Relevant bibliographies by topics / Hydroamination

Academic literature on the topic 'Hydroamination'

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Published: 4 June 2021
Last updated: 22 June 2024

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Journal articles on the topic "Hydroamination"

1

Tobisch, Sven. "CuH-catalysed hydroamination of arylalkynes with hydroxylamine esters – a computational scrutiny of rival mechanistic pathways." Chemical Science 8, no. 6 (2017): 4410–23. http://dx.doi.org/10.1039/c7sc01107e.

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An in-depth computational mechanistic probe of the CuH-mediated hydroamination of internal arylalkynes with amine electrophile and hydrosilane defines the most accessible pathways for rival avenues of direct and reductive hydroamination, from which a general understanding of the factors controlling formal hydroamination catalysis emerges.
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Li, Ping, Boon Chong Lee, Ming Joo Koh, and Xiaoxiang Zhang. "Base-Mediated Site-Selective Hydroamination of Alkenes." Synthesis 54, no. 06 (October 28, 2021): 1566–76. http://dx.doi.org/10.1055/a-1681-4720.

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AbstractWe present a base-mediated hydroamination protocol, using substoichiometric amounts of a hydrosilane and potassium tert-butoxide­, that operates under mild conditions at 30 °C. Many aryl- and heteroatom-substituted olefins as well as arylamines are tolerated, affording the desired products with complete regioselectivity. Preliminary mechanistic investigations reveal a non-radical pathway for hydroamination. A sequential remote hydroamination strategy involving an initial Fe-catalysed olefin isomerisation followed by our base-mediated hydroamination was also developed to directly access β-arylamines from terminal aliphatic alkenes.
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Yang, Song, Quan-Zhe Li, Chen Xu, Qin Xu, and Min Shi. "Rhodium-catalyzed asymmetric hydroamination and hydroindolation of keto-vinylidenecyclopropanes." Chemical Science 9, no. 22 (2018): 5074–81. http://dx.doi.org/10.1039/c8sc01595c.

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A novel rhodium-catalyzed asymmetric hydroamination and hydroindolation of keto-vinylidenecyclopropanes has been developed, affording the hydroamination and hydroindolation products in good to excellent yields with outstanding ee values through a new TMM–Rh model complex.
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Tobisch, Sven. "Aluminium-catalysed intramolecular hydroamination of aminoalkenes: computational perusal of alternative pathways for aminoalkene activation." Dalton Transactions 44, no. 27 (2015): 12169–79. http://dx.doi.org/10.1039/c5dt00121h.

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Rival mechanistic pathways for CC bond activation in aluminium-catalysed hydroamination: computational mechanistic analysis reveals that a catalytically relevant [(pda)Al(NHR)] compound promotes hydroamination through a stepwise σ-bond insertive mechanism with turnover-limiting aminolysis.
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Palchak, Zachary L., Daniel J. Lussier, Conor J. Pierce, Hoseong Yoo, and Catharine H. Larsen. "Catalytic Tandem Markovnikov Hydroamination-Alkynylation and Markovnikov Hydroamination-Hydrovinylation." Advanced Synthesis & Catalysis 357, no. 2-3 (January 30, 2015): 539–48. http://dx.doi.org/10.1002/adsc.201401037.

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Suleymanov, Yury. "Anti-Markovnikov hydroamination." Science 366, no. 6467 (November 14, 2019): 834.2–834. http://dx.doi.org/10.1126/science.366.6467.834-b.

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Hong, Sukwon, and Tobin J. Marks. "Organolanthanide-Catalyzed Hydroamination." Accounts of Chemical Research 37, no. 9 (September 2004): 673–86. http://dx.doi.org/10.1021/ar040051r.

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Ogasawara, M., T. Takahashi, W. Lin, A. Hu, T. Sakamoto, A. Okada, and K. Nakajima. "Intermolecular Asymmetric Hydroamination." Synfacts 2007, no. 1 (January 2007): 0049. http://dx.doi.org/10.1055/s-2006-955723.

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9

Shibuya, Masatoshi, Shohei Kawano, Shoji Fujita, and Yoshihiko Yamamoto. "Boron‐Catalyzed Hydroamination/Hydroallylation and Hydroamination/Hydrocyanation of Unactivated Alkynes." Asian Journal of Organic Chemistry 8, no. 7 (May 21, 2019): 1075–79. http://dx.doi.org/10.1002/ajoc.201900165.

