(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-ETHYL-ZINC-IODIDE
Compound with spectra: 1 NMR
![(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-ETHYL-ZINC-IODIDE](/api/compound/4cLB84fKRfA.png?ph=true&h=300&w=458 "(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-ETHYL-ZINC-IODIDE")
| SpectraBase Compound ID | 4cLB84fKRfA |
|---|---|
| InChI | InChI=1S/C12H22O2.C2H5.HI.Zn/c1-11(2)8-6-7-12(11,3)10(14-5)9(8)13-4;1-2;;/h8-10H,6-7H2,1-5H3;1H2,2H3;1H;/q;;;+1/p-1/t8-,9-,10-,12+;;;/m1.../s1 |
| InChIKey | WXZQQYXYKZZPMU-LFXSUNLRSA-M |
| Mol Weight | 419.65 g/mol |
| Molecular Formula | C14H27IO2Zn |
| Exact Mass | 418.034717 g/mol |
| Parent InChIKey | FXNJLZWGSNHJEQ-VJVGBEBFSA-M |
| Enantiomer InChIKey | WXZQQYXYKZZPMU-JJLGXLETSA-M |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-IODIDE;ISOMER-#-IODIDE;ISOMER-#1
(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-ETHYL-(IODOMETHYL)-ZINC
Euchrenone b(16)
Methyl ester fo (3.alpha.,5.beta.,7.beta.,12.alpha.)-3,12-bis(acetyloxy)-7-chlorocholan-24-oic acid
Androstane-11,17-dione, 3-[(trimethylsilyl)oxy]-, 17-[O-(phenylmethyl)oxime], (3.alpha.,5.alpha.)-
4a,5a-Dibromo-5a-cholestan-3-one
Parvixanthone I
trans-7-(1-(4-bromophenyl)vinyl)-4-methyl-3-phenyl-5-tosyl-4,5,6,7-tetrahydro[1,2,3]triazolo[1,5-a]pyrazine
cis-7-(1-(4-bromophenyl)vinyl)-4-methyl-3-phenyl-5-tosyl-4,5,6,7-tetrahydro[1,2,3]triazolo[1,5-a]pyrazine
ent-19-Hydroxygibberell-2,16-diene
| Title | Journal or Book | Year |
|---|---|---|
| Enantioselective Cyclopropanation of Allylic Alcohols. The Effect of Zinc Iodide | The Journal of Organic Chemistry | 1997 |