about
Chemical methods of DNA and RNA fluorescent labelingInterception of teicoplanin oxidation intermediates yields new antimicrobial scaffoldsSubstrate and Reaction Specificity of Mycobacterium tuberculosis Cytochrome P450 CYP121: INSIGHTS FROM BIOCHEMICAL STUDIES AND CRYSTAL STRUCTURESEnzyme-substrate intermediate formation at lysine 329 of human deoxyhypusine synthaseThe metabolism of amphetamine in vitro by rabbit liver preparations: a comparison of R(-) and S(+) enantiomers3-Formyl-1-butyl pyrophosphate A novel mycobacterial metabolite-activating human gammadelta T cells.Synthesis and biological evaluation of a targeted library of protein phosphatase inhibitors.Synthesis of new 2-(aminomethyl)-4-phenylpyrrolo[1,2-a]-quinoxalines and their preliminary in-vivo central dopamine antagonist activity evaluation in mice.Sugar-based tertiary amino gemini surfactants with a vesicle-to-micelle transition in the endosomal pH range mediate efficient transfection in vitro.Solid-phase synthesis of 7-substituted 3H-imidazo[2,1-i]purines.Short and efficient diastereoselective synthesis of pyrrolidinone-containing dipeptide analogues.A mass spectrometric analysis of 4-hydroxy-2-(E)-nonenal modification of cytochrome c.delta(13)C and delta(2)H isotope ratios in amphetamine synthesized from benzaldehyde and nitroethane.Intra-tRNA distance measurements for nucleocapsid proteindependent tRNA unwinding during priming of HIV reverse transcription.Lysine methylation is an endogenous post-translational modification of tau protein in human brain and a modulator of aggregation propensity.A dynamic combinatorial approach for identifying side groups that stabilize DNA-templated supramolecular self-assemblies.pH-regulated formation of side products in the reductive amination approach for differential labeling of peptides in relative quantitative experiments.Kinetic mechanism of protein N-terminal methyltransferase 1.DNA-catalyzed reductive aminationSynthesis and antibacterial activity of Schiff bases and amines derived from alkyl 2-(2-formyl-4-nitrophenoxy)alkanoates.Location of biomarkers and reagents within agarose beads of a programmable bio-nano-chip.eIF4E, the mRNA cap-binding protein: from basic discovery to translational research.Direct quantitation of psychosine from alkaline-treated lipid extracts with a semi-synthetic internal standard.Goniomitine: an overview on the chemistry of this indole alkaloid.Albumin-drug conjugates in the treatment of hepatic disorders.A convenient oxidation of natural glycosphingolipids to their "ceramide acids" for neoglycoconjugation. Bovine serum albumin-glycosylceramide acid conjugates as investigative probes for HIV gp120 coat protein-glycosphingolipid interactions.Cellulose carbonates: a platform for promising biopolymer derivatives with multifunctional capabilities.Developments and recent advancements in the field of endogenous amino acid selective bond forming reactions for bioconjugation.Importance of the 6'-hydroxy group and its configuration for apramycin activity.Total synthesis of indole-derived allocolchicine analogues exhibiting strong apoptosis-inducing activity.Endogenous lectins and drug targeting.T4 endonuclease V. Perspectives on catalysis.Synthesis and Evaluation of Ciprofloxacin-Nitroxide Conjugates as Anti-Biofilm Agents.BACE1- and BACE2-expressing human cells: characterization of beta-amyloid precursor protein-derived catabolites, design of a novel fluorimetric assay, and identification of new in vitro inhibitors.Isolation of animal cell mutants defective in long-chain fatty aldehyde dehydrogenase. Sensitivity to fatty aldehydes and Schiff's base modification of phospholipids: implications for Sj-ogren-Larsson syndrome.Eco-contribution for the production of N-arylnitrones: solvent-free and assisted by microwaves.Gemini alkyldeoxy-D-glucitolammonium salts as modern surfactants and microbiocides: synthesis, antimicrobial and surface activity, biodegradation.Irreversible inhibition of GABA-T by halogenated analogues of beta-alanine.Metabolism of N-(5-pyrrolidinopent-3-ynyl)-succinimide (BL 14) in rat liver preparations. Characterization of four oxidative reactions.Photodynamic therapy of fullerene modified with pullulan on hepatoma cells.
P2860
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P2860
description
1971 nî lūn-bûn
@nan
1971 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1971 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1971年の論文
@ja
1971年論文
@yue
1971年論文
@zh-hant
1971年論文
@zh-hk
1971年論文
@zh-mo
1971年論文
@zh-tw
1971年论文
@wuu
name
Cyanohydridoborate anion as a selective reducing agent
@ast
Cyanohydridoborate anion as a selective reducing agent
@en
type
label
Cyanohydridoborate anion as a selective reducing agent
@ast
Cyanohydridoborate anion as a selective reducing agent
@en
prefLabel
Cyanohydridoborate anion as a selective reducing agent
@ast
Cyanohydridoborate anion as a selective reducing agent
@en
P2093
P356
P1476
Cyanohydridoborate anion as a selective reducing agent
@en
P2093
H. Dupont Durst
Mark D. Bernstein
Richard F. Borch
P304
P356
10.1021/JA00741A013
P407
P577
1971-06-01T00:00:00Z