imidazoles through CBr4-Mediated Tandem Cyclization of Amidines with 1,3-Dicarbonyl Compounds or Ketones
2. New protocols to access imidazoles and their ring fused analogues: synthesis from N-propargylamines
3. Synthesis of 2,4,5-trisubstituted imidazoles over reusable CoFe2O4nanoparticles: an efficient and green sonochemical process
4. Recent Developments of p38α MAP Kinase Inhibitors as Antiinflammatory Agents Based on the Imidazole Scaffolds
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