Mild oxidation of allylic and benzylic alcohols with 5-arylidene barbituric acid derivatives as a model of redox coenzymes.
Author:
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/34/9/34_9_3945/_pdf
Cited by 17 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Assessing the potential of para-donor and para-acceptor substituted 5-benzylidenebarbituric acid derivatives as push–pull electronic systems: Experimental and quantum chemical study;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2021-05
2. Acid catalyzed Knoevenagel condensation of thiobarbituric acid and aldehyde at room temperature;Synthetic Communications;2020-04-27
3. Gated Decoupling 13C NMR Application to Determine Conformation and Unambiguous Chemical Shift of Arylidene Barbiturates;Applied Magnetic Resonance;2015-03-26
4. Reaction of 6-aminouracils with aldehydes in water as both solvent and reactant under FeCl3·6H2O catalysis: towards 5-alkyl/arylidenebarbituric acids;RSC Adv.;2014
5. Hydrogen bond donor–acceptor–donor organocatalysis for conjugate addition of benzylidene barbiturates via complementary DAD–ADA hydrogen bonding;RSC Adv.;2014
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