Acylation of 2-benzylpyridine N-oxides and subsequent in situ [3,3]-sigamatropic rearrangement reaction
Author:
Funder
China Postdoctoral Science Foundation
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. Synthesis of Pyridine and Dihydropyridine Derivatives by Regio- and Stereoselective Addition toN-Activated Pyridines
2. The developability of heteroaromatic and heteroaliphatic rings – do some have a better pedigree as potential drug molecules than others?
3. Copper-Catalyzed α-Methylenation of Benzylpyridines Using Dimethylacetamide as One-Carbon Source
4. Chemistry of the Benzylpyridines. II. Nuclear Substituted 2-Benzylpyridines1
5. Stereochemical aspects of antihistamine action. 4. Absolute configuration of carbinoxamine antipodes
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1. Deoxygenation of N-heterocyclic N-oxides using isopropanol as a recyclable reductant;Organic Chemistry Frontiers;2024
2. [3,3]-Sigmatropic rearrangements: a variety of methods and recent advances;Russian Chemical Reviews;2022
3. Microwave‐Assisted 1,3‐Dioxa‐[3,3]‐Sigmatropic Rearrangement of Substituted Allylic Carbamates: Application to the Synthesis of Novel 1,3‐Oxazine‐2,4‐dione Derivatives;European Journal of Organic Chemistry;2021-11-19
4. Six-membered ring systems: pyridines and benzo derivatives;Progress in Heterocyclic Chemistry;2021
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