(3AR,4S)-4-(TRI-O-ACETYL-D-ERYTHRO-TRIOL-1-YL)-2-TOSYL-2,3,3A,4-TETRAHYDRO-1H-CYCLOPENTA-[C]-PYRROLE-5-ONE
Compound with spectra: 1 NMR
![(3AR,4S)-4-(TRI-O-ACETYL-D-ERYTHRO-TRIOL-1-YL)-2-TOSYL-2,3,3A,4-TETRAHYDRO-1H-CYCLOPENTA-[C]-PYRROLE-5-ONE](/api/compound/CTp7ik6jhWs.png?ph=true&h=300&w=458 "(3AR,4S)-4-(TRI-O-ACETYL-D-ERYTHRO-TRIOL-1-YL)-2-TOSYL-2,3,3A,4-TETRAHYDRO-1H-CYCLOPENTA-[C]-PYRROLE-5-ONE")
| SpectraBase Compound ID | CTp7ik6jhWs |
|---|---|
| InChI | InChI=1S/C23H27NO10S/c1-13-5-7-18(8-6-13)35(29,30)34-24-10-17-9-20(28)22(19(17)11-24)23(33-16(4)27)21(32-15(3)26)12-31-14(2)25/h5-9,19,21-23H,10-12H2,1-4H3/t19-,21-,22+,23+/m0/s1 |
| InChIKey | BZGUVMQOGFLGAT-KZKAQZJJSA-N |
| Mol Weight | 509.53 g/mol |
| Molecular Formula | C23H27NO10S |
| Exact Mass | 509.135567 g/mol |
| Enantiomer InChIKey | BZGUVMQOGFLGAT-LGKPFJOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3aS,4R)-4-(Tri-O-acetyl-D-erythro-triol-1-yl)-2-(tert-butoxycarbonylamine)-2,3,3a,4-tetrahydro-1H-cyclopenta[c]pyrrole-5-one
(3aR,4S)-4-(Tri-O-acetyl-D-erythro-triol-1-yl)-2-(tert-butoxycarbonylamine)-2,3,3a,4-tetrahydro-1H-cyclopenta[c]pyrrole-5-one
(3AR,4S)-4-(TRI-O-ACETYL-D-ERYTHRO-TRIOL-1-YL)-2-(TERT.-BUTYLOXYCARBONYLAMINE)-(2,3,3A,4-TETRAHYDRO)-1H-CYCLOPENTA-[C]-PYRROLE-5-ONE
(3AS,4R)-4-(TRI-O-ACETYL-D-ERYTHRO-TRIOL-1-YL)-2-(TERT.-BUTYLOXYCARBONYLAMINE)-(2,3,3A,4-TETRAHYDRO)-1H-CYCLOPENTA-[C]-PYRROLE-5-ONE
2',3',4',5',6'-pentakis(O-Acetyl)-aldehydo-D-galactose-[1-acetyl-1-(3"-ethyl-4"-oxoquinazolin-2"-yl)]-hydrazone
XBBLLENRTSUTSP-PEGIKPHUSA-N
(1S,3S,4R)-PARA-MENTHANE-3-YL-2,6-DI-O-(BETA-D-GLUCOPYRANOSYL)-BETA-D-GLUCOPYRANOSIDE-DECAACETATE
9,10-Anhydro-cumambrin A
CUMAMBRIN A,9,10-DEHYDRO
| Title | Journal or Book | Year |
|---|---|---|
|
Synthesis of Enantiopure 3-Azabicyclo[3.3.0]octen-7-one Derivatives via Intramolecular Pauson−Khand Cycloaddition Reaction Using Tri-O-acetyl- |
The Journal of Organic Chemistry | 2002 |