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dc.contributor.authorJAMDADE, AKASH BANDUen_US
dc.contributor.authorSUTAR, DASHRAT VISHAMBARen_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.date.accessioned2022-07-22T10:55:28Z
dc.date.available2022-07-22T10:55:28Z
dc.date.issued2022-06en_US
dc.identifier.citationOrganic Letters, 24(24), 4394–4398.en_US
dc.identifier.issn1523-7052en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttps://doi.org/10.1021/acs.orglett.2c01617en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7249
dc.description.abstractHerein, we have developed a new approach for the synthesis of 11 to 21-membered macrolactones via intramolecular dehydrogenative coupling of primary alcohols by using Ru-MACHO as a catalyst and Cs2CO3 as a base. This protocol generated 11–21-ring-sized macrocycles (26 derivatives), free from an external oxidant or an additive, eliminating stoichiometric reagents and producing only hydrogen as a byproduct.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectAlcoholsen_US
dc.subjectCatalystsen_US
dc.subjectChemical reactionsen_US
dc.subjectHydrocarbonsen_US
dc.subjectHydrogenen_US
dc.subject2022-JUL-WEEK2en_US
dc.subjectTOC-JUL-2022en_US
dc.subject2022en_US
dc.titleDehydrogenative Intramolecular Macrolactonization of Dihydroxy Compounds Using Ru-MACHO Catalysten_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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