摘要:
Compounds of formula (I) wherein the other substituents HetAr, R1, R2, R3, R4, R5, R6, R7 and R8 are as defined in claim 1, and their use in compositions and methods for the control and/or prevention of microbial infection, particularly fungal infection, in plants and to processes for the preparation of these compounds.
摘要:
The present invention provides an organic compound represented by following Formula:
wherein each of R 1 to R 14 is independently selected from hydrogen, substituted or non-substituted C 6 to C 12 aryl, substituted or non-substituted C 3 to C 11 heteroaryl, substituted or non-substituted C 1 to C 10 alkyl, substituted or non-substituted C 1 to C 10 alkoxy, ether, cyano group (CN), fluorine, tri-fluoro methyl, tri-fluoro methoxy and trimethylsilyl, and at least one of R 1 to R 10 is the cyano group, and wherein at least one of R 11 to R 14 is the cyano group, and A is selected from substituted or non-substituted C 6 to C 30 aryl and substituted or non-substituted C 3 to C 30 heteroaryl. The present invention also provides an organic light emitting diode (D) and an organic light emitting display device (100) including the organic compound.
摘要:
The present invention relates to the technical field of medicine, and specifically relates to the carboxylic acid compound represented by the chemical formula I or chemical formula II, and a pharmaceutically acceptable salt, a prodrug, and a solvate thereof, and a method for preparation thereof, as well as a pharmaceutical composition containing the described substances, and a use thereof.
摘要:
Described herein are compounds that are deubiquitinase inhibitors, methods of making pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders that would benefit from inhibition of deubiquitinase activity.
摘要:
The present invention relates to a process for preparing compound 1 that is useful as an antifungal agent. In particular, the invention seeks to provide new methodology for preparing compound 1 and substituted derivatives thereof.
摘要:
A process for fluorination of aromatic compounds employing iodonium ylides and applicable to radiofluorination using 18F is described. Processes, intermediates, reagents and radiolabelled compounds are described.