| dc.contributor.author | ANAND, NITYA | |
| dc.contributor.author | JAIN, P C | |
| dc.date.accessioned | 2010-04-29T05:00:50Z | |
| dc.date.available | 2010-04-29T05:00:50Z | |
| dc.date.issued | 1968 | |
| dc.identifier.citation | Indian Journal of Chemistry, 6,1968,767,768 | en |
| dc.identifier.uri | http://hdl.handle.net/123456789/547 | |
| dc.description.abstract | I-P-D-Ribofuranosyl-5-ethoxycarbonyl-4-hydroxy- 1,2-dihydropyrid-2-one has been synthesized starting from 2,4-dihydroxy-5-. The monomercury derivative of the starting compound on condensation with 2,3,5-tri-O-chloride affords which on debenzoylation in the presence of catalytic amount of sodium methoxide in the furnishes the desired nucleoside. | en |
| dc.format.extent | 795740 bytes | |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | en | en |
| dc.subject | methanol | en |
| dc.subject | ethoxycarbonylpyridine | en |
| dc.subject | benzoylated nucleoside | en |
| dc.subject | benzoylribofuranosyl | en |
| dc.title | Synthesis of I-p-D-Ribofuranosyl-5-ethoxycarbonyl-4- hydroxy -l,2-dihydropyrid-2-one. | en |
| dc.type | Article | en |