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N-METHOXYCARBONYL-3-TRIMETHYLSILYLOXY-8-AZABICYCLO-[3.2.1]-OCT-2-ENE;ROTAMER-#2

Compound with spectra: 2 NMR

N-METHOXYCARBONYL-3-TRIMETHYLSILYLOXY-8-AZABICYCLO-[3.2.1]-OCT-2-ENE;ROTAMER-#2
SpectraBase Compound ID HPUZcMEVEUx
InChI InChI=1S/C12H21NO3Si/c1-15-12(14)13-9-5-6-10(13)8-11(7-9)16-17(2,3)4/h7,9-10H,5-6,8H2,1-4H3/t9-,10+/m0/s1
InChIKey IRGUIURMZIHCSG-VHSXEESVSA-N
Mol Weight 255.39 g/mol
Molecular Formula C12H21NO3Si
Exact Mass 255.12907 g/mol
Enantiomer InChIKey IRGUIURMZIHCSG-ZJUUUORDSA-N

View Spectrum of N-METHOXYCARBONYL-3-TRIMETHYLSILYLOXY-8-AZABICYCLO-[3.2.1]-OCT-2-ENE;ROTAMER-#2

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

View Spectrum of N-METHOXYCARBONYL-3-TRIMETHYLSILYLOXY-8-AZABICYCLO-[3.2.1]-OCT-2-ENE;ROTAMER-#2

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • N-METHOXYCARBONYL-3-TRIMETHYLSILYLOXY-8-AZABICYCLO-[3.2.1]-OCT-2-ONE;ROTAMER-#1
9-Azabicyclo[3.3.1]non-2-ene-9-carboxylic acid, 6-hydroxy-, ethyl ester, endo-
[(1S,4S)-4-(Benzyloxycarbonyl-but-3-enyl-amino)-6-tert-butylsilanyloxy-cyclohept-2-enyl]-but-3-enyl-carbamic acid benzyl ester
N-(ethoxycarbonyl)-3-exo-ethyl-2-azabicyclo[2.2.2]oct-5-ene
(1R*,5S*)-2-METHYLENE-3-OXO-8-AZABICYCLO-[3.2.1]-OCTANE-8-CARBOXYLIC-ACID-ETHYLESTER
(5S,8aS)-5-((R)-1-Hydroxy-3-methylbutyl)-1,5,6,8a-tetrahydro-3H-oxazolo[3,4-a]pyridin-3-one
(5S,8aS)-5-((S)-1-Hydroxy-3-methylbutyl)-1,5,6,8a-tetrahydro-3H-oxazolo[3,4-a]pyridin-3-one
(5R,8aS)-5-(1-Hydroxy-3-methylbutyl)-1,5,6,8a-tetrahydro-3H-oxazolo[3,4-a]pyridin-3-one
(5S,8aS)-5-((R)-1-Hydroxyhexyl)-1,5,6,8a-tetrahydro-3H-oxazolo[3,4-a]pyridin-3-one
(5S,8aS)-5-((S)-1-Hydroxyhexyl)-1,5,6,8a-tetrahydro-3H-oxazolo[3,4-a]pyridin-3-one
(5R,8aS)-5-(1-Hydroxyhexyl)-1,5,6,8a-tetrahydro-3H-oxazolo[3,4-a]pyridin-3-one
Title Journal or Book Year
The total synthesis of the analgesic alkaloid epibatidine Journal of the Chemical Society, Perkin Transactions 1 1998
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