(1R,3S,6S)-6-[(E)-2-(TRIBUTYLSTANNYL)-ETHENYL]-1,5,5-TRIMETHYL-7-OXA-BICYCLO-[4.1.0]-HEPTAN-3-OL
Compound with spectra: 1 NMR
![(1R,3S,6S)-6-[(E)-2-(TRIBUTYLSTANNYL)-ETHENYL]-1,5,5-TRIMETHYL-7-OXA-BICYCLO-[4.1.0]-HEPTAN-3-OL](/api/compound/9FvcVquZ3wS.png?ph=true&h=300&w=458 "(1R,3S,6S)-6-[(E)-2-(TRIBUTYLSTANNYL)-ETHENYL]-1,5,5-TRIMETHYL-7-OXA-BICYCLO-[4.1.0]-HEPTAN-3-OL")
| SpectraBase Compound ID | 9FvcVquZ3wS |
|---|---|
| InChI | InChI=1S/C11H17O2.3C4H9.Sn/c1-5-11-9(2,3)6-8(12)7-10(11,4)13-11;3*1-3-4-2;/h1,5,8,12H,6-7H2,2-4H3;3*1,3-4H2,2H3;/t8-,10+,11-;;;;/m0..../s1 |
| InChIKey | DQKLCVHOHXWQRM-PPCMEYCYSA-N |
| Mol Weight | 471.3 g/mol |
| Molecular Formula | C23H44O2Sn |
| Exact Mass | 472.236333 g/mol |
| Enantiomer InChIKey | DQKLCVHOHXWQRM-WTRVLYBYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
7-Oxabicyclo[4.1.0]heptane, retinal deriv.
(1R,3S,6S)-6-[(1E,3E,5E,7E)-3,7-dimethyl-9-oxidanyl-nona-1,3,5,7-tetraenyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol
(9'Z,3S,5S,6R,3'S,5'S,6'R)-5,6:5',6'-Diepoxy-5,6,5',6'-tetrahydro-beta,beta-carotene-3,3'-diol
(3S,5R,6S,3'S,5'R,6'S)-13-CIS-VIOLAXANTHIN
(3S,5R,6S,3'S,5'R,6'S)-VIOLAXANTHIN
(1S,6R)-1,5,5-trimethyl-6-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethyl-1-cyclohexenyl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-7-oxabicyclo[4.1.0]heptane
.beta.,.beta.-Carotene, 5,6-epoxy-5,6-dihydro-
.beta.,.epsilon.-Carotene, 5,6-epoxy-5,6-dihydro-, (5S,6R,6'R)-
(3R,5S,6S,7E,9R)-5,6-DIHYDRO-5-HYDROXY-3,6-EPOXY-BETA-IONOL
CROTALIONOL-C
| Title | Journal or Book | Year |
|---|---|---|
| The Stille Reaction in the Synthesis of Carotenoid Butenolides: Synthesis of 6‘-epi-Peridinin | Organic Letters | 2005 |