3′-Sialyl-Lewis X → HCID 70698323, compound

HRID 977509Notes

Reaction equation

[OH:1][C:2]([C@@:4]1([O:50][C@@H:49]([C@@H:51]([C@@H:53]([CH2:55][OH:56])[OH:54])[OH:52])[C@H:44]([NH:45][C:46]([CH3:48])=[O:47])[C@@H:42]([OH:43])[CH2:41]1)[O:5][C@H:6]1[C@@H:36]([OH:37])[C@@H:35]([CH2:38][OH:39])[O:34][C@@H:8]([O:9][C@@H:10]2[C@@H:16]([CH2:17][OH:18])[O:15][CH:13]([OH:14])[C@H:12]([NH:19][C:20]([CH3:22])=[O:21])[C@H:11]2[O:23][C@@H:24]2[O:32][C@@H:31]([CH3:33])[C@@H:29]([OH:30])[C@@H:27]([OH:28])[C@@H:25]2[OH:26])[C@@H:7]1[OH:40])=[O:3].C[C@@H]1O[C@@H](O[C@@H]([C@H]([O:78][C@@H:79]2[O:84][C@H:83]([CH2:85][OH:86])[C@H:82]([OH:87])[C@H:81](O[C@@]3(C(O)=O)O[C@@H]([C@H](O)[C@H](O)CO)[C@H](NC(C)=O)[C@@H](O)C3)[C@H:80]2[OH:109])[C@H](O)CO)[C@@H](NC(C)=O)C=O)[C@@H](O)[C@H](O)[C@@H]1O>>[OH:3][C:2]([C@@:4]1([O:50][C@@H:49]([C@@H:51]([C@@H:53]([CH2:55][OH:56])[OH:54])[OH:52])[C@H:44]([NH:45][C:46]([CH3:48])=[O:47])[C@@H:42]([OH:43])[CH2:41]1)[O:5][C@H:6]1[C@@H:36]([OH:37])[C@@H:35]([CH2:38][OH:39])[O:34][C@@H:8]([O:9][C@@H:10]2[C@@H:16]([CH2:17][OH:18])[O:15][C@@H:13]([O:14][C@H:81]3[C@@H:82]([OH:87])[C@@H:83]([CH2:85][OH:86])[O:84][C@@H:79]([OH:78])[C@@H:80]3[OH:109])[C@H:12]([NH:19][C:20]([CH3:22])=[O:21])[C@H:11]2[O:23][C@@H:24]2[O:32][C@@H:31]([CH3:33])[C@@H:29]([OH:30])[C@@H:27]([OH:28])[C@@H:25]2[OH:26])[C@@H:7]1[OH:40])=[O:1]

Participants

Reactant 2

HCID 6439903′-Sialyl-Lewis X

HCID 11828886HCID 11828886, compound

Product 1

HCID 70698323HCID 70698323, compound

Procedure

NeuAcα2→3Galβ1→4(Fucα1→3)GlcNAc=Slex.

Sources & evidence

ORD record: ord-a184fb735b3345a98e00cae5ec5c8aee
Source dataset: uspto-grants-1997_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05614615

Reaction notes

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