METHYL-(3S,7AS)-3-TERT.-BUTYL-7-[(1R)-1-HYDROXYBUTYL]-5-OXO-1H-PYRROLO-[1,2-C]-[1,3]-OXAZOLE-7A-(5H)-CARBOXYLATE
Compound with spectra: 1 NMR
![METHYL-(3S,7AS)-3-TERT.-BUTYL-7-[(1R)-1-HYDROXYBUTYL]-5-OXO-1H-PYRROLO-[1,2-C]-[1,3]-OXAZOLE-7A-(5H)-CARBOXYLATE](/api/compound/4ZqHG1d9D1Z.png?ph=true&h=300&w=458 "METHYL-(3S,7AS)-3-TERT.-BUTYL-7-[(1R)-1-HYDROXYBUTYL]-5-OXO-1H-PYRROLO-[1,2-C]-[1,3]-OXAZOLE-7A-(5H)-CARBOXYLATE")
| SpectraBase Compound ID | 4ZqHG1d9D1Z |
|---|---|
| InChI | InChI=1S/C16H25NO5/c1-6-7-11(18)10-8-12(19)17-13(15(2,3)4)22-9-16(10,17)14(20)21-5/h8,11,13,18H,6-7,9H2,1-5H3/t11-,13-,16-/m0/s1 |
| InChIKey | IGTSSZCDYRMBNT-RBOXIYTFSA-N |
| Mol Weight | 311.38 g/mol |
| Molecular Formula | C16H25NO5 |
| Exact Mass | 311.173273 g/mol |
| Enantiomer InChIKey | IGTSSZCDYRMBNT-AXAPSJFSSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2-[4-(6,6-dimethyl-8-oxo-4,5,6,7,8,9-hexahydro[1,2,4]triazolo[5,1-b]quinazolin-9-yl)-2-methoxyphenoxy]acetamide
4-GERANYL-6-(2,6-DIMETHYLHEPTA-1,5-DIENYL)-2-HYDROXY-6-H-BENZO-[C]-CHROMENE-7,10-DIONE
(3R,6S,7aR)-3-tert-butyl-6-hydroxy-5,7-diketo-6-methyl-1,3-dihydropyrrolo[1,2-c]oxazole-7a-carboxylic acid methyl ester
(2R,5R,7S)-2-TERT.-BUTYL-7-HYDROXY-5-METHOXYCARBONYL-7-METHYL-6,8-DIOXO-1-AZA-3-OXABICYClO-[3.3.0]-OCTANE
24-BETA-ETHYL-7-BETA-METHOXY-24-BETA-ETHYL-CHOLEST-5-ENE;SCHLEICHEOL-1
(3S,7R,8S,9S,10R,13R,14S,17R)-17-[(1R,4R)-4-ethyl-1,5-dimethyl-hexyl]-7-methoxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
7-BETA-METHOXYSTIGMAST-5-EN-3-BETA-OL
9-(2-chlorophenyl)-6,6-dimethyl-5,6,7,9-tetrahydro[1,2,4]triazolo[5,1-b]quinazolin-8(4H)-one
GUSANLUNG_A
2a,6b-Dibromo-cholest-4-en-3-one
| Title | Journal or Book | Year |
|---|---|---|
| The Preparation of Nonracemic Secondary α-(Carbamoyloxy)alkylzinc and Copper Reagents. A Versatile Approach to Enantioenriched Alcohols | Organic Letters | 2001 |