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Casnati, Alessandra, Aleksandr Voronov, Damiano Giuseppe Ferrari, Raffaella Mancuso, Bartolo Gabriele, Elena Motti, and Nicola Della Ca’. "PdI2 as a Simple and Efficient Catalyst for the Hydroamination of Arylacetylenes with Anilines." Catalysts 10, no. 2 (February 2, 2020): 176. http://dx.doi.org/10.3390/catal10020176.

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The hydroamination reaction is a convenient alternative strategy for the formation of C–N bonds. Herein, we report a new versatile and convenient protocol for the hydroamination of arylacetylenes with anilines using palladium iodide in the absence of any added ligand as catalyst. Mild conditions, excellent regio- and stereoselectivity, and high functional group tolerance are the main features of this methodology. A subsequent reduction step gives access to a wide variety of secondary aromatic amines.
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Dissertations / Theses on the topic "Hydroamination"

1

Shasha, Adelle. "Metal-Catalysed Hydroamination." Science. School of Chemistry, 2007. http://hdl.handle.net/2123/1710.

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Doctor of Philosophy(PhD),
This thesis describes the synthesis of terminal and internal amino and amidoalkynes and their hydroamination (cyclisation) catalysed by the complex (bis(N-methylimidazol-2-yl)methane)dicarbonylrhodium(I) tetraphenylborate (1). A series of analogous palladium complexes were also prepared and investigated for catalytic hydroamination. The scope of the rhodium(I) complex (1) for the intramolecular hydroamination of more complex amino and amidoalkyne substrates was investigated. This was made possible with the synthesis of aliphatic substrates, namely, 4 pentyn 1 amide (3) and 5 hexyn 1 amide (4) and a number of aromatic substrates, namely, 1, 4 diamino-2, 5 diethynylbenzene (5), 1, 4-diamino-2, 5 bis(phenylethynyl)benzene (6), 2, 3-diamino-1, 4-diethynylbenzene (7), 2, 3-diamino-1, 4-bis(phenylethynyl)benzene (8), 1, 5-bis(acetamido)-2, 4-diethynylbenzene (9), N-(acetyl)-2-ethynylbenzylamine (10) and N-(acetyl)-2-(phenylethynyl)benzylamine (11). The rhodium(I) complex (1) catalytically cyclised the aliphatic 4 pentyn 1 amide (3) regioselectively to the 6 membered ring, 3, 4 dihydro 2 pyridone (64) as the sole product. Attempts to cyclise 5 hexyn 1 amide (4) to produce either the 6 or 7 membered ring were unsuccessful. Compounds 5, 6, 7 and 8 were doubly cyclised to 1, 5 dihydro pyrrolo[2, 3 f]indole (71), 1, 5-dihydro-2, 6-diphenyl-pyrrolo[2, 3 f]indole (73), 1, 8-dihydro-pyrrolo[2, 3 g]indole (74) and 1, 8-dihydro-2, 7-diphenyl-pyrrolo[2, 3 g]indole (75) respectively. The aromatic amides with terminal acetylenes 9 and 10 cyclised to give 1, 7 diacetyl pyrrolo[3, 2 f]indole (76) and N (acetyl) 1, 2 dihydroisoquinoline (77) respectively. However, attempts to cyclise 11 were unsuccessful. Thus the rhodium(I) complex (1) successfully catalysed via hydroamination both terminal and internal acetylenic amine and amide substrates, to give pyridones, indoles and isoquinolines. Cationic and neutral palladium complexes incorporating the bidentate heterocyclic nitrogen donor ligand bis(N-methylimidazol-2-yl)methane (bim; 2) were synthesised: [Pd(bim)Cl2] (15), [Pd(bim)2][BF4]2 (17) [Pd(bim)(Cl)(CH3)] (14), [Pd(bim)(CH3)(NCCH3)][BF4] (16). All of the complexes were active as catalysts for the intramolecular hydroamination reaction, using the cyclisation of 4 pentyn 1 amine (21) to 2 methyl 1 pyrroline (22) as the model test reaction. Percentage conversions, turnover numbers and reaction profiles for each complex were compared to the rhodium(I) complex (1). These studies have shown that the catalytic activity was not significantly dependent on the bim donor ligand or the choice of metal. Substitution of the bim (2) ligand with the COD ligand and the use of methanol as the solvent did impact significantly on the efficiency of the hydroamination reactions.
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Shasha, Adelle. "Metal-Catalysed Hydroamination." Thesis, The University of Sydney, 2006. http://hdl.handle.net/2123/1710.

