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  2. 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) Nicotinic acid (3-pyridinecarboxylic acid), also known as Niacin; Isonicotinic acid (4-pyridinecarboxylic acid)

  3. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    IUPAC name: Common name: Structural formula butanoic acid: butyric acid propanecarboxylic acid: CH 3 (CH 2) 2 COOH : 2-methylpropanoic acid: isobutyric acid isobutanoic acid

  4. Tris(pentafluorophenyl)borane - Wikipedia

    en.wikipedia.org/wiki/Tris(pentafluorophenyl)borane

    B(C 6 F 5) 3 forms a strong Lewis adduct with water, [5] which was shown to be a strong Brønsted acid having an acidity comparable to hydrochloric acid (in acetonitrile). [6] In consequence, even traces of moisture are able to deactivate B(C 6 F 5 ) 3 and remaining catalytic activity might only be due to the Brønsted acidity of the water adduct.

  5. 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]

  6. Protodeboronation - Wikipedia

    en.wikipedia.org/wiki/Protodeboronation

    This protocol has proved useful in the cross-coupling of some notoriously unstable boronic acids, such as the 2-pyridine boronic acid. [ 16 ] [ 17 ] This ensures that the boronic acid concentration is low during the cross-coupling reaction, which in turn minimises the potential for side reactions.

  7. Borylation - Wikipedia

    en.wikipedia.org/wiki/Borylation

    [5] B2pin2 and B2cat2. 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.

  8. Pyridinedicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Pyridinedicarboxylic_acid

    Pyridinedicarboxylic acid is a group of organic compounds which are dicarboxylic derivatives of pyridine. Pyridinedicarboxylic acid comes in several isomers: Quinolinic acid (2,3-pyridinedicarboxylic acid) Lutidinic acid (2,4-pyridinedicarboxylic acid) Isocinchomeronic acid (2,5-pyridinedicarboxylic acid) Dipicolinic acid (2,6 ...

  9. Borinic acid - Wikipedia

    en.wikipedia.org/wiki/Borinic_acid

    Hydrolysis then results in the boronic acid (R 2 BOH). [5] Trialkylborates [(RO) 3 B] or trialkoxyboroxine [(ROBO) 3] can be reduced to borinic acid by us of a Grignard reagent. Grignard reagents can also reduce a boronic ester [RB(OR') 2] to a borinic ester. [5] Bu 3 B + N2CHCOR → BuCH=C(R)OBBu 2 Bu 3 B + CH2=CHCOCH 3 → BuCH 2 CH=C(CH 3)OBBu 2

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