JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0002077
Submitter
The Noguchi Institute
Reaction ID
R-0000-002077
Regist Date
2012/06/21 18:32:06
REACTANT
MOLECULE ID
JCGG-COM0002713 (Reaction Tree)
Reactant Type
(containing ca. 4 wt % triethylammonium dichloroacetate)
Weight
0.219 g
MOLECULE ID
JCGG-COM0002699
Reactant Type
TEA*3HF
Mol
2.7 mmol
PRODUCT
MOLECULE ID
JCGG-COM0002714 (Reaction Tree)
Product Type
intermediate
Yield
41%(at least)
REACTION DETAIL
Reaction Time
44 hours
Reaction Temp
40 degree C
Solvent
dry THF
COMMENT
Keywords: alpha-D-glycosyl boranophosphate, phosphoramidite, condensation, boronation, terminal deprotection, Leishmania glycocalyx lipophosphoglycans
REFERENCE
Reference Id
REF-0000-000315
Issn
Electronic
Doi
10.1021/jo102584g
PubMed ID
21381786
Journal Name
The Journal of organic chemistry. (2011) 76 (8): 2648-59.
Article Title
Synthesis of oligo(α-D-glycosyl phosphate) derivatives by a phosphoramidite method via boranophosphate intermediates.
Author
Shoichi, Fujita; Natsuhisa, Oka; Fumiko, Matsumura; Takeshi, Wada
Affiliation
Department of Medical Genome Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Bioscience Building 702, 5-1-5 Kashiwanoha, Kashiwa, Chiba 277-8562, Japan.
Reference Id
REF-0000-000316
Source
J. Org. Chem. 2011, 76, 2648-2659
Doi
10.1021/jo102584g

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