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dc.contributor.authorZhang, Hong
dc.contributor.authorRuiz-Castillo, Paula
dc.contributor.authorSchuppe, Alexander W
dc.contributor.authorBuchwald, Stephen L
dc.date.accessioned2022-02-14T18:41:30Z
dc.date.available2022-02-14T18:41:30Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/140330
dc.description.abstractCopyright © 2020 American Chemical Society. An improved protocol for the Pd-catalyzed C-O cross-coupling of secondary alcohols is described. The use of biaryl phosphine L2 as the ligand was key to achieving efficient cross-coupling of (hetero)aryl chlorides with only a 20% molar excess of the alcohol. Additionally, we observed an unusual reactivity difference between an electron-rich aryl bromide and the analogous aryl chloride, and deuterium-labeling suggested that currently unidentified pathways for reduction play an important role in explaining this disparity.en_US
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionof10.1021/ACS.ORGLETT.0C01668en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleImproved Process for the Palladium-Catalyzed C–O Cross-Coupling of Secondary Alcoholsen_US
dc.typeArticleen_US
dc.identifier.citationZhang, Hong, Ruiz-Castillo, Paula, Schuppe, Alexander W and Buchwald, Stephen L. 2020. "Improved Process for the Palladium-Catalyzed C–O Cross-Coupling of Secondary Alcohols." Organic Letters, 22 (14).
dc.relation.journalOrganic Lettersen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-02-14T18:38:25Z
dspace.orderedauthorsZhang, H; Ruiz-Castillo, P; Schuppe, AW; Buchwald, SLen_US
dspace.date.submission2022-02-14T18:38:26Z
mit.journal.volume22en_US
mit.journal.issue14en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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