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Synthesis of Macrolactams from Macrolactones Using Ru-/Ir-Catalytic System under Neutral Conditions

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dc.contributor.author JAMDADE, AKASH B. en_US
dc.contributor.author SUTAR, DASHRAT V. en_US
dc.contributor.author GNANAPRAKASAM, BOOPATHY en_US
dc.date.accessioned 2024-01-24T04:25:48Z
dc.date.available 2024-01-24T04:25:48Z
dc.date.issued 2023-12 en_US
dc.identifier.citation Organic Letters, 25(50), 9058–9063. en_US
dc.identifier.issn 1523-7060 en_US
dc.identifier.issn 1523-7052 en_US
dc.identifier.uri https://doi.org/10.1021/acs.orglett.3c03885 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8405
dc.description.abstract Herein, 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.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Alcohols en_US
dc.subject Amides en_US
dc.subject Catalysts en_US
dc.subject Chemical reactions en_US
dc.subject Organic reactions en_US
dc.subject 2024-JAN-WEEK1 en_US
dc.subject TOC-JAN-2024 en_US
dc.subject 2023 en_US
dc.title Synthesis of Macrolactams from Macrolactones Using Ru-/Ir-Catalytic System under Neutral Conditions 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


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