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  2. 4-Formylphenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/4-Formylphenylboronic_acid

    4-Formylphenylboronic acid (4-FPBA) is an organoboron compound with the formula (HO) 2 BC 6 H 4 CO 2 H. As a bifunctional molecule, it is used as a building block in the synthesis of other organic compounds.

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  5. You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  6. CBS catalyst - Wikipedia

    en.wikipedia.org/wiki/CBS_catalyst

    The general outline for the organic synthesis of a CBS catalyst is shown below. The first leg of the reaction sequence starts from the azeotropic dehydration of a boronic acid (1) such as one based on toluene to a boroxine (2). This boroxine reacts with the proline derivative (3d) to form the basic oxazaborolidine CBS catalyst (4).

  7. 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.

  8. Kulinkovich reaction - Wikipedia

    en.wikipedia.org/wiki/Kulinkovich_reaction

    Complex 4 obtained is a tetraalkyloxytitanium compound able to play a part similar to that of the starting tetraisopropyloxytitanate, which closes the catalytic cycle. At the end of the reaction, the product is mainly in the shape of the magnesium alcoholate 5 , giving the cyclopropanol after hydrolysis by the reaction medium.

  9. Seyferth–Gilbert homologation - Wikipedia

    en.wikipedia.org/wiki/Seyferth–Gilbert...

    Safe and scalable synthesis of alkynes from aldehydes Recently a safer and more scalable approach has been developed for the synthesis of alkynes from aldehydes. This protocol takes advantage of a stable sulfonyl azide, rather than tosyl azide, for the in situ generation of the Ohira−Bestmann reagent.