A convenient route to synthesize N2-(isobutyryl)-9-(carboxymethyl)guanine for aeg-PNA backbone

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