3′-Sialyl-Lewis X → HCID 44456859, compound

HRID 355327Notes

Reaction equation

O([C@H]1[C@H](O)[C@@H](CO)OC(O)[C@@H]1NC(C)=O)[C@@H]1O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]1O.[CH3:26][C@@H:27]1[O:32][C@@H:31]([O:33][C@@H:34]([C@H:42]([O:47][C@@H:48]2[O:53][C@H:52]([CH2:54][OH:55])[C@H:51]([OH:56])[C@H:50]([O:57][C@@:58]3([C:75]([OH:77])=[O:76])[O:63][C@@H:62]([C@H:64]([OH:69])[C@H:65]([OH:68])[CH2:66][OH:67])[C@H:61]([NH:70][C:71]([CH3:73])=[O:72])[C@@H:60]([OH:74])[CH2:59]3)[C@H:49]2[OH:78])[C@H:43]([OH:46])[CH2:44][OH:45])[C@@H:35]([NH:38][C:39]([CH3:41])=[O:40])[CH:36]=[O:37])[C@@H:30]([OH:79])[C@H:29]([OH:80])[C@@H:28]1[OH:81]>>[OH:76][C:75]([C@@:58]1([O:63][C@@H:62]([C@@H:64]([C@@H:65]([CH2:66][OH:67])[OH:68])[OH:69])[C@H:61]([NH:70][C:71]([CH3:73])=[O:72])[C@@H:60]([OH:74])[CH2:59]1)[O:57][C@H:50]1[C@@H:51]([OH:56])[C@@H:52]([CH2:54][OH:55])[O:53][C@@H:48]([O:47][C@@H:42]2[C@@H:43]([CH2:44][OH:45])[O:46][C@@H:36]([OH:37])[C@H:35]([NH:38][C:39]([CH3:41])=[O:40])[C@H:34]2[O:33][C@@H:31]2[O:32][C@@H:27]([CH3:26])[C@@H:28]([OH:81])[C@@H:29]([OH:80])[C@@H:30]2[OH:79])[C@@H:49]1[OH:78])=[O:77]

Participants

Reactant 2

HCID 6439903′-Sialyl-Lewis X

HCID 52921582HCID 52921582, compound

Product 1

HCID 44456859HCID 44456859, compound

Procedure

NeuAcα2→3Galβ1→4(Fucα1→3GlcNAc=Slex.

Sources & evidence

ORD record: ord-2a8e163a04cb4ffd9718428bd96d5d71
Source dataset: uspto-grants-1998_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05830871

Reaction notes

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