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(5S)-2,2-DIMETHYL-8-OXO-1-AZA-3-OXA-BICYCLO-[3.3.0]-OCTANE

Compound with spectra: 2 NMR, and 1 MS (GC)

(5S)-2,2-DIMETHYL-8-OXO-1-AZA-3-OXA-BICYCLO-[3.3.0]-OCTANE
SpectraBase Compound ID HAVZh9mVLlw
InChI InChI=1S/C8H13NO2/c1-8(2)9-6(5-11-8)3-4-7(9)10/h6H,3-5H2,1-2H3/t6-/m0/s1
InChIKey YTXXRLXVAZGQAL-LURJTMIESA-N
Mol Weight 155.2 g/mol
Molecular Formula C8H13NO2
Exact Mass 155.094629 g/mol
Enantiomer InChIKey YTXXRLXVAZGQAL-ZCFIWIBFSA-N
Racemate InChIKey YTXXRLXVAZGQAL-UHFFFAOYSA-N

View Spectrum of (5S)-2,2-DIMETHYL-8-OXO-1-AZA-3-OXA-BICYCLO-[3.3.0]-OCTANE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-66-8840-12

View Spectrum of (5S)-2,2-DIMETHYL-8-OXO-1-AZA-3-OXA-BICYCLO-[3.3.0]-OCTANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (5S)-2,2-DIMETHYL-8-OXO-1-AZA-3-OXA-BICYCLO-[3.3.0]-OCTANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (5S)-2,2-DIMETHYL-3-OXA-1-AZA-BICYCLO-[3.3.0]-OCTAN-8-ONE
  • (7aS)-3,3-dimethyl-1,6,7,7a-tetrahydropyrrolo[1,2-c]oxazol-5-one
FCSNOHQZMHLLPG-UHFFFAOYSA-N
(5S)-1-benzyl-5-(methoxymethyl)-2-pyrrolidone
Levetiracetam-M/A (-NH2,+OCH(CH3)2)
4-t-Butyl-N-(propanoyl)oxazolidinone
Benzyl 2-(isopropoxymethyl)-pyrrolidine-1-carboxylate
5-(Hydroxymethyl)-1-(4-methylphenyl)pyrrolidin-2-one
L-Proline, 1-(5-amino-5-carboxypentyl)-5-oxo-, (S)-
1-Azetidineacetic acid, .alpha.-(2-methylpropyl)-2-oxo-, ethyl ester
6,7,8,8a-tetrahydro-1H-pyrrolo[1,2-d][1,4]oxazine-3,4-quinone
5H-Oxazolo[3,2-a]pyridin-3(2H)-one, 6,7,8,8a-tetrahydro-2-methyl-, cis-
Title Journal or Book Year
Synthetic Studies Towards the Core Structure of Nakadomarin A by a Thioamide-Based Strategy European Journal of Organic Chemistry 2013
Electrophilic Fluorination of Pyroglutamic Acid Derivatives:  Application of Substrate-Dependent Reactivity and Diastereoselectivity to the Synthesis of Optically Active 4-Fluoroglutamic Acids The Journal of Organic Chemistry 2001
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