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This thesis describes the synthesis of terminal and internal amino and amidoalkynes and their hydroamination (cyclisation) catalysed by the complex (bis(N-methylimidazol-2-yl)methane)dicarbonylrhodium(I) tetraphenylborate (1). A series of analogous palladium complexes were also prepared and investigated for catalytic hydroamination. The scope of the rhodium(I) complex (1) for the intramolecular hydroamination of more complex amino and amidoalkyne substrates was investigated. This was made possible with the synthesis of aliphatic substrates, namely, 4 pentyn 1 amide (3) and 5 hexyn 1 amide (4) and a number of aromatic substrates, namely, 1, 4 diamino-2, 5 diethynylbenzene (5), 1, 4-diamino-2, 5 bis(phenylethynyl)benzene (6), 2, 3-diamino-1, 4-diethynylbenzene (7), 2, 3-diamino-1, 4-bis(phenylethynyl)benzene (8), 1, 5-bis(acetamido)-2, 4-diethynylbenzene (9), N-(acetyl)-2-ethynylbenzylamine (10) and N-(acetyl)-2-(phenylethynyl)benzylamine (11). The rhodium(I) complex (1) catalytically cyclised the aliphatic 4 pentyn 1 amide (3) regioselectively to the 6 membered ring, 3, 4 dihydro 2 pyridone (64) as the sole product. Attempts to cyclise 5 hexyn 1 amide (4) to produce either the 6 or 7 membered ring were unsuccessful. Compounds 5, 6, 7 and 8 were doubly cyclised to 1, 5 dihydro pyrrolo[2, 3 f]indole (71), 1, 5-dihydro-2, 6-diphenyl-pyrrolo[2, 3 f]indole (73), 1, 8-dihydro-pyrrolo[2, 3 g]indole (74) and 1, 8-dihydro-2, 7-diphenyl-pyrrolo[2, 3 g]indole (75) respectively. The aromatic amides with terminal acetylenes 9 and 10 cyclised to give 1, 7 diacetyl pyrrolo[3, 2 f]indole (76) and N (acetyl) 1, 2 dihydroisoquinoline (77) respectively. However, attempts to cyclise 11 were unsuccessful. Thus the rhodium(I) complex (1) successfully catalysed via hydroamination both terminal and internal acetylenic amine and amide substrates, to give pyridones, indoles and isoquinolines. Cationic and neutral palladium complexes incorporating the bidentate heterocyclic nitrogen donor ligand bis(N-methylimidazol-2-yl)methane (bim; 2) were synthesised: [Pd(bim)Cl2] (15), [Pd(bim)2][BF4]2 (17) [Pd(bim)(Cl)(CH3)] (14), [Pd(bim)(CH3)(NCCH3)][BF4] (16). All of the complexes were active as catalysts for the intramolecular hydroamination reaction, using the cyclisation of 4 pentyn 1 amine (21) to 2 methyl 1 pyrroline (22) as the model test reaction. Percentage conversions, turnover numbers and reaction profiles for each complex were compared to the rhodium(I) complex (1). These studies have shown that the catalytic activity was not significantly dependent on the bim donor ligand or the choice of metal. Substitution of the bim (2) ligand with the COD ligand and the use of methanol as the solvent did impact significantly on the efficiency of the hydroamination reactions.
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Penzien, Jochen. "New heterogeneous catalysts for hydroamination reactions." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=964639076.

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Jiménez, Silva Oriol. "Novel heterogeneous catalysts for intermolecular hydroamination reactions." [S.l.] : [s.n.], 2006. http://mediatum2.ub.tum.de/doc/601479/document.pdf.

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Couce, Ríos Almudena. "Mechanistic insights into metal-catalyzed hydroamination reactions." Doctoral thesis, Universitat Autònoma de Barcelona, 2017. http://hdl.handle.net/10803/403762.

