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Glucuronic Acid → Iduronic Acid

HRID 843510
Notes
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Reaction equation

HRID 843510 reaction equation
[O:1]=[CH:2][C@@H:3]([C@H:5]([C@@H:7]([C@@H:9]([C:11]([OH:13])=[O:12])[OH:10])[OH:8])[OH:6])[OH:4].O=C[C@@H]([C@H]([C@H]([C@@H](C(O)=O)O)O)O)O>>[O:1]=[CH:2][C@H:3]([C@@H:5]([C@H:7]([C@@H:9]([C:11]([OH:13])=[O:12])[OH:10])[OH:8])[OH:6])[OH:4]
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 65041Glucuronic AcidHCID 84740Galacturonic Acid

Product 1

HCID 18845Iduronic Acid

Procedure

As the standards for PA hexuronic acids, use is made of those prepared by pyridyl-(2)-amination of glucuronic acid manufactured by Sigma Chemical Co., galacturonic acid manufactured by Wako Pure Chemical Industries, Ltd., iduronic acid obtained by hydrolyzing 4-methylumbelliferyl-α-L-iduronide manufactured by Sigma Chemical Co., and mannuronic acid and guluronic acid obtained by hydrolyzing alginic acid (mfd. by Wako Pure Chemical Industries, Ltd.) in accordance with the method described in Acta Chemica Scandinavicaj, 15, 1397-1398 (1961) followed by the separation with an anion exchange resin.

Sources & evidence

ORD record
ord-97533bed5bce49298d85408d12dbf593
Source dataset
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06379947B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes