SEARCH Articles Figures Tables Acetals alkali labile Acid labile Acid labile sulfide formation Acid-labile acetal Acid-labile aldehyde Acid-labile anchors Acid-labile epoxides Acid-labile glycoconjugates Acid-labile groups Acid-labile hydrazone linkage Acid-labile isotope-coded extractants Acid-labile linkers Acid-labile liposome Acid-labile precursors Acid-labile sulfide Acid-labile surfactants Action of Labile Nitrogen Alkali lability Alkali-labile site Alkali-labile surfactants Alkali-lability, dextrins Amide labilizing effect Amine labilization Amines acid-labile linkers Amines base-labile linkers Amino acids catalysis by labile metal ions Analysis, structure, and reactivity labile terpenoid aroma precursors Anchoring acid labile Anions, configurationally labile Base Labile Sulfones Base labile Base-labile carboxylic esters Base-labile ester linkers Base-labile linkers Base-labile resins Biocatalyzed Reactions on Polymeric Supports Enzyme-Labile Linker Groups Biologically labile Blocking groups, acid labile Bond lability Bromide lability Carbon labilizing effect Carbonyls lability Carboxylic acid-labile linkers Catalysts lability effect Chemically labile Chloride lability Clathrate lability Cleavage acid labile linkers Cluster labile Cobalt , labile groups Cobalt labile Complex ions labile Complex lability Complexes, quasi labile Complexes, slowly labile Concentration Profiles in Ideally Labile Systems Concentration Profiles in Systems of Limited Lability Criteria for the Thermally Labile Coblock Crystallization labile region Cyanide labilizing effect DKR of Configurationally Labile Anions Decarboxylation labile metal ions Decomposition lability toward E. coli heat-labile enterotoxin E. coli heat-labile toxin Emotional lability Enol acid-labile Enzyme-labile phosphate Enzyme-labile protecting groups Enzyme-labile safety catch linkers Equilibrium, labile Escherichia coli labile enterotoxin Escherichia coli labile enterotoxin subunit Ester lability Ester lability steric effects Esters acid-labile linkers Ethylenediamine labilization Exchange of labile bonded hydrogen Explanation of Inert versus Labile Complexes Factors Affecting Biological Lability Formation Labile Cations Functional groups, acid-labile linker Generation and Trapping of Labile Anions Glycosides alkali-lability HMGA biochemical modifications a labile regulatory code Halogens, labile bonded Heat-labile bodies Heat-labile enterotoxin Heat-labile sites Hemi-labile coordination Heterobifunctional reagents acid labile Highly labile metal centers Hydrogen atom, labile Hydrolysis catalysis by labile metal ions Hydrolytically labile Hydrolytically labile poly Hydrolytically labile polyesters Hydrolytically labile polyurethanes Hydroxide lability INDEX lability Inert and Labile Compounds Inert metal complexes induced lability Inert metal complexes inherent lability Isocyanides lability Kerogen labile Kinetic lability Kinetically Inert and Labile Complexes Kinetically labile Kinetically labile complexes Labile Labile Labile Complexes as Anion Hosts Labile H atoms Labile Sulfur Contents Labile aliphatic molecules Labile aluminium Labile analytes Labile and Inert Coordination Compounds Labile atmospheric pollutants, sampling Labile atom Labile atropisomers Labile bicyclic Labile biomass Labile carbohydrates Labile carbon Labile carbonyl groups Labile cells Labile chloride ligands Labile cluster mechanism Labile cluster nucleation hypothesis Labile complex formation Labile complex formation Eigen mechanism Labile complexes Labile complexes 5-lactam Labile complexes, mass transfer coupled Labile components Labile compounds Labile compounds, analysis Labile compounds, preparation Labile compounds, preparation under protective conditions Labile coordination compounds Labile copper Labile dissolved organic Labile dissolved organic carbon Labile enterotoxin Labile forms Labile fraction Labile functionality Labile group Labile hydrogens Labile hypertension Labile intermediates