Single S:1640-39-7,15h,100°C Reactants:2,Solvents:1,Steps:1,Stages:1,Moststagesinanyonestep:1Near-InfraredFluorescenceProbesforEnzymesBasedonBindingAffinityModulationofSquaryliumDyeScaffoldByOushiki,DaihietFromyticalChemistry(Washington,DC,UnitedStates),84(10),4404-4410;2012CASREACT?:Copyright?2012AmericanChemicalSociety.s.CASREACTcontainsreactionsfromCASandfrom:ZIC/VINITIdatabase(1974-1999)providedbyInfoChem;INPIdatapriorto1986;BiotransformationsdatabasecompiledunderthedirectionofProfessorDr.KlausKieslich;organicreactions,portionscopyright1996-2006JohnWiley&Sons, .,JohnWileyandSons,.,OrganicReactions.,andOrganicSyntheses.Reproducedunderlicense. s.Single 5h,95°C nosolvent,Reactants:2,Steps:1,Stages:1,Moststagesinanyonestep:1MethodforEnhancingCellPrationofGd3+-basedMRIContrastAgentsbyByYamane,TakehiroetFromBioconjugateChemistry,22(11),2236;CASREACT?:Copyright?2012AmericanChemicalSociety.s.CASREACTcontainsreactionsfromCASandfrom:ZIC/VINITIdatabase(1974-1999)providedbyInfoChem;INPIdatapriorto1986;BiotransformationsdatabasecompiledunderthedirectionofProfessorDr.KlausKieslich;organicreactions,portionscopyright1996-2006JohnWiley&Sons, .,JohnWileyandSons,.,OrganicReactions.,andOrganicSyntheses.Reproducedunderlicense. s.Single S:PhMe,3h,100°C Reactants:2,Solvents:1,Steps:1,Stages:1,Moststagesinanyonestep:1Resettable,Multi-ReadoutLogicGatesBasedonControllablyReversibleAggregationofByLiu, Edition,50(18),4103-4107,S4103/1-S4103/16;CASREACT?:Copyright?2012AmericanChemicalSociety.s.CASREACTcontainsreactionsfromCASandfrom:ZIC/VINITIdatabase(1974-1999)providedbyInfoChem;INPIdatapriorto1986;BiotransformationsdatabasecompiledunderthedirectionofProfessorDr.KlausKieslich;organicreactions,portionscopyright1996-2006JohnWiley&Sons, .,JohnWileyandSons,.,OrganicReactions.,andOrganicSyntheses.Reproducedunderlicense. s.Single 3h,80°C Reactants:2,Steps:1,Stages:1,Moststagesinanyonestep:1SwitchableaffinitybindersandmethodsandkitsforbindingandreleasingbiologicalBySood,AnupetFromPCTInt.Appl., ,26AugExperimentalExample13PreparationofCD34-SPantibodyconjugatesllbindingandreleaseSP-NHSSynthesis:AmodifiedversionoftheprotocoloriginallypublishedbyAizawa,etal.wasusedtosynthesizethespiropyranprecursormoleculeSP.Toaflaskequippedwithamaicstirbarwereadded2,3,3-trimethylindolenine(3.2mL,20mmol)and-iodopropionicacid(4.0g,20mmol).Theresultingmixturewasheatedat80°Cfor3hbeforebeingcooledtoroomtemperature(rt)anddilutedwithmethanol(30-50mL).Additionofethylacetate(150mL)inducedprecipitationofthedesired1-carboxyethyl-2,3,3-trimethylindoleniumiodideproduct(TM).Thispinksolidwasfurtherwashedseveraltimeswithexcessethylacetate,driedunderreducedpressure,andusedwithoutfurtherpurification.ProductidentityandtherelativepuritywereconfirmedusingTLC(5%MeOH/95%CASREACT?:Copyright?2012AmericanChemicalSociety.s.CASREACTcontainsreactionsfromCASandfrom:ZIC/VINITIdatabase(1974-1999)providedbyInfoChem;INPIdatapriorto1986;BiotransformationsdatabasecompiledunderthedirectionofProfessorDr.KlausKieslich;organicreactions,portionscopyright1996-2006JohnWiley&Sons, .,JohnWileyandSons,.,OrganicReactions.,andOrganicSyntheses.Reproducedunderlicense. s.Single 