JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
 JCGG-RAC0002759
Submitter
 The Noguchi Institute
Reaction ID
 R-0000-002759
Regist Date
 2012/06/21 19:46:05
REACTANT
MOLECULE ID
 JCGG-COM0003605 (Reaction Tree)
Skeleton
JCGG-STR032527
Mol
 less than 0.173 mmol
MOLECULE ID
 JCGG-COM0000647
Reactant Type
 Na2CO3
Weight
 1.3 mg
MOLECULE ID
 JCGG-COM0000418
Reactant Type
 NaOH
Mol
 7 mmol
PRODUCT
MOLECULE ID
 JCGG-COM0003599 (Reaction Tree)
Skeleton
JCGG-STR032527
Yield
 37%
MOLECULE ID
 JCGG-COM0003600 (Reaction Tree)
Skeleton
JCGG-STR032527
Yield
 52%
MOLECULE ID
 JCGG-COM0003602 (Reaction Tree)
Yield
 27%
MOLECULE ID
 JCGG-COM0003603 (Reaction Tree)
Yield
 12%
MOLECULE ID
 JCGG-COM0003606 (Reaction Tree)
Yield
 7%
MOLECULE ID
 JCGG-COM0003607 (Reaction Tree)
Yield
 7%
REACTION DETAIL
Reaction Time
 4.5 hours
Reaction Temp
 NOT specified
Solvent
 H2O (34.6mL)
Reaction Type
 photochemical cleavage
Comment
 irradiation of UV light
COMMENT
Keywords: trityl, photolabile, PPGs, electron-donating substituents, m-dimethylamino, photochemical deprotection
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)