[(R)-4-(TERT.-BUTYLDIMETHYLSILYLOXY)-2,6,6-TRIMETHYLCYCLOHEX-1-ENYL]-METHANOL
Compound with spectra: 1 NMR
![[(R)-4-(TERT.-BUTYLDIMETHYLSILYLOXY)-2,6,6-TRIMETHYLCYCLOHEX-1-ENYL]-METHANOL](/api/compound/BdDEhuitR3D.png?ph=true&h=300&w=458 "[(R)-4-(TERT.-BUTYLDIMETHYLSILYLOXY)-2,6,6-TRIMETHYLCYCLOHEX-1-ENYL]-METHANOL")
| SpectraBase Compound ID | BdDEhuitR3D |
|---|---|
| InChI | InChI=1S/C16H32O2Si/c1-12-9-13(10-16(5,6)14(12)11-17)18-19(7,8)15(2,3)4/h13,17H,9-11H2,1-8H3/t13-/m1/s1 |
| InChIKey | FPEHVLBHYQJKMO-CYBMUJFWSA-N |
| Mol Weight | 284.5 g/mol |
| Molecular Formula | C16H32O2Si |
| Exact Mass | 284.217157 g/mol |
| Enantiomer InChIKey | FPEHVLBHYQJKMO-ZDUSSCGKSA-N |
| Racemate InChIKey | FPEHVLBHYQJKMO-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3,3'-Dimethoxy.beta.-carotene
Crocusatin H
(E)-METHYL-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-7-(3-METHOXYPROPYL)-10-METHYL-2-(NITROMETHYL)-UNDECA-7,9-DIENOATE;MAJOR-DIASTEREOMER
(1E,3R,4R,5E,7S,9S,11S)-9-((tert-Butyldimethylsilyl)oxy)-1-(dimethyl(phenyl)silyl)-4,7,11-trimethyl-13-((triethylsilyl)oxy)trideca-1,5-dien-3-ol
[(4R,6S)-4-[tert-butyl(dimethyl)silyl]oxy-6-fluoranyl-cyclohexen-1-yl]methyl 2-phenylselanylethanoate
2-[(1S,3S,5R)-5-[tert-butyl(dimethyl)silyl]oxy-3-hydroxy-2-methylene-cyclohexyl]acetic acid methyl ester
6S,8S,10S,13R,14R,E)-8-((tert-Butyldimethylsilyl)oxy)-14-((E)-2-iodovinyl)-6,10,13-trimethyloxacyclotetradec-11-en-3-yn-2-one
tert-Butyl(((5S,7S,9S,10E,12R,13R,14E)-15-iodo-13-((4-methoxybenzyl)oxy)-5,9,12-trimethylpentadeca-10,14- dien-2-yn-7-yl)oxy)dimethylsilane
(1R,2R)-4-[(3R)-3-Hydroxybutyl]-3,3,5-trimethylcyclohex-4-ene-1,2-diol
(2R,3R,9R)-2,3,9-TRIHYDROXY-MEGASTIGMAN-5-ENE
| Title | Journal or Book | Year |
|---|---|---|
| The Stille Reaction in the Synthesis of Carotenoid Butenolides: Synthesis of 6‘-epi-Peridinin | Organic Letters | 2005 |