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El tema de esta tesis es el estudio DFT del mecanismo de hidroaminaciones intermoleculares catalizadas por catalizadores de rodio y oro. Los compuestos que contienen nitrógeno son muy valiosos y tienen muchos usos que van desde productos farmacéuticos hasta productos químicos. La reacción de hidroaminación es la vía más económica para sintetizar aminas sustituidas. Los catalizadores metálicos que han sido desarrollados para la hidroaminación directa incluyen tanto lantánidos como metales de transición tempranos y tardíos. Los catalizadores más versátiles para la hidroaminación intermolecular se basan en metales de transición tardíos. Hay muchos estudios publicados en los últimos años acerca de esta reacción, pero a pesar del esfuerzo algunas preguntas permanecen abiertas. Los principales retos de las reacciones de hidroaminación son el uso de aminas simples y sustratos inactivados, la versión intermolecular, el control de la regioselectividad (especialmente la versión anti-Markovnikov) y la versión asimétrica. En esta tesis nos hemos centrado principalmente en el estudio del control de la regioselectividad en la versión intermolecular de esta reacción y en un proceso asimétrico. El primer y segundo capítulo son una introducción al tema y una explicación teórica de todos los temas utilizados en esta tesis. En el tercer capítulo se recogen los puntos que este trabajo pretende lograr, en el cuarto capítulo se estudió una reacción de hidroaminación anti-Markovnikov de alquenos catalizada por un catalizador de rodio desarrollado por Hartwig et al. El quinto capítulo trata de la reacción de hidroaminación enantioselectiva de alenos catalizados por un catalizador de rodio. El sistema desarrollado por Breit y compañeros ha sido elegido para nuestro estudio. El sexto capítulo está dedicado a la reacción de hidroaminación de alquinos, alquenos y alenos con hidracina catalizada por tres catalizadores catiónicos de oro diferentes desarrollados por los grupos de Bertrand y Hasmi. En el séptimo capítulo estudiamos una reacción de hidroaminación anti-Markovnikov catalizada por oro. El sistema de Widenhoefer ha sido seleccionado ya que es el único ejemplo presente en la literatura. El último capítulo de esta tesis incluye una breve conclusión y un resumen del resultado del trabajo realizado.
The topic of this thesis is the DFT study of the mechanism of intermolecular hydroaminations catalyzed by rhodium and gold catalyst. The nitrogen-containing compounds are very valuable and have a lot of uses ranging from pharmaceutical to chemical. The hydroamination reaction is the most economical pathway to synthesize substituted amines. Metal catalysts developed for direct hydroamination includes lanthanides, as well as early and late transition metals. The most versatile catalysts for the intermolecular hydroamination are based on late transition metals. There are a lot of studies published in recent years about this reaction, but despite the effort some questions remain open. The main challenges of hydroamination reactions are the use of simple amines and unactivated substrates, the intermolecular version, the control of regioselectivity (especially the anti-Markovnikov version) and the asymmetrical version. In this thesis we mainly focused on the study of the control of regioselectivity in the intermolecular version of this reaction and an asymmetric process. The first and second chapters are an introduction to the subject and a theoretical explanation of all the topics used in this thesis. In the third chapter are collected the points this work pretends to achieve, in the fourth chapter we studied an anti-Markovnikov hydroamination of alkenes catalyzed by a rhodium catalyst developed by Hartwig et al. The fifth chapter deals with the enantioselective hydroamination of allenes catalyzed by a rhodium catalyst. The system developed by Breit and coworkers has been chosen for our study. The sixth chapter is devoted to the hydroamination reaction of alkynes, alkenes and allenes with hydrazine catalyzed by three different cationic gold catalysts developed by Bertrand and Hasmi’s groups. In the seventh chapter we studied an Au-catalyzed anti-Markovnikov hydroamination. The Widenhoefer system has been selected since is the only example in the literature. The last chapter of this thesis includes a brief conclusion and summary of the outcome of the work carried out.
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Shanbhag, G. V. "Studies on hydroamination reactions using heterogeneous catalysts." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2008. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2626.

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Abadie, Marc-Antoine. "Hydroamination intramoléculaire asymétrique d'alcènes catalysée à l'or." Thesis, Lille 1, 2014. http://www.theses.fr/2014LIL10065/document.

