11 Oxidation of Amines and N-Hetarenes
Buch
Herausgeber: Muniz, K.
Titel: Catalytic Oxidation in Organic Synthesis
Print ISBN: 9783132012318; Online ISBN: 9783132403710; Buch-DOI: 10.1055/b-003-129345
1st edition © 2018. Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Fachgebiete: Organische Chemie;Chemische Reaktionen, Katalyse;Organometallchemie;Chemische Labormethoden, Stöchiometrie
Science of Synthesis Reference Libraries
Übergeordnete Publikation
Titel: Science of Synthesis
DOI: 10.1055/b-00000101
Reihenherausgeber: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Koch, G.; Molander, G. A.; Schaumann, E.; Shibasaki, M.; Thomas, E. J.; Trost, B. M.
Typ: Mehrbändiges Werk
Abstract
The oxidation of amines and hetarenes are significant transformations that have been widely applied in synthetic organic chemistry. In this chapter, the oxidation of primary, secondary, and tertiary amines, affording imines, nitriles, amides, carbonyls, oximes, nitro compounds, diazenes and their oxides, nitrones, hydrazines, and N-oxides, as well as the oxidation of hetarenes including pyridines, azoles, pyrroles, indoles, guanines, and adenines, are comprehensively discussed. In addition to traditional organometallic catalysis to fulfill these oxidation reactions, some advanced approaches such as photocatalysis, biochemical catalysis, and biomimetic catalysis are also described.
Schlüsselwörter
oxidation of amines - oxidation of hetarenes - organometallic catalysis - photocatalysis - biomimetic catalysis-
18 Cristian L, Nica S, Pavel O D, Mihailciuc C, Almasan V, Coman S M, Hardacre C, Parvulescu V I. Catal. Sci. Technol. 2013; 3: 2646
-
19 Pavel O D, Goodrich P, Cristian L, Coman S M, Pârvulescu V I, Hardacre C. Catal. Sci. Technol. 2015; 5: 2696
-
39 Jayachandran B, Sasidharan M, Sudalai A, Ravindranathan T. J. Chem. Soc., Chem. Commun. 1995; 1523
-
44 Choudary B M, Bharathi B, Reddy C V, Kantam M L, Raghavan K V. Chem. Commun. (Cambridge) 2001; 1736
-
61 Abrantes M, Gonçalves I S, Pillinger M, Vurchio C, Cordero F M, Brandi A. Tetrahedron Lett. 2011; 52: 7079
-
80 Suresh S, Joseph R, Jayachandran B, Pol A V, Vinod M P, Sudalai A, Sonawane H R, Ravindranathan T. Tetrahedron 1995; 51: 11305
-
84 Benedini F, Nali M, Rindone B, Tollari S, Cenini S, La Monica G, Porta F. J. Mol. Catal. 1984; 34: 155
-
92 Ma H, Li W, Wang J, Xiao G, Gong Y, Qi C, Feng Y, Li X, Bao Z, Cao W, Sun Q, Veaceslav C, Wang F, Lei Z. Tetrahedron 2012; 68: 8358
-
125 Veerakumar P, Balakumar S, Velayudham M, Lu K-L, Rajagopal S. Catal. Sci. Technol. 2012; 2: 1140
-
126 Larionov O V, Stephens D, Mfuh A M, Arman H D, Naumova A S, Chavez G, Skenderi B. Org. Biomol. Chem. 2014; 12: 3026
-
140 Crossley M J, Burn P L, Langford S J, Pyke S M, Stark A G. J. Chem. Soc., Chem. Commun. 1991; 1567
-
142 Carvalho C M B, Neves M G P M S, Tomé A C, Paz F A A, Silva A M S, Cavaleiro J A S. Org. Lett. 2011; 13: 130
-
149 Sriram R, Kumar C N S S P, Raghunandan N, Ramesh V, Sarangapani M, Rao V J. Synth. Commun. 2012; 42: 3419
-
155 Choi S, Cooley R B, Hakemian A S, Larrabee Y C, Bunt R C, Maupas S D, Muller J G, Burrows C J. J. Am. Chem. Soc. 2004; 126: 591