480439-44-9Relevant articles and documents
ALLOSTERIC CHROMENONE INHIBITORS OF PHOSPHOINOSITIDE 3-KINASE (PI3K) FOR THE TREATMENT OF DISEASES ASSOCIATED WITH P13K MODULATION
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Paragraph 1139; 1162, (2021/10/11)
The disclosure relates to compounds of Formula (I) as allosteric chromenone inhibitors of phosphoinositide 3-kinase (PI3K) useful in the treatment of diseases or disorders associated with PI3K modulation, Formula (I), or a prodrug, solvate, enantiomer, st
Regioselectivity in palladium-catalyzed C-H activation/oxygenation reactions
Kalyani, Dipannita,Sanford, Melanie S.
, p. 4149 - 4152 (2007/10/03)
(Chemical Equation Presented) Palladium-catalyzed directed C-H activation/oxygenation reactions have been explored in a series of meta-substituted aryl pyridine and aryl amide derivatives. These transformations tolerate a diverse array of electron-donatin
Successful development and scale-up of a palladium-catalysed amination process in the manufacture of ZM549865
Robinson, Graham E.,Cunningham, Oliver R.,Dekhane, Mouloud,McManus, Julie C.,O'Kearney-McMullan, Anne,Mirajkar, Abdurrazzaque M.,Mishra, Vikas,Norton, Alison K.,Venugopalan,Williams, Emyr G.
, p. 925 - 930 (2013/09/03)
Key steps in the synthesis of ZM549865 (a 5-HT receptor antagonist) are the palladium-catalysed amination of ethyl 8-bromo-6-fluoro-4-oxo-4H-2- chromenecarboxylate and subsequent hydrolysis of the ester group. The development of a simple, robust process c