An Expedient Approach to Internally Functionalized Chiral Dendrimers: Synthesis of a Dendritic Molecule Incorporating Furanoside Skeleton
IR@IICB: CSIR-Indian Institute of Chemical Biology, Kolkata
View Archive Info| Field | Value | |
| Title |
An Expedient Approach to Internally
Functionalized Chiral Dendrimers:
Synthesis of a Dendritic Molecule
Incorporating Furanoside Skeleton
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| Creator |
Ghorai, Subir
Bhattacharjya, Anup Basak, Ajoy Mitra, Abhijit Williamson, R Thomas |
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| Subject |
Chemistry
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| 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.
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| Publisher |
American Chemical Society
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| Date |
2003
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| Type |
Article
PeerReviewed |
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| Format |
application/pdf
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| Identifier |
http://www.eprints.iicb.res.in/609/1/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. |
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| Relation |
http://dx.doi.org/10.1021/jo0264168 CCC: $25.00
http://www.eprints.iicb.res.in/609/ |
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