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α-Aminobutyric acid (AABA), also known as homoalanine in biochemistry, is a non-proteinogenic alpha amino acid with chemical formula C 4 H 9 NO 2. The straight two carbon side chain is one carbon longer than alanine, hence the prefix homo-. Homoalanine is biosynthesised by transaminating oxobutyrate, a metabolite in isoleucine biosynthesis.
β-Aminobutyric acid (BABA) is an isomer of the amino acid aminobutyric acid with the chemical formula C 4 H 9 NO 2.It has two isomers, α-aminobutyric acid and γ-aminobutyric acid (GABA), a neurotransmitter in animals that is also found in plants, where it may play a role in signalling.
The first row shows the reaction, which some authors label R and some leave blank. The second row, labeled I, has the initial conditions: the nominal concentration of acid is C a and it is initially undissociated, so the concentrations of A − and H + are zero. The third row, labeled C, specifies the change that occurs during the reaction.
The Strecker amino acid synthesis, also known simply as the Strecker synthesis, is a method for the synthesis of amino acids by the reaction of an aldehyde with cyanide in the presence of ammonia. The condensation reaction yields an α-aminonitrile, which is subsequently hydrolyzed to give the desired amino acid.
Example Bjerrum plot: Change in carbonate system of seawater from ocean acidification.. A Bjerrum plot (named after Niels Bjerrum), sometimes also known as a Sillén diagram (after Lars Gunnar Sillén), or a Hägg diagram (after Gunnar Hägg) [1] is a graph of the concentrations of the different species of a polyprotic acid in a solution, as a function of pH, [2] when the solution is at ...
These plots were first introduced in a 1970 paper by R. A. More O’Ferrall to discuss mechanisms of β-eliminations [2] and later adopted by W. P. Jencks in an attempt to clarify the finer details involved in the general acid-base catalysis of reversible addition reactions to carbon electrophiles such as the hydration of carbonyls.
In diagrams which indicate this, the new bond formed between the base and the proton is shown by an arrow that starts on an electron pair from the base and ends at the hydrogen ion (proton) that will be transferred: In this case, the water molecule is the conjugate acid of the basic hydroxide ion after the latter received the hydrogen ion from ...
The tert-butyloxycarbonyl protecting group or tert-butoxycarbonyl protecting group [1] (BOC group) is an acid-labile protecting group used in organic synthesis. The BOC group can be added to amines under aqueous conditions using di- tert -butyl dicarbonate in the presence of a base such as sodium hydroxide :