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  2. Borane dimethylsulfide - Wikipedia

    en.wikipedia.org/wiki/Borane_dimethylsulfide

    Borane dimethylsulfide (BMS) is a chemical compound with the chemical formula BH 3 ·S(CH 3) 2. It is an adduct between borane molecule ( BH 3 ) and dimethyl sulfide molecule ( S(CH 3 ) 2 ). It is a complexed borane reagent that is used for hydroborations and reductions .

  3. 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]

  4. Borane–tetrahydrofuran - Wikipedia

    en.wikipedia.org/wiki/Borane–tetrahydrofuran

    Borane–tetrahydrofuran is an adduct derived from borane and tetrahydrofuran (THF). These solutions, which are colorless, are used for reductions and hydroboration, reactions that are useful in synthesis of organic compounds. A common alternative to BHF•THF is borane–dimethylsulfide, which has a longer shelf life and effects similar ...

  5. Corey–Itsuno reduction - Wikipedia

    en.wikipedia.org/wiki/Corey–Itsuno_reduction

    X-ray crystal structures and 11 B NMR spectroscopic analyses of the coordinated catalyst-borane complex 2 have provided support for this initial step. [5] [7] Subsequently, the endocyclic boron of the catalyst coordinates to the ketone at the sterically more accessible electron lone pair (i.e. the lone pair closer to the smaller substituent, Rs).

  6. Dimethyl sulfide - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfide

    It is used is for the production of borane dimethyl sulfide from diborane: [19] B 2 H 6 + 2 (CH 3) 2 S → 2 BH 3 ·S(CH 3) 2. Oxidation of dimethyl sulfide gives the solvent dimethyl sulfoxide. Further oxidation affords dimethyl sulfone. As illustrated above by the formation of its adduct with borane, dimethyl sulfide is a Lewis base.

  7. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    It is obtained by hydroboration of (−)‐α‐pinene with borane dimethyl sulfide. [7] Dialkylboranes are also rare for small alkyl groups. One common way of preparing them is the reduction of dialkylhalogenoboranes with metal hydrides. [8]

  8. Borane - Wikipedia

    en.wikipedia.org/wiki/Borane

    Borane(5) is the dihydrogen complex of borane. Its molecular formula is BH 5 or possibly BH 3 (η 2-H 2). [19] It is only stable at very low temperatures and its existence is confirmed in very low temperature. [20] [21] Borane(5) and methanium (CH 5 +) are isoelectronic. [22] Its conjugate base is the borohydride anion.

  9. Boron compounds - Wikipedia

    en.wikipedia.org/wiki/Boron_compounds

    These compounds do not occur in nature. Many of the boranes readily oxidise on contact with air, some violently. The parent member BH 3 is called borane, but it is known only in the gaseous state, and dimerises to form diborane, B 2 H 6. The larger boranes all consist of boron clusters that are polyhedral, some of which exist as isomers.