简介：Treatmentof4-amino-3-(1-aryl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-1,2,4-triazoles/2-amino-5-(1-aryl-5-methyl-1,2,3-triazole-4-yl)-1,3,4-thiadiazoleswithbenzaldehyde,acetoneandω-bromoacetophenonewastestedandcompared.ThetitlecompoundsSchiffbases,amides,imidazolo[2,1-b]-1,3,4-thiadiazolesand7H-s-triazolo[3,4-b]-1,3,4-thiadiazineshavebeenconfirmedbyelementalanalyses,^1HNMR,IRandMSspectra.AllthecompoundshavealsobeenscreenedfortheirantibacterialactivitiesagainstB.subtilis,S.aureusandE.coli.
简介：Fourteennew1-acyl-5-arylbiuretsweresynthesizedbythereactionofarylureaswithacylisocynantes.Thelatterwasobtainedfromacylchlorideandleadcyanateindichloromethane,usingpyridineascatalyst.Thestructuresofcompounds3a-nwereconfirmedbyIR,1HNMRandMSspectra.
简介：Thereactionof1-phenyl-3-methyl-4-benzoyl-2,5-dihydro-1H-pyrazol-5-one(PMBP)andmethyldithiocarbazate(mdtc)inmethanolresultsinformationofayellowcrystallinesolid,adductof1-phenyl-3-methyl-4benzoyl-2,5-dihydro-lH-pyrazol-5-oneandmethyldithiocarbazate.Whentheyellowsolidsweredissolvedinamixtureofmethanolandether(1:4),aredcrystal,whichisanoxidationproductoftheformer,wasobtainedbyallowingsolventtoevaporateforafewdaysatroomtemperature.TheX-rayanalysisoftheredcrystalindicatesthatitisanoveldisulfidewithaspecialstructurelikea“U”conformationinthesolidstate.
简介：ＳＴＵＤＹＯＮＴＨＥＲＥＡＲＲＡＮＧＥＭＥＮＴＲＥＡＣＴＩＯＮＯＦ５－ＡＭＩＮＯ－１－ＡＭＩＮＯＣＡＲＢＯＮＹＬ－１，２，ＡＮＤＩＴＳＡＮＡＬＯＧＵＥＳ￥ＲｏｎｇＪｉａｎＬＵ；ＨｕａＺｈｅｎｇＹＡＮＧ；ＢａｏＹｉｎｇＱＩＡＮ；ＨａｉＹａｎＤＥＮＧ（Ｎ...
简介：AseriesofnovelN-（3-furan-2-yl-1-phenyl-1H-pyrazol-5-yl）amidesderivativesweredesignedandsynthesized.Theirstructureswereconfirmedby1HNMR,13CNMRandHRMS.Alltitlecompoundswereevaluatedfortheirherbicidalandantifungalactivities.Preliminarybioassayresultsindicatedthatthetitlecompoundsshowedgoodtomoderateherbicidalactivityat1000mg/L.Compound6qpresentedthebestactivityagainstDigitariasanguinalis（L）Scop.,AmaranthusretroflexusL.andArabidopsisthalianawithaninhibitiondegreeoffive.Compound6dalsoshowedaninhibitiondegreeoffiveagainstD.sanguinalis.Inaddition,at50mg/L,mostcompoundsexhibitedgoodinvitroantifungalactivityagainstSclerotiniasclerotiorum,withcompound6cshowingover90%antifungalactivityagainstS.sclerotiorumandPelliculariasasakii.
简介：ＩｎｔｒｏｄｕｃｔｉｏｎＩｎｒｅｃｅｎｔｙｅａｒｓ，Ｌａｎｇｍｕｉｒ－Ｂｌｏｄｇｅｔ（ＬＢ）ｆｉｌｍｓｈａｖｅａｔｒａｃｔｅｄｍｕｃｈａｔｅｎｔｉｏｎｂｅｃａｕｓｅｏｆｔｈｅｉｒｐｏｓｉｂｉｌｉｔｉｅｓａｓｆｕｎｃｔｉｏｎａｌｍｏｌｅｃｕｌａｒｄｅｖ...
简介：Thesynthesisofanewtypeofhetero-macrocyclicpolyether2,3-henzo-1,4,7,13-tetraoxa-10-selenacyclopentadeca-2-eneisdeseribed.
简介：Novelsulfur-containingcompounds(3a–3c,4a–4c)wereobtainedinethanolwith1,3-diphenyl-2-propanoneasthestartingmaterial.Theadvantagesofthisprocedureweremildreactionconditions,simpleprotocol,andhighyields.ThestructuresoftheproductswerecharacterizedbyIR,1HNMR,MSandelementaryanalysis.Thecrystalofthenewcompound4abelongstomonoclinic,spacegroupC2witha=18.727(3),b=6.5179(9),c=13.7576(18),b=131.0610(10)°,V=1266.2(3)A3,Z=2,Dc=2.136g/cm3,μ=1.078mm-1,F(000)=843,R=0.0490andwR=0.1247for3211observedreflectionwithI>2δ(I).X-rayanalysisrevealsthatthemoleculeisnotsymmetrical,themolecularstructureisstabilizedbyweakp–pstackinginteractions,andnoclassicalhydrogenbondscanbeobserved.
