(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
Compound with spectra: 1 NMR
![(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](/api/compound/FyEScskjlaO.png?ph=true&h=300&w=458 "(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")
| SpectraBase Compound ID | FyEScskjlaO |
|---|---|
| InChI | InChI=1S/2C21H29NO9/c2*1-11(23)28-10-17(29-12(2)24)19(30-13(3)25)18-15-9-22(8-14(15)7-16(18)26)20(27)31-21(4,5)6/h2*7,15,17-19H,8-10H2,1-6H3/t2*15-,17-,18+,19-/m11/s1 |
| InChIKey | WARMKFTWRYCZCD-MXCJCTAXSA-N |
| Mol Weight | 878.92 g/mol |
| Molecular Formula | C42H58N2O18 |
| Exact Mass | 878.368463 g/mol |
| Enantiomer InChIKey | WARMKFTWRYCZCD-FSHZPGIISA-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-TOSYL-2,3,3A,4-TETRAHYDRO-1H-CYCLOPENTA-[C]-PYRROLE-5-ONE
(2S,3S)-3-benzyl-2-(4-bromophenyl)-2H-benzo[4,5]thiazolo[3,2-a]pyrimidin-4(3H)-one
3-[3',4'-Dimethoxy-.alpha.-R-(methoxymethoxy)benzyl]-4-[(trityloxy)methyl]-5-(3",4"-methylenedioxyphenyl)-tetrahydrofuran-2-one
DENDOCARBIN-D
2-Acetoxy-3-(diethylaminocarbonyl)-8,9-dimethoxy-2H-1,2,3,4,4a,10a-hexahydro-dibenzo[a,c]piperidine
1-(3,5-DI-O-BENZOYL-2-O-PHENOXYTHIO-CARBONYL-BETA-D-XYLOFURANOSYL)-URACILE
(1R,3R,5S,6R,7S,8Z)-6-ACETOXY-8-METHYL-5-(2',3'-DIACETOXY-1',5'-DIMETHYLHEX-4'-ENYL)-2-METHYLENEBICYClO-[5.3.0]-DEC-8-EN-3-OL
| 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 |