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La catalyse de la réaction d'hydroamination intramoléculaire asymétrique d'aminoalcènes a été étudiée en utilisant différents complexes d'Au(I) et (III) activés par un sel d'argent. Parmi les ligands phosphorés et diaminocarbènes testés, les complexes mononucléaires d'Au(I) composés de ligands phosphoramidites dérivés du BINOL ont d'abord présenté les meilleurs résultats. Ces ligands ont été améliorés par l'addition de substituants stériquement encombrants sur le fragment BINOL. L'utilisation de ces ligands pour la catalyse à l'Au(I) de l'hydroamination asymétrique des aminoalcènes a donné de bonnes conversions et des excès énantiomériques notables à température ambiante. Par la suite, des complexes binucléaires d'Au(I) ont aussi été étudiés comme catalyseurs pour la réaction d'hydroamination intramoléculaire asymétrique d'aminoalcènes. Un complexe binucléaire d'Au(I) basé sur une diphosphine sélectionnée et combiné à un sel d'argent a permis d'obtenir de bonnes conversions et énantiosélectivités à température ambiante et en présence d'eau. Les deux énantiomères du produit de réaction ont pu être obtenus en contrôlant les paires d'ions du catalyseur via la polarité du solvant de réaction employé. Le complexe actif a été caractérisé à l'état solide par diffraction des rayons X et en solution par RMN DOSY 1H. Aucun atome d'argent ne prend part au mode de coordination de ce complexe
The intramolecular gold catalyzed asymmetric hydroamination of alkenes was studied screening a series of mononuclear gold(I) and (III) complexes in combination with silver salts. Among the various chiral phosphine and diaminocarbene ligands tried, the best catalysts arose from mononuclear gold(I) complexes synthesized from BINOL based phosphoramidite ligands. The latest were improved by addition of bulky substituents at specific positions of the BINOL scaffold. The resulting gold(I) complexes were combined with selected silver salts to afford efficient catalysts for intramolecular hydroamination of alkenes at mild temperatures, with good conversions and average enantioselectivities. Afterwards binuclear gold(I) complexes were investigated as catalysts for the intramolecular asymmetric hydroamination of alkenes. When combined to a silver salt, selected diphosphine binuclear gold(I) chloride complex afforded chiral amines for the first time in high conversions and enantioselectivities, within mild conditions and the presence of water. Both enantiomers of the products could be obtained by controlling the molecular ion-pairs through the solvent polarity. The gold(I) cationic active species was characterized for the first time unambiguously at the solid state by X-ray analysis and in solution by DOSY 1H NMR experiments. No contribution of silver chloride was observed on the bonding mode of the catalyst
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Abadie, Marc-Antoine. "Hydroamination intramoléculaire asymétrique d'alcènes catalysée à l'or." Electronic Thesis or Diss., Lille 1, 2014. http://www.theses.fr/2014LIL10065.

