Direct functionalization of 4,5-dichloropyridazin-6-one
Author:
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570360413/fullpdf
Reference6 articles.
1. Retro-ene reaction. V. Functionalization of 4,5-dihalopyridazin-6-ones using 1-hydroxymethyl-4,5-dihalopyridazin-6-ones as 1-0, 3-n, 5-0 ene-adducts
2. Retro-Ene reaction.VI.Functionalization of 4,5-dihalopyridazin-6-ones using 1-acetyloxymethyl-4,5-dihalopyridazin-6-ones as the 1-O, 3-N, 5-O ene-adduct
3. Functionalization of 4,5-dihalopyridazin-6-ones using 1-(1,1-dibromo-2-oxopropyl) derivatives
4. A large scale synthesis of 3-chloro-5-methoxypyridazine
5. Pyridazines with heteroatom substituents in position 3 and 5, part 1: 5-Hydroxy-3(2H)-pyridazinone and its derivatives
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1. Recent Progress in the Chemistry of Pyridazinones for Functional Group Transformations;The Journal of Organic Chemistry;2017-12-11
2. A green expedient synthesis of pyridopyrimidine-2-thiones and their antitubercular activity;Bioorganic & Medicinal Chemistry Letters;2011-05
3. A “Click and Activate” Approach in One-Pot Synthesis of a Triazolyl-Pyridazinone Library;Organic Letters;2011-02-25
4. ChemInform Abstract: Direct Functionalization of 4,5-Dichloropyridazin-6-one.;ChemInform;2010-06-11
5. Pyridazines and their Benzo Derivatives;Comprehensive Heterocyclic Chemistry III;2008
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