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  2. Phenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylboronic_acid

    Phenylboronic acid or benzeneboronic acid, abbreviated as PhB(OH) 2 where Ph is the phenyl group C 6 H 5 - and B(OH) 2 is a boronic acid containing a phenyl substituent and two hydroxyl groups attached to boron. Phenylboronic acid is a white powder and is commonly used in organic synthesis.

  3. Benzoyl group - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_group

    Benzoyl esters and amides are common in organic chemistry. The esters are used as a protecting groups in organic synthesis, [4] which can be easily removed by hydrolysis in dilute basic solution. Benzoyl-β-D-glucoside is a natural substance that can be found in Pteris ensiformis.

  4. 4-Formylphenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/4-Formylphenylboronic_acid

    4-Formylphenyl boronic acid crystallizes in colorless needles [1] or is obtained as an odorless, whitish powder, which dissolves little in cold but better in hot water. The compound is quite stable [3] and readily forms dimers and cyclic trimeric anhydrides, which complicate purification and tend to protodeboronize, a secondary reaction that occurs frequently in the Suzuki coupling, with ...

  5. Neopentyl glycol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_glycol

    Similarly it gives boronic acid esters, which can be useful in the cross coupling reactions. [3] [4] A condensation reaction of neopentyl glycol with 2,6-di-tert-butylphenol gives CGP-7930. Neopentyl glycol is a precursor to Neopentyl glycol diglycidyl ether. The sequence begins with alkylation with epichlorohydrin using a Lewis acid catalyst.

  6. 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]

  7. Organotrifluoroborate - Wikipedia

    en.wikipedia.org/wiki/Organotrifluoroborate

    Organotrifluoroborates are tolerant of air and moisture [1] and are easy to handle and purify. [2] They are often used in organic synthesis as alternatives to boronic acids (RB(OH) 2), boronate esters (RB(OR′) 2), and organoboranes (R 3 B), particularly for Suzuki-Miyaura coupling. [3] [4]

  8. Bis(pinacolato)diboron - Wikipedia

    en.wikipedia.org/wiki/Bis(pinacolato)diboron

    The B-B bond adds across alkenes and alkynes to give the 1,2-diborylated alkanes and alkenes. Using various organorhodium or organoiridium catalysts, it can also be installed onto saturated hydrocarbons: [3] CH 3 (CH 2) 6 CH 3 + [pinB] 2 → pinBH + CH 3 (CH 2) 7 Bpin. These reactions proceed via boryl complexes. Bis(pinacolato)diboron can also ...

  9. Dibromo neopentyl glycol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Dibromo_neopentyl_glycol...

    Dibromo neopentyl glycol diglycidyl ether is a brominated version of neopentyl glycol diglycidyl ether. It is an aliphatic organic chemical in the glycidyl ether family that is used in epoxy resin formulations. It has the molecular formula C 11 H 18 Br 2 O 4