Access to Highly Substituted Pyrimidine N-Oxides and 4-Acetoxymethyl-Substituted Pyrimidines via the LANCA Three-Component Reaction–Cyclocondensation Sequence
Author:
Affiliation:
1. Institut für Chemie und Biochemie, Freie Universität Berlin
2. Department of Chemistry, Indian Institute of Engineering Science and Technology
Abstract
Funder
Bayer HealthCare
Deutsche Forschungsgemeinschaft
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry,Catalysis
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0040-1706020.pdf
Reference13 articles.
1. Pyrimidine Derivatives with Terminal Pyridyl Heterocycles: Facile Synthesis and Their Antiproliferative Activities
2. Synthesis and structure–activity relationship of fused-pyrimidine derivatives as a series of novel GPR119 agonists
3. Dual M3 antagonists-PDE4 inhibitors. Part 2: Synthesis and SAR of 3-substituted azetidinyl derivatives
4. Development and Scale-up of a Route to ATR Inhibitor AZD6738
5. FeCl3-Assisted Niobium-Catalyzed Cycloaddition of Nitriles and Alkynes: Synthesis of Alkyl- and Arylpyrimidines Based on Independent Functions of NbCl5 and FeCl3 Lewis Acids
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1. The Boekelheide Rearrangement of Pyrimidine N‐oxides as a Case Study of Closed or Open Shell Reactions ‐ Experimental and Computational Evidence for the Participation of Radical Intermediates;Chemistry – A European Journal;2023-03-22
2. A Proline and 4‐Hydroxyproline Based Approach to Enantiopure Pyrrolidin‐2‐yl‐Substituted Pyridine and Pyrimidine Derivatives;European Journal of Organic Chemistry;2021-09-03
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