(SYN)-1-[(4S,5R)-5-[(S)-2-(BENZYLOXYMETHOXY)-3-METHYLBUTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER
Compound with spectra: 1 NMR
![(SYN)-1-[(4S,5R)-5-[(S)-2-(BENZYLOXYMETHOXY)-3-METHYLBUTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER](/api/compound/BXjZZZlvVEw.png?ph=true&h=300&w=458 "(SYN)-1-[(4S,5R)-5-[(S)-2-(BENZYLOXYMETHOXY)-3-METHYLBUTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER")
| SpectraBase Compound ID | BXjZZZlvVEw |
|---|---|
| InChI | InChI=1S/C23H29BO5/c1-17(2)21(27-16-26-15-19-10-6-4-7-11-19)14-22-23(18(3)25)29-24(28-22)20-12-8-5-9-13-20/h4-13,17,21-23H,14-16H2,1-3H3/t21-,22+,23+/m0/s1 |
| InChIKey | OPYSCWSPLLPZBI-YTFSRNRJSA-N |
| Mol Weight | 396.3 g/mol |
| Molecular Formula | C23H29BO5 |
| Exact Mass | 396.210804 g/mol |
| Enantiomer InChIKey | OPYSCWSPLLPZBI-VJBWXMMDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(ANTI)-1-[(4R,5S)-5-[(R)-2-(BENZYLOXYMETHOXY)-PENTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER
(SYN)-1-[(4S,5R)-5-[(R)-2-(BENZYLOXYMETHOXY)-PENTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER
THREITOL, 1,3-DI-O-BENZOYL-2,4-O-(PHENYLBORANDIYL)-
[(4R,5R)-2-phenyl-5-(phenylcarbonyloxy)-1,3,2-dioxaborinan-4-yl]methyl benzoate
RIBOPYRANOSIDE, METHYL, CYCLIC 2,4-BENZENEBORONATE, beta-D-
6-Methoxy-3-phenyl-2,4,7-trioxa-3-borabicyclo[3.3.1]nonan-9-ol
2-(CYCLOHEXYLAMINO)-2-OXO-1-PHENYLETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZOATE
(4S,5R)-2,4,5-triphenyl-1,3,2-dioxaborinane
trans-2,4,5-Triphenyl-1,3-dioxa-2-boracyclohexane
| Title | Journal or Book | Year |
|---|---|---|
| Stereocontrolled Synthesis of 1,3,5-Triols by an Iteration of Asymmetric Dihydroxylation and Deoxygenation | European Journal of Organic Chemistry | 2010 |