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  2. 2-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/2-Methylpyridine

    2-Methylpyridine, or 2-picoline, is the compound described with formula C 6 H 7 N. 2-Picoline is a colorless liquid that has an unpleasant odor similar to pyridine. It is mainly used to make vinylpyridine and the agrichemical nitrapyrin .

  3. Picoline - Wikipedia

    en.wikipedia.org/wiki/Picoline

    He recognized the acid from β–picoline as Nicotinsäure (nicotinic acid or "niacin"), [12] which Weidel had discovered in 1873. [13] When Weidel decarboxylated the carboxylic acid of each isomer – by dry distilling its calcium salt with calcium oxide – the reaction yielded pyridine, thus showing that picoline was a mixture of three ...

  4. Picolinic acid - Wikipedia

    en.wikipedia.org/wiki/Picolinic_acid

    Picolinic acid is an organic compound with the formula NC 5 H 4 CO 2 H. It is a derivative of pyridine with a carboxylic acid (COOH) substituent at the 2-position. It is an isomer of nicotinic acid and isonicotinic acid , which have the carboxyl side chain at the 3- and 4-positions, respectively.

  5. Protodeboronation - Wikipedia

    en.wikipedia.org/wiki/Protodeboronation

    Basic heteroaromatic boronic acids (boronic acids that contain a basic nitrogen atom, such as 2-pyridine boronic acid) display additional protodeboronation mechanisms. [4] A key finding shows the speciation of basic heteroaromatic boronic acids to be analogous to that of simple amino acids , with zwitterionic species forming under neutral pH ...

  6. Boronic acid - Wikipedia

    en.wikipedia.org/wiki/Boronic_acid

    Boronic acids are known to bind to active site serines and are part of inhibitors for porcine pancreatic lipase, [2] subtilisin [3] and the protease Kex2. [4] Furthermore, boronic acid derivatives constitute a class of inhibitors for human acyl-protein thioesterase 1 and 2, which are cancer drug targets within the Ras cycle. [5]

  7. Borylation - Wikipedia

    en.wikipedia.org/wiki/Borylation

    [2] [3] Boronic acids, and boronic esters are common boryl groups incorporated into organic molecules through borylation reactions. [4] Boronic acids are trivalent boron-containing organic compounds that possess one alkyl substituent and two hydroxyl groups. Similarly, boronic esters possess one alkyl substituent and two ester groups.

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  9. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    One example is [B 12 (CH 3) 12] 2-and its radical derivative [B 12 (CH 3) 12] −. [14] Related cluster compounds with carbon vertices are carboranes; the best known is orthocarborane, C 2 B 10 H 12. Carboranes have few commercial applications. Anionic derivatives such as [C 2 B 9 H 11] 2−, called dicarbollides, ligate similarly to ...