(2R,5R)-2-TERT.-BUTYL-5-METHOXYCARBONYL-7-METHYL-6,8-DIOXO-1-AZA-3-OXABICYClO-[3.3.0]-OCTANE;MINOR-ENOL-TAUTOMERE
Compound with spectra: 1 NMR
![(2R,5R)-2-TERT.-BUTYL-5-METHOXYCARBONYL-7-METHYL-6,8-DIOXO-1-AZA-3-OXABICYClO-[3.3.0]-OCTANE;MINOR-ENOL-TAUTOMERE](/api/compound/De58YtV0yWg.png?ph=true&h=300&w=458 "(2R,5R)-2-TERT.-BUTYL-5-METHOXYCARBONYL-7-METHYL-6,8-DIOXO-1-AZA-3-OXABICYClO-[3.3.0]-OCTANE;MINOR-ENOL-TAUTOMERE")
| SpectraBase Compound ID | De58YtV0yWg |
|---|---|
| InChI | InChI=1S/C13H19NO5/c1-7-8(15)13(11(17)18-5)6-19-10(12(2,3)4)14(13)9(7)16/h10,15H,6H2,1-5H3/t10-,13-/m0/s1 |
| InChIKey | KATOFSQFUYEKFD-GWCFXTLKSA-N |
| Mol Weight | 269.3 g/mol |
| Molecular Formula | C13H19NO5 |
| Exact Mass | 269.126323 g/mol |
| Enantiomer InChIKey | KATOFSQFUYEKFD-ZWNOBZJWSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3S,7aR)-6,6-Dibenzyl-3-tert-butyl-1,6,7,7a-tetrahydro-5-oxopyrrolo[1,2-c]oxazolidine-7a-carboxylic acid 7a-methyl ester
(3R,7S,7aR)-7-acetoxy-3-tert-butyl-5-keto-1,3,6,7-tetrahydropyrrolo[1,2-c]oxazole-7a-carboxylic acid methyl ester
NPLHCGRFPLFETM-UXJNMKMCSA-N
16 HYDROXY-3,4B-EPOXY-5B,10B-cis-17A,20A-CLERODA-15-OL
ENT-3-BETA,4-BETA-EPOXY-ClEROD-13E-EN-15-OL
ethyl 4-[(3aR,6aS)-3-(2-chlorophenyl)-4,6-dioxo-3a,4,6,6a-tetrahydro-5H-pyrrolo[3,4-d]isoxazol-5-yl]benzoate
5.alpha.,14.beta.-Pregnan-15-one, 20-methyl-
5.alpha.-Pregnan-15-one, 20-methyl-
(2aS,5R,5aR,6S,8aR,8bR)-6-Hydroxy-2a-methyl-2a,3,4,5,5a,6,7,8,8a,8b-decahydro-2H-cyclopropa[4,4a]naphtho[1,8-bc]furan-2-one
GPCXQNNOCYGKIY-GZBFAFLISA-N
| Title | Journal or Book | Year |
|---|---|---|
| Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |