Document Type
Showing 1-14 of 14 results for "deprotonations"
Product Information Sheet - M8878
Methylimidazole has been utilized in the synthesis of inorganic complexes, ionic liquids, and catalytic deprotonation reagents.3-5 The use of 1-methylimidazole in the preparation of GDP-hexanolamine for the purification
Data Sheet - D5905
tablets added directly to buffer solutions. Buffer pH will also affect solubility. High pH will deprotonate DAB to its free base, which is not water-soluble. Storage/Stability Store the tablets at –
Product Information Sheet - G1626
acid is commonly referred to as "glutamate", because its carboxylic acid side chain will be deprotonated and thus negatively charged in its anionic form at physiological pH. In amino acid metabolism
Product Information Sheet - G1251
acid is commonly referred to as "glutamate", because its carboxylic acid side chain will be deprotonated and thus negatively charged in its anionic form at physiological pH. In amino acid metabolism
Product Information Sheet - G2128
acid is commonly referred to as "glutamate", because its carboxylic acid side chain will be deprotonated and thus negatively charged in its anionic form at physiological pH. In amino acid metabolism
Buchwald Portfolio - Precatalysts and Ligands
Pd NH2 X Deprotonation Pd NH Reductive elimination Base N H LPd(0) Active Catalyst L L Reductive elimination LPd(0) Active Catalyst Deprotonation References listed
Acta Volume 49 Number 3
F F F – e – H+ 4m C–F arylation product oxidation oxidation deprotonation deprotonation (4l) 14 15a 15b Path A Path B R ...
Asymmetric Synthesis
application in asymmetric synthesis serving, for instance, as chiral bases in enantioselective deprotonation reactions32 or being valuable substances for resolving racemic mixtures of acids. Additionally
Acta Interactive Archive Vol 51
protonated heteroarene in a regioselective manner. The ensuing radical cation is further oxidized and deprotonated to give the monoacylated heteroarene. Hexafluoroisopropanol was found to be a key additive
"Amidine-Based Catalysts (ABCs)- Design, Development, and Applications"
suggested that we offer bis[(pinacolato)- boryl]methane. This reagent provides, through simple deprotonation– alkylation reaction sequences, a simple entry point into a diverse array of substituted geminal
ChemFiles 6.2
compounds (Conia-ene reaction) provides access to methylenecyclopentanes without the need for deprotonation. However, the synthetic utility of this reaction is limited due to the high temperatures required
ChemFiles Vol. 5 No. 12
Use of triethylamine can be added to ensure that the target amino groups of the peptide are deprotonated, which is required for the labeling procedure. Table 1 shows a selection of our fluorescent
Aldrichimica Acta Volume 50 Number 1
following different enzymatic pathways that involve the formation of cis-(4S)-d-Hyp (C3DHyp) via deprotonation of the Ca chiral carbon and racemization. Hydroxyprolines have also been detected in nonribosomal
Aldrichimica Acta Volume 50 Number 2
members of this class of crosslinkers were synthesized by Staros.52 The sulfonic acid group is deprotonated under all pH conditions useful for coupling with amines, and its resulting strongly polar character

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