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Book Chapter: Oxidation by Metals (Nitrene)

TitleOxidation by Metals (Nitrene)
Authors
KeywordsAziridination
C-H insertion
Enantioselectivity
Iminoiodinanes
Metal-imido intermediates
Nitrene transfer
Organic azides
Oxycarbamates
Issue Date2014
PublisherElsevier Ltd.
Citation
Oxidation by Metals (Nitrene). In Knochel, P & Molander, GA (Eds.), Comprehensive Organic Synthesis (2 ed.), v. 7, p. 26-85. Amsterdam: Elsevier Ltd., 2014 How to Cite?
AbstractRecent surge of interest in metal-catalyzed nitrene transfer reactions reflects the high importance of such reactions in organic synthesis. Nitrene transfer reaction, the analogous to carbene and oxo transfer reactions, involves the formation of a new covalent X–N bond, where X is mainly C atom for most of the metal-catalyzed nitrene transfer and insertion reactions. This class of reactions can also be viewed as oxidation due to the higher electronegativity of nitrogen atom than carbon atom. In this chapter, the focus is on the transition metal-catalyzed nitrene transfer and insertion reactions reported since the year 2000. A brief description of earlier studies is provided. Mechanistic studies including the preparation and characterization of the reaction intermediates and the identification of short-lived reactive species are discussed. The recent important findings in transition metal-catalyzed alkene aziridination, C–H amidation/amination, and sulfimidation reactions are highlighted in this chapter.
Persistent Identifierhttp://hdl.handle.net/10722/198946
ISBN

 

DC FieldValueLanguage
dc.contributor.authorChe, CM-
dc.contributor.authorLo, KY-
dc.contributor.authorZhou, C-
dc.date.accessioned2014-07-21T09:54:55Z-
dc.date.available2014-07-21T09:54:55Z-
dc.date.issued2014-
dc.identifier.citationOxidation by Metals (Nitrene). In Knochel, P & Molander, GA (Eds.), Comprehensive Organic Synthesis (2 ed.), v. 7, p. 26-85. Amsterdam: Elsevier Ltd., 2014-
dc.identifier.isbn9780080977430-
dc.identifier.urihttp://hdl.handle.net/10722/198946-
dc.description.abstractRecent surge of interest in metal-catalyzed nitrene transfer reactions reflects the high importance of such reactions in organic synthesis. Nitrene transfer reaction, the analogous to carbene and oxo transfer reactions, involves the formation of a new covalent X–N bond, where X is mainly C atom for most of the metal-catalyzed nitrene transfer and insertion reactions. This class of reactions can also be viewed as oxidation due to the higher electronegativity of nitrogen atom than carbon atom. In this chapter, the focus is on the transition metal-catalyzed nitrene transfer and insertion reactions reported since the year 2000. A brief description of earlier studies is provided. Mechanistic studies including the preparation and characterization of the reaction intermediates and the identification of short-lived reactive species are discussed. The recent important findings in transition metal-catalyzed alkene aziridination, C–H amidation/amination, and sulfimidation reactions are highlighted in this chapter.-
dc.languageeng-
dc.publisherElsevier Ltd.-
dc.relation.ispartofComprehensive Organic Synthesis (2 ed.)-
dc.subjectAziridination-
dc.subjectC-H insertion-
dc.subjectEnantioselectivity-
dc.subjectIminoiodinanes-
dc.subjectMetal-imido intermediates-
dc.subjectNitrene transfer-
dc.subjectOrganic azides-
dc.subjectOxycarbamates-
dc.titleOxidation by Metals (Nitrene)en_US
dc.typeBook_Chapteren_US
dc.identifier.emailChe, CM: cmche@hku.hk-
dc.identifier.emailLo, KY: vanessal@hkusua.hku.hk-
dc.identifier.emailZhou, C: cyzhou@hku.hk-
dc.identifier.doi10.1016/B978-0-08-097742-3.00703-5-
dc.identifier.scopuseid_2-s2.0-84903509232-
dc.identifier.hkuros231500-
dc.identifier.volume7-
dc.identifier.spage26-
dc.identifier.epage85-
dc.publisher.placeAmsterdam-

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