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5-DEOXY-1,2-O-ISOPROPYLIDENE-5-(1,6,6-TRIMETHYL-3-AZABICYClO-[3.2.1]-OCTAN-3-YL)-ALPHA-D-XYLOFURANOSE

Compound with spectra: 1 NMR

5-DEOXY-1,2-O-ISOPROPYLIDENE-5-(1,6,6-TRIMETHYL-3-AZABICYClO-[3.2.1]-OCTAN-3-YL)-ALPHA-D-XYLOFURANOSE
SpectraBase Compound ID Eduu46N2Xun
InChI InChI=1S/C17H29NO4/c1-16(2)6-10-5-11(16)8-18(7-10)9-12-13(19)14-15(20-12)22-17(3,4)21-14/h10-15,19H,5-9H2,1-4H3/t10-,11-,12-,13+,14-,15-/m1/s1
InChIKey UNLYGPMIIJCSMT-PLJUSGQGSA-N
Mol Weight 311.42 g/mol
Molecular Formula C17H29NO4
Exact Mass 311.209658 g/mol
Enantiomer InChIKey UNLYGPMIIJCSMT-SOAFEQHCSA-N

View Spectrum of 5-DEOXY-1,2-O-ISOPROPYLIDENE-5-(1,6,6-TRIMETHYL-3-AZABICYClO-[3.2.1]-OCTAN-3-YL)-ALPHA-D-XYLOFURANOSE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Desoxy-5-O-isopropylidene-1,2-(methyl-1-p-nitrophenyl-3-triazen-2-yl-1)-5-alpha-D-xylofurannose
6-O-ACETYL-5-AZIDO-5-DEOXY-1,2-0-ISOPROPYLIDENE-BETA-L-IDOFURANOSE
5,6-Dideoxy-1,2-O-isopropylidene-5-[(R and S)-(methoxy)phenylphosphinyl]-.beta.-D-arabino-hexofuranose
5'-O-[(TERT.-BUTYL)-DIPHENYLSILYL]-1',2'-O-ISOPROPYLIDENE-BETA-D-ARABINOFURANOSIDE
5-O-TERT.-BUTYLDIPHENYLSILYL-1,2-O-ISOPROPYLIDENE-ALPHA-D-XYLOFURANOSE
6-DEOXY-7-CYCLOHEXYL-1,2-O-ISOPROPYLIDENE-ALPHA-D-XYLO-HEPTAFURANOS-5-ULOSE
6-Deoxy-7-cyclohexyl-1,2-O-(isopropylidene)-.alpha.-D-xyloheptofuranos-5-ulose
1-[(3aR,5S,6R,6aR)-2,2-dimethyl-6-oxidanyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-3-oxidanyl-3-phenyl-propan-1-one
6-DEOXY-1,2-O-ISOPROPYLIDENE-7-PHENYL-ALPHA-D-XYLO-HEPTAFURANOS-5-ULOSE
Ethyl 5,6-Dideoxy-1,2-O-isopropylidene-3-O-(S-methylthiocarbonate)-.alpha.,D-xylo-heptofuranuronate
Title Journal or Book Year
Catalytic enantioselective reaction. Part 9. 1,2-O-Isopropylidene-5-deoxy-5-N,N-dialkyl (or -N-monoalkyl)amino-α-D-xylofuranose derivatives as highly effective chiral catalysts for enantioselective addition of diethylzinc to aliphatic and aromatic aldehydes J. Chem. Soc., Perkin Trans. 1 1996
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