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  2. Boronic acid - Wikipedia

    en.wikipedia.org/wiki/Boronic_acid

    The general structure of a boronic acid, where R is a substituent. A boronic acid is an organic compound related to boric acid (B(OH) 3) in which one of the three hydroxyl groups (−OH) is replaced by an alkyl or aryl group (represented by R in the general formula R−B(OH) 2). [1]

  3. Pyrimidine - Wikipedia

    en.wikipedia.org/wiki/Pyrimidine

    Pyrimidine (C 4 H 4 N 2; / p ɪ ˈ r ɪ. m ɪ ˌ d iː n, p aɪ ˈ r ɪ. m ɪ ˌ d iː n /) is an aromatic, heterocyclic, organic compound similar to pyridine (C 5 H 5 N). [3] One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has nitrogen atoms at positions 1 and 3 in the ring.

  4. Borinic acid - Wikipedia

    en.wikipedia.org/wiki/Borinic_acid

    Borinic acid, also known as boronous acid, is an oxyacid of boron with formula H 2 BOH. Borinate is the associated anion of borinic acid with formula H 2 BO −; however, being a Lewis acid, the form in basic solution is H 2 B(OH) − 2. Borinic acid can be formed as the first step in the hydrolysis of diborane: [1] BH 3 + H 2 O → H 2 BOH + H 2

  5. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    For example, in Nicolaou's epothilones synthesis, asymmetric allylboration (with an allylborane derived from chiral alpha-pinene) is the first step in a two-carbon homologation to acetogenin: [41] Trifluoroborate salts are stabler than boronic acids and selectively alkylate aldehydes: [42]

  6. Boron compounds - Wikipedia

    en.wikipedia.org/wiki/Boron_compounds

    The mean oxidation number for the boron atoms is then simply the ratio of hydrogen to boron in the molecule. For example, in diborane B 2 H 6, the boron oxidation state is +3, but in decaborane B 10 H 14, it is 7 / 5 or +1.4. In these compounds the oxidation state of boron is often not a whole number.

  7. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.

  8. CBS catalyst - Wikipedia

    en.wikipedia.org/wiki/CBS_catalyst

    The first leg of the reaction sequence starts from the azeotropic dehydration of a boronic acid (1) such as one based on toluene to a boroxine (2). This boroxine reacts with the proline derivative ( 3d ) to form the basic oxazaborolidine CBS catalyst ( 4 ).

  9. Brønsted–Lowry acid–base theory - Wikipedia

    en.wikipedia.org/wiki/Brønsted–Lowry_acid...

    [5] [6] [7] In the Brønsted–Lowry theory acids and bases are defined by the way they react with each other, generalising them. This is best illustrated by an equilibrium equation. acid + base ⇌ conjugate base + conjugate acid. With an acid, HA, the equation can be written symbolically as: