(1R,6S,7S,8R,9S)-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,6S,7S,8R,9S)-8-PHENYL-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-4-AZA-3,5-DIOXATRICYCLO-[5.2.1.0(4,9)]-DECANE](/api/compound/KZYJ6uxI4T8.png?ph=true&h=300&w=458 "(1R,6S,7S,8R,9S)-8-PHENYL-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-4-AZA-3,5-DIOXATRICYCLO-[5.2.1.0(4,9)]-DECANE")
| SpectraBase Compound ID | KZYJ6uxI4T8 |
|---|---|
| InChI | InChI=1S/C25H29NO3/c1-3-9-17(10-4-1)20-13-7-8-14-22(20)28-25-21-15-19-16-27-26(29-25)24(19)23(21)18-11-5-2-6-12-18/h1-6,9-12,19-25H,7-8,13-16H2/t19-,20+,21-,22-,23-,24+,25-/m1/s1 |
| InChIKey | OQBDWYWFARAKDH-OPVIGOKSSA-N |
| Mol Weight | 391.51 g/mol |
| Molecular Formula | C25H29NO3 |
| Exact Mass | 391.214744 g/mol |
| Enantiomer InChIKey | OQBDWYWFARAKDH-JRIVBUFDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C6D6 |
METHYL-(2S,2AS,6AS,9S)-9-[(1R,2S)-2-PHENYLCYCLOHEXYLOXY]-1,10-DIOXA-10A-AZACYCLOHEX-[C]-INDENE-2-CARBOXYLATE
GLOMERATOSE-D;3-O-[(E)-3,4,5-TRIMETHOXYCINNAMOYL]-BETA-D-FRUCTOFURANOSYL-(2->1)-[3-O-(E)-3,4,5-TRIMETHOXYCINNAMOYL]-ALPHA-D-GLUCOPYRANOSIDE
3a-(4-Chloro-phenyl)-3,3,6,6-tetramethyl-tetrahydro-furo[3,2-b]furan-2,5-dione
Amoenolide A - 19-acetate
BUDDLENOL_A
4-(methoxymethyl)-6-methyl-3-[(2-piperidinoacetyl)amino]thieno[2,3-b]pyridine-2-carboxylic acid ethyl ester
DIOSFEBOSIDE_B
WAHLENBERGIOSIDE-PERACETATE
.alpha.-Estradiol diacetate
1-Anilino-N-(4-chloro-phenyl)-2-methyl-4,5-diphenyl-3-pyrrolecarboxamide
| 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 |