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dc.contributor.authorKumar, Dalip-
dc.date.accessioned2021-10-27T04:20:06Z-
dc.date.available2021-10-27T04:20:06Z-
dc.date.issued2015-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/B9780128000700000141?via%3Dihub-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3036-
dc.description.abstractFacile and metal-free syntheses of natural and natural product-inspired bioactive heterocycles are of paramount importance in drug discovery program; therefore, it is highly desirable to develop efficient protocols to generate a diverse library of drug-like molecules. In recent years, organohypervalent iodines have played a vital role as eco-friendly recyclable reagents to construct a variety of bioactive heterocycles, particularly with five- and six-membered ring systems. Due to readily accessible, easy-to-use and shorter reaction times, organohypervalent iodine reagents have gained special attention as versatile and benign oxidants in several organic transformations. Moreover, in a multistep synthesis of natural bioactive heterocycles, organohypervalent iodine reagents are important source to achieve key intermediates for being safer alternatives to hazardous and metal-based reagents. This chapter summarizes the recent trends adapted by organic chemists mainly in the synthesis of biologically relevant five- and six-membered heterocycles using such diverse organohypervalent iodine reagents.en_US
dc.language.isoenen_US
dc.publisherElsieveren_US
dc.subjectChemistryen_US
dc.subject(Diacetoxy)iodobenzeneen_US
dc.subjectBioactive heterocyclesen_US
dc.subjectDess–Martin periodinaneen_US
dc.titleOrganohypervalent Iodine Reagents in the Synthesis of Bioactive Heterocyclesen_US
dc.typeBook chapteren_US
Appears in Collections:Department of Chemistry

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