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(+)-(1S,2S,4R,5S,6S)-5-ENDO-(BENZYLOXY)-6-EXO-[(TERT.-BUTOXY)-CARBONYLAMINO]-3-OXO-7-OXABICYCLO-[2.2.1]-HEPT-2-EXO-YL-3-CHLOROBENZOATE

Compound with spectra: 1 NMR

(+)-(1S,2S,4R,5S,6S)-5-ENDO-(BENZYLOXY)-6-EXO-[(TERT.-BUTOXY)-CARBONYLAMINO]-3-OXO-7-OXABICYCLO-[2.2.1]-HEPT-2-EXO-YL-3-CHLOROBENZOATE
SpectraBase Compound ID FHTeKcHPc0W
InChI InChI=1S/C25H26ClNO7/c1-25(2,3)34-24(30)27-17-19(31-13-14-8-5-4-6-9-14)21-18(28)22(20(17)32-21)33-23(29)15-10-7-11-16(26)12-15/h4-12,17,19-22H,13H2,1-3H3,(H,27,30)/t17-,19-,20+,21+,22+/m0/s1
InChIKey QGLKXOPUTABAOJ-XBJCXQGOSA-N
Mol Weight 487.94 g/mol
Molecular Formula C25H26ClNO7
Exact Mass 487.13978 g/mol
Enantiomer InChIKey QGLKXOPUTABAOJ-ICGSVKGVSA-N

View Spectrum of (+)-(1S,2S,4R,5S,6S)-5-ENDO-(BENZYLOXY)-6-EXO-[(TERT.-BUTOXY)-CARBONYLAMINO]-3-OXO-7-OXABICYCLO-[2.2.1]-HEPT-2-EXO-YL-3-CHLOROBENZOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
D-epi-4-Inosose, 2,5-anhydro-1-deoxy-1-[[(1,1-dimethylethoxy)carbonyl]amino]-6-O-(phenylmethyl)-, 3-(3-chlorobenzoate)
2-ACETAMIDO-1-AZI-3-O-BENZYL-4,6-O-BENZYLIDENE-1,2-DIDEOXY-D-ALLOPYRANOSE
3,4,6,7-TETRA-O-BENZYL-N-BENZYLOXYCARBONYLAMINO-2,5-DIDEOXY-2,5-IMINO-D-GLYCERO-D-GLUCO-HEPTONONITRILE
.beta.-O-Methyl-7,8-dideoxy-7-azido-galacto-octan-pyranoside 2,3,4-tribenzoate 6-mesylate
3-AZIDOPROPYL-3-O-ACETYL-4,6-O-BENZILIDENE-2-DEOXY-2-(2,2,2-TRICHLOROETHOXYCARBONYL-AMINO)-ALPHA-D-GALACTOPYRANOSIDE
6-PHTHALIMIDOHEXYL 2-O-(3-O-ACETYL-2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-3,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSIDE
3-CHLOROPROPYL-3-O-ACETYL-4,6-O-BENZILIDENE-2-DEOXY-2-(2,2,2-TRICHLOROETHOXYCARBONYL-AMINO)-ALPHA-D-GALACTOPYRANOSIDE
3,4,6-TRI-O-ACETYL-2-ALLYLOXY-CARBONYLAMINO-2-DEOXY-alpha-D-GLUCOPYRANOSYL)-TRICHLORO-ACETIMIDATE
3,4,6-TRI-O-ACETYL-2-ALLYLOXY-CARBONYLAMINO-2-DEOXY-beta-D-GLUCOPYRANOSYL)-TRICHLORO-ACETIMIDATE
(2S)-2-HYDROXY-2-METHYL-3-TOSYLOXYPROPYL-2-ACETAMIDO-3-O-BENZYL-4,6-O-(R)-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSIDE
Title Journal or Book Year
Acid-Catalyzed Rearrangement of 3-Aza-8-oxatricyclo[3.2.1. 02,4]octan-6-one Acetals. Highly Stereoselective Total Synthesis of 3-Amino-3-deoxy-D-altrose and Derivatives Helvetica Chimica Acta 1989
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