Stereoselective Synthesis of 2'-Deoxynucleoside Analogues as Building Blocks for Deoxynucleoside Chemistry

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dc.contributor.author Pal, Pinki
dc.contributor.author Singh, Pragya
dc.contributor.author Kumar, Brijesh
dc.contributor.author Guniyal, H M
dc.contributor.author Shaw, A K
dc.date.accessioned 2011-09-30T10:50:56Z
dc.date.available 2011-09-30T10:50:56Z
dc.date.issued 2011
dc.identifier.citation Tetrahedron Asymmetry (2011), 22(9), 992-999 en
dc.identifier.uri http://hdl.handle.net/123456789/726
dc.description.abstract Three pairs of enantiomeric 2'-deoxy nucleoside analogues (4a, 4b), (4c, 4e) and (4d, 4f) respectively have been synthesized from enantiomerically pure highly functionalized furanoid glycals 2a-d by involving the similar synthetic strategy. These analogues with various well defined chiral centres are useful building blocks for deoxynucleoside chemistry. en
dc.format.extent 547448 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CDRI communication no. 8080 en
dc.subject Enantiomeric 2 en
dc.subject deoxy nucleoside analogues en
dc.subject furanoid glycols en
dc.subject deoxynucleoside chemistry en
dc.title Stereoselective Synthesis of 2'-Deoxynucleoside Analogues as Building Blocks for Deoxynucleoside Chemistry en
dc.type Article en


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