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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 ...

  3. Protodeboronation - Wikipedia

    en.wikipedia.org/wiki/Protodeboronation

    Protodeboronation is a well-known undesired side reaction, and frequently associated with metal-catalysed coupling reactions that utilise boronic acids (see Suzuki reaction). [1] For a given boronic acid, the propensity to undergo protodeboronation is highly variable and dependent on various factors, such as the reaction conditions employed and ...

  4. 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]

  5. 4-Formylphenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/4-Formylphenylboronic_acid

    4-Formylphenyl boronic acid crystallizes in colorless needles [2] or is obtained as an odorless, whitish powder, which dissolves little in cold but better in hot water. The compound is quite stable [4] 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 ...

  6. tert-Butyloxycarbonyl protecting group - Wikipedia

    en.wikipedia.org/wiki/Tert-butyloxycarbonyl...

    The tert-butyloxycarbonyl protecting group or tert-butoxycarbonyl protecting group [1] (BOC group) is an acid-labile protecting group used in organic synthesis. The BOC group can be added to amines under aqueous conditions using di- tert -butyl dicarbonate in the presence of a base such as sodium hydroxide :

  7. 1-Boc-4-AP - Wikipedia

    en.wikipedia.org/wiki/1-Boc-4-AP

    1-Boc-4-AP (tert-butyl 4-(phenylamino)piperidine-1-carboxylate) is a compound used as an intermediate in the manufacture of fentanyl, as well as various related derivatives such as butyrylfentanyl, furanylfentanyl, benzylfentanyl and homofentanyl, among others.

  8. Jennifer Lopez Will Keep 8.5-Carat Green Diamond ... - AOL

    www.aol.com/lifestyle/jennifer-lopez-keep-8-5...

    Jennifer Lopez will keep her diamond engagement ring in her divorce settlement with Ben Affleck. Affleck, 52, proposed to Lopez, 53, with an 8.5-carat green diamond engagement ring after they ...

  9. 3-Aminobiphenyl - Wikipedia

    en.wikipedia.org/wiki/3-Aminobiphenyl

    3-Aminobiphenyl is an organic compound with the formula C 6 H 5 C 6 H 4 NH 2. It is one of three monoamine derivatives of biphenyl. It is a colorless solid, although aged samples can appear colored. It is obtained from 3-bromoaniline and phenylboronic acid by Suzuki coupling. [1]