|
Glycan Syntheses |
JCGG ID |
JCGG-RAC0002739 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-002739
|
||||
Regist Date |
2012/06/21 19:44:37 | ||||
| REACTANT | |||||
|
|
|
||||
Reactant Type |
PPG reagent | ||||
Mol |
0.10 mmol | ||||
|
|
|
||||
Reactant Type |
MoO2Cl2 | ||||
Mol |
0.001 mmol | ||||
|
|
|
||||
Reactant Type |
Ac2O | ||||
Mol |
0.15 mmol | ||||
|
|
|
||||
Reactant Type |
TEA | ||||
Mol |
0.10 mmol | ||||
| PRODUCT | |||||
MOLECULE ID |
|
|
|||
Product Type |
intermediate | ||||
Yield |
89% | ||||
| REACTION DETAIL | |||||
Reaction Time |
2 hours | ||||
Reaction Temp |
120 degree C | ||||
Solvent |
PhCH3 (0.1mL) | ||||
| COMMENT | |||||
| Keywords: trityl, photolabile, PPGs, electron-donating substituents, m-dimethylamino, photochemical deprotection | |||||
| The product was used for the next reaction. (without purification) | |||||
| REFERENCE | |||||
Reference Id |
REF-0000-000365 | ||||
Issn |
Electronic | ||||
Doi |
10.1021/jo200692c | ||||
PubMed ID |
21612261 | ||||
Journal Name |
The Journal of organic chemistry. (2011) 76 (15): 5873-81. | ||||
Article Title |
Development of trityl-based photolabile hydroxyl protecting groups. | ||||
Author |
Lei, Zhou; Haishen, Yang; Pengfei, Wang | ||||
Affiliation |
Department of Chemistry, University of Alabama at Birmingham, 901 14th Street South, Birmingham, Alabama 35294, USA. | ||||
Reference Id |
REF-0000-000366 | ||||
Source |
J. Org. Chem. 2011, 76, 5873-5881 | ||||
Doi |
10.1021/jo200692c | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
|