The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C-H activation

dc.citation.issue14
dc.citation.volume12
dc.contributor.authorTewari S
dc.contributor.authorMungalpara MN
dc.contributor.authorPatel S
dc.contributor.authorRowlands GJ
dc.coverage.spatialEngland
dc.date.accessioned2024-01-10T00:37:15Z
dc.date.accessioned2024-07-25T06:51:49Z
dc.date.available2022-03-17
dc.date.available2024-01-10T00:37:15Z
dc.date.available2024-07-25T06:51:49Z
dc.date.issued2022-03-17
dc.description.abstractPlanar chiral [2.2]paracyclophanes are resolved through the direct C-H arylation of enantiopure oxazolines, providing a convenient route to ligands and chiral materials. Preliminary results show that hydrolysis followed by decarboxylative phosphorylation leads to enantiopure [2.2]paracyclophane derivatives that are otherwise challenging to prepare.
dc.description.confidentialfalse
dc.format.pagination8588-8591
dc.identifier.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/35424822
dc.identifier.citationTewari S, Mungalpara MN, Patel S, Rowlands GJ. (2022). The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C-H activation.. RSC Adv. 12. 14. (pp. 8588-8591).
dc.identifier.doi10.1039/d2ra01075e
dc.identifier.eissn2046-2069
dc.identifier.elements-typejournal-article
dc.identifier.issn2046-2069
dc.identifier.piid2ra01075e
dc.identifier.urihttps://mro.massey.ac.nz/handle/10179/71051
dc.languageeng
dc.publisherRoyal Society of Chemistry
dc.publisher.urihttps://pubs.rsc.org/en/content/articlelanding/2022/RA/D2RA01075E
dc.relation.isPartOfRSC Adv
dc.rights(c) 2022 The Author/s
dc.rightsCC BY-NC 3.0
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/
dc.titleThe concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C-H activation
dc.typeJournal article
pubs.elements-id452567
pubs.organisational-groupOther
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