JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0002607
Submitter
The Noguchi Institute
Reaction ID
R-0000-002607
Regist Date
2012/06/21 19:30:49
REACTANT
MOLECULE ID
JCGG-COM0003386 (Reaction Tree)
Mol
0.16 mmol
MOLECULE ID
JCGG-COM0000426
Reactant Type
DIEA
Volume
0.5 mL
PRODUCT
MOLECULE ID
JCGG-COM0003387 (Reaction Tree)
Yield
67%
REACTION DETAIL
Reaction Time
14 hours, overnight
Reaction Temp
0 degree C, room temp
Solvent
MeOH/H2O = 5mL/1mL, MeOH/H2O = 5mL/1mL
Comment
1) +all, 2) temperature change
COMMENT
Keywords: carbamyl glucuronidation, metabolism, secondary amine drugs, glucuronyl p-nitrophenyl carbonates
There are multiple phases in this reaction.
REFERENCE
Reference Id
REF-0000-000357
Issn
Electronic
Doi
10.1021/jo200238d
PubMed ID
21598979
Journal Name
The Journal of organic chemistry. (2011) 76 (13): 5429-32.
Article Title
Reagents for stereoselective preparation of N-carbamyl β-D-glucuronides.
Author
William H, Bunnelle
Affiliation
Abbott Laboratories, Neuroscience Research, Building AP9A, Department R4MN, 100 Abbott Park Road, Abbott Park, Illinois 60064-6117, United States. william.h.bunnelle@abbott.com
Reference Id
REF-0000-000358
Source
J. Org. Chem. 2011, 76, 5429-5432
Doi
10.1021/jo200238d

©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)