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  2. α-Aminobutyric acid - Wikipedia

    en.wikipedia.org/wiki/Α-aminobutyric_acid

    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.

  3. β-Aminobutyric acid - Wikipedia

    en.wikipedia.org/wiki/Β-Aminobutyric_acid

    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.

  4. Strecker amino acid synthesis - Wikipedia

    en.wikipedia.org/wiki/Strecker_amino_acid_synthesis

    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.

  5. tert-Butyloxycarbonyl protecting group - Wikipedia

    en.wikipedia.org/wiki/Tert-butyloxycarbonyl...

    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 :

  6. Aminonaphthalenesulfonic acids - Wikipedia

    en.wikipedia.org/wiki/Aminonaphthalenesulfonic_acids

    reduction of 1-nitroonaphthalene-8-sulfonic acid, precursor to C.I. Acid Blue 113 Notes: Peri-acid dehydrates to the sultam . Via the Bucherer reaction , heating periacid with anilinium salts gives the N-phenyl derivative, precursor to Acid Blue 113.

  7. Schotten–Baumann reaction - Wikipedia

    en.wikipedia.org/wiki/Schotten–Baumann_reaction

    Schotten–Baumann reaction also refers to the conversion of acid chloride to esters. The reaction was first described in 1883 by German chemists Carl Schotten and Eugen Baumann. [1] [2] The name "Schotten–Baumann reaction conditions" often indicate the use of a two-phase solvent system, consisting of water and an organic solvent.

  8. Metal ions in aqueous solution - Wikipedia

    en.wikipedia.org/wiki/Metal_ions_in_aqueous_solution

    A water molecule in the first solvation shell of an aqua ion may exchange places with a water molecule in the bulk solvent. It is usually assumed that the rate-determining step is a dissociation reaction. [M(H 2 O) n] z+ → [M(H 2 O) n-1] z+ * + H 2 O. The * symbol signifies that this is the transition state in a chemical reaction. The rate of ...

  9. 4-aminobutyrate transaminase - Wikipedia

    en.wikipedia.org/wiki/4-aminobutyrate_transaminase

    In enzymology, 4-aminobutyrate transaminase (EC 2.6.1.19), also called GABA transaminase or 4-aminobutyrate aminotransferase, or GABA-T, is an enzyme that catalyzes the chemical reaction: 4-aminobutanoate + 2-oxoglutarate ⇌ {\displaystyle \rightleftharpoons } succinate semialdehyde + L-glutamate