简介：Anovelseriesofpyrido[1,2-e]purin-4(3H)-onederivativescontainingpolarsubstituentson5'-positionweredesignedandpreparedaspotentialPDE5inhibitors.Thispaperreportsthesyntheticroutes,1H-NMRdata,andthePDE5inhibitoryactivitiesofthetargetcompounds.Thepolarpiperazinylgroupcontained(on5'-position)compound,3B2,showedthehighestactivityamongthetestedderivativesbutlesspotencythansildenafil1.
简介：Thetitlecomplex,[La(baec)1/2(H2btec)1/2(H2O)]n(H4btec=1,2,4,5-benzenetetracarboxylicacid)(1)wassynthesizedbythehydrothermalreactionof1,2,4,5-benzenetetracarboxylicdianhydridewithLa(NO3)3·6H2OinH2O,andcrystallizesinthetriclinicsystem,spacegroupP-1withα=0.64403(3)nm,b=0.94500(4)nm,c=0.96380(5)nm,α=88.535(2)°,β=100.314(2)°,γ=76.6470(10)°,V=1.69968(10)nm^3,Z=2,andfinalR=0.0274,Rw=0.0735.In1,eachLa(Ⅲ）ioniscoordinatedbyeightoxygenatomsfromsixcarboxylategroupsandonecoordinatedwatermolecule.TwodifferentcoordinstionmodesofH4btecwerePresentinthestructure,oneofwhichcontainstwoprotonatedcarboxylategrougpstobalancethecharge.
客服QQ：30444492琼网文【2021】1550-113号
增值电信业务经营许可证：琼B2-20210322
出版物经营许可证：新出发龙华出字第(2021)009号
广播电视节目制作经营许可证：(琼)字第00779号
版权所有 ©2002-2024 期刊网(www.qikanchina.com) 琼ICP备2021005105号
![Synthesis and Evaluation of PDE<b style='color:red'>5</b> Inhibitory Activity of Novel Pyrido[2＇,<b style='color:red'>1</b>＇：<b style='color:red'>5</b>,<b style='color:red'>1</b>]pyrazolo[4,3-d]pyrimidin-4-one Derivatives](/image/thesis2 "Synthesis and Evaluation of PDE<b style='color:red'>5</b> Inhibitory Activity of Novel Pyrido[2＇,<b style='color:red'>1</b>＇：<b style='color:red'>5</b>,<b style='color:red'>1</b>]pyrazolo[4,3-d]pyrimidin-4-one Derivatives")
![Crystal Structure of Bis{<b style='color:red'>1</b>-methylthio-<b style='color:red'>1</b>-[<b style='color:red'>1</b>-phenyl-<b style='color:red'>1</b>-（<b style='color:red'>1</b>-phenyl3-methyl-<b style='color:red'>5</b>-oxo-4,5-dihydropyrazol-4-ylene）-methylamino]iminomethyl} Disulfide with the “U” Conformation](/image/thesis3 "Crystal Structure of Bis{<b style='color:red'>1</b>-methylthio-<b style='color:red'>1</b>-[<b style='color:red'>1</b>-phenyl-<b style='color:red'>1</b>-（<b style='color:red'>1</b>-phenyl3-methyl-<b style='color:red'>5</b>-oxo-4,5-dihydropyrazol-4-ylene）-methylamino]iminomethyl} Disulfide with the “U” Conformation")
![<b style='color:red'>1</b>-[2-（2-Methoxyphenylthio） benzyl]-4-arylpiperazines derivatives： Synthesis and evaluation for dual <b style='color:red'>5</b>-HT<b style='color:red'>1</b>A/SSRI activities](/image/thesis8 "<b style='color:red'>1</b>-[2-（2-Methoxyphenylthio） benzyl]-4-arylpiperazines derivatives： Synthesis and evaluation for dual <b style='color:red'>5</b>-HT<b style='color:red'>1</b>A/SSRI activities")
![Design and Synthesis of Pyrido[<b style='color:red'>1</b>,2-e]purin-4（3H）-one Derivatives as Potential PDE <b style='color:red'>5</b> Inhibitors](/image/thesis16 "Design and Synthesis of Pyrido[<b style='color:red'>1</b>,2-e]purin-4（3H）-one Derivatives as Potential PDE <b style='color:red'>5</b> Inhibitors")
![Hydrothermal Synthesis and Structure of a New 3D Lanthanide—Carboxylate Framework,[La（btec）<b style='color:red'>1</b>／2（H2btec）<b style='color:red'>1</b>／2（H2O）]n（H4btec=<b style='color:red'>1</b>,2,4,<b style='color:red'>5</b>—Benzeneteracarboxylic acid）](/image/thesis17 "Hydrothermal Synthesis and Structure of a New 3D Lanthanide—Carboxylate Framework,[La（btec）<b style='color:red'>1</b>／2（H2btec）<b style='color:red'>1</b>／2（H2O）]n（H4btec=<b style='color:red'>1</b>,2,4,<b style='color:red'>5</b>—Benzeneteracarboxylic acid）")
