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You searched for subject:(Hypervalent iodine). Showing records 1 – 30 of 69 total matches.

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University of Minnesota

1. Maskaev, Andrey Viktorovich. Preparation, structural studies and chemical properties of new hypervalent iodine compounds.

Degree: MS, Chemistry, 2013, University of Minnesota

University of Minnesota M.S. thesis. August 2013. Major: Chemistry. Advisor: Viktor Zhdankin. 1 computer file (PDF); ix, 116 pages, appendices p. 79-116.

This work describes… (more)

Subjects/Keywords: Benziodoxaborole; Hypervalent iodine; Iodylarene

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APA (6th Edition):

Maskaev, A. V. (2013). Preparation, structural studies and chemical properties of new hypervalent iodine compounds. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/160238

Chicago Manual of Style (16th Edition):

Maskaev, Andrey Viktorovich. “Preparation, structural studies and chemical properties of new hypervalent iodine compounds.” 2013. Masters Thesis, University of Minnesota. Accessed April 03, 2020. http://purl.umn.edu/160238.

MLA Handbook (7th Edition):

Maskaev, Andrey Viktorovich. “Preparation, structural studies and chemical properties of new hypervalent iodine compounds.” 2013. Web. 03 Apr 2020.

Vancouver:

Maskaev AV. Preparation, structural studies and chemical properties of new hypervalent iodine compounds. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2020 Apr 03]. Available from: http://purl.umn.edu/160238.

Council of Science Editors:

Maskaev AV. Preparation, structural studies and chemical properties of new hypervalent iodine compounds. [Masters Thesis]. University of Minnesota; 2013. Available from: http://purl.umn.edu/160238


University of Minnesota

2. Maskaev, Andrey Viktorovich. Preparation, structural studies and chemical properties of new hypervalent iodine compounds.

Degree: MS, Chemistry, 2013, University of Minnesota

 This work describes two independent research projects. The first one is focused on preparation of a new class of heterocyclic hypervalent iodine (III) compounds, the… (more)

Subjects/Keywords: Benziodoxaborole; Hypervalent iodine; Iodylarene

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APA (6th Edition):

Maskaev, A. V. (2013). Preparation, structural studies and chemical properties of new hypervalent iodine compounds. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/160238

Chicago Manual of Style (16th Edition):

Maskaev, Andrey Viktorovich. “Preparation, structural studies and chemical properties of new hypervalent iodine compounds.” 2013. Masters Thesis, University of Minnesota. Accessed April 03, 2020. http://purl.umn.edu/160238.

MLA Handbook (7th Edition):

Maskaev, Andrey Viktorovich. “Preparation, structural studies and chemical properties of new hypervalent iodine compounds.” 2013. Web. 03 Apr 2020.

Vancouver:

Maskaev AV. Preparation, structural studies and chemical properties of new hypervalent iodine compounds. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2020 Apr 03]. Available from: http://purl.umn.edu/160238.

Council of Science Editors:

Maskaev AV. Preparation, structural studies and chemical properties of new hypervalent iodine compounds. [Masters Thesis]. University of Minnesota; 2013. Available from: http://purl.umn.edu/160238


University of Minnesota

3. Middleton, Kyle Richard. Recyclable reagents and Catalytic systems based on hypervalent iodine Chemistry.

Degree: MS, Chemistry, 2013, University of Minnesota

 Hofmann rearrangement of carboxamides to carbamates using Oxone® as an oxidant can be efficiently catalyzed by iodobenzene. This reaction involves hypervalent Iodine species generated in… (more)

Subjects/Keywords: Aziridine; Hofmann; Hypervalent; Iodine; Oxidation

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APA (6th Edition):

Middleton, K. R. (2013). Recyclable reagents and Catalytic systems based on hypervalent iodine Chemistry. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/162372

Chicago Manual of Style (16th Edition):

Middleton, Kyle Richard. “Recyclable reagents and Catalytic systems based on hypervalent iodine Chemistry.” 2013. Masters Thesis, University of Minnesota. Accessed April 03, 2020. http://hdl.handle.net/11299/162372.

MLA Handbook (7th Edition):

Middleton, Kyle Richard. “Recyclable reagents and Catalytic systems based on hypervalent iodine Chemistry.” 2013. Web. 03 Apr 2020.

Vancouver:

Middleton KR. Recyclable reagents and Catalytic systems based on hypervalent iodine Chemistry. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/11299/162372.

Council of Science Editors:

Middleton KR. Recyclable reagents and Catalytic systems based on hypervalent iodine Chemistry. [Masters Thesis]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/162372


University of Minnesota

4. Jarvi, Melissa. Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition.

Degree: MS, Chemistry, 2019, University of Minnesota

 Isoxazole is a five membered heterocyclic compound containing oxygen and nitrogen atoms in the 1,2 positions. Isoxazole rings are found in natural products, such as… (more)

Subjects/Keywords: Cycloaddition; Hypervalent iodine(III); Isoxazole

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APA (6th Edition):

Jarvi, M. (2019). Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/208932

Chicago Manual of Style (16th Edition):

Jarvi, Melissa. “Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition.” 2019. Masters Thesis, University of Minnesota. Accessed April 03, 2020. http://hdl.handle.net/11299/208932.

MLA Handbook (7th Edition):

Jarvi, Melissa. “Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition.” 2019. Web. 03 Apr 2020.

Vancouver:

Jarvi M. Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition. [Internet] [Masters thesis]. University of Minnesota; 2019. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/11299/208932.

Council of Science Editors:

Jarvi M. Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition. [Masters Thesis]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/208932


University of Minnesota

5. Shea, Michael. Preparation, Structure, and Reactivity of the First Bicyclic Benziodazole and its Monocyclic Analogue.

Degree: MS, Chemistry, 2019, University of Minnesota

 Nitrogen containing mono-heterocyclic hypervalent iodine(III) compounds, benziodazoles, have been investigated by several research groups as well as ours. These compounds are commonly used as efficient… (more)

Subjects/Keywords: Amide; Benziodazole; Ester; Hypervalent; Iodine

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APA (6th Edition):

Shea, M. (2019). Preparation, Structure, and Reactivity of the First Bicyclic Benziodazole and its Monocyclic Analogue. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/208961

Chicago Manual of Style (16th Edition):

Shea, Michael. “Preparation, Structure, and Reactivity of the First Bicyclic Benziodazole and its Monocyclic Analogue.” 2019. Masters Thesis, University of Minnesota. Accessed April 03, 2020. http://hdl.handle.net/11299/208961.

MLA Handbook (7th Edition):

Shea, Michael. “Preparation, Structure, and Reactivity of the First Bicyclic Benziodazole and its Monocyclic Analogue.” 2019. Web. 03 Apr 2020.

Vancouver:

Shea M. Preparation, Structure, and Reactivity of the First Bicyclic Benziodazole and its Monocyclic Analogue. [Internet] [Masters thesis]. University of Minnesota; 2019. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/11299/208961.

Council of Science Editors:

Shea M. Preparation, Structure, and Reactivity of the First Bicyclic Benziodazole and its Monocyclic Analogue. [Masters Thesis]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/208961


University of Cambridge

6. Nelson, Jennifer Emily. Selective Protein Functionalisation at Methionine.

Degree: PhD, 2019, University of Cambridge

 The development of novel bioconjugation strategies for the functionalisation of polypeptides and proteins has been of great benefit to the fields of chemical biology and… (more)

Subjects/Keywords: Bioconjugation; Protein functionalisation; Methionine; Hypervalent iodine

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APA (6th Edition):

Nelson, J. E. (2019). Selective Protein Functionalisation at Methionine. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/296920

Chicago Manual of Style (16th Edition):

Nelson, Jennifer Emily. “Selective Protein Functionalisation at Methionine.” 2019. Doctoral Dissertation, University of Cambridge. Accessed April 03, 2020. https://www.repository.cam.ac.uk/handle/1810/296920.

MLA Handbook (7th Edition):

Nelson, Jennifer Emily. “Selective Protein Functionalisation at Methionine.” 2019. Web. 03 Apr 2020.

Vancouver:

Nelson JE. Selective Protein Functionalisation at Methionine. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Apr 03]. Available from: https://www.repository.cam.ac.uk/handle/1810/296920.

Council of Science Editors:

Nelson JE. Selective Protein Functionalisation at Methionine. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/296920


Université de Grenoble

7. Brenet, Simon. Nouvelle structure BINOL-Maléimide. Applications en catalyse d'oxydation asymétrique : New Structure BINOL-Fused Maleimide. Applications in Catalysed Asymmetric Oxidations.

Degree: Docteur es, Chimie organique, 2013, Université de Grenoble

Les réactions asymétriques catalysées constituent une approche élégante au problème de l'introduction de centres stéréogène pour la synthèse de molécules complexes. Dans ce contexte, les… (more)

Subjects/Keywords: Oxydation; Catalyse; Chimie radicalaire; Iode hypervalent; Nhpi; Oxidation; Catalysis; Radical chemistry; Hypervalent iodine; Nhpi

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APA (6th Edition):

Brenet, S. (2013). Nouvelle structure BINOL-Maléimide. Applications en catalyse d'oxydation asymétrique : New Structure BINOL-Fused Maleimide. Applications in Catalysed Asymmetric Oxidations. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2013GRENV050

Chicago Manual of Style (16th Edition):

Brenet, Simon. “Nouvelle structure BINOL-Maléimide. Applications en catalyse d'oxydation asymétrique : New Structure BINOL-Fused Maleimide. Applications in Catalysed Asymmetric Oxidations.” 2013. Doctoral Dissertation, Université de Grenoble. Accessed April 03, 2020. http://www.theses.fr/2013GRENV050.

MLA Handbook (7th Edition):

Brenet, Simon. “Nouvelle structure BINOL-Maléimide. Applications en catalyse d'oxydation asymétrique : New Structure BINOL-Fused Maleimide. Applications in Catalysed Asymmetric Oxidations.” 2013. Web. 03 Apr 2020.

Vancouver:

Brenet S. Nouvelle structure BINOL-Maléimide. Applications en catalyse d'oxydation asymétrique : New Structure BINOL-Fused Maleimide. Applications in Catalysed Asymmetric Oxidations. [Internet] [Doctoral dissertation]. Université de Grenoble; 2013. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2013GRENV050.

Council of Science Editors:

Brenet S. Nouvelle structure BINOL-Maléimide. Applications en catalyse d'oxydation asymétrique : New Structure BINOL-Fused Maleimide. Applications in Catalysed Asymmetric Oxidations. [Doctoral Dissertation]. Université de Grenoble; 2013. Available from: http://www.theses.fr/2013GRENV050


Université Paris-Sud – Paris XI

8. Nocquet-Thibault, Sophie. La difonctionnalisation d’énamides en utilisant des dérivés d’iode (III) hypervalent : Oxidative difonctionnalization of enamides.

Degree: Docteur es, Chimie, 2014, Université Paris-Sud – Paris XI

 Lors de ce travail de thèse qui visait à développer une méthode générale d’introduction d’halogénures et de pseudo-halogénures en se basant sur l’utilisation de réactifs… (more)

Subjects/Keywords: Difonctionnalisation; Enamides; Iode hypervalent; (pseudo)-halogénures; Difunctionalization; Enamides; Hypervalent iodine; (pseudo)-halides

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APA (6th Edition):

Nocquet-Thibault, S. (2014). La difonctionnalisation d’énamides en utilisant des dérivés d’iode (III) hypervalent : Oxidative difonctionnalization of enamides. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA112270

Chicago Manual of Style (16th Edition):

Nocquet-Thibault, Sophie. “La difonctionnalisation d’énamides en utilisant des dérivés d’iode (III) hypervalent : Oxidative difonctionnalization of enamides.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed April 03, 2020. http://www.theses.fr/2014PA112270.

MLA Handbook (7th Edition):

Nocquet-Thibault, Sophie. “La difonctionnalisation d’énamides en utilisant des dérivés d’iode (III) hypervalent : Oxidative difonctionnalization of enamides.” 2014. Web. 03 Apr 2020.

Vancouver:

Nocquet-Thibault S. La difonctionnalisation d’énamides en utilisant des dérivés d’iode (III) hypervalent : Oxidative difonctionnalization of enamides. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2014PA112270.

Council of Science Editors:

Nocquet-Thibault S. La difonctionnalisation d’énamides en utilisant des dérivés d’iode (III) hypervalent : Oxidative difonctionnalization of enamides. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA112270

9. Peilleron, Laure. Nouvelle approche synthétique vers des analogues de l'avibactam et cyclisations de N-alkoxyurées insaturées initiées par des réactifs d’iode(III) hypervalent : New synthetic approach towards avibactam analogues and hypervalent iodine(III)-mediated cyclizations of unsaturated N-alkoxyureas.

Degree: Docteur es, Chimie, 2019, Université Paris-Saclay (ComUE)

La situation très préoccupante due aux résistances antimicrobiennes incite les chimistes à concevoir de nouvelles molécules capables de lutter contre ces résistances. Les inhibiteurs de… (more)

Subjects/Keywords: Antibiotiques; Résistances; Avibactam; Iode Hypervalent; Cyclisation; Antibiotic; Resistance; Avibactam; Hypervalent Iodine; Cyclization

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APA (6th Edition):

Peilleron, L. (2019). Nouvelle approche synthétique vers des analogues de l'avibactam et cyclisations de N-alkoxyurées insaturées initiées par des réactifs d’iode(III) hypervalent : New synthetic approach towards avibactam analogues and hypervalent iodine(III)-mediated cyclizations of unsaturated N-alkoxyureas. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS408

Chicago Manual of Style (16th Edition):

Peilleron, Laure. “Nouvelle approche synthétique vers des analogues de l'avibactam et cyclisations de N-alkoxyurées insaturées initiées par des réactifs d’iode(III) hypervalent : New synthetic approach towards avibactam analogues and hypervalent iodine(III)-mediated cyclizations of unsaturated N-alkoxyureas.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 03, 2020. http://www.theses.fr/2019SACLS408.

MLA Handbook (7th Edition):

Peilleron, Laure. “Nouvelle approche synthétique vers des analogues de l'avibactam et cyclisations de N-alkoxyurées insaturées initiées par des réactifs d’iode(III) hypervalent : New synthetic approach towards avibactam analogues and hypervalent iodine(III)-mediated cyclizations of unsaturated N-alkoxyureas.” 2019. Web. 03 Apr 2020.

Vancouver:

Peilleron L. Nouvelle approche synthétique vers des analogues de l'avibactam et cyclisations de N-alkoxyurées insaturées initiées par des réactifs d’iode(III) hypervalent : New synthetic approach towards avibactam analogues and hypervalent iodine(III)-mediated cyclizations of unsaturated N-alkoxyureas. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2019SACLS408.

Council of Science Editors:

Peilleron L. Nouvelle approche synthétique vers des analogues de l'avibactam et cyclisations de N-alkoxyurées insaturées initiées par des réactifs d’iode(III) hypervalent : New synthetic approach towards avibactam analogues and hypervalent iodine(III)-mediated cyclizations of unsaturated N-alkoxyureas. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS408


NSYSU

10. Lin, Chun-yu. (1) C-H Oxidation with Hypervalent Iodine (III) at Benzylic Position without Undergoing SET(Single Electron Transfer) (2) Chemistry and Biology of Triazole-pyrrole: Click Chemistry and DNA Interaction.

Degree: PhD, Chemistry, 2013, NSYSU

 There are two parts in this dissertation. Part I : benzylic C-H oxidation of methyl aromatic compounds is a useful reaction. We found that the… (more)

Subjects/Keywords: hypervalent iodine reagents; triazole-tripyrrole compounds; triazole; iodine (III) reagents; benzylic C-H oxidation

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APA (6th Edition):

Lin, C. (2013). (1) C-H Oxidation with Hypervalent Iodine (III) at Benzylic Position without Undergoing SET(Single Electron Transfer) (2) Chemistry and Biology of Triazole-pyrrole: Click Chemistry and DNA Interaction. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0705113-220151

Chicago Manual of Style (16th Edition):

Lin, Chun-yu. “(1) C-H Oxidation with Hypervalent Iodine (III) at Benzylic Position without Undergoing SET(Single Electron Transfer) (2) Chemistry and Biology of Triazole-pyrrole: Click Chemistry and DNA Interaction.” 2013. Doctoral Dissertation, NSYSU. Accessed April 03, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0705113-220151.

MLA Handbook (7th Edition):

Lin, Chun-yu. “(1) C-H Oxidation with Hypervalent Iodine (III) at Benzylic Position without Undergoing SET(Single Electron Transfer) (2) Chemistry and Biology of Triazole-pyrrole: Click Chemistry and DNA Interaction.” 2013. Web. 03 Apr 2020.

Vancouver:

Lin C. (1) C-H Oxidation with Hypervalent Iodine (III) at Benzylic Position without Undergoing SET(Single Electron Transfer) (2) Chemistry and Biology of Triazole-pyrrole: Click Chemistry and DNA Interaction. [Internet] [Doctoral dissertation]. NSYSU; 2013. [cited 2020 Apr 03]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0705113-220151.

Council of Science Editors:

Lin C. (1) C-H Oxidation with Hypervalent Iodine (III) at Benzylic Position without Undergoing SET(Single Electron Transfer) (2) Chemistry and Biology of Triazole-pyrrole: Click Chemistry and DNA Interaction. [Doctoral Dissertation]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0705113-220151


NSYSU

11. Hsu, Wen-Ting. Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect.

Degree: Master, Chemistry, 2013, NSYSU

 An intramolecular cyclization of N-([1,1'-biphenyl]-2-yl)pyridin-2-amines catalyzed by hypervalent iodine(III) via C-H activation / C-N formation was investigated. The influence of electronic effect regarding the cyclization… (more)

Subjects/Keywords: electronic effect; benzimidazole; C-H bond activation; carbazole; hypervalent iodine(III)

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APA (6th Edition):

Hsu, W. (2013). Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0616113-135655

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hsu, Wen-Ting. “Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect.” 2013. Thesis, NSYSU. Accessed April 03, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0616113-135655.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hsu, Wen-Ting. “Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect.” 2013. Web. 03 Apr 2020.

Vancouver:

Hsu W. Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect. [Internet] [Thesis]. NSYSU; 2013. [cited 2020 Apr 03]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0616113-135655.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hsu W. Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0616113-135655

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


NSYSU

12. Wu, Yi-hua. I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation.

Degree: Master, Chemistry, 2014, NSYSU

 The first chapter summaries present that the hypervalent iodine(III) reagents induced the direct intramolecular C-N cyclization of N-(biphenyl)pyridin-2-amines to establisha variety of 6-arylbenzimidazoles and N-pyridinyl-9H-carbazoles.We… (more)

Subjects/Keywords: carbazole; C-H bond activation; benzimidazol; Hypervalent Iodine(III)

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APA (6th Edition):

Wu, Y. (2014). I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0526114-094415

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wu, Yi-hua. “I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation.” 2014. Thesis, NSYSU. Accessed April 03, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0526114-094415.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wu, Yi-hua. “I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation.” 2014. Web. 03 Apr 2020.

Vancouver:

Wu Y. I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation. [Internet] [Thesis]. NSYSU; 2014. [cited 2020 Apr 03]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0526114-094415.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wu Y. I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation. [Thesis]. NSYSU; 2014. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0526114-094415

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Cambridge

13. Male, Henry Peter John. Towards the Development, Application and Understanding of Copper-Catalysed Alkene Functionalisation Processes Using Iodonium Salts.

Degree: PhD, 2018, University of Cambridge

 This thesis comprises three projects focused on the use of the combination of catalytic copper and iodonium salts towards the functionalisation of alkenes. Chapter 2… (more)

Subjects/Keywords: Catalysis; Copper; Enantioselectivity; Total Synthesis; Regiodivergence; Hypervalent Iodine; High Valent Copper

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APA (6th Edition):

Male, H. P. J. (2018). Towards the Development, Application and Understanding of Copper-Catalysed Alkene Functionalisation Processes Using Iodonium Salts. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/273476

Chicago Manual of Style (16th Edition):

Male, Henry Peter John. “Towards the Development, Application and Understanding of Copper-Catalysed Alkene Functionalisation Processes Using Iodonium Salts.” 2018. Doctoral Dissertation, University of Cambridge. Accessed April 03, 2020. https://www.repository.cam.ac.uk/handle/1810/273476.

MLA Handbook (7th Edition):

Male, Henry Peter John. “Towards the Development, Application and Understanding of Copper-Catalysed Alkene Functionalisation Processes Using Iodonium Salts.” 2018. Web. 03 Apr 2020.

Vancouver:

Male HPJ. Towards the Development, Application and Understanding of Copper-Catalysed Alkene Functionalisation Processes Using Iodonium Salts. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2020 Apr 03]. Available from: https://www.repository.cam.ac.uk/handle/1810/273476.

Council of Science Editors:

Male HPJ. Towards the Development, Application and Understanding of Copper-Catalysed Alkene Functionalisation Processes Using Iodonium Salts. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/273476


University of Waterloo

14. Tran, Richard. Gem-Difluorination of α-Diazo Amides Using (Difluoroiodo)toluene.

Degree: 2017, University of Waterloo

 Fluorination chemistry is a branch of study that appeals to the pharmaceutical and agricultural industries. Drawbacks of popular methods of forming carbon-fluorine bonds include high… (more)

Subjects/Keywords: Organic chemistry; fluorination; diazo; (difluoro)iodotoluene; hypervalent iodine

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APA (6th Edition):

Tran, R. (2017). Gem-Difluorination of α-Diazo Amides Using (Difluoroiodo)toluene. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/12451

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tran, Richard. “Gem-Difluorination of α-Diazo Amides Using (Difluoroiodo)toluene.” 2017. Thesis, University of Waterloo. Accessed April 03, 2020. http://hdl.handle.net/10012/12451.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tran, Richard. “Gem-Difluorination of α-Diazo Amides Using (Difluoroiodo)toluene.” 2017. Web. 03 Apr 2020.

Vancouver:

Tran R. Gem-Difluorination of α-Diazo Amides Using (Difluoroiodo)toluene. [Internet] [Thesis]. University of Waterloo; 2017. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10012/12451.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tran R. Gem-Difluorination of α-Diazo Amides Using (Difluoroiodo)toluene. [Thesis]. University of Waterloo; 2017. Available from: http://hdl.handle.net/10012/12451

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

15. St-Onge Carle, Myriam. Use of (Dihaloiodo)arene Reagents in Halogenation Reactions.

Degree: 2017, University of Waterloo

 Halogenation of organic molecules is a fundamental transformation in organic chemistry. Introducing halogens into substrates can be a challenge since most methods for introducing fluorine… (more)

Subjects/Keywords: Organic chemistry; Hypervalent iodine

…104 ix List of Figures Figure 1.1 – Reactivity profile of hypervalent iodine molecules… …Koser’s reagent xiv HVI Hypervalent iodine IBX 2-Iodoxybenzoic acid in-situ In place or… …Chapter 1 – Hypervalent iodine and fluorination reactions 1.0 Introduction to iodine Iodine is… …the other stable halogens, iodine can form polyvalent compounds known as hypervalent iodine… …were discovered over a century ago, the chemistry of hypervalent iodine has only been rapidly… 

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APA (6th Edition):

St-Onge Carle, M. (2017). Use of (Dihaloiodo)arene Reagents in Halogenation Reactions. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/12394

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

St-Onge Carle, Myriam. “Use of (Dihaloiodo)arene Reagents in Halogenation Reactions.” 2017. Thesis, University of Waterloo. Accessed April 03, 2020. http://hdl.handle.net/10012/12394.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

St-Onge Carle, Myriam. “Use of (Dihaloiodo)arene Reagents in Halogenation Reactions.” 2017. Web. 03 Apr 2020.

Vancouver:

St-Onge Carle M. Use of (Dihaloiodo)arene Reagents in Halogenation Reactions. [Internet] [Thesis]. University of Waterloo; 2017. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10012/12394.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

St-Onge Carle M. Use of (Dihaloiodo)arene Reagents in Halogenation Reactions. [Thesis]. University of Waterloo; 2017. Available from: http://hdl.handle.net/10012/12394

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

16. Eljo, Jasmin. LIGAND TRANSFER REACTIONS OF HYPERVALENT IODINE REAGENTS WITH PHOSPHORUS COMPOUNDS.

Degree: 2018, University of Waterloo

 Many hypervalent iodine compounds are used as versatile reagents in synthetic organic chemistry. Hypervalent iodine reagents are capable of oxidizing trivalent phosphorus compounds into pentavalent,… (more)

Subjects/Keywords: ORGANIC CHEMISTRY; HYPERVALENT IODINE

…Figure 1.3: Main classes of some hypervalent iodine reagents… …mass spectrometry gem Geminal HVI Hypervalent iodine in situ In the reaction mixture… …p-(Difluoroiodo)toluene xiv Chapter 1: Hypervalent Iodine Reagents and… …Triphenylphosphine 1.1 Introduction to Hypervalent Iodine Compounds Iodine is the heaviest, non radioactive… …atom in higher oxidation states are termed as hypervalent iodine (HVI) compounds… 

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APA (6th Edition):

Eljo, J. (2018). LIGAND TRANSFER REACTIONS OF HYPERVALENT IODINE REAGENTS WITH PHOSPHORUS COMPOUNDS. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/12932

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Eljo, Jasmin. “LIGAND TRANSFER REACTIONS OF HYPERVALENT IODINE REAGENTS WITH PHOSPHORUS COMPOUNDS.” 2018. Thesis, University of Waterloo. Accessed April 03, 2020. http://hdl.handle.net/10012/12932.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Eljo, Jasmin. “LIGAND TRANSFER REACTIONS OF HYPERVALENT IODINE REAGENTS WITH PHOSPHORUS COMPOUNDS.” 2018. Web. 03 Apr 2020.

Vancouver:

Eljo J. LIGAND TRANSFER REACTIONS OF HYPERVALENT IODINE REAGENTS WITH PHOSPHORUS COMPOUNDS. [Internet] [Thesis]. University of Waterloo; 2018. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10012/12932.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Eljo J. LIGAND TRANSFER REACTIONS OF HYPERVALENT IODINE REAGENTS WITH PHOSPHORUS COMPOUNDS. [Thesis]. University of Waterloo; 2018. Available from: http://hdl.handle.net/10012/12932

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Clemson University

17. Lex, Timothy R. Developing Iodoarene Derivatives for Useful Oxidative Transformations and Biodegradable X-ray Materials.

Degree: PhD, Chemistry, 2019, Clemson University

  This thesis discloses two distinct applications of synthesized iodoarene-containing compounds: as hypervalent iodine (HI) organocatalysts and as biodegradable X-ray contrasting agents. This thesis also… (more)

Subjects/Keywords: asymmetric synthesis; contrast imaging agents; diazacyclobutenes; Hypervalent iodine; organocatalysis; X-ray

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APA (6th Edition):

Lex, T. R. (2019). Developing Iodoarene Derivatives for Useful Oxidative Transformations and Biodegradable X-ray Materials. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/2460

Chicago Manual of Style (16th Edition):

Lex, Timothy R. “Developing Iodoarene Derivatives for Useful Oxidative Transformations and Biodegradable X-ray Materials.” 2019. Doctoral Dissertation, Clemson University. Accessed April 03, 2020. https://tigerprints.clemson.edu/all_dissertations/2460.

MLA Handbook (7th Edition):

Lex, Timothy R. “Developing Iodoarene Derivatives for Useful Oxidative Transformations and Biodegradable X-ray Materials.” 2019. Web. 03 Apr 2020.

Vancouver:

Lex TR. Developing Iodoarene Derivatives for Useful Oxidative Transformations and Biodegradable X-ray Materials. [Internet] [Doctoral dissertation]. Clemson University; 2019. [cited 2020 Apr 03]. Available from: https://tigerprints.clemson.edu/all_dissertations/2460.

Council of Science Editors:

Lex TR. Developing Iodoarene Derivatives for Useful Oxidative Transformations and Biodegradable X-ray Materials. [Doctoral Dissertation]. Clemson University; 2019. Available from: https://tigerprints.clemson.edu/all_dissertations/2460


University of Minnesota

18. Klasen, Scott. Hypervalent Iodine Reagents for Tosyl Transfer Reactions in Organic Synthesis.

Degree: MS, Chemistry, 2015, University of Minnesota

 In recent years, organohypervalent iodine compounds have emerged as environmentally friendly and efficient reagents for various synthetically useful oxidative transformations. The purpose of this research… (more)

Subjects/Keywords: HTI; HTIB; Hypervalent Iodine; Koser's Reagent; Organic Synthesis; Tosyloxylation

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APA (6th Edition):

Klasen, S. (2015). Hypervalent Iodine Reagents for Tosyl Transfer Reactions in Organic Synthesis. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/174792

Chicago Manual of Style (16th Edition):

Klasen, Scott. “Hypervalent Iodine Reagents for Tosyl Transfer Reactions in Organic Synthesis.” 2015. Masters Thesis, University of Minnesota. Accessed April 03, 2020. http://hdl.handle.net/11299/174792.

MLA Handbook (7th Edition):

Klasen, Scott. “Hypervalent Iodine Reagents for Tosyl Transfer Reactions in Organic Synthesis.” 2015. Web. 03 Apr 2020.

Vancouver:

Klasen S. Hypervalent Iodine Reagents for Tosyl Transfer Reactions in Organic Synthesis. [Internet] [Masters thesis]. University of Minnesota; 2015. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/11299/174792.

Council of Science Editors:

Klasen S. Hypervalent Iodine Reagents for Tosyl Transfer Reactions in Organic Synthesis. [Masters Thesis]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/174792


University of Minnesota

19. Moon, Nicholas. 2,5-Cyclohexadienones as a Useful Launching Point for the Synthesis of the Briarane Diterpenoids and A Hypervalent Iodine-Mediated Synthesis of Oxazolines.

Degree: PhD, Chemistry, 2015, University of Minnesota

 The briarane diterpenoids are a large class of natural products derived from gorgonians and other corals from throughout the world. Despite the extremely large number… (more)

Subjects/Keywords: 2; 5-Cyclohexadienones; Briaranes; Hypervalent Iodine; Methodology; Total Synthesis

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APA (6th Edition):

Moon, N. (2015). 2,5-Cyclohexadienones as a Useful Launching Point for the Synthesis of the Briarane Diterpenoids and A Hypervalent Iodine-Mediated Synthesis of Oxazolines. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/175267

Chicago Manual of Style (16th Edition):

Moon, Nicholas. “2,5-Cyclohexadienones as a Useful Launching Point for the Synthesis of the Briarane Diterpenoids and A Hypervalent Iodine-Mediated Synthesis of Oxazolines.” 2015. Doctoral Dissertation, University of Minnesota. Accessed April 03, 2020. http://hdl.handle.net/11299/175267.

MLA Handbook (7th Edition):

Moon, Nicholas. “2,5-Cyclohexadienones as a Useful Launching Point for the Synthesis of the Briarane Diterpenoids and A Hypervalent Iodine-Mediated Synthesis of Oxazolines.” 2015. Web. 03 Apr 2020.

Vancouver:

Moon N. 2,5-Cyclohexadienones as a Useful Launching Point for the Synthesis of the Briarane Diterpenoids and A Hypervalent Iodine-Mediated Synthesis of Oxazolines. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/11299/175267.

Council of Science Editors:

Moon N. 2,5-Cyclohexadienones as a Useful Launching Point for the Synthesis of the Briarane Diterpenoids and A Hypervalent Iodine-Mediated Synthesis of Oxazolines. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/175267


University of Minnesota

20. Chau Nguyen, Khiem. Pseudocyclic benziodoxole triflate as an effective reagent for the catalytic oxidative cycloadditions of aldoximes with nitriles and maleimides.

Degree: MS, Chemistry, 2017, University of Minnesota

 A novel hypervalent iodine(III) compound - pseudocyclic benziodoxole triflate (IBAOTf) - was prepared, isolated, identified and tested for its reactivity over various reactions in our… (more)

Subjects/Keywords: 1; 2; 4-oxadiazole; benziodoxole triflate; cycloaddition; hypervalent iodine; pyrrolo-isoxazole

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APA (6th Edition):

Chau Nguyen, K. (2017). Pseudocyclic benziodoxole triflate as an effective reagent for the catalytic oxidative cycloadditions of aldoximes with nitriles and maleimides. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/190611

Chicago Manual of Style (16th Edition):

Chau Nguyen, Khiem. “Pseudocyclic benziodoxole triflate as an effective reagent for the catalytic oxidative cycloadditions of aldoximes with nitriles and maleimides.” 2017. Masters Thesis, University of Minnesota. Accessed April 03, 2020. http://hdl.handle.net/11299/190611.

MLA Handbook (7th Edition):

Chau Nguyen, Khiem. “Pseudocyclic benziodoxole triflate as an effective reagent for the catalytic oxidative cycloadditions of aldoximes with nitriles and maleimides.” 2017. Web. 03 Apr 2020.

Vancouver:

Chau Nguyen K. Pseudocyclic benziodoxole triflate as an effective reagent for the catalytic oxidative cycloadditions of aldoximes with nitriles and maleimides. [Internet] [Masters thesis]. University of Minnesota; 2017. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/11299/190611.

Council of Science Editors:

Chau Nguyen K. Pseudocyclic benziodoxole triflate as an effective reagent for the catalytic oxidative cycloadditions of aldoximes with nitriles and maleimides. [Masters Thesis]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/190611


University of Minnesota

21. Fuchs, Jonathan. Water-Triggered Benzyne Generation Using Pseudocyclic Arylbenziodoxaboroles.

Degree: MS, Chemistry, 2018, University of Minnesota

Hypervalent iodine compounds are a broad and hot topic in synthetic organic chemistry. They are much cheaper, more environmentally friendly, and safer to handle then… (more)

Subjects/Keywords: Aryne; Benzyne; Hypervalent Iodine; Pseudocyclic Arylbenziodoxaboroles; Water-Triggered

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APA (6th Edition):

Fuchs, J. (2018). Water-Triggered Benzyne Generation Using Pseudocyclic Arylbenziodoxaboroles. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/201006

Chicago Manual of Style (16th Edition):

Fuchs, Jonathan. “Water-Triggered Benzyne Generation Using Pseudocyclic Arylbenziodoxaboroles.” 2018. Masters Thesis, University of Minnesota. Accessed April 03, 2020. http://hdl.handle.net/11299/201006.

MLA Handbook (7th Edition):

Fuchs, Jonathan. “Water-Triggered Benzyne Generation Using Pseudocyclic Arylbenziodoxaboroles.” 2018. Web. 03 Apr 2020.

