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#12;2-[2-[2-[2-(HYDROXY)-ETHOXY]-ETHOXY]-ETHYL-6-O-(2-ACETAMIDO-3,4-DI-O-BENZYL-2-DEOXY-6-O-THEXYLDIMETHYLSILYL-5A-CARBA-ALPHA-D-MANNOPYRANOSYL-PHOSPHONATO)-2-

Compound with spectra: 2 NMR

#12;2-[2-[2-[2-(HYDROXY)-ETHOXY]-ETHOXY]-ETHYL-6-O-(2-ACETAMIDO-3,4-DI-O-BENZYL-2-DEOXY-6-O-THEXYLDIMETHYLSILYL-5A-CARBA-ALPHA-D-MANNOPYRANOSYL-PHOSPHONATO)-2-
SpectraBase Compound ID E8kSTSfDne
InChI InChI=1S/C62H91N2O16PSi.C6H15N/c1-45(2)62(5,6)82(7,8)79-44-53-38-55(57(64-47(4)67)61(77-42-51-27-19-12-20-28-51)59(53)75-40-49-23-15-10-16-24-49)80-81(68,69)78-43-52-37-54(73-36-35-72-34-33-71-32-31-70-30-29-65)56(63-46(3)66)60(76-41-50-25-17-11-18-26-50)58(52)74-39-48-21-13-9-14-22-48;1-4-7(5-2)6-3/h9-28,45,52-61,65H,29-44H2,1-8H3,(H,63,66)(H,64,67)(H,68,69);4-6H2,1-3H3/t52-,53-,54+,55+,56-,57-,58-,59-,60-,61-;/m1./s1
InChIKey XUBZVLHHITYNKX-FMIPREFWSA-N
Mol Weight 1280.7 g/mol
Molecular Formula C68H106N3O16PSi
Exact Mass 1279.707998 g/mol
Parent InChIKey QLBGTSMTKXGZRM-OQRKVEOISA-N
Enantiomer InChIKey XUBZVLHHITYNKX-RBJKIWRYSA-N

View Spectrum of #12;2-[2-[2-[2-(HYDROXY)-ETHOXY]-ETHOXY]-ETHYL-6-O-(2-ACETAMIDO-3,4-DI-O-BENZYL-2-DEOXY-6-O-THEXYLDIMETHYLSILYL-5A-CARBA-ALPHA-D-MANNOPYRANOSYL-PHOSPHONATO)-2-

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O

View Spectrum of #12;2-[2-[2-[2-(HYDROXY)-ETHOXY]-ETHOXY]-ETHYL-6-O-(2-ACETAMIDO-3,4-DI-O-BENZYL-2-DEOXY-6-O-THEXYLDIMETHYLSILYL-5A-CARBA-ALPHA-D-MANNOPYRANOSYL-PHOSPHONATO)-2-

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#11;2-[2-[2-[2-(PARA-METHOXYBENZYLOXY)-ETHOXY]-ETHOXY]-ETHYL-6-O-(2-AZIDO-3,4-DI-O-BENZYL-2-DEOXY-6-O-THEXYLDIMETHYLSILYL-5A-CARBA-ALPHA-D-MANNOPYRANOSYL-PHOSP
TERT.-BUTYL-5-ACETAMIDO-2-C-(ACETOXYMETHYL)-2,6-ANHYDRO-4,7,8,9-TETRA-O-BENZYL-3,5-DIDESOXY-D-ERYTHRO-L-GLUCO-NONONATE
ALLYL-[3,4,6-TRI-O-BENZYL-2-DEOXY-2-TRICHLOROACETAMIDO-BETA-D-GALACTOPYRANOSYL-(1->4)]-2-O-BENZOYL-3-O-BENZYL-ALPHA-D-MANNOPYRANOSIDE
TERT.-BUTYL-5-ACETAMIDO-2,6-ANHYDRO-2-C-(AZIDOMETHYL)-4,7,8,9-TETRA-O-BENZYL-3,5-DIDESOXY-D-ERYTHRO-L-MANNO-NONONATE
(5S,10bS)-(-)-5-Benzyloxymethyl-8,9-dimethoxy-10b-methyl-1,5,6,10b-tetrahydropyrrolo[2,1-a]isoquinolin-3-one
2-O-(3,4,6-TRI-O-ACETYL-2-ALLYLOXYCARBONYLAMINO-2-DESOXY-BETA-D-GLUCOPYRANOSYL)-1,6-ANHYDRO-4-O-BENZOYL-BETA-D-MANNOPYRANOSE
ALLYL-(3,4,6-TRI-O-ACETYL-2-DEOXY-2-TRICHLOROACETAMIDO-BETA-D-GLUCOPYRANOSYL)-(1->2)-3,4-DI-O-BENZYL-ALPHA-L-RHAMNOPYRANOSIDE
8-(1-adamantyl)-2,3,3a,4,5,6-hexahydro-1H-pyrazino[3,2,1-jk]carbazol-3-ium chloride
8a-tert-Butyldimethylsilyloxy-3-oxo-4,6,11b,5,7aH-eudesm-1-en-6,12-olide
#18;2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL-(1->4)-3,6-DI-O-ACETYL-2-DEOXY-2-TRIFLUOROACETAMIDO-ALPHA-D-GLUCOPYRANOSYL-PHOSPHATE-MONO-(TRI
Title Journal or Book Year
A Strategy for Multivalent Presentation of Carba Analogues fromN. meningitidisA Capsular Polysaccharide European Journal of Organic Chemistry 2014
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