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  2. 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.

  3. 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]

  4. Pyridinium - Wikipedia

    en.wikipedia.org/wiki/Pyridinium

    As pyridine is often used as an organic base in chemical reactions, pyridinium salts are produced in many acid-base reactions. Its salts are often insoluble in the organic solvent, so precipitation of the pyridinium leaving group complex is an indication of the progress of the reaction.

  5. 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

  6. Borylation - Wikipedia

    en.wikipedia.org/wiki/Borylation

    The boron atom of a boronic ester or acid is sp 2 hybridized possessing a vacant p orbital, enabling these groups to act as Lewis acids. The C–B bond of boronic acids and esters are slightly longer than typical C–C single bonds with a range of 1.55-1.59 Å.

  7. Boron compounds - Wikipedia

    en.wikipedia.org/wiki/Boron_compounds

    As anticipated by its hydride clusters, boron forms a variety of stable compounds with formal oxidation state less than three. B 2 F 4 and B 4 Cl 4 are well characterized. [6] Ball-and-stick model of superconductor magnesium diboride. Boron atoms lie in hexagonal aromatic graphite-like layers, with a charge of −1 on each boron atom.

  8. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    Pyridine is a basic heterocyclic organic compound with the chemical formula C 5 H 5 N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom (=N−). It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.

  9. Pyridinecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Pyridinecarboxylic_acid

    A pyridinecarboxylic acid is any member of a group of organic compounds which are monocarboxylic derivatives of pyridine. Pyridinecarboxylic acid comes in three isomers : Picolinic acid (2-pyridinecarboxylic acid)