A convenient regioselective synthesis of (2E)-2-[2,3,6-triarylpyrimidin-4(3H)-ylidene]acetonitriles through ring transformation reactions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference36 articles.
1. A novel strategy for the expeditious synthesis of aryl-tethered highly congested 2-hydroxybenzyl alcohols from 2-pyranones
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1. Base Promoted Synthesis of 2-((5-methoxynaphthalen-1-yl)methyl)-3-methyl-5-sec-amino-[1,1′-biphenyl]-4-carbonitrilederivatives: Photophysical, Solvatochromic and DFT studies;Journal of Molecular Structure;2021-02
2. Recent Development on the Ring Transformation Reactions: Synthesis of Functionalized Benzenes, N-Heterocycles and Fused Ring Systems;HETEROCYCLES;2021
3. Synthesis, photophysical, solvatochromic and DFT studies of (Z)-2-(2-Phenyl-4H-benzo[4,5]thiazolo[3,2-a]pyrimidin-4-ylidene)acetonitrile derivatives;Journal of Luminescence;2019-06
4. 2H-Pyran-2-ones and their annelated analogs as multifaceted building blocks for the fabrication of diverse heterocycles;Tetrahedron;2017-05
5. ChemInform Abstract: A Convenient Regioselective Synthesis of (2E)-2-[2,3,6-Triarylpyrimidin-4(3H)-ylidene]acetonitriles Through Ring Transformation Reactions.;ChemInform;2013-04-11
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