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La catalyse de la réaction d'hydroamination intramoléculaire asymétrique d'aminoalcènes a été étudiée en utilisant différents complexes d'Au(I) et (III) activés par un sel d'argent. Parmi les ligands phosphorés et diaminocarbènes testés, les complexes mononucléaires d'Au(I) composés de ligands phosphoramidites dérivés du BINOL ont d'abord présenté les meilleurs résultats. Ces ligands ont été améliorés par l'addition de substituants stériquement encombrants sur le fragment BINOL. L'utilisation de ces ligands pour la catalyse à l'Au(I) de l'hydroamination asymétrique des aminoalcènes a donné de bonnes conversions et des excès énantiomériques notables à température ambiante. Par la suite, des complexes binucléaires d'Au(I) ont aussi été étudiés comme catalyseurs pour la réaction d'hydroamination intramoléculaire asymétrique d'aminoalcènes. Un complexe binucléaire d'Au(I) basé sur une diphosphine sélectionnée et combiné à un sel d'argent a permis d'obtenir de bonnes conversions et énantiosélectivités à température ambiante et en présence d'eau. Les deux énantiomères du produit de réaction ont pu être obtenus en contrôlant les paires d'ions du catalyseur via la polarité du solvant de réaction employé. Le complexe actif a été caractérisé à l'état solide par diffraction des rayons X et en solution par RMN DOSY 1H. Aucun atome d'argent ne prend part au mode de coordination de ce complexe
The intramolecular gold catalyzed asymmetric hydroamination of alkenes was studied screening a series of mononuclear gold(I) and (III) complexes in combination with silver salts. Among the various chiral phosphine and diaminocarbene ligands tried, the best catalysts arose from mononuclear gold(I) complexes synthesized from BINOL based phosphoramidite ligands. The latest were improved by addition of bulky substituents at specific positions of the BINOL scaffold. The resulting gold(I) complexes were combined with selected silver salts to afford efficient catalysts for intramolecular hydroamination of alkenes at mild temperatures, with good conversions and average enantioselectivities. Afterwards binuclear gold(I) complexes were investigated as catalysts for the intramolecular asymmetric hydroamination of alkenes. When combined to a silver salt, selected diphosphine binuclear gold(I) chloride complex afforded chiral amines for the first time in high conversions and enantioselectivities, within mild conditions and the presence of water. Both enantiomers of the products could be obtained by controlling the molecular ion-pairs through the solvent polarity. The gold(I) cationic active species was characterized for the first time unambiguously at the solid state by X-ray analysis and in solution by DOSY 1H NMR experiments. No contribution of silver chloride was observed on the bonding mode of the catalyst
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Ng, Peter J. "Directed Organocatalytic Intermolecular Cope-type Hydroamination of Alkenes." Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/19895.

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Intermolecular reactions are inherently more difficult than intramolecular reactions, and several transformations can only occur as cyclizations, often to form 5-membered rings. The use of directing or tethering groups allowing preassociation with a reagent or catalyst is a common strategy to overcome such low reactivity, which can lead to increases in the rate, regioselectivity and stereoselectivity of intermolecular reactions. Typically, such preassociation involves hydrogen bonds, coordination to a metal ion/catalyst or stepwise installation of a temporary tether. As part of ongoing investigations on metal-free hydroaminations, it was speculated that a simple organic molecule could allow the formation of a temporary tether and enable directed intermolecular Cope-type hydroaminations to proceed at room temperature. Recently, it was found that alkylhydroxylamines add to allylic amines regioselectively in the presence of an aldehyde catalyst. This thesis presents the background material, design elements, optimization and scope of this reactivity.
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Rizk, Toni. "Synthesis of pyridines and pyrazines using intramolecular hydroamination." Thesis, University of Ottawa (Canada), 2010. http://hdl.handle.net/10393/28453.

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Despite recent progress, the scope and efficiency of intramolecular hydroamination has not yet reached its full synthetic potential. In particular, cyclizations to form 6-membered rings and applications in the synthesis of aromatic nitrogen heterocycles remain rare, despite the potential to access a variety of medicinally relevant heterocycles. The intramolecular hydroamination of alkynes presented offers a general approach to such nitrogen heterocycles from appropriately substituted acyclic precursors, in which the oxime functionality allows for a milder cyclization event and allows subsequently for the installation of one additional unsaturation (via loss of H2O). The discovery and optimization of an acid-catalyzed, hydroamination-isomerization-aromatization route for the synthesis of pyridines and pyrazines will be presented and discussed.* *Please refer to dissertation for diagrams.
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Books on the topic "Hydroamination"

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Antonio, Togni, and Grützmacher Hansjörg, eds. Catalytic heterofunctionalization: From hydroanimation [i.e. hydroamination] to hydrozirconation. Weinheim: Wiley-VCH, 2001.

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Hultzsch, K. C. Hydroamination and Hydroaminoalkylation Reaction. Wiley & Sons, Limited, John, 2021.

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Togni, Antonio, and Hansjörg Grützmacher. Catalytic Heterofunctionalization: From Hydroamination to Hydrozirconization. Wiley & Sons, Incorporated, John, 2001.

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Togni, Antonio, and Hansjörg Grützmacher. Catalytic Heterofunctionalization: From Hydroamination to Hydrozirconization. Wiley & Sons, Incorporated, John, 2020.

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Book chapters on the topic "Hydroamination"

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Reznichenko, Alexander L., and Kai C. Hultzsch. "Asymmetric Hydroamination." In Chiral Amine Synthesis, 341–75. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527629541.ch11.

