JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
 JCGG-RAC0002136
Submitter
 The Noguchi Institute
Reaction ID
 R-0000-002136
Regist Date
 2012/06/21 18:37:15
REACTANT
MOLECULE ID
 JCGG-COM0002776 (Reaction Tree)
MOLECULE ID
 JCGG-COM0002777
Reactant Type
 (i-Pr2N)2PCl
MOLECULE ID
 JCGG-COM0000426
Reactant Type
 DIPEA
PRODUCT
MOLECULE ID
 JCGG-COM0002778 (Reaction Tree)
Skeleton
JCGG-STR008690
Yield
 32%
REACTION DETAIL
Reaction Time
 NOT specified
Reaction Temp
 room temp
Solvent
 CH2Cl2
Comment
 MS 4A was included in the solvent.
Very few were described regarding this reaction.
COMMENT
Keywords: mannose-6-phosphate, M6P, N-linked glycans, eukaryotic cells, N-acetylglucosamine, GlcNAc, sequential deprotection
The procedure regarding this reaction is discussed in another paper in References.
REFERENCE
Reference Id
 REF-0000-000321
Issn
 Electronic
Doi
 10.1021/jo2010999
PubMed ID
 21955083
Journal Name
 The Journal of organic chemistry. (2011) 76 (21): 8682-9.
Article Title
 Chemical synthesis of N-linked glycans carrying both mannose-6-phosphate and GlcNAc-mannose-6-phosphate motifs.
Author
 Yunpeng, Liu; Gong, Chen
Affiliation
 Department of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Reference Id
 REF-0000-000322
Source
 J. Org. Chem., 2011, 76 (21), pp 8682-8689
Doi
 10.1021/jo2010999
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)