Synthesis and Enzymatic Incorporation of a Responsive Ribonucleoside Probe That Enables Quantitative Detection of Metallo-Base Pairs

dc.contributor.author	MANNA, SUDESHNA	en_US
dc.contributor.author	SRIVATSAN, SEERGAZHI G.	en_US
dc.date.accessioned	2019-06-25T08:50:11Z
dc.date.available	2019-06-25T08:50:11Z
dc.date.issued	2019-06	en_US
dc.identifier.citation	Organic Letters, 21(12), 4646-4650.	en_US
dc.identifier.issn	1523-7060	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3108
dc.identifier.uri	https://doi.org/10.1021/acs.orglett.9b01544	en_US
dc.description.abstract	Synthesis of a highly responsive fluorescent ribonucleoside analogue based on a 5-methoxybenzofuran uracil core, enzymatic incorporation of its triphosphate substrate into RNA transcripts, and its utility in the specific detection and estimation of Hg2+-ion-mediated metallo-base pair formation in DNA–RNA and RNA–RNA duplexes are described.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Chemistry	en_US
dc.subject	TOC-JUN-2019	en_US
dc.subject	2019	en_US
dc.title	Synthesis and Enzymatic Incorporation of a Responsive Ribonucleoside Probe That Enables Quantitative Detection of Metallo-Base Pairs	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Organic Letters	en_US
dc.publication.originofpublisher	Foreign	en_US