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  2. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    Structure of a rare monomeric boron hydride, R = i-Pr. [4] The most-studied class of organoboron compounds has the formula BR n H 3−n. These compounds are catalysts, reagents, and synthetic intermediates. The trialkyl and triaryl derivatives feature a trigonal-planar boron center that is typically only weakly Lewis acidic.

  3. Hydroboration–oxidation reaction - Wikipedia

    en.wikipedia.org/wiki/Hydroboration–oxidation...

    The boron reagent is converted to boric acid. The reaction was originally described by H.C. Brown in 1957 for the conversion of 1-hexene into 1-hexanol. [3] Hexanol synthesis. Knowing that the group containing the boron will be replaced by a hydroxyl group, it can be seen that the initial hydroboration step determines the regioselectivity.

  4. Hydroboration - Wikipedia

    en.wikipedia.org/wiki/Hydroboration

    Borane dimethylsulfide (BMS) is a complexed borane reagent that is widely used for hydroborations. [4] Much of the original work on hydroboration employed diborane as a source of BH 3. Usually however, borane dimethylsulfide complex BH 3 S(CH 3) 2 (BMS) is used instead. [5] It can be obtained in highly concentrated forms. [6]

  5. Bakthan Singaram - Wikipedia

    en.wikipedia.org/wiki/Bakthan_Singaram

    Singaram also worked in and directed the laboratory of Nobel Prize-winning chemist Herbert Brown, who shared the 1979 Nobel prize in chemistry 1979 with Georg Wittig "for their development of the use of boron- and phosphorus-containing compounds, respectively, into important reagents in organic synthesis". [1]

  6. Borylation - Wikipedia

    en.wikipedia.org/wiki/Borylation

    The origin of selectivity for aliphatic C–H borylation using rhodium catalysts was probed using a type of mechanistic study called hydrogen–deuterium exchange. H/D exchanged showed that regioselectivity of the overall process shown below results from selective cleavage of primary over secondary C–H bonds and selective functionalization of ...

  7. Trimethyl borate - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_borate

    It is a useful reagent in organic synthesis, as a precursor to boronic acids, which are used in Suzuki couplings. These boronic acids are prepared via reaction of the trimethyl borate with Grignard reagents followed by hydrolysis:. [3] [4] ArMgBr + B(OCH 3) 3 → MgBrOCH 3 + ArB(OCH 3) 2 ArB(OCH 3) 2 + 2 H 2 O → ArB(OH) 2 + 2 HOCH 3

  8. Boranes - Wikipedia

    en.wikipedia.org/wiki/Boranes

    A borane is a compound with the formula BR x H y although examples include multi-boron derivatives. A large family of boron hydride clusters is also known. In addition to some applications in organic chemistry , the boranes have attracted much attention as they exhibit structures and bonding that differs strongly from the patterns seen in ...

  9. Organozinc chemistry - Wikipedia

    en.wikipedia.org/wiki/Organozinc_chemistry

    The two most common zinc functional group interconversion reactions are with halides and boron, which is catalyzed by copper iodide (CuI) or base. The boron intermediate is synthesized by an initial hydroboration reaction followed by treatment with diethyl zinc. This synthesis shows the utility of organozinc reagents by displaying high ...