(1S,4S,5S,8S,9S)-9-[4'-(HEPT-6''-YN-YL)-1H-1',2',3'-TRIAZOL-1'-YL]-4-(HYDROXYMETHYL)-3,3-DIMETHYL-2,6-DIOXA-BICYCLO-[3.2.2]-NONAN-8-OL
Compound with spectra: 1 NMR
![(1S,4S,5S,8S,9S)-9-[4'-(HEPT-6''-YN-YL)-1H-1',2',3'-TRIAZOL-1'-YL]-4-(HYDROXYMETHYL)-3,3-DIMETHYL-2,6-DIOXA-BICYCLO-[3.2.2]-NONAN-8-OL](/api/compound/F0L3ZkZAgpI.png?ph=true&h=300&w=458 "(1S,4S,5S,8S,9S)-9-[4'-(HEPT-6''-YN-YL)-1H-1',2',3'-TRIAZOL-1'-YL]-4-(HYDROXYMETHYL)-3,3-DIMETHYL-2,6-DIOXA-BICYCLO-[3.2.2]-NONAN-8-OL")
| SpectraBase Compound ID | F0L3ZkZAgpI |
|---|---|
| InChI | InChI=1S/C19H29N3O4/c1-4-5-6-7-8-9-13-10-22(21-20-13)16-17(24)15-12-25-18(16)14(11-23)19(2,3)26-15/h1,10,14-18,23-24H,5-9,11-12H2,2-3H3/t14-,15-,16-,17+,18-/m0/s1 |
| InChIKey | PDFPGBHGOJCCCC-TXTZMMAHSA-N |
| Mol Weight | 363.46 g/mol |
| Molecular Formula | C19H29N3O4 |
| Exact Mass | 363.215806 g/mol |
| Enantiomer InChIKey | PDFPGBHGOJCCCC-HSFUPAIVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
KESAOQNOWUTRIH-IECFSIQFSA-N
GUCSTIGJWALRPV-HOKCYDHUSA-N
#24;(2S,3S,4R,5S,6S)-6-(HYDROXYMETHYL)-7,7-DIMETHYL-4-[4'-(PENT-4''-YN-YL)-1H-1',2',3'-TRIAZOL-1'-YL]-2-[[4'-(PENT-4''-YN-YL)-1H-1',2',3'-TRIAZOL-1'-YL]-METHYL
(1S,2S,3R,4R,6S)-4-(ACETOXYMETHYL)-6-(4-PENTYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE
QNNLHEVWPUVESR-PLACYPQZSA-N
(1R,3R,4S,5R) 4-Acetoxy-3-benzyloxy-5-(1,2-diacetoxyethyl)-6,7,8-triazabicyclo[4.3.0.]non-1(9),7-dien
(1R,2S,3R,4R)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-2,3-ISOPROPYLIDENE-DIOXY-1-(4-METHOXYCARBONYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOPENTANE
(1R,2S,3R,4R)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-2,3-ISOPROPYLIDENE-DIOXY-1-(4-PHENYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOPENTANE
(1R,2S,3R,4R)-1-[4-(ACETOXYMETHYL)-1H-1,2,3-TRIAZOL-1-YL]-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-2,3-ISOPROPYLIDENE-DIOXY-CYCLOPENTANE
2-(.alpha.-Benzyloxy)-4-acetyl-12-phenyl-1-aza-1,6,9,11-tetraoxatricyclo[8.4.3.1(9,13).0(3,7)]tridecane
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of Di- and Trivalent Carbohydrate Mimetics with Oxepane Substructure by Employing Copper-Catalyzed [3+2] Cycloadditions of Alkynes with Azidooxepanes | European Journal of Organic Chemistry | 2014 |