Alkylboranes
Alkylboranes are a class of organoboron compounds characterized by the presence of an alkyl group bonded to a boron atom. These materials are widely used in organic synthesis due to their unique reactivity and stability. Typically, alkylboranes possess a borane moiety, which can participate in various chemical reactions, including reductions, coupling reactions, and alkylation processes. Notably, the use of alkylboranes is often favored for their mild conditions, broad functional group tolerance, and high chemoselectivity. They are particularly valuable in pharmaceuticals, fine chemicals, and polymer synthesis industries where controlled transformations and mild reaction conditions are crucial.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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bromodimethylborane | 5158-50-9 | C2H6BBr |
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L-Selectride Solution (1.0M in THF) | 38721-52-7 | C12H27BLi |
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trihexylborane | 1188-92-7 | C18H39B |
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N-Selectride Solution (1.0M in THF) | 67276-04-4 | C12H27BNa |
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Lithium Triethylhydroborate Tetrahydrofuran Solution | 22560-16-3 | C6H15BLi |
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Borane, tripropyl- | 1116-61-6 | C9H21B |
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Borate(1-),triethylhydro-, sodium (1:1), (T-4)- | 17979-81-6 | C6H15BNa |
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Borane, tridodecyl- | 14245-38-6 | C36H75B |
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Tri-sec-butylborane | 1113-78-6 | C12H27B |
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Borane, (1,1,2-trimethylpropyl)- | 3688-24-2 | C6H13B |
Related Literature
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J. M. Granadino-Roldán,M. Fernández-Gómez,A. Navarro,T. Pe?a Ruiz,U. A. Jayasooriya Phys. Chem. Chem. Phys., 2004,6, 1133-1143
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James D. Kirkham,Patrick M. Delaney,George J. Ellames,Eleanor C. Row,Joseph P. A. Harrity Chem. Commun., 2010,46, 5154-5156
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