简介：AnefficientroutetoprepareL-glucoseandL-galactoseisdescribed.TheL-sugarsareachievedbyusingthestrategyofswitchingthefunctionalgroupsatC1andC5ofD-glucoseandD-mannose.TheoxidationandreductionofthesilylenoletheratC1andthelead(IV)tetraacetatemediatedoxidativedecarboxylationatC5arethekeysteps.L-GlucoseandL-galactosearepreparedinaconvenientandinexpensiveway.

简介：NineteenL-N-2-hydroxyethylaminoacidsandL-N,N-bis(2-hydroxyethyl)aminoacidswerepreparedfromthereactionofchlorohydrinwithL-alanine,L-valine,L-leucine,L-isoleucine,L-phenylalanine,L-serine,L-thrcunine,L-glutamicacid,L-asparticacidandglycine.L-N,N,N’,N’-tetra(2-hydroxyethyl)cystinewaspreparedbythereactionofL-cystinewithchlorohydrin.

简介：Anewbiflavonoid,stelleranol,wasisolatedfromtherootsofStellerachamaejasmeL..ItsstructurewasdeterminedbytheanalysisofMSandNMRdata,especially2DNMRspectra.

简介：新奇sesquiterpenoid，pterisemipol，从PterissemipinnataL被孤立。它的骨骼，也就是pterisane，被认为从protoilludane被重排，它的结构根据分光镜的分析被阐明。

简介：ByusingOH-terminatedpolyaryletherdendrimerandN-Fmoc-glycineasrawmaterials,thedendriticpolyarylether2-aminoacetate(G3-NH2)wassynthesizedviatwostepreactions.G3-NH2asamacroinitiatorforthering-openingpolymerizationofγ-benzylL-glutamateN-carboxyanhydridewasinvestigated.Itisfoundthattheresultingcopolymerspossessedrelativelyhighmolecularweightandnarrowmolecularweightdistribution(1.12

简介：ConformationofL-lysineinaqueoussolutionwasinvestigatedbylanthanideshiftprobes（Dy,Ho,Er,TmandYb）.Reilley’smethodwasemployedtoseparatethecontactanddipolarcom-ponentsofthe13Cparamagneticshifts.ThisstudyrevealsthatCαshifthasthelargestcontactcon-tributionwhiletheothercarbonshiftsaredominatedbythedipolarcontribution.TheaverageoverallconformationofL-lysineinaqueoussolutionisextendedwiththemolecularbackboneintransform.Inthecomplex,lanthanideioncoordinatestothecarboxylgroupwithLn—Obondlength2.2/nandthewholeligandislocatedoutsidethezero-dipolarshiftconeofthelanthanideion.Theelectronicspindensitydistributionontheligandnucleishowsthatthespinpolarizationisthepredominantmech-anismofthecontactinteractionfornucleiincloseproximitytotheboundlanthanideion.

简介：ThesolidcomplexesofCr(AA)2Cl3·nH2OofCrCl3withL-α-aminoacids(AA=Val,Len,Thr,Met,Arg,Phe,TryandHis)havebeenpreparedin95?EtOHmedium,andcharacterizedstructurallybyelementalanalysis,chemicalanalysis,IRspectraandTG-DTG.Theconstant-volumecombustionenergiesofthecomplexeshavebeendetermimedbyRBC-Ⅱtyperotating-bombcalorimeter.Thestandardenthalpiesofformationofthecomplexeshavebeencalculatedaswell,hwichare(-2543.16±3.71)(Val),(-2561.32±4.06)(Leu),(-2284.02±2.95)(Thr),(-1418.77±4.60)(Met(,(-3218.91±4.67)(Arg),(-2643.90±5.02)(Phe),(-1707.18±3.23)(Try)and(-2838.05±3.45)(His)kJ/mol,respectively.

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简介：借助于G03W程序包,对系列氨基羧酸分子的羰基铼配合物进行了结构优化,并对其中的相关能量、键长、键角、布局数等进行了研究.计算结果表明：各配合物相对于羰基铼中间体均具有一定的稳定性;配体分子结构中含有杂环或者较多数目杂原子时,有形成相对更稳定配合物的趋势;配体分子结构中应含有适宜的间隔体,否则需经较大的结构扭转或局部原子的拥挤方可形成相应配合物.

简介：OpticallypureL-butyllactatewassynthesizedbynormaltransesterificationusingnafion-Hcatalystinmoderateyield.Variousreactionconditionswereinvestigated,includingthereactiontemperature,reactiontime,ratioofthestartingmaterialandamountofthenafioncatalyst.