1.1S:o-Dichlorobenzene liturepreparation,Reactants:2,Solvents:1,Steps:1,Stages:1,Moststagesinanyonestep:1MolecularDesignStrategiesforNear-InfraredRatiometricFluorescentProbesBasedontheUniqueSpectralPropertiesofAminocyaninesByKiyose,KazukietFromChemistry--AEuropeanJournal,15(36),9191-9200,S9191/1-S9191/7;2009CASREACT?:Copyright?2012AmericanChemicalSociety.s.CASREACTcontainsreactionsfromCASandfrom:ZIC/VINITIdatabase(1974-1999)providedbyInfoChem;INPIdatapriorto1986;BiotransformationsdatabasecompiledunderthedirectionofProfessorDr.KlausKieslich;organicreactions,portionscopyright1996-2006JohnWiley&Sons, .,JohnWileyandSons,.,OrganicReactions.,andOrganicSyntheses.Reproducedunderlicense. s.Single ,48h,reflux Reactants:2,Solvents:1,Steps:1,Stages:1,Moststagesinanyonestep:1FlexiblezoxidesolarcellssensitizedbystyryldyesByDentani,TakuyaetFromDyesandments,77(1),59-69;CASREACT?:Copyright?2012AmericanChemicalSociety.s.CASREACTcontainsreactionsfromCASandfrom:ZIC/VINITIdatabase(1974-1999)providedbyInfoChem;INPIdatapriorto1986;BiotransformationsdatabasecompiledunderthedirectionofProfessorDr.KlausKieslich;organicreactions,portionscopyright1996-2006JohnWiley&Sons, .,JohnWileyandSons,.,OrganicReactions.,andOrganicSyntheses.Reproducedunderlicense. s.Single S:EtC(=O)Me,3h,100°C Reactants:2,Solvents:1,Steps:1,Stages:1,Moststagesinanyonestep:1ReversiblefluorescencemodulationthroughenergytransferwithABCtriblockcopolymermicellesasscaffoldsByChen,JiFromChemicalCommunications(Cambridge,UnitedKingdom),(43),5580-5582;2008CASREACT?:Copyright?2012AmericanChemicalSociety.s.CASREACTcontainsreactionsfromCASandfrom:ZIC/VINITIdatabase(1974-1999)providedbyInfoChem;INPIdatapriorto1986;BiotransformationsdatabasecompiledunderthedirectionofProfessorDr.KlausKieslich;organicreactions,portionscopyright1996-2006JohnWiley&Sons, .,JohnWileyandSons,.,OrganicReactions.,andOrganicSyntheses.Reproducedunderlicense. s.Single rt;4h,95°C Reactants:2,Steps:1,Stages:1,Moststagesinanyonestep:1Inctionsbetweenspiropyransandroom-temperatureionicliquids:photochromismandByWu,YusongetFromJournalofPhysicalChemistryB,112(25),7530-7536;2008Experimental(3)1-(nitrobenzospiropyran(SP-I):Step1:3.29g(0.02mol)of2,3,3-trimethylindolenineof(1)wasdispersedin4.00g(0.02mol)of3-iddopropanicacidfollowedbyheatingunderN2atmospherefor4hat95°C.Theobtainedviscousliquidwasdissolvedinwater,andthepossibleimpuritieswereextractedwithchloroform.Afterremovalofwaterbydistillation,theresiduewasdissolvedinacetoneandre-precipitatedbyethertoobtain5.41gyellowpowderc(Yield83.2%,c,Yield(5.41g,83.2%)(mp:208~210°C).CASREACT?:Copyright?2012AmericanChemicalSociety.s.CASREACTcontainsreactionsfromCASandfrom:ZIC/VINITIdatabase(1974-1999)providedbyInfoChem;INPIdatapriorto1986;BiotransformationsdatabasecompiledunderthedirectionofProfessorDr.KlausKieslich;organicreactions,portionscopyright1996-2006JohnWiley&Sons, .,JohnWileyandSons,.,OrganicReactions.,andOrganicSyntheses.Reproducedunderlicense. s.Single S:EtC(=O)Me,3h,100°C inthedark,Reactants:2,Solvents:1,Steps:1,Stages:1,Moststagesinanyonestep:1Acore-snanoparticleapproachtophotoreversiblefluorescencemodulationofahydrophobicdyeinaqueousmediaByChen, FromChemistry--AEuropeanJournal,14(16),4851-4860;2008CASREACT?:Copyright?2012AmericanChemicalSociety.s.CASREACTcontainsreactionsfromCASandfrom:ZIC/VINITIdatabase(1974-1999)providedbyInfoChem;INPIdatapriorto1986;BiotransformationsdatabasecompiledunderthedirectionofProfessorDr.KlausKieslich;organicreactions,portionscopyright1996-2006JohnWiley&Sons, .,JohnWileyandSons,.,OrganicReactions.,andOrganicSyntheses.Reproducedunderlicense. s.1S:1640-39-7,15h,100°C2,1,1,1,Squarylium：OushikiDaihi（美國華盛頓特區(qū)），84(10),4404-4410；2012CASREACT.： 。2012年美國化學(xué)會(huì)。 。CASREACT包含來自CAS和InfoChem提供的ZIC/VINITI數(shù)據(jù)庫(1974-1999)的反應(yīng)；1986年之前的INPI數(shù)據(jù)；在KlausKieslich教授博士的指導(dǎo)下編制的生物轉(zhuǎn)化數(shù)據(jù)庫；有機(jī)反應(yīng)，部分 1996-2006JohnWiley&Sons,.、JohnWileyandSons,.、OrganicReactions.和OrganicSyntheses.經(jīng)許可轉(zhuǎn)載。 1.15小時(shí)，95°C無溶劑，反應(yīng)物：2，步驟：1，階段：1，任一步驟中的大多數(shù)階段：1參考文獻(xiàn)MethodforEnhancingCellPrationofGd3+-basedMRIContrastAgentsbyConjugationwithHydrophobicFluorescentDyesByYamane,TakehiroetalFromBioconjugateChemistry,22(11),2227-2236；2011年CASREACT.： 。2012年美國化學(xué)會(huì)。 。CASREACT包含來自CAS和InfoChem提供的ZIC/VINITI數(shù)據(jù)庫(1974-1999)的反應(yīng)；1986年之前的INPI數(shù)據(jù)；在KlausKieslich教授博士的指導(dǎo)下編制的生物轉(zhuǎn)化數(shù)據(jù)庫；有機(jī)反應(yīng)，部分 1996-2006JohnWiley&Sons,.、JohnWileyandSons,.、OrganicReactions.和OrganicSyntheses.經(jīng)許可轉(zhuǎn)載。 1.1S:PhMe，3100°C2，溶劑：1，步驟：1，階段：1，自AngewandteChemie，國際版，50(18),4103-4107,S4103/1-S4103/16；2011CASREACT.： 。2012年美國化學(xué)會(huì)。 。CASREACT包含來自CAS和InfoChem提供的ZIC/VINITI數(shù)據(jù)庫(1974-1999)的反應(yīng)；1986年之前的INPI數(shù)據(jù)；在KlausKieslich教授博士的指導(dǎo)下編制的生物轉(zhuǎn)化數(shù)據(jù)庫；有機(jī)反應(yīng)，部分 1996-2006JohnWiley&Sons,.、JohnWileyandSons,.、OrganicReactions.和OrganicSyntheses.經(jīng)許可轉(zhuǎn)載。 1.1380°C：2，步驟：1，階段：1等人，來自PCTInt。申請(qǐng) ,2010年8月2613SP-NHSαCD34-SP減壓干燥，并且無需進(jìn)一步純化即可使用。使用TLC（5%MeOH/95%CH2Cl2）確認(rèn)產(chǎn)品身份和相對(duì)CASREACT 。CASREACT包含來自CAS和ZIC/VINITI1974-1999)1986INPIKieslich教授博士的指導(dǎo)下編制的生物轉(zhuǎn)化數(shù)據(jù)庫；有機(jī)反應(yīng)，部分 1996-2006JohnWiley&Sons,.、JohnWileyandSons, .、OrganicReactions .和Organic .經(jīng)許可轉(zhuǎn)載。 KiyoseKazuki，來自Chemistry--AEuropeanJournal,15(36),9191-9200,S9191/1-S9191/7；2009年CASREACT.： 。2012年美國化學(xué)會(huì)。 。CASREACT包含來自CAS和InfoChem提供的ZIC/VINITI數(shù)據(jù)庫(1974-1999)的反應(yīng)；1986年之前的INPI數(shù)據(jù)；在KlausKieslich教授博士的指導(dǎo)下編制的生物轉(zhuǎn)化數(shù)據(jù)庫；有機(jī)反應(yīng)，部分 1996-2006JohnWiley&Sons,.、JohnWileyandSons,.、OrganicReactions.和OrganicSyntheses.經(jīng)許可轉(zhuǎn)載。 和顏料，77(1),59-69；2007年CASREACT.： 。2012年美國化學(xué)會(huì)。 。CASREACT包含來自CAS和InfoChem提供的ZIC/VINITI數(shù)據(jù)庫(1974-1999)的反應(yīng)；1986年之前的INPI數(shù)據(jù)；在KlausKieslich教授博士的指導(dǎo)下編制的生物轉(zhuǎn)化數(shù)據(jù)庫；有機(jī)反應(yīng)，部分 1996-2006JohnWiley&Sons,.、JohnWileyandSons,.、OrganicReactions.和OrganicSyntheses.經(jīng)許可轉(zhuǎn)載。 1.1S:EtC(=O)Me，3，100°C2，溶劑：1，步驟：1，