Acid-Catalyzed Condensation of 1,3,5-Triphenylpentane-1,5-dione with Benzaldehyde—A New Domino Reaction-Reference-Cited by-同舟云学术

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Acid-Catalyzed Condensation of 1,3,5-Triphenylpentane-1,5-dione with Benzaldehyde—A New Domino Reaction

Published:2004-04 Issue:4 Volume:40 Page:479-481
ISSN:1070-4280
Container-title:Russian Journal of Organic Chemistry
language:en
Short-container-title:Russian Journal of Organic Chemistry

Author:

Bagrina N. P.,Vysotskii V. I.,Sergeeva S. A.,Denisenko V. A.,Gerasimenko A. V.

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry

Cited by 5 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. Regioselective Synthesis of Unsymmetrical 3-(Quinolin-3-yl)Pentane-1,5-Diones in the Aqueous Medium through Montmorillonite KSF Catalysis;Polycyclic Aromatic Compounds;2020-05-03

2. In situ formed acetals facilitated direct Michael addition of unactivated ketones;New Journal of Chemistry;2017

3. TiO2 nano crystallites catalyzed water mediated microwave assisted regioselective three component domino hydrolysis/aldol condensation/Michael addition reaction of 3-(1,5-dioxo-1,5-diphenylpentan-3-yl)quinolin-2(1H)-one;RSC Adv.;2014

4. Facile Microwave-Assisted Michael Addition of Diphenacyl Sulfides to Chalcones Under Solvent-Free Conditions: Generation of Symmetrical and Unsymmetrical 1,5-Diketones;Synthetic Communications;2012-09-05

5. Acid-Catalyzed Condensation of 1,3,5-Triphenylpentane-1,5-dione with Benzaldehyde — A New Domino Reaction.;ChemInform;2004-11-09

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