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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | DATTA, DHRUBAJYOTI | en_US |
| dc.date.accessioned | 2022-06-13T04:29:00Z | - |
| dc.date.available | 2022-06-13T04:29:00Z | - |
| dc.date.issued | 2020-08 | en_US |
| dc.identifier.citation | Nucleosides, Nucleotides & Nucleic Acids, 39(4) , 530-541. | en_US |
| dc.identifier.issn | 1525-7770 | en_US |
| dc.identifier.issn | 1532-2335 | en_US |
| dc.identifier.uri | https://doi.org/10.1080/15257770.2019.1666139 | en_US |
| dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7029 | - |
| dc.description.abstract | Synthesis of exclusive N2-(isobutyryl)-9-(carboxymethyl)guanine, an important moiety for peptide nucleic acid synthesis has been reported through a high-yielding reaction scheme starting from 6-chloro-2-amino purine. Crystal structures of two intermediates confirmed the formation of N9-regioisomer. This new synthetic route can potentially replace the conventional tedious method with moderate overall yield. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Taylor & Francis | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | 2020 | en_US |
| dc.title | A convenient route to synthesize N2-(isobutyryl)-9-(carboxymethyl)guanine for aeg-PNA backbone | en_US |
| dc.type | Article | en_US |
| dc.contributor.department | Dept. of Chemistry | en_US |
| dc.identifier.sourcetitle | Nucleosides, Nucleotides & Nucleic Acids | en_US |
| dc.publication.originofpublisher | Foreign | en_US |
| Appears in Collections: | JOURNAL ARTICLES | |
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