Record Details

An Expedient Approach to Internally Functionalized Chiral Dendrimers: Synthesis of a Dendritic Molecule Incorporating Furanoside Skeleton

EPrints@IICB

View Archive Info
 
 
Field Value
 
Title An Expedient Approach to Internally Functionalized Chiral Dendrimers: Synthesis of a Dendritic Molecule Incorporating Furanoside Skeleton
 
Creator Ghorai, Subir
Bhattacharjya, Anup
Basak, Ajoy
Mitra, Abhijit
Williamson, R Thomas
 
Subject Chemistry
 
Description In an approach to chiral dendritic molecules, a
dendrimer incorporating pentose units in the interior and
hexose units in the periphery is built up on a 1, 3, 5-trisubstituted aromatic core by using 1,2:5,6-diisopropylidene glucose as the carbohydrate precursor and a 3, 5-disubstituted aromatic unit as the branching block. The carbohydrate moiety also provides internal functionalities in the form of hemiacetal moiety of the furanoside ring.
 
Date 2003
 
Type Article
PeerReviewed
 
Format application/pdf
 
Identifier http://www.eprints.iicb.res.in/934/1/JOURNAL_OF_ORGANIC_CHEMISTRY%2C__68(_2)%2C_617%2D620[84].pdf
Ghorai, Subir and Bhattacharjya, Anup and Basak, Ajoy and Mitra, Abhijit and Williamson, R Thomas (2003) An Expedient Approach to Internally Functionalized Chiral Dendrimers: Synthesis of a Dendritic Molecule Incorporating Furanoside Skeleton. The Journal of Organic Chemistry, 68 (2). pp. 617-620.
 
Relation http://dx.doi.org/10.1021/jo0264168
http://www.eprints.iicb.res.in/934/