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(2R,5S)-6-AMINO-2-TERT.-BUTYL-8-OXO-1-AZA-3-OXABICYClO-[3.3.0]-OCT-6-ENE

Compound with spectra: 1 NMR

(2R,5S)-6-AMINO-2-TERT.-BUTYL-8-OXO-1-AZA-3-OXABICYClO-[3.3.0]-OCT-6-ENE
SpectraBase Compound ID DJVxWflMc3G
InChI InChI=1S/C10H16N2O2/c1-10(2,3)9-12-7(5-14-9)6(11)4-8(12)13/h4,7,9H,5,11H2,1-3H3/t7-,9-/m0/s1
InChIKey YJRKDOZBAJDHJW-CBAPKCEASA-N
Mol Weight 196.25 g/mol
Molecular Formula C10H16N2O2
Exact Mass 196.121178 g/mol
Enantiomer InChIKey YJRKDOZBAJDHJW-VXNVDRBHSA-N

View Spectrum of (2R,5S)-6-AMINO-2-TERT.-BUTYL-8-OXO-1-AZA-3-OXABICYClO-[3.3.0]-OCT-6-ENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(3R,7aS)-7-amino-3-tert-butyl-3,7a-dihydro-1H-pyrrolo[1,5-c][1,3]oxazol-5-one
(2R,4S)-2-TERT.-BUYL-3-CYANOACETYL-4-METHOXYCARBONYL-1,3-OXAZOLIDINE
(3R,7aR)-3-tert-butyl-3,7a-dihydro-1H-pyrrolo[1,5-c]oxazole-5,7-quinone
(2R,5R)-2-TERT.-BUTYL-6,8-DIOXO-1-AZA-3-OXABICYClO-[3.3.0]-OCTANE
3-t-Butyl-dihydro-pyrrolo[1,2-c]oxazole-1,5-dione
(S,RS)-3-Isopropyl-7a-methyl-2,3-dihydropyrrolo[2,1-b][1,3]oxazol-5(7aH)-one
(3R,7aS)-7a-methyl-3-propan-2-yl-2,3-dihydropyrrolo[5,1-b][1,3]oxazol-5-one
Bicyclic lactam
1-Aza-7-oxa-9-phenylbicyclo[4.3.0]nonan-2-one
2-(t-Butyl)-3-[(phenyloxy)carbonyl]-4-methyl-1,3-oxazolidin-5-one
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
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