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CCCXI.—A synthesis of acacetin and certain other derivatives of flavone

Robert Robinson, +1 more
- 01 Jan 1926 - 
- Vol. 129, pp 2344-2348
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This article is published in Journal of The Chemical Society (resumed).The article was published on 1926-01-01. It has received 22 citations till now. The article focuses on the topics: Acacetin.

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Pd-catalyzed copper-free carbonylative Sonogashira reaction of aryl iodides with alkynes for the synthesis of alkynyl ketones and flavones by using water as a solvent.

TL;DR: The Pd-catalyzed copper-free carbonylative Sonogashira coupling reaction to synthesize alkynyl ketones from terminal alkynes and aryl iodides was achieved by using water as a solvent and was successfully applied to the synthesis of flavones.
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Regiospecific Carbonylative Annulation of Iodophenol Acetates and Acetylenes To Construct the Flavones by a New Catalyst of Palladium−Thiourea−dppp Complex

TL;DR: Regiospecific carbonylative annulation of o-iodophenol acetates and acetylenes mediated by palladium-thiourea-dppp complex in the presence of base at 40 degrees C under a balloon pressure of CO generates diversified flavones in high yields.
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Transition‐Metal‐Free Intramolecular Ullmann‐Type O‐Arylation: Synthesis of Chromone Derivatives

TL;DR: The unexpected transition-metal-free intramolecular Ullmann-type O-arylation leading to chromone derivatives is reported, which shows that transition- metal catalysts seem to be necessary in O-arylations.
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Synthesis of Novel 3,7-Substituted-2-(3‘,4‘-dihydroxyphenyl)flavones with Improved Antioxidant Activity

TL;DR: A series of 3,7-disubstituted-2-(3',4'-dihydroxyphenyl)flavones was synthesized as potential cardioprotective agents in doxorubicin antitumor therapy and the 3-substituting flavones were the most potent compounds in the LPO assay.
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