(1R,3R,4S,5R,6S,7R)-5,6-(ISOPROPYLIDENEDIOXY)-3-METHOXY-2-OXABICYCLO-[2.2.1]-HEPTANE-7-ACETIC-ACID,ETHYLESTER
Compound with spectra: 1 NMR
![(1R,3R,4S,5R,6S,7R)-5,6-(ISOPROPYLIDENEDIOXY)-3-METHOXY-2-OXABICYCLO-[2.2.1]-HEPTANE-7-ACETIC-ACID,ETHYLESTER](/api/compound/DoxHpqDG8K3.png?ph=true&h=300&w=458 "(1R,3R,4S,5R,6S,7R)-5,6-(ISOPROPYLIDENEDIOXY)-3-METHOXY-2-OXABICYCLO-[2.2.1]-HEPTANE-7-ACETIC-ACID,ETHYLESTER")
| SpectraBase Compound ID | DoxHpqDG8K3 |
|---|---|
| InChI | InChI=1S/C14H22O6/c1-5-17-8(15)6-7-9-11-12(20-14(2,3)19-11)10(7)18-13(9)16-4/h7,9-13H,5-6H2,1-4H3/t7?,9-,10+,11+,12-,13+/m0/s1 |
| InChIKey | HCSFGRLYZLCYDZ-UKDGZIMKSA-N |
| Mol Weight | 286.32 g/mol |
| Molecular Formula | C14H22O6 |
| Exact Mass | 286.141638 g/mol |
| Enantiomer InChIKey | HCSFGRLYZLCYDZ-KPEPVWKFSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3aR,5R,5aS,8aS,8bR)-2,2,7,7-tetramethyl-5-(2,4,6-trimethylbenzyl)tetrahydro-3aH-bis[1,3]dioxolo[4,5-b:4',5'-d]pyran
(2S,2'S,3'R,4'R,5'R,6'R)-2-HYDROXY-2-[2'-(3',4',5',6'-DI-O-ISOPROPYLIDENE)-TETRAHYDROPYRANYL]-ACETIC-ACID-METHYLESTER
(2R,2'S,3'R,4'R,5'R,6'R)-2-HYDROXY-2-[2'-(3',4',5',6'-DI-O-ISOPROPYLIDENE)-TETRAHYDROPYRANYL]-ACETIC-ACID-METHYLESTER
1-(METHYL-2-O-BENZYL-4,6-O-BENZYLIDENE-3-DEOXY-ALPHA-D-ALTROPYRANOSID-3-YL)-4-PHENYL-BUT-3-YN-2-ONE
METHYL 2,3-O-ISOPROPYLIDENE-4-O-(2,3,4-TRI-O-ACETYL-BETA-D-XYLOPYRANOSYL)-ALPHA-L-RHAMNOPYRANOSIDE
(1R,5R,6S,7R,8S)-6-AZIDO-7,8-ISOPROPYLIDENE-DIOXY-2-OXABICYCLO-[3.3.0]-OCTAN-3-ONE
YSXGCABZBQXROW-LLJVEVAISA-N
PCKHREPDCQMYHX-DFILTRRMSA-N
2-Amino-3,7-anhydro-1,2-dideoxy-1-(diethylamino)-4,5;6,8-di-O-isopropylidene-D-erythro-L-gluco-octitol
NRRYXARMDIMXKT-ZQQMXMEDSA-N
| Title | Journal or Book | Year |
|---|---|---|
| Radical cyclization routes to bridged pyranosides as precursors of densely functionalized cycloalkanes | The Journal of Organic Chemistry | 1992 |