124854-96-2Relevant academic research and scientific papers
Antioxidant-Based Inhibitors of Leukotriene Biosynthesis. The Discovery of 6--1-propen-3-yl>-2,3-dihydro-5-benzofuranol, a Potent Topical Antiinflammatory Agent
Hammond, Milton L.,Zambias, Robert A.,Chang, Michael N.,Jensen, Norman P.,McDonald, John,et al.
, p. 909 - 918 (2007/10/02)
The leukotrienes, metabolites of arachidonic acid produced through the action of the enzyme 5-lipoxygenase, are important mediators of immediate hypersensitivity and inflammation.Among the variety of diseases in which the leukotrienes may play a symptomat
Synthesis of 6-(3-Aryl-2-propenyl)-2,3-dihydro-5-hydroxybenzofuran Derivatives by Cross Coupling Reactions
Alabaster, Ramon J.,Cottrell, Ian F.,Hands, David,Humphrey, Guy R.,Kennedy, Derek J.,et al.
, p. 598 - 603 (2007/10/02)
The synthesis of 6-(3-aryl-2-propenyl)-2,3-dihydro-5-hydroxybenzofuran derivatives by cross coupling between 6-bromo-2,3-dihydrobenzofurans and cinnamyl halides via organo-metallic compounds has been explored.Palladium catalysed reaction between benzofury
Substituted cinnamyl-2,3-dihydrobenzofuran and analogs useful as anti-inflammatory agents
-
, (2008/06/13)
Substituted cinnamyl-2,3-dihydrobenzofurans and analogs were prepared from the nucleophlic substitution of a cinnamylhalide with a 2,3-dihydrobenzofuran anion or an analog thereof. These compounds were found to be potent topical anti-inflammatory agents.
Substituted cinnamyl-2,3-dihydrobenzofuran and analogs useful as anti-inflammatory agents
-
, (2008/06/13)
Substituted cinnamyl-2,3-dihydrobenzofurans and analogs were prepared from the nucleophilic substitution of a cinnamylhalide with a 2,3-dihydrobenzofuran anion or an analog thereof. These compounds were found to be potent topical anti-inflammatory agents.
