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Glycan Syntheses |
JCGG ID |
JCGG-RAC0001842 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001842
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Regist Date |
2012/06/21 18:08:14 | |||||||
| REACTANT | ||||||||
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Mol |
25.7 mmol | |||||||
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Reactant Type |
DBTO | |||||||
Mol |
56.6 mmol | |||||||
| PRODUCT | ||||||||
MOLECULE ID |
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Product Type |
stannane | |||||||
Yield |
82%(at least) | |||||||
| REACTION DETAIL | ||||||||
Reaction Time |
1 hour | |||||||
Reaction Temp |
70 degree C | |||||||
Solvent |
dry MeOH | |||||||
| COMMENT | ||||||||
| Keywords: synthesis, methyl 2,6-di-O-benzyl-alpha-D-glucopyranoside | ||||||||
| The reaction is the 1st part of the sequence. | ||||||||
| REFERENCE | ||||||||
Reference Id |
REF-0000-000253 | |||||||
Source |
Essentials of Carbohydrate Chemistry and Biochemistry | |||||||
Reference Id |
REF-0000-000254 | |||||||
Source |
ISBN 978-3-527-31528-4 | |||||||
Reference Id |
REF-0000-000267 | |||||||
Source |
Tetrahedron Lett. 11, 3503 (1976) | |||||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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