(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-ETHYL-(IODOMETHYL)-ZINC
Compound with spectra: 1 NMR
![(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-ETHYL-(IODOMETHYL)-ZINC](/api/compound/C6hxf2GZQ1a.png?ph=true&h=300&w=458 "(R)-(1L,2L,3U,4U)-2,3-DIMETHOXY-4,7,7-TRIMETHYLBICYCLO-[2.2.1]-HEPTANE-ETHYL-(IODOMETHYL)-ZINC")
| SpectraBase Compound ID | C6hxf2GZQ1a |
|---|---|
| InChI | InChI=1S/C12H22O2.C2H5.CH2I.Zn/c1-11(2)8-6-7-12(11,3)10(14-5)9(8)13-4;2*1-2;/h8-10H,6-7H2,1-5H3;1H2,2H3;1H2;/t8-,9-,10-,12+;;;/m1.../s1 |
| InChIKey | LEJJURSKLOEVIR-LFXSUNLRSA-N |
| Mol Weight | 433.68 g/mol |
| Molecular Formula | C15H29IO2Zn |
| Exact Mass | 432.050367 g/mol |
| Enantiomer InChIKey | LEJJURSKLOEVIR-JJLGXLETSA-N |
| 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-ZINC-IODIDE
1-[1-(20-OXOPREGNA-3,5-DIEN-3-YL)-VINYL]-2-AZEPANONE
METHYL-HISPANONATE
(1R*,2R*,4S*,2'R*)-1-Propyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-norbornen-2,2'-sultone
CUDRATRICUSXANTHONE_M;1,3,6,7-TETRAHYDROXY-4-(1,1-DIMETHYLALLYL)-8-(3-HYDROXY-3-METHYLBUTYL)-XANTHONE
(2R,3R)-6-butyl-2-[(3S,8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxidanyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]decane-2,3,6-triol
6β-Hydroxyprogesterone acetate
17a-Hydroxy-20-hydroxymethyl-pregna-4,20-dien-3-one
16-[(1,3-dimethyl-1H-pyrazol-4-yl)methylene]androst-5-ene-3,17-diol
| Title | Journal or Book | Year |
|---|---|---|
| Enantioselective Cyclopropanation of Allylic Alcohols. The Effect of Zinc Iodide | The Journal of Organic Chemistry | 1997 |