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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3179
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dc.contributor.authorKumar, Indresh-
dc.date.accessioned2021-10-27T04:28:09Z-
dc.date.available2021-10-27T04:28:09Z-
dc.date.issued2012-02-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S095741661200105X?via%3Dihub-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3179-
dc.description.abstractThe intramolecular alkyne–azide Huisgen [3+2] cycloaddition reaction as a ‘click-chemistry’ reaction without a metal catalyst has been studied under aerobic conditions. The synthesis of various pyrrolidine–triazole hybrid compounds has also been achieved by using this intramolecular cycloaddition reaction in water with complete 1,5-regioselectivity.en_US
dc.language.isoenen_US
dc.publisherElsieveren_US
dc.subjectChemistryen_US
dc.subjectPyrrolidine–triazolesen_US
dc.subjectSynthesisen_US
dc.subjectIntramolecular Huisgenen_US
dc.titleIntramolecular Huisgen [3+2] cycloaddition in water: synthesis of fused pyrrolidine–triazolesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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