Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8405
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dc.contributor.authorJAMDADE, AKASH B.en_US
dc.contributor.authorSUTAR, DASHRAT V.en_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.date.accessioned2024-01-24T04:25:48Z
dc.date.available2024-01-24T04:25:48Z
dc.date.issued2023-12en_US
dc.identifier.citationOrganic Letters, 25(50), 9058–9063.en_US
dc.identifier.issn1523-7060en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttps://doi.org/10.1021/acs.orglett.3c03885en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8405
dc.description.abstractHerein, we report the Ru-/Ir-catalyzed synthesis of valuable macrolactams from macrolactones and esters. The ring-opening of the macrolactones was efficaciously facilitated by the Ru catalyst to generate 32 amides in the first step. In the second step, intramolecular N-alkylative ring closure of amides with alcohols was succeeded by Ir catalyst to provide a series of 22 macrolactams and gave water as a byproduct. Moreover, this approach proceeded under neutral conditions and avoided the use of external additives.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectAlcoholsen_US
dc.subjectAmidesen_US
dc.subjectCatalystsen_US
dc.subjectChemical reactionsen_US
dc.subjectOrganic reactionsen_US
dc.subject2024-JAN-WEEK1en_US
dc.subjectTOC-JAN-2024en_US
dc.subject2023en_US
dc.titleSynthesis of Macrolactams from Macrolactones Using Ru-/Ir-Catalytic System under Neutral Conditionsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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