54669-73-7Relevant academic research and scientific papers
Sunlight-driven synthesis of γ-diketones via oxidative coupling of enamines with silyl enol ethers catalyzed by [Ru(bpy)3]2+
Yasu, Yusuke,Koike, Takashi,Akita, Munetaka
supporting information; experimental part, p. 5355 - 5357 (2012/06/30)
A photosensitizer [Ru(bpy)3]2+ catalyzes oxidative coupling reaction of enamines with silyl enol ethers under visible light irradiation by a Xe lamp or sunlight to produce γ-diketones. A 2e-oxidation process involved in this reaction
The cascade carbo-carbonylation of unactivated alkenes catalyzed by an organocatalyst and a transition metal catalyst: A facile approach to γ-diketones and γ-carbonyl aldehydes from arylalkenes under air
Xie, Jin,Huang, Zhi-Zhen
supporting information; experimental part, p. 1947 - 1949 (2010/06/21)
A novel cascade carbo-carbonylation reaction of unactivated arylalkenes with ketones or aldehydes was catalyzed by an organocatalyst and a transition metal catalyst via a SOMO-enamine under air, affording a simple approach to γ-diketones and γ-carbonyl aldehydes. The Royal Society of Chemistry 2010.
Substituted N-aminoalkylpyrroles
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, (2008/06/13)
Substituted N-aminoalkylpyrroles of the formula: STR1 IN WHICH X, Z, R1, -R5 and n are as defined below, and their physiologically tolerable acid addition salts are disclosed to have antiarrhythmic, central nervous system depressant,
Method of treatment with and compositions containing condensed pyrroles bearing an N-phenyl substituent
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, (2008/06/13)
Novel N-phenylpyrroles are disclosed that are effective in the treatment of inflammation and pain in mammals and have the formula SPC1 Wherein R is hydrogen, alkyl of one to six carbon atoms, thienyl, phenyl or phenyl substituted by halogen, trifluorometh
