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ENDO-3-AZA-3-(3-TERT.-BUTYL-1,3,2-OXAZAPHOSPHORYL)-2-OXO-2-THIABICYCLO-[2.2.2]-OCT-5-ENE;MAJOR-ISOMER

Compound with spectra: 2 NMR

ENDO-3-AZA-3-(3-TERT.-BUTYL-1,3,2-OXAZAPHOSPHORYL)-2-OXO-2-THIABICYCLO-[2.2.2]-OCT-5-ENE;MAJOR-ISOMER
SpectraBase Compound ID GtQbMw5LHjG
InChI InChI=1S/C13H23N2O3PS/c1-13(2,3)14-9-4-10-18-19(14,16)15-11-5-7-12(8-6-11)20(15)17/h5,7,11-12H,4,6,8-10H2,1-3H3/t11-,12+,19?,20?/m1/s1
InChIKey JAIPRULUCRLRHV-CVFNZVRXSA-N
Mol Weight 318.37 g/mol
Molecular Formula C13H23N2O3PS
Exact Mass 318.116701 g/mol
Enantiomer InChIKey JAIPRULUCRLRHV-ZRVKLJFSSA-N

View Spectrum of ENDO-3-AZA-3-(3-TERT.-BUTYL-1,3,2-OXAZAPHOSPHORYL)-2-OXO-2-THIABICYCLO-[2.2.2]-OCT-5-ENE;MAJOR-ISOMER

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of ENDO-3-AZA-3-(3-TERT.-BUTYL-1,3,2-OXAZAPHOSPHORYL)-2-OXO-2-THIABICYCLO-[2.2.2]-OCT-5-ENE;MAJOR-ISOMER

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • ENDO-3-AZA-3-(3-TERT.-BUTYL-1,3,2-OXAZAPHOSPHORYL)-2-OXO-2-THIABICYCLO-[2.2.2]-OCT-5-ENE;MINOR-ISOMER
methyl 2-[(2,5-dimethyl-3-furoyl)amino]-4-(2,4-dimethylphenyl)-5-methyl-3-thiophenecarboxylate
10-Hydroxy-2,5-dimethoxy-7-methyl-1,4-anthracenedione
Naphtho[1,2-c]furan-1,3-dione, 3a,4,6,7,8,9,9a,9b-octahydro-5-methyl-4-phenyl-, (3a.alpha.,4.beta.,9a.alpha.,9b.alpha.)-
4-(1-(4-bromophenyl)-6,7-diethoxy-3-oxo-3,4-dihydro-2(1H)-isoquinolinyl)benzoic acid
1-((4R,5S)-3-hydroxy-5-(2-oxopropyl)-4,5-diphenylcyclopent-2-enylidene)pyrrolidinium chloride
1-((4S,5S)-3-hydroxy-5-(2-oxopropyl)-4,5-diphenylcyclopent-2-enylidene)pyrrolidinium chloride
3-(2-methoxyphenyl)-2-[(E)-2-(1-naphthyl)ethenyl]-4(3H)-quinazolinone
5,7-Dimethoxy-3-(1-hydroxy-6,6-dimethylbenzo[b]pyran-2-yl)-6-(isopent-2-en-1-yl)dihydrobenzo[b]pyran
6-Amino-4-chloro-1-phenol-2-sulfonacid->1-butyl-4-hydroxycarbostyril
MICHAOLIDE-K
Title Journal or Book Year
Reactivity and Diastereoselectivity in the Thermal and Lewis Acid-Catalyzed Diels−Alder Reactions of N-Sulfinylphosphoramidates1 The Journal of Organic Chemistry 1998
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