简介：新alkylenedihydrofuranglycoside(1)从根被孤立桑属albaL.吠叫，与moracinM-3鈥?O-尾-一起d-glucopyranoside(2)，和moracinM-6，3鈥?di-O-尾-d-glucopyranoside(3)。化合物1作为2-methylene-3-methoxy-2被识别，5-dihydrofuran-4-O-尾-d-glucopyranoside根据包括1D和2DNMR的化学、分光镜的数据光谱分析。另外，1的抗氧化剂活动用1,1-diphenyl-2-picrylhydrazyl(DPPH)和2,2鈥?azinobis-3-ethylbenzothiazoline-6-sulphonic被评估酸(ABTS)试金。IC50价值分别地是2.49和0.45mg/mL。

简介：　　Enantioimericallypure1,l'-bi-2-naphthol(BINOL)1anditsderivativesareimportantchiralligandsandauxiliariesforanumberofasymmetrictransformations1suchasaldolcondensations,alkylations,Diels-Alderreactions,Michaeladditions,epoxidations,etc.Opticallypure1andtheirderivativeshavealsobeenusedextensivelyinchiralrecognition,chiralseparationandintheconstructionoffunctionalisedmaterials2.Furthermore,(R)-and(S)-BINOLarealsofundamentalstartingmaterialsforthesynthesisofalargevarietyofotherchiralbinaphthylssuchasMOP(2c),NOBIN(2d)andBINAP(2e).Asaresultthedevelopmentofefficientandeconomicmethodsforthepreparationofopticallypure1hasattractedmuchattentioninrecentyears3andnovelmethodsfortheresolutionof(±)-1continuetobedeveloped.……

简介：TwoseriesofterritremBanalogues(10a-10cand18)havebeendesignedandsynthesizedfromjujubogenin5awhichwaspreparedfromjujubogeninglycosides5bobtainedfromtheleavesofZizyphusjujuba.Thestructuresofthenewcompoundswereconfirmedby1H-,13C-NMRandMSdata.Compounds10cand18showedweakinhibitoryeffectonAChEat10^-4mol/E.

简介：由di-(2,4,4-trimethylpentyl)的L本氨基丙酸的抽取行为phosphinic酸，di-(2,4,4-trimethylpentyl)-monothiophosphinic酸和di-(2-ethylhexyl)磷的酸分别地在二阶段、三阶段的系统被学习。为这些抽取反应的平衡常数是计算的。

简介：基于乙醇/水溶液体系结晶纯化制备了Fmoc-L-亮氨酸.通过HRMS,IR和1HNMR对该化合物进行了化学结构分析.被测化合物相对分子质量与Fmoc-L-亮氨酸理论相对分子质量一致,含有芴环、酰胺键和苯环等Fmoc-L-亮氨酸特征基团,其结构与目标化合物的分子结构一致.

简介：GinsenosidesRg1,Re,Rb1,Rc,Rb2,Rb3,andRdindifferentpartsoftheAmericanginsengplantwereinvestigated.Theextractionprocesswasapressurizedmicrowave-assistedextraction(PMAE).Thesevenginsenosideswereseparatedanddeterminedbyhigh-performanceliquidchromatography(HPLC)withaultraviolet(UV)detector,at203nm.TheexperimentresultsshowedsignificantvariationsintheindividualginsenosidecontentsoftheAmericanginsengindifferentpartsandagesoftheplant.Theresultsdemonstratedthattheleaves,roothairs,andrhizomesofPanaxquinquefoliusL.containedhigherginsenosidecontents,followedbythemainrootsandstems.TheleavescontaineddramaticallyhigherlevelsofginsenosideRg1,Rb3,andRdthantheotherfourparts.HighercontentsofRb1andRewerepresentinthemainroots,roothairs,andrhizomes.Theamountofginsenosidecontentinthestemswasthelowest.Thetotalcontentofthesevenginsenosidesinmainroots,roothairsandrhizomesincreasedwiththeageoftheplant.Incontrast,theginsenosidecontentsintheleavesandstemsdecreasedwithayearofgrowth.

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简介：Anewcerebroside,1-O-(β-D-glucopyranosyloxy)-(2S,3R,4E,8Z)-2-[(2′R)-2’-hydroxylignoceranoylamino]-4,8-tetradecene-3-diolwasisolatedfromthe60%EtOHextractoftraditionalChinesemedicalplantCyperusrotundusL.Itsstructurewasdeterminedonthebasisofspectroscopicdata.Thisnewcompoundshowedanti-proliferationeffectonvascularsmoothmusclecells(VSMCs).

简介：TheternaryCu(Ⅱ）complexwith2,2′-bipyridyl(bipy)andL-methioninte(L-Met)hasbeensynthesizedandcharacterizedbyelementalanalysis,molarconductivity,UV-Visspectra,IRspectraandpH-potentiometrictitrationmethods.Thestructureofthecomplex[Cu(L-Met)(bipy)(H2O)]ClO4·3/8H2OwascharacterizedbytheX-raydiffractionanalysis.Itcrystallizesinthetriclinicsystem,spacegroupP1withfourmoleculesinaunitcellofdimensions,a=0.7656(2)nm,b=1.3142(3)nm,c=2.0596(4)nm,α=97.70(3)°,β=97.96(3)°,γ=94.33(3)°，V=2.0244(8)nm^3,R1=0.0441andwR2=0.0678,Thecrystalcontainsfourcrystallographicallyindependent[Cu(L-Met)(bipy)(H2O)]^+complexes(Cu1-Cu4),havingadistortedsquare-pyramidalgeometrywiththesamecoordinatedatomsaroundeachcoppercenter.Thebaseplaneisoccupiedbytwonitrogenatomsofonebipy,theaminonitrogenatomandonecarboxylateoxygenatomfromeachindependentL-Metmoiety,andonewateroxygenatanaxialposition.CulandCu3areessentiallyenantiomersofCu2andCu4.Thefourmoleculesarepackedwitheachotherbyintermolecularhydrogen-bondingandaromatic-ringstackinginteractions.