摘要：Nine C2-symmetric chiral disulfonamldes were designed and synthesized from L-valine, L-phenylalanine and L-leucine respectively via one-pot ring opening of aziridines. The application of these disulfonamides as catalyst in the addition of diethyl zinc to benzaldehyde in three reagent systems: Ligand-Ti(OiPr)4-Et2Zn; Ligand-Ti(OiPr)4-H2O-Et2Zn; Ligand-Et2Zn was also described.

摘要：The development of two highly reactive electrophilic trifluoromethylating reagents(trifluoromethyl)(4-nitrophenyl)bis(carbometh-oxy)methylide(1g)and(trifluoromethyl)(3-chlorophenyl)bis(carbomethoxy)methylide(1j)through structure-activity study was *** mild conditions,reagent 1g reacted with β-ketoesters and silyl enol ethers to give α-trifluoromethylated-β-ketoesters or α-trifluoromethylated ketones in high *** addition,reagent 1g could serve as a trifluoromethyl radical for a variety of trifluo-romethylative transformations under visible light irradiation,including radical trifluoromethylation of electron-rich indoles and pyrroles and sodium aryl sulfinates as well as trifluoromethylative difunctionalization with styrene *** the other hand,as a complimentary,under reductive coupling conditions,reagent 1j reacted with a variety of(hetero)aryl iodides for the formation of tri-fluoromethylated(hetero)arenes.

摘要：A novel gem-difluoromethylenated castanospermine analogue B was designed and synthesized, starting from 3-bromo-3,3-difluoropropene and L-（-）-malic acid. The key steps involve substitution cyclization reaction and RCM reaction to construct the aza fused bicyclic framework.

摘要：Chiral phosphorus ligands have played a crucial role for the recent advances in asymmetric *** review summarizes chiral phosphorus ligands developed from the Laboratory of Professor Xumu Zhang in the latest 25 years.A number of iconic phosphorus ligands including bisphosphorus ligands with rigid chiral backbone such as BICP,PennPhos,TunePhos,and f-Binaphane,P-chiral bisphosphorus ligands TangPhos,Binapine,and DuanPhos,phosphine-phosphoramidte ligand YanPhos,noncovalent interaction-assisted ferrocenyl phosphorus ligand ZhaoPhos and WudaPhos,and tridentate ferrocenyl phosphorus ligands f-amphox are introduced,and their applications in asymmetric hydrogenation are emphasized.

摘要：We present the design and synthesis of polyoxazole-based macrocycles containing a phosphonate group.A reliable route was established that allows for convenient and versatile incorporation of various phosphonate functionalities such as phosphonate ester,acid,and salt at the macrocyclic ring *** unprecedented macrocyclic compounds are anticipated to be appealing candidates as telomerase inhibitors.

摘要：Main observation and conclusion Amicetin and congeners constitute a small family of complex pyrimidine nucleosides,which exhibit strong antibiotic activities against Gram-positive bacteria and notably against strains of Mycobacterium ***,we report chemical synthesis of a series of disaccharide congeners of the amicetin family,including amicetin,plicacetin,and cytosaminomycin A—*** is the first time for successful synthesis of amicetin,the prototypical member,and *** synthetic approach employs glycosyl N-phenyltrifluoroacetimidate and thioglycoside donors to construct the characteristic aminodeoxydisaccharides consisting ofα-(1→4)-glycosidic linkage,uses gold(I)-catalyzed N-glycosylation to furnish 2-deoxy-β-nucleosides,and finally exploits amidation and global deprotection to complete the *** is noteworthy that the 3-O-protecting group in the 2-deoxydisaccharide donors is found to be crucial for a successful N-glycosylation to assemble the cytosaminomycin disaccharide nucleosides.

摘要：A novel strategy for site-selective benzylic C–H oxidation has been developed through mediated electrolysis.A bulky maleimide N-oxyl radical(MINO)generated by proton-coupled electrochemical oxidation of N-hydroxymaleimide(NHMI),serves as a hydrogen atom-transfer ***-to-excellent site selectivity was observed among different substrates,providing a practical approach for site-selective benzylic C–H ***,the hydrogen-atom transfer mechanism for C–H electrochemical oxidation allows the oxidation to proceed at much lower anode potentials relative to direct electrolysis and with minimal reliance on the substrate's electronic properties.

摘要：Perfluorooctanoic acid(PFOA) or perfluorooctane sulphonate(PFOS) was one of the most prominent fluorosurfactants and applied widely in firefighting and daily chemical, etc. However, these surfactants have recently been identified as toxic and undegradability in the environment. Developing an efficient approach to environment-friendly fluorosurfactants is essential. A fluorocarbon branched chain strategy was adopted to develop/PFOS substitutes. A series of intermediates of novel branched fluorinated surfactants with CF_3 CF_2CF_2C(CF3)_2 group were synthesized from perfluoro-2-methyl-2-pentene. All the steps were mild, easy-handled and cheap. It is expected to be a very significant direction for the development of non-bioaccumulable alternatives of PFOA or PFOS.

摘要：A series of novel 4,5-disubstituted-3-S-（β-D-acetylglycosyl）-l,2,4-triazole derivatives was designed and synthesized via the strategy of introducing S-β-D-acetylglycosyl fragments into 1,2,4-triazole ring. The structures of 17 target compounds were characterized by means of lH NMR, 13C NMR and high-resolution mass spectrometer （HRMS）. The results of insecticidal activity indicated that compound 5a displayed 60% lethality rate at 100 mg/L concentration. More importantly, the introduction of the carbohydrate fragment to the 1,2,4-triazole core could im- prove the insecticidal activities since the insecticidal activities of compounds 5 were better than those of compounds 4 and this result was also supported by calcium imaging technique. The antifungal activity of the target compounds showed that some novel compounds displayed moderate to good inhibition rate against Sclerotinia sclerotiorum and Botrytis cinerea, in which compound 5p exhibited 78.8% inhibition rate against Sclerotinia sclerotiorum and 68.6% inhibition rate against Botrytis cinerea. The herbicidal activities of compounds 5 against Brassica campestris indi- cated that most of the target compounds showed moderate to good activities, especially compound 5g which showed 52.9% herbicidal activity at the concentration of 200 mg/L.

摘要：A new compound based on immobilizing of Pd6(RuL3)8(BF4)28 (L=2-(pyridin-3-yl)-1H-imidazo [4,5-f][1,10]-phenanthroline) cage (MOC-16) on g-C3N4 was synthesized. Infrared spectrum and powder X-ray diffraction were used to characterize structure of hybrid MOC-16/g-C3N4, as well as UV-vis absorption spectrum and X-ray photoelectron spectroscopy were carried out to unveil photocatalytic mechanism. With the introduction of MOC-16, the absorption edge of MOC-16/g-C3N4 in UV-vis spectrum extended apparently to long-wavelength region compared with pristine g-C3N4. H2 evolution yielded with MOC-16/g-C3N4 in aqueous solution containing TEOA was much higher than that with RuL3/g-C3N4, Pd/RuL3/g-C3N4 and mixture of MOC-16 and g-C3N4, showing that the octahedral cage structure with high-efficient electron transfer and the interface interaction between MOC-16 and g-C3N4 were significant for improvement of H2 evolution.