Titre de série :	Comprehensive Chirality
Titre :	Vol.5 : Synthetic methods IV – Asymmetric oxidation reduction, C–N
Type de document :	texte imprimé
Auteurs :	Erick M. Carreira, Éditeur scientifique ; Hisashi Yamamoto, Éditeur scientifique ; Keiji Maruoka, Éditeur scientifique
Editeur :	Amsterdam : Elsevier
Année de publication :	2012
Collection :	Comprehensive Chirality
Importance :	xxvi, 599 p.
Format :	28 cm
ISBN/ISSN/EAN :	978-0-08-095167-6
Langues :	Anglais (eng)
Note de contenu :	"* Asymmetric Baeyer–Villiger oxidation * Oxidation: C–O bond formation by C–H activation * Oxidation: Epoxidation (allylic alcohol, homoallylic alcohol, simple C=C, electron deficient C=C) * Oxidation: ?-hydroxylation of carbonyls * Oxidation: C–N bond formation by oxidation: C–H bond activation * Oxidation: C–N bond formation by oxidation (aziridines) * Oxidation: C–N bond formation by oxidation: Dinitrogen addition to double bond (diamino) * Asymmetric S–O bond formation by oxidation * Oxidation: C–X bond formation (X=Halogen, S, Se) * Reduction – hydrogenation: C=C; chemoselective * Reduction – hydrogenation: C=O; chemoselective * Asymmetric hydrogenation of prochiral C=N bonds * Reduction: Hydrosilylation * Reduction: Hydroformylation C–H and C–C * Reduction: Hydrocyanation of C=C * Reduction: Enantioselective hydrovinylation of alkenes * Reduction: Pinacol coupling * Addition reaction: Kinetic resolution * Addition reaction: 1,4 addition heteroatom * Addition reaction: Cycloaddition involving oxidation (N=N, N=O; No C–C bond formed) * Desymmetrization of meso diols * Desymmetrization of meso epoxide * Desymmetrization of meso anhydride."
Cote :	EXCLU (SdL)
Num_Inv :	3294

Comprehensive Chirality. Vol.5 : Synthetic methods IV – Asymmetric oxidation reduction, C–N [texte imprimé] / Erick M. Carreira, Éditeur scientifique ; Hisashi Yamamoto, Éditeur scientifique ; Keiji Maruoka, Éditeur scientifique . - Amsterdam : Elsevier, 2012 . - xxvi, 599 p. ; 28 cm. - (Comprehensive Chirality) .
ISBN : 978-0-08-095167-6
Langues : Anglais (eng)

Note de contenu :	"* Asymmetric Baeyer–Villiger oxidation * Oxidation: C–O bond formation by C–H activation * Oxidation: Epoxidation (allylic alcohol, homoallylic alcohol, simple C=C, electron deficient C=C) * Oxidation: ?-hydroxylation of carbonyls * Oxidation: C–N bond formation by oxidation: C–H bond activation * Oxidation: C–N bond formation by oxidation (aziridines) * Oxidation: C–N bond formation by oxidation: Dinitrogen addition to double bond (diamino) * Asymmetric S–O bond formation by oxidation * Oxidation: C–X bond formation (X=Halogen, S, Se) * Reduction – hydrogenation: C=C; chemoselective * Reduction – hydrogenation: C=O; chemoselective * Asymmetric hydrogenation of prochiral C=N bonds * Reduction: Hydrosilylation * Reduction: Hydroformylation C–H and C–C * Reduction: Hydrocyanation of C=C * Reduction: Enantioselective hydrovinylation of alkenes * Reduction: Pinacol coupling * Addition reaction: Kinetic resolution * Addition reaction: 1,4 addition heteroatom * Addition reaction: Cycloaddition involving oxidation (N=N, N=O; No C–C bond formed) * Desymmetrization of meso diols * Desymmetrization of meso epoxide * Desymmetrization of meso anhydride."
Cote :	EXCLU (SdL)
Num_Inv :	3294