Accessing a small library of pluripotent 1,4,5-trisubstituted 1H-1,2,3-triazoles via diversity oriented synthesis

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dc.contributor.author Ajay, Arya
dc.contributor.author Gupt, M P
dc.contributor.author Devender, N
dc.contributor.author Tripathi, R P
dc.date.accessioned 2013-07-25T10:16:11Z
dc.date.available 2013-07-25T10:16:11Z
dc.date.issued 2012
dc.identifier.citation Molecular Diversity, 2012, 16(2), 335-350 en
dc.identifier.uri http://hdl.handle.net/123456789/1116
dc.description.abstract Diversity oriented synthesis of structurally diverse, novel and small drug like molecules based on 1,4,5-trisubstituted 1,2,3-triazoles is developed in a streamlined sequence of different sets of reactions. The method involves the use of simple, readily available and highly economical substrates and reagents. The molecules developed herein have potential to be exploited either as chemotherapeutic agents or as scaffolds for other biologically active compounds. en
dc.format.extent 1046041 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CSIR-CDRI communication no 8204 en
dc.subject β-Amino alocohol en
dc.subject Benzooxazoles en
dc.subject Dipolar cycloaddition en
dc.subject Diversity oriented synthesis en
dc.subject 1,4,5-Trisubstituted-1H-1,2,3-,Triazoles en
dc.title Accessing a small library of pluripotent 1,4,5-trisubstituted 1H-1,2,3-triazoles via diversity oriented synthesis en
dc.type Article en


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