JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0002596
Submitter
The Noguchi Institute
Reaction ID
R-0000-002596
Regist Date
2012/06/21 19:29:46
REACTANT
MOLECULE ID
JCGG-COM0003370 (Reaction Tree)
Skeleton
JCGG-STR007826
MOLECULE ID
JCGG-COM0000530
Reactant Type
NaOMe
PRODUCT
MOLECULE ID
JCGG-COM0003371 (Reaction Tree)
Skeleton
JCGG-STR007826
Yield
NOT specified
REACTION DETAIL
Reaction Time
NOT specified
Reaction Temp
NOT specified
Solvent
MeOH
Comment
Very few were described regarding this reaction.
COMMENT
Keywords: 2-methylchromone-7-O-rutinosides, cytotoxicity, human tumor cell lines, acidic labile, 2-methylchromone aglycon
REFERENCE
Reference Id
REF-0000-000355
Issn
Electronic
Doi
10.1021/jo102325s
PubMed ID
21366286
Journal Name
The Journal of organic chemistry. (2011) 76 (7): 2265-8.
Article Title
Concise synthesis of 5-methoxy-6-hydroxy-2-methylchromone-7-O- and 5-hydroxy-2-methylchromone-7-O-rutinosides. Investigation of their cytotoxic activities against several human tumor cell lines.
Author
Baolin, Wu; Wenpeng, Zhang; Zhonghua, Li; Li, Gu; Xin, Wang; Peng George, Wang
Affiliation
Department of Chemistry, The Ohio State University, 484 West 12th Avenue, Columbus, Ohio 43210, USA.
Reference Id
REF-0000-000356
Source
J. Org. Chem. 2011, 76, 2265-2268
Doi
10.1021/jo102325s

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