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N(ALPHA)-FMOC-TYR-[AC(4)-ALPHA-D-GLC-(1->4)-AC(3)-BETA-D-GLC]-OPFP

Compound with spectra: 1 NMR

N(ALPHA)-FMOC-TYR-[AC(4)-ALPHA-D-GLC-(1->4)-AC(3)-BETA-D-GLC]-OPFP
SpectraBase Compound ID ASsNGUxTLMG
InChI InChI=1S/C56H54F5NO22/c1-24(63)72-22-39-46(75-26(3)65)49(76-27(4)66)52(79-30(7)69)55(82-39)84-47-40(23-73-25(2)64)81-54(51(78-29(6)68)50(47)77-28(5)67)80-32-18-16-31(17-19-32)20-38(53(70)83-48-44(60)42(58)41(57)43(59)45(48)61)62-56(71)74-21-37-35-14-10-8-12-33(35)34-13-9-11-15-36(34)37/h8-19,37-40,46-47,49-52,54-55H,20-23H2,1-7H3,(H,62,71)/t38-,39-,40+,46-,47+,49+,50-,51+,52-,54+,55-/m0/s1
InChIKey RFSPKXPBXHSTEJ-ZDXKPNKTSA-N
Mol Weight 1188.0 g/mol
Molecular Formula C56H54F5NO22
Exact Mass 1187.305763 g/mol
Enantiomer InChIKey RFSPKXPBXHSTEJ-AJBFMZITSA-N

View Spectrum of N(ALPHA)-FMOC-TYR-[AC(4)-ALPHA-D-GLC-(1->4)-AC(3)-BETA-D-GLC]-OPFP

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
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
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-ser penta-F-phenyl ester
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
N(ALPHA)-(9-FLUORENYLMETHYLOXYCARBONYL)-THREONINE-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSE)-O-PENTAFLUOROPHENYLESTER
N(ALPHA)-(FLUOREN-9-YL-METHOXYCARBONYL)-O-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-L-THREONINE-PENTAFLUOROPHENYLESTER
O-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-beta-D-GLUCOPYRANOSYL)-N-(FLUOREN-9-YL-METHOXYCARBONYL)-L-TREONINE-PENTAFLUOROPHENYLESTER
NYDSVGLDIZVUMA-NQMWAKAJSA-N
#8;4-METHOXYPHENYL-(2-AZIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-ALPHA-D-GLUCOPYRANOSYL)-(1->3)-(2,4-DI-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->4)-(2,3-DI-O-ACETYL-6-O-BEN
No Name
Title Journal or Book Year
Glycosylation of phenols: preparation of 1,2-cis and 1,2-trans glycosylated tyrosine derivatives to be used in solid-phase glycopeptide synthesis Journal of the Chemical Society, Perkin Transactions 1 1993
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Unknown Identification

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