Directed ortho‐Metalation of Aryl Amides, O‐Carbamates, and Methoxymethoxy Systems: Directed Metalation Group Competition and Cooperation

dc.contributor.authorMiah, M.A.J.
dc.contributor.authorSibi, M.P.
dc.contributor.authorChattopadhyay, S.
dc.contributor.authorFamiloni, O.B.
dc.contributor.authorSnieckus, V.
dc.date.accessioned2019-09-05T08:41:33Z
dc.date.available2019-09-05T08:41:33Z
dc.date.issued2017-09-20
dc.descriptionStaff publicationsen_US
dc.description.abstractA systematic study on the competitive metalation of derivatives containing four directed metalation groups (DMGs), namely, Cl, OMe, methoxymethoxy (OMOM), and CONEt2, in comparison with the OCONEt2 DMG is described. In addition, the anionic ortho‐Fries (AoF) rearrangement, the double metalation–electrophile quench of 1,2‐ and 1,4‐O‐carbamates, and iterative metalation procedures are presented. The results provide new methodologies for the synthesis of contiguously functionalized 1,2,3‐ and 1,2,3,4‐substituted aromatic derivatives of difficult accessibility and potential broad utility. A comparison of the present methodology with previously developed routes is provided for selected examples with emphasis on such substituted compounds.en_US
dc.identifier.citationMiah, M. J., [Et...al] (2018). Directed ortho‐Metalation of Aryl Amides, O‐Carbamates, and Methoxymethoxy Systems: Directed Metalation Group Competition and Cooperation. European Journal of Organic Chemistry, 2018(4), 447-454pp.en_US
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/5127
dc.language.isoenen_US
dc.publisherWiley Online Libraryen_US
dc.relation.ispartofseries. European Journal of Organic Chemistry,;
dc.subjectResearch Subject Categories::NATURAL SCIENCES::Chemistry::Organic chemistryen_US
dc.subjectMethoxymethoxy (OMOM)en_US
dc.subjectMetalation groupsen_US
dc.subjectOCONEt2 DMGen_US
dc.titleDirected ortho‐Metalation of Aryl Amides, O‐Carbamates, and Methoxymethoxy Systems: Directed Metalation Group Competition and Cooperationen_US
dc.typeArticleen_US
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