Abstract
An efficient and convenient method for thiazolo[3,2-a]pyrimidines from cyclization reaction of dihydropyrimidine- thiones with α-bromoacetone in aqueous media is described.
Keywords: 5H-Thiazolo[3,2-a]pyrimidines, 3,4-dihydropyrimidinones, α-bromoacetone, aqueous media
Letters in Organic Chemistry
Title: Efficient Synthesis of 5H-Thiazolo[3,2-a]pyrimidines from Reactions of 3,4-Dihydropyrimidine-thiones with α-Bromoacetone in Aqueous Media
Volume: 4 Issue: 5
Author(s): Xi-Cun Wang, Zheng-Jun Quan, Zhang Zhang, Ya-Juan Liu and Peng-Yan Ji
Affiliation:
Keywords: 5H-Thiazolo[3,2-a]pyrimidines, 3,4-dihydropyrimidinones, α-bromoacetone, aqueous media
Abstract: An efficient and convenient method for thiazolo[3,2-a]pyrimidines from cyclization reaction of dihydropyrimidine- thiones with α-bromoacetone in aqueous media is described.
Export Options
About this article
Cite this article as:
Xi-Cun Wang , Zheng-Jun Quan , Zhang Zhang , Ya-Juan Liu and Peng-Yan Ji , Efficient Synthesis of 5H-Thiazolo[3,2-a]pyrimidines from Reactions of 3,4-Dihydropyrimidine-thiones with α-Bromoacetone in Aqueous Media, Letters in Organic Chemistry 2007; 4 (5) . https://dx.doi.org/10.2174/157017807781212139
DOI https://dx.doi.org/10.2174/157017807781212139 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers