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  2. Triethylborane - Wikipedia

    en.wikipedia.org/wiki/Triethylborane

    [7] [8] The Et stands for ethyl group CH 3 CH 2 −. It is used in the Barton–McCombie deoxygenation reaction for deoxygenation of alcohols. In combination with lithium tri-tert-butoxyaluminum hydride it cleaves ethers. For example, THF is converted, after hydrolysis, to 1-butanol. It also promotes certain variants of the Reformatskii ...

  3. 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 ...

  4. Triethyloxonium tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Triethyloxonium_tetrafluo...

    where the Et stands for ethyl. The trimethyloxonium salt is available from dimethyl ether via an analogous route. [6] These salts do not have long shelf-lives at room temperature. They degrade by hydrolysis: [Et 3 O] + [BF 4] − + H 2 O → Et 2 O + EtOH + H + [BF 4] −. The propensity of trialkyloxonium salts for alkyl-exchange can be ...

  5. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    Bis(norbornyl)borane and 9-BBN are often hydroboration reagents for this reason — only the hydroborated olefin is likely to migrate upon nucleophilic activation. Migration retains configuration at the migrant carbon [ 33 ] and inverts it at the (presumably sp 3 -hybridized ) terminus. [ 34 ]

  6. Borylation - Wikipedia

    en.wikipedia.org/wiki/Borylation

    They found out that the chiral amino alcohols would react with borane to form aloxyl-amine-borane complexes. The complexes are proposed to contain a relatively rigid five member-ring system which makes them thermal and hydrolytic stable and soluble in a wide variety of protic and aprotic solvents.

  7. Triethyl borate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_borate

    Triethyl borate is a colorless liquid with the formula B(OCH 2 CH 3) 3.It is an ester of boric acid and ethanol.It has few applications. [1]It is a weak Lewis acid (AN = 17 as measured by the Gutmann–Beckett method). [2]

  8. 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]

  9. Borate - Wikipedia

    en.wikipedia.org/wiki/Borate

    Borate ions occur, alone or with other anions, in many borate and borosilicate minerals such as borax, boracite, ulexite (boronatrocalcite) and colemanite.Borates also occur in seawater, where they make an important contribution to the absorption of low frequency sound in seawater.