hydrolysis at pH 8 to nearly inert at pH 1, and that the Taft parameter of the orthoester substituent allows an adequate prediction of the reaction kinetics. Moreover, the synthesis of an alkyne-capped cryptand enabled the post-functionalization of orthoester cryptands by Sonogashira and CuAAC “click” reactions. The methylation of the resulting triazole furnished a cryptate that was kinetically inert towards
[EN] CONDENSED PYRIDINE DERIVATIVES USEFUL AS A28 ADENOSINE RECEPTOR ANTAGONISTS<br/>[FR] DERIVES DE PYRIDINE CONDENSES UTILES COMME ANTAGONISTES DU RECEPTEUR DE L'ADENOSINE A28
申请人:ALMIRALL PRODESFARMA SA
公开号:WO2005100353A1
公开(公告)日:2005-10-27
The present invention relates to new antagonists of the A2B adenosine receptor represented by formula (I). Those compounds are useful for treating a subject afflicted with a pathological condition or disease susceptible to amelioration by antagonism of the A2B adenosine receptor such as asthma, bronchoconstriction, allergic diseases, hypertension, atherosclerosis, reperfusion injury, myocardial ischemia, retinopathy, inflammation, gastrointestinal tract disorders, cell proliferation disorders, diabetes mellitus, and/or autoimmune diseases.
METAL COMPLEXES COMPRISING DIAZABENZIMIDAZOLOCARBENE LIGANDS AND THE USE THEREOF IN OLEDS
申请人:Molt Oliver
公开号:US20130032766A1
公开(公告)日:2013-02-07
The present invention relates to metal-carbene complexes comprising a central atom selected from iridium and platinum, and diazabenzimidazolocarbene ligands, to organic light diodes which comprise such complexes, to light-emitting layers comprising at least one such metal-carbene complex, to a device selected from the group comprising illuminating elements, stationary visual display units and mobile visual display units comprising such an OLED and to the use of such a metal-carbene complex in OLEDs, for example as emitter, matrix material, charge transport material and/or charge or exciton blocker.
An efficient [3+2] cycloaddition for the synthesis of substituted pyrazolo[1,5-c]quinazolines
作者:Tao Wang、Ailong Shao、Haiyan Feng、Shuwu Yang、Meng Gao、Jun Tian、Aiwen Lei
DOI:10.1016/j.tet.2015.03.019
日期:2015.7
and efficient [3+2] cycloaddition reaction between N-iminoquinazolinium ylide and nitroolefins was developed. From a synthetic point of view, this protocol represents an efficient way to pyrazolo[1,5-c]quinazolines derivatives.
开发了N-亚氨基喹唑啉鎓叶立德和硝基烯烃之间简单有效的[3 + 2]环加成反应。从综合的观点来看,该方案代表了吡唑并[1,5- c ]喹唑啉衍生物的有效方法。