JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0001525
Submitter
The Noguchi Institute
Reaction ID
R-0000-001525
Regist Date
2012/06/21 17:16:56
REACTANT
MOLECULE ID
JCGG-COM0001937 (Reaction Tree)
MOLECULE ID
JCGG-COM0000647
Reactant Type
Na2CO3
MOLECULE ID
JCGG-COM0000414
Reactant Type
H2
MOLECULE ID
JCGG-COM0001026
Reactant Type
Pd-C
MOLECULE ID
JCGG-COM0000086
Reactant Type
Ac2O
PRODUCT
MOLECULE ID
JCGG-COM0001938 (Reaction Tree)
Yield
59%
REACTION DETAIL
Reaction Time
NOT specified, NOT specified, NOT specified
Reaction Temp
NOT specified, NOT specified, NOT specified
Solvent
MeOH, Et3N/AcOEt, pyridine
Comment
1) bromide+Na2CO3, 2) +H2, Pd-C, 3) +Ac2O
Very few were described regarding this reaction.
COMMENT
Keywords: The synthesis of 2-deoxy-glycoside, stereoselectivity control using C-2 substitution group
There are multiple steps in this reaction.
The reaction is the 3rd part of the sequence.
REFERENCE
Reference Id
REF-0000-000073
Source
第4版 実験化学講座 (26), 丸善
Reference Id
REF-0000-000074
Source
ISBN 4-621-03702-1
Reference Id
REF-0000-000165
Source
J. Thiem and M. Gerken, J. Carbohydr. Chem., 1, 229 (1982)

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