With the volume and accessibility of scientific research increasing across the world, it has never been more important to continue building the reputation for quality and ethical publishing we’ve spent the past two centuries establishing. 523-27-3, Name is 9,10-Dibromoanthracene, SMILES is BrC1=C2C=CC=CC2=C(Br)C3=CC=CC=C13, in an article , author is Wedek, Volker, once mentioned of 523-27-3, Application In Synthesis of 9,10-Dibromoanthracene.
The use of a new class of unsymmetrical cinchona-alkaloid-based, phthalazine-bridged organocatalysts enabled the highly enantioselective dichlorination of unfunctionalized alkenes. In combination with the electrophilic chlorinating agent 1,3-dichloro-5,5-dimethylhydantoin (DCDMH) and triethylsilyl chloride (TES-Cl) as the source of nucleophilic chloride, 1-aryl-2-alkyl alkenes were dichlorinated with enantioselectivities of up to 94:6 er. Initial mechanistic investigations suggest that no free chlorine is formed, and by replacement of the chloride by fluoride, enantioselective chlorofluorinations of alkenes are possible.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 523-27-3, you can contact me at any time and look forward to more communication. Application In Synthesis of 9,10-Dibromoanthracene.
Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem