SEARCH Articles Figures Tables 2-Oxazolines activating groups 5- Nitropyrimidine, ring transformation reaction with active methylene groups A-Aminosulfonic acid amides groups, active Acetonitrile, carboxylic group activation Acidic groups biological activity Activate neighboring functional groups Activated alkyl groups and polynuclear aromatics Activated carbon acidic groups Activated carbon basic groups Activated carbon pyrone groups Activated carbon surface functional groups Activated halogen groups Activated halogen groups, compounds Activated vinyl group Activating Oxygen as a Leaving Group Activating and deactivating groups Activating group (aromatic acidity and Activating group (aromatic explanation Activating group characteristics Activating group effects Activating group explanation Activating group methoxycarbonyl Activating groups Activating groups Activating groups Substituents that, when Activating groups addition Activating groups in electrophilic aromatic Activating groups meta directors Activating groups ortho—para directors Activating groups substituents Activating groups substitution Activating groups, aromatic substitution Activation amino groups Activation by amino group Activation effects groups Activation energies amino group restricted rotation Activation energy group Activation of Carbonyl Groups and Alcohols Activation of Dioxygen by Cobalt Group Activation of Dioxygen by Cobalt Group Metal Complexes Activation of carbonyl groups by iminium ion formation Activation of the carbonyl group Activation target groups Active Group exchange Active Group identification Active groups Active groups Active methylene group Active site group theories Active transport group translocation Activity coefficient group contribution model Activity coefficients, limiting group Activity group VIII metals supported Activity, glycosyl group Activity-based probes reactive groups Acylamino group, activating effects Alcohols hydroxy group activation Aldehydes from activated methyl groups Alkyl groups, activating effect Alkyl polysilane, optically active groups Amino group activated, peptide Amino groups activation parameters Amino groups active-esters methods Anomeric Activating Groups and Stereoselectivity Anomeric activating groups Antioxidative activity hydroxyl groups kinds Antitumor activity group 12 Arenes and Hetarenes Activated by the Nitro Group Arenium ions activating groups Aromatic compounds, activation groups Aromatic, activating groups Azine substitution , activation acyl groups, electronic effects Azine substitution , activation acyloxy groups, electronic effects Azine substitution , activation acylthio group, electronic effects Azine substitution , activation alkyl leaving groups Azine substitution , activation alkylsulfonyl leaving groups Azine substitution , activation alkylthio group, electronic effects Azine substitution , activation alkylthio leaving groups Azine substitution , activation amino leaving groups Azine substitution , activation ammonio groups, displacement Azine substitution , activation aryl groups, electronic effects Azine substitution , activation aryloxy groups, electronic effects Azines—continued bicyclic, activation by benzo group Basicity, silanol group activation Biotin-Hydrazide Modification of Bisulfite-Activated Cytosine Groups Blood group B-active Blood-group active glycolipids Blood-group active glycoproteins Carbonyl groups, activation Carboxy group activation Carboxy group activation esterification Carboxy group activation mechanism Carboxy group, activated Carboxyl group activation Carboxyl group, activated Carboxyl groups active site Carboxylic acids hydroxy group activation Catalyst activity and functional group Catalyst activity and functional group tolerance Catalytic groups, active site Catalytically active group Chemically-active surface groups Compounds with Activated Methyl, Methylene and Methine Groups Compounds with activated halogen groups Control groups active Cyano group activating effects Diphenylphosphinoyl group, activation Effects of Activating Groups Electrochemical Properties of Active Groups Electrochemical Properties of Protein Macromolecules and Their Active Groups Enzyme biological activity, sulfhydryl groups Formate, active methyl groups from Functional group activation Functional group activation bioactivation Functional group activation carbonyl compounds, unsaturated Functional group activation carboxylic acids Functional group activation hydrazines Functional group activation reactive intermediates Glycol groups, activation Glycosphingolipids group-active Glycosyl groups, active Group Learning Activities Group NMR active nuclei Group VIII metals dehydrogenation activities Group VIII metals hydrogenation activities Group VIII metals hydrogenolysis activities Group VIII metals methanation activity Group biological activity values Group-transfer reactions active carriers Herbicide groups, structure-activity Herbicide groups, structure-activity relationships Hydrogenolysis of activated keto groups Hydroxy group activation Hydroxy group activation ester synthesis Hydroxyl groups activation with Imidazoles 2-silyl groups, active LC Copolymers Containing Both Nematogenic (or Smectogenic) and Active Side Groups Leaving group activation, peptide hydrolysis Leaving group selective activation Leaving groups, active Light-active donor group Mesylates hydroxy group activation Metabolic activation, organic functional groups Methoxycarbonyl as activating group Methyl and methylene groups, active Methyl groups activating effects Methyl groups active Methylene groups, activated Methylene groups, activated Michael-type addition Methylene groups, activated aldol condensation Methylene groups, activated alkylation Methylene groups, activated iodination Methylene groups, activated periodate oxidation Near-infrared activated groups Nitrile group activation Nitro compounds Methyl groups, active Nitro group activating effects Nitro group, activation Nitrogen-Activating Group Effects Nitroso compounds reaction with active methylene groups Nucleophilic aromatic substitution activating groups, effects Nucleophilic aromatic substitution nitro-group activated Of activated methylene group Of blood group I active Of the active groups Oligothiophenes containing redox-active groups Oligothiophenes containing surface-active groups Optical activity space-groups Oxidation of active methylene groups Oxidation, oxazole reactions activating group Oxirane polymerization active groups Oxygen Bridge Activation by an Electron-Donating Group at the Bridgehead Carbon Ozonolysis activating group Peptide amido groups active) Perfluoroacetone, reaction with methylene groups, activ Perfluoroalkyl group, activation Periodate oxidation active methylene groups Phosphorus with methylene groups, active Phosphoryl group transfer active carriers Photo-active groups Platinum, catalytic activity with functional groups Preparation of polymethylphenylsiloxanes with active hydrogen atoms and vinyl groups at the silicon atom Pyrrole activated methylene groups Quaternary N groups and anticholinesterase activity quaternization Reactions of azides with active methylene groups Redox active groups Redox-active prosthetic groups Reduction of activated carbonyl groups Remote chiral groups, optically active Ruthenium, catalytic activity with functional groups Selective activation with three leaving groups Solubility group activity) Special Activity Group on Accident Special Activity Group on Accident Reduction Stereochemical Activity of Lone Pairs in Heavier Main-group Element Compounds Structure-activity relationship groups Structure-activity relationship substituent groups Structure-activity relationships specific substituent groups Substitution SnAt, activating groups Sulfhydryl groups activity Sulfhydryl groups, metal binding active site Sulfonation hydroxy group activation Sulfonium salts groups, active Surface active agents hydrophilic group Surface active agents hydrophobic group Surface active agents lipophilic group Surface active agents lipophobic group Surface hydroxyl groups activation Surface-active functional groups Surface-active groups Target groups of activation Thermally activated phenyl group Thermo-active group Thioesters to activate carboxyl groups Tosylates hydroxy group activation Transformation of active end-groups Transition Metals as Protecting, Activating, and Directing Groups Triflates hydroxy group activation Trifluoromethyl groups nitro displacement activation UNIFAC method functional group activity coefficient Universal Functional Group Activity Universal Functional Group Activity UNIFAC)