(R)-PINACOL-(1-PHENYLETHYL)-BORONATE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | IsyM2FlXkNC |
|---|---|
| InChI | InChI=1S/C14H21BO2/c1-11(12-9-7-6-8-10-12)15-16-13(2,3)14(4,5)17-15/h6-11H,1-5H3/t11-/m1/s1 |
| InChIKey | VNYHYPMNRXFAAP-LLVKDONJSA-N |
| Mol Weight | 232.1 g/mol |
| Molecular Formula | C14H21BO2 |
| Exact Mass | 232.16346 g/mol |
| Enantiomer InChIKey | VNYHYPMNRXFAAP-NSHDSACASA-N |
| Racemate InChIKey | VNYHYPMNRXFAAP-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-butanoate
Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-butanoate
2-cyclooct-4-en-1-yl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-(2-deuterio-2-phenyl-ethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
(Z)-4,4,5,5-tetramethyl-2-(1-phenylprop-1-en-2-yl)-1,3,2-dioxaborolane
2-(4-(tert-Butyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-(3-Dibenzylaminopropan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
4-(1-methyl)propylphenylboronic acid pinacol ester
| Title | Journal or Book | Year |
|---|---|---|
| Catalytic Asymmetric Hydrocarboxylation and Hydrohydroxymethylation. A Two-Step Approach to the Enantioselective Functionalization of Vinylarenes | The Journal of Organic Chemistry | 1999 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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