About: DBDMH is a research topic. Over the lifetime, 66 publications have been published within this topic receiving 562 citations. The topic is also known as: 1,3-Dibromo-5,5-dimethylhydantoin.
TL;DR: In this article, a useful method for oxidation of various thiols to their corresponding disulfides with 1,3-dibromo-5,5-dimethylhydantoin (DBDMH) in very short reaction times and mild conditions under both solution and solvent-free conditions is described.
Abstract: A useful method for oxidation of various thiols to their corresponding disulfides with 1,3-dibromo-5,5-dimethylhydantoin (DBDMH) in very short reaction times and mild conditions under both solution and solvent-free conditions is described.
TL;DR: In this paper, the authors report the facile fabrication of N-Br bond-containing N-halamine nanofibers using the electrospinning method for antibacterial usages.
Abstract: N-Halamine compounds have attracted great attention because they are recognized as promising antibacterial agents to control microbial contamination; however, most of the research interests were focused on N-halamines that contain N–Cl bond(s) rather than N–Br bond(s). In this contribution, we report the facile fabrication of N–Br bond-containing N-halamine nanofibers using the electrospinning method for antibacterial usages. The as-produced N–Br bond-containing N-halamine nanofibers (i.e., DBDMH/PAN nanofibers) comprise an antibacterial component of 1,3-dibromo-5,5-dimethylhydantoin (DBDMH) and a support component of polyacrylonitrile (PAN). When systematic characterizations were carried out, the as-obtained DBDMH/PAN nanofibers were proven to exhibit well-defined fiber-like morphology and be highly efficient in the killing of the selected model bacteria (Escherichia coli). Their morphology and size could be well governed by tuning the concentration of electrospinning precursor and the mass ratio of PAN ...
TL;DR: Intramolecular alkene electrophilic bromination initiated dearomative cyclization has been realized in the presence of DBDMH to provide functionalized azaspirocyclohexadienones in excellent yields under mild conditions.
TL;DR: A new industrial process, involving only two isolation and drying steps, for 10-methoxyiminostilbene (MISB), an advance intermediate of widely prescribed antiepileptic drug, oxcarbazepine, has been developed as discussed by the authors.