Pyrimidine compounds (Formula I), or their pharmaceutically acceptable salts, hydrates, solvates, crystal forms and individual diastereomers, and pharmaceutical compositions including the same, which are inhibitors of tyrosine kinase enzymes, and as such are useful in the prophylaxis and treatment of protein tyrosine kinase-associated disorders, such as immune diseases, hyperproliferative disorders and other diseases in which inappropriate protein kinase action is believed to play a role, such as cancer, angiogensis, atheroscelerosis, graft rejection, rheumatoid arthritis and psoriasis.
Compounds of Formula (I): or pharmaceutically acceptable salts, solvates, or esters thereof, are useful in treating diseases or conditions mediated by CB1 receptors, such as metabolic syndrome and obesity, neuroinflammatory disorders, cognitive disorders and psychosis, addiction (e.g., smoking cessation), gastrointestinal disorders, and cardiovascular conditions.
[EN] SUBSTITUTED PIPERAZINES AS CB1 ANTAGONISTS<br/>[FR] PIPÉRAZINES À SUBSTITUTION SERVANT D'ANTAGONISTES DES RÉCEPTEURS CB1
申请人:SCHERING CORP
公开号:WO2009005671A2
公开(公告)日:2009-01-08
Compounds of Formula (I): or pharmaceutically acceptable salts, solvates, or esters thereof, are useful in treating diseases or conditions mediated by CB1 receptors, such as metabolic syndrome and obesity, neuroinflammatory disorders, cognitive disorders and psychosis, addiction (e.g., smoking cessation), gastrointestinal disorders, and cardiovascular conditions.
Full chirality transfer in the synthesis of hindered tertiary boronic esters under in situ lithiation–borylation conditions
作者:D. J. Blair、S. Zhong、M. J. Hesse、N. Zabaleta、E. L. Myers、V. K. Aggarwal
DOI:10.1039/c6cc00536e
日期:——
Using non-cryogenic lithiation-borylation, sterically hindered tertiary neopentyl glycol boronicesters can be prepared from secondary benzylic carbamates with full chirality transfer.