Labile iron pool Labile junctions Labile lactam ethers Labile lactamase Labile ligand Labile lipids Labile metal determinations Labile metals Labile metals bioavailable fraction Labile metals column elution Labile metals seawater Labile natural products Labile nickel Labile nitrogen Labile octahedral complexes Labile organic matter Labile organometallic complex Labile pharmaceuticals Labile phosphate Labile photoproducts Labile plasma iron Labile proteins Labile protons Labile reactions Labile region Labile s. Unstable Labile species, encapsulation Labile state Labile stereocenters Labile structure Labile substances Labile substrate Labile systems Labile systems redox reactions Labile systems substitution reactions Labile terpenoid aroma precursors Labile toxin Labile transition-metal ions, ligand Labile transition-metal ions, ligand substitution Labile tricyclic Labile zinc Labile/unstable species Lability and Inertness in Octahedral Complexes Lability definition Lability of complexes Lability of proteins Lability synthesis Lability, nonleaving ligand, effect Lability, stereochemical Labilization, ligands Large Heat-Labile Proteins (Class III) Lewis acid kinetically labile Ligand Substitution on Labile Transition-Metal Ions Ligand lability Ligand substitution labile terminal ligands Ligand-directed labilization Ligand-directed labilizations Light labile Linkages lability Linker acid-labile Linker oxidatively labile Linker photo-labile Linkers, nucleophile-labile Loss of fine particulates, volatile and labile components Manganese complexes lability Metabolic lability Metabolically labile drugs Metal ions labile Microtubule labile Nature of Labile Sulfur Nickel complexes, lability Nickel complexes, lability coordinated water Nitrite labilizing effect Nitro group, lability Nitroglycerine, labile form Nucleosides lability Nucleotides acid-labile phosphate Octahedral Substitution Reactions. Labile and Inert Complexes Optically labile racemates Other Acid-Labile Carbamates Other Base-Labile Carbamates Oxygen atoms, lability PH lability Patterns of Dissolved Organic Matter Lability among Systems Peptides acid-labile linkers Peptides catalysis by labile metal ions Peptides nucleophile-labile resins Phosphorus compounds, labile Phosphorus labile forms Photolysis-labile anchor Preparation of Labile Compounds under Protective Conditions. Chromium (II) Salts Pressurized fluid extraction thermal lability Protected polymers having acid-labile groups Protecting enzyme labile Protecting groups acid-labile Protecting groups base labile Protecting groups basic-labile Protecting groups oxidation-labile Protecting groups reduction-labile Protective group, base-labile Protective group, base-labile acid resistant Protein amino acid lability Protein lability Protein peptide lability Pulse radiolysis ligand labilization Pyridine labile” adducts from dimethyl Racemate, kinetically labile Racemic compounds chirally labile Reactions at Labile Transition Metal Centers Remove Labile Groups First Reviews on Enzyme-Labile Protecting Groups Reviews on Photo-Labile Protecting Groups Ribose lability SPPS acid-labile resins SPPS base-labile resins Safety-catch acid-labile Self-assembly labile complexes Semi-labile complexes, lability Solid base-labile resins Solid nucleophile-labile resins Solid-phase linkers acid-labile Solid-phase peptide synthesis acid labile linkers Spacers acid-labile linkers Starch alkali lability Sterically Deactivated and Base-labile Alcohols Substitution inert labile complexes Substitutional lability Sulfite labilizing effect Sulfone base labile group in crosslinkers Sulphate labile organic Sulphur labile forms Thermal lability Thermal stability and kinetic lability Thermally labile compounds Thermally labile materials Thermally labile products Thermally labile samples Thermally labile substance, examination Thermo-labile Tosylethyl Esters and Related Base-Labile Groups Trans labilizing effect Trans-labilization Trans-labilizing activity