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Reznichenko, Alexander L., Agnieszka J. Nawara-Hultzsch, and Kai C. Hultzsch. "Asymmetric Hydroamination." In Stereoselective Formation of Amines, 191–260. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/128_2013_500.

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Li, Tianshu, Jelena Wiecko, and Peter W. Roesky. "Zinc-Catalyzed Hydroamination Reactions." In Zinc Catalysis, 83–118. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527675944.ch5.

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Nishina, Naoko, and Yoshinori Yamamoto. "Late Transition Metal-Catalyzed Hydroamination." In Hydrofunctionalization, 115–43. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/3418_2012_31.

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Schafer, Laurel L., Jacky C. H. Yim, and Neal Yonson. "Transition-Metal-Catalyzed Hydroamination Reactions." In Metal-Catalyzed Cross-Coupling Reactions and More, 1135–258. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527655588.ch15.

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Chen, Zhiwei, and Vy M. Dong. "Rhodium(I)-Catalyzed Hydroformylation and Hydroamination." In Rhodium Catalysis in Organic Synthesis, 49–62. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2019. http://dx.doi.org/10.1002/9783527811908.ch3.

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Färber, T., Arno Behr, and Andreas J. Vorholt. "Hydroamination and Telomerisation of β-Myrcene." In Catalysis by Metal Complexes, 177–89. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-54161-7_10.

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Arcadi, Antonio. "Gold-Catalyzed Synthesis of Nitrogen Heterocyclic Compounds via Hydroamination Reactions." In Topics in Heterocyclic Chemistry, 53–85. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_5001.

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Jimenez, Oriol, Thomas E. Müller, and Johannes A. Lercher. "Tailoring Adsorption-Desorption Properties of Hydroamination Catalysts with Ionic Liquids." In ACS Symposium Series, 267–80. Washington, DC: American Chemical Society, 2007. http://dx.doi.org/10.1021/bk-2007-0950.ch021.

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Julian, Lisa D. "Synthesis of Saturated Heterocycles via Metal-Catalyzed Alkene Hydroamination or Hydroalkoxylation Reactions." In Topics in Heterocyclic Chemistry, 109–55. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/7081_2013_105.

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Conference papers on the topic "Hydroamination"

1

Seijas, Julio, M. Vazquez-Tato, Luis Barreiro-Castro, and Raquel Romero-Van-der-Schoot. "Hydroamination of Cinnamyl Alcohol." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01736.

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Seijas, Julio, M. Vazquez-Tato, and M. Martinez. "Microwave Enhanced Hydroamination of Styrene." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01733.

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Lavilla, Rodolfo, Federica Catti, Davide Bello, and Edgar Báguena. "Hydroamination of alkynes as a new source of Imines for Ugi MCRs - Scope and Limitations." In The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01231.

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Merican, Zulkifli, Bao Khanh Vu, Vera A. Solovyeva, Valentin O. Rodionov, Cheng Seong Khe, Sokkalingam Rajalingam, and Pandian Vasant. "Fluorocarbon compatibilized gold-silica nanocomposites for recyclable regioselective hydroamination of alkynes in a fluorous biphasic system." In 4TH INTERNATIONAL CONFERENCE ON FUNDAMENTAL AND APPLIED SCIENCES (ICFAS2016). Author(s), 2016. http://dx.doi.org/10.1063/1.4968079.

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Reports on the topic "Hydroamination"

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Hovey, Megan. Ligand strategies for green chemistry. Catalysts for amide reduction and hydroamination. Office of Scientific and Technical Information (OSTI), January 2014. http://dx.doi.org/10.2172/1226561.

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2

Bertrand, Guy. Ammonia and hydrazine. Transition-metal-catalyzed hydroamination and metal-free catalyzed functionalization. Office of Scientific and Technical Information (OSTI), June 2012. http://dx.doi.org/10.2172/1253630.

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Manna, Kuntal. Transition metal complexes of oxazolinylboranes and cyclopentadienyl-bis(oxazolinyl)borates: Catalysts for asymmetric olefin hydroamination and acceptorless alcohol decarbonylation. Office of Scientific and Technical Information (OSTI), December 2012. http://dx.doi.org/10.2172/1082975.

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