Cramer’s rule over residue class rings of Bézout domains

Cramer’s rule over residue class rings of Bézout domains is given.     

Symplectic Self-adjointness of Infinite Dimensional Hamiltonian Operators

Symplectic self-adjointness of infinite dimensional Hamiltonian operators is studied, the necessary and sufficient conditions are given. Using the relatively bounded perturbation, the sufficient conditions about symplectic self-adjointness are shown.     

Cross‐coupling reactions using porous multipod Cu2O microcrystals as recoverable catalyst in aqueous media

Porous multipod Cu₂O microcrystals were found to be an efficient, highly recyclable and eco‐friendly catalyst for the cross‐coupling reactions of aryl halides and terminal alkynes with high yields in aqueous media. Noteworthy, the Cu₂O catalyst can be reused for several times without significant decrease in catalytic activity.     

Graphyne-oxide supported Pd catalyst with ten times higher nitrobenzenes reduction activity than Pd/C

Research on Chemical Intermediates - Upon oxidation, a graphyne-like porous carbon-rich network (GYLPC), which is a two-dimensional carbon material consisting of sp- and sp2-hybridized carbon atoms...     

Highly efficient antimicrobial electrospun PVP/CS/PHMGH nanofibers membrane: preparation,antimicrobial activity and in vitro evaluations

Research on Chemical Intermediates - A highly efficient oligomer antimicrobial agent, polyhexamethylene guanidine hydrochloride (PHMGH), is added to mixtures of polyvinylpyrrolidone (PVP)/chitosan...     

Reaction mechanism of NH3-SCR denitrification over rare-earth concentrate

Research on Chemical Intermediates - A rare-earth concentrate obtained from Bayan Obo tailings was used as catalyst for low-temperature selective catalytic reduction (SCR) of NOx. X-ray powder...     

An efficient stereoselective synthesis of aminocyclohexenes from 7-azanorbornenes via LiAlH4 mediated tandem double bond migration-ring opening sequence

hNav1.7 had received great interest in the past decade owing to its attractive mechanism of actions in pain processing pathway. More recently, we developed a series of efficacious hNav1.7 inhibitors for analgesic, which were characterized with a novel aminocyclohexene as pharmacophore. Herein, we reported our synthetic efforts to construct the unique scaffold, which can be rapidly accessed from readily available 7-azanorbornenes via an unexpected catalyst-free, LiAlH₄ mediated tandem double bond migration-ring opening sequence. A probable mechanism was proposed to illuminate the good regio- and stereoselectivity.