(1R,6R,7S,8R,9S)-9-METHYL-8-PHENYL-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-4-AZA-3,5-DIOXATRICYCLO-[5.2.1.0(4,9)]-DECANE
Compound with spectra: 1 NMR
![(1R,6R,7S,8R,9S)-9-METHYL-8-PHENYL-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-4-AZA-3,5-DIOXATRICYCLO-[5.2.1.0(4,9)]-DECANE](/api/compound/HwgyLDeH6WF.png?ph=true&h=300&w=458 "(1R,6R,7S,8R,9S)-9-METHYL-8-PHENYL-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-4-AZA-3,5-DIOXATRICYCLO-[5.2.1.0(4,9)]-DECANE")
| SpectraBase Compound ID | HwgyLDeH6WF |
|---|---|
| InChI | InChI=1S/C26H31NO3/c1-26-20-16-22(24(26)19-12-6-3-7-13-19)25(30-27(26)28-17-20)29-23-15-9-8-14-21(23)18-10-4-2-5-11-18/h2-7,10-13,20-25H,8-9,14-17H2,1H3/t20-,21-,22+,23+,24-,25-,26-/m0/s1 |
| InChIKey | GXMJJKHUQSNKNH-XMDZHUTCSA-N |
| Mol Weight | 405.54 g/mol |
| Molecular Formula | C26H31NO3 |
| Exact Mass | 405.230394 g/mol |
| Enantiomer InChIKey | GXMJJKHUQSNKNH-UBZGLVDWSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C6D6 |
#21;(2S,2AS,4AS,5S,6S,7AR,7BR)-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-OCTAHYDRO-7B-METHYL-1,7-DIOXA-7A-AZACYCLOPENT-[CD]-INDANE-2-CARBOXYLIC-ACID-METHYLESTER
SENBURISIDE-IV
CANDESALVONE_B_METHYLESTER
(1-R,2-R,3-S)-1-(4-HYDROXY-3,5-DIMETHOXYPHENYL)-6,7-METHYLENEDIOXY-8-METHOXY-1,2,3,4-TETRAHYDRONAPHTHALENE-2,3-DIMETHANOL-DIACETATE
2-benzyl-8-(3,4-dichlorophenyl)-1,3,4-trimethyl-2H-dipyrrolo[1,2-b:3,4-d]pyridazine
3-(3'-methylindol-2'-yl)-1-Dichloroacetyl-3-methylindole
1H-pyrazolo[3,4-b]pyridine, 4-(difluoromethyl)-6-(1-ethyl-3-methyl-1H-pyrazol-4-yl)-1-(2-fluorophenyl)-3-methyl-
methyl 2-({[3-bromo-5-(4-methoxyphenyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-2-yl]carbonyl}amino)-4-ethyl-5-methyl-3-thiophenecarboxylate
| Title | Journal or Book | Year |
|---|---|---|
| Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. Asymmetric Synthesis of Highly Functionalized Aminocyclopentanes Using the Bridged Mode (β-Tether) Process | The Journal of Organic Chemistry | 1998 |