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#23;(+/-)-(1R,4S,5R,6S)-7-TERT.-BUTOXYCARBONYL-5-ENDO-[(1S,4R)-CAMPHANOYLOXY]-6-ENDO-PARA-TOLUENESULFONYL-7-AZABICYCLO-[2.2.1]-HEPT-2-ENE;TERT.-BUTYL-(1

Compound with spectra: 1 NMR

#23;(+/-)-(1R,4S,5R,6S)-7-TERT.-BUTOXYCARBONYL-5-ENDO-[(1S,4R)-CAMPHANOYLOXY]-6-ENDO-PARA-TOLUENESULFONYL-7-AZABICYCLO-[2.2.1]-HEPT-2-ENE;TERT.-BUTYL-(1
SpectraBase Compound ID 5oxMee3GB5n
InChI InChI=1S/C28H35NO8S/c1-16-8-10-17(11-9-16)38(33,34)21-19-13-12-18(29(19)24(32)37-25(2,3)4)20(21)35-23(31)28-15-14-27(7,22(30)36-28)26(28,5)6/h8-13,18-21H,14-15H2,1-7H3/t18-,19+,20+,21-,27+,28-/m0/s1
InChIKey UEHCNECYSCFJHP-HLUDKYKISA-N
Mol Weight 545.6 g/mol
Molecular Formula C28H35NO8S
Exact Mass 545.208338 g/mol
Enantiomer InChIKey UEHCNECYSCFJHP-JUQHHJMMSA-N

View Spectrum of #23;(+/-)-(1R,4S,5R,6S)-7-TERT.-BUTOXYCARBONYL-5-ENDO-[(1S,4R)-CAMPHANOYLOXY]-6-ENDO-PARA-TOLUENESULFONYL-7-AZABICYCLO-[2.2.1]-HEPT-2-ENE;TERT.-BUTYL-(1

13C NMR Spectrum
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Solvent CDCl3
#22;(+/-)-(1S,4R,5S,6R)-7-TERT.-BUTOXYCARBONYL-5-ENDO-[(1S,4R)-CAMPHANOYLOXY]-6-ENDO-PARA-TOLUENESULFONYL-7-AZABICYCLO-[2.2.1]-HEPT-2-ENE;TERT.-BUTYL-(1
Title Journal or Book Year
Synthesis of Enantiomerically Pure 1,2-Diamine Derivatives of 7-Azabicyclo[2.2.1]heptane. New Leads as Glycosidase Inhibitors and Rigid Scaffolds for the Preparation of Peptide Analogues The Journal of Organic Chemistry 2003
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