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#2A;(2R,5R,6R,7S)-5-[[[[(9H-FLUOREN-9-YL)-METHOXY]-CARBONYL]-OXY]-METHYL]-2-[[2-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-4-METHOXYBENZYL]-OXY]-2-PHENYLTETRAHYDRO-3AH-[

Compound with spectra: 1 NMR

#2A;(2R,5R,6R,7S)-5-[[[[(9H-FLUOREN-9-YL)-METHOXY]-CARBONYL]-OXY]-METHYL]-2-[[2-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-4-METHOXYBENZYL]-OXY]-2-PHENYLTETRAHYDRO-3AH-[
SpectraBase Compound ID LeUanDXjOKm
InChI InChI=1S/C56H56O13Si/c1-55(2,3)70(5,6)69-46-32-40(60-4)31-30-38(46)33-63-56(39-24-14-9-15-25-39)67-50-49(66-52(58)37-22-12-8-13-23-37)48(65-51(57)36-20-10-7-11-21-36)47(64-53(50)68-56)35-62-54(59)61-34-45-43-28-18-16-26-41(43)42-27-17-19-29-44(42)45/h7-32,45,47-50,53H,33-35H2,1-6H3/t47-,48-,49+,50-,53-,56?/m1/s1
InChIKey PFJSVRBMYJPBMB-SYXFLPMJSA-N
Mol Weight 965.1 g/mol
Molecular Formula C56H56O13Si
Exact Mass 964.349018 g/mol
Enantiomer InChIKey PFJSVRBMYJPBMB-LEDFGKKISA-N

View Spectrum of #2A;(2R,5R,6R,7S)-5-[[[[(9H-FLUOREN-9-YL)-METHOXY]-CARBONYL]-OXY]-METHYL]-2-[[2-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-4-METHOXYBENZYL]-OXY]-2-PHENYLTETRAHYDRO-3AH-[

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
No Name
N(ALPHA)-FMOC-TYR-[AC(4)-ALPHA-D-GLC-(1->4)-AC(3)-BETA-D-GLC]-OPFP
N-(Fluoren-9-yl-meo-carbonyl)-O-(3,4,6-tri-O-ac-2-O-<2,3,4,6-tetra-O-ac-A-D-man-P>-A-D-man-P)-L-thr penta-F-phenyl ester
NYDSVGLDIZVUMA-NQMWAKAJSA-N
No Name
#4;N-(9H-FLUOREN-9-YL)-METHOXYCARBONYL-[BETA-2,3,4,6-TETRA-O-ACETYL-GALACTOPYRANOSYL)-(1->3)-(ALPHA-2-ACETAMIDO-4,6-DI-O-ACETYL-2-DEOXY-GALACTOPYRANOSYL)]-BETA
No Name
1',2,3,3',4',6'-HEXA-O-ACETYL-4,6-O-(3-ETHOXYCARBONYL-BUTYLIDENE)-SUCROSE
1',2,3,3',4',6'-HEXY-O-ACETYL-4,6-O-(3-CARBOXY-BUTYLIDENE)-SUCROSE
PHENYL-2,3,4-TRI-O-BENZOYL-6-O-9-FLUORENYLMETHYLOXYCARBOXYL-BETA-D-GLUCOPYRANOSYL-(1->6)-2,3,4-TRI-O-BENZOYL-1-THIO-BETA-D-GLUCOPYRANOSIDE
Title Journal or Book Year
Glycosylation of a Newly Functionalized Orthoester Derivative Molecules 2014
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