Vancouver:

Fuchs J. Water-Triggered Benzyne Generation Using Pseudocyclic Arylbenziodoxaboroles. [Internet] [Masters thesis]. University of Minnesota; 2018. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/11299/201006.

Council of Science Editors:

Fuchs J. Water-Triggered Benzyne Generation Using Pseudocyclic Arylbenziodoxaboroles. [Masters Thesis]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/201006


Université Paris-Sud – Paris XI

22. Dequirez, Geoffroy. Transferts de nitrène catalysés par les métaux de transition. Développement de nouvelles réactions pour la difonctionnalisation d’alcènes et application en synthèse : Transition metal catalyzed nitrene transfers. Development of new reactions for the difunctionalization of alkenes and application in synthesis.

Degree: Docteur es, Chimie, 2013, Université Paris-Sud – Paris XI

Cette thèse décrit le développement de nouvelles réactions de difonctionnalisation catalytique d’oléfines impliquant des transferts de nitrène médiés par des complexes de dirhodium(II).La première partie… (more)

Subjects/Keywords: Nitrène; Rhodium; Difonctionnalisation d’alcènes; Indole; Oxyamination; Diamination; Iode hypervalent; Nitrene; Rhodium; Difunctionalization of alkenes; Indole; Oxyamination; Diamination; Hypervalent iodine

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APA (6th Edition):

Dequirez, G. (2013). Transferts de nitrène catalysés par les métaux de transition. Développement de nouvelles réactions pour la difonctionnalisation d’alcènes et application en synthèse : Transition metal catalyzed nitrene transfers. Development of new reactions for the difunctionalization of alkenes and application in synthesis. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA112256

Chicago Manual of Style (16th Edition):

Dequirez, Geoffroy. “Transferts de nitrène catalysés par les métaux de transition. Développement de nouvelles réactions pour la difonctionnalisation d’alcènes et application en synthèse : Transition metal catalyzed nitrene transfers. Development of new reactions for the difunctionalization of alkenes and application in synthesis.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed April 03, 2020. http://www.theses.fr/2013PA112256.

MLA Handbook (7th Edition):

Dequirez, Geoffroy. “Transferts de nitrène catalysés par les métaux de transition. Développement de nouvelles réactions pour la difonctionnalisation d’alcènes et application en synthèse : Transition metal catalyzed nitrene transfers. Development of new reactions for the difunctionalization of alkenes and application in synthesis.” 2013. Web. 03 Apr 2020.

Vancouver:

Dequirez G. Transferts de nitrène catalysés par les métaux de transition. Développement de nouvelles réactions pour la difonctionnalisation d’alcènes et application en synthèse : Transition metal catalyzed nitrene transfers. Development of new reactions for the difunctionalization of alkenes and application in synthesis. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2013PA112256.

Council of Science Editors:

Dequirez G. Transferts de nitrène catalysés par les métaux de transition. Développement de nouvelles réactions pour la difonctionnalisation d’alcènes et application en synthèse : Transition metal catalyzed nitrene transfers. Development of new reactions for the difunctionalization of alkenes and application in synthesis. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA112256

23. Soulard, Marine. Approche synthétique vers la synthèse totale de l’epicocconone, étude de la réaction de désaromatisation oxydante à l’aide d’iode hypervalent (III) ou (V) : Synthetic approach toward the total synthesis of epicocconone, studies of oxydative dearomatization mediated by I(III) or I(V).

Degree: Docteur es, Chimie organique, 2014, Rouen, INSA

L'epicocconone est un produit naturel tricyclique, de la famille des azaphilones, isolé en 2003 d'un champignon Epicoccum nigrum. Ce composé se lie de façon covalente… (more)

Subjects/Keywords: Epicocconone; Marqueur fluorescent; Acylcétènes; Désaromatisation oxydante; Iode hypervalent; Epicocconone; Fluorescent proteins stain; Acylketenes; Dearomatization; Hypervalent iodine

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APA (6th Edition):

Soulard, M. (2014). Approche synthétique vers la synthèse totale de l’epicocconone, étude de la réaction de désaromatisation oxydante à l’aide d’iode hypervalent (III) ou (V) : Synthetic approach toward the total synthesis of epicocconone, studies of oxydative dearomatization mediated by I(III) or I(V). (Doctoral Dissertation). Rouen, INSA. Retrieved from http://www.theses.fr/2014ISAM0005

Chicago Manual of Style (16th Edition):

Soulard, Marine. “Approche synthétique vers la synthèse totale de l’epicocconone, étude de la réaction de désaromatisation oxydante à l’aide d’iode hypervalent (III) ou (V) : Synthetic approach toward the total synthesis of epicocconone, studies of oxydative dearomatization mediated by I(III) or I(V).” 2014. Doctoral Dissertation, Rouen, INSA. Accessed April 03, 2020. http://www.theses.fr/2014ISAM0005.

MLA Handbook (7th Edition):

Soulard, Marine. “Approche synthétique vers la synthèse totale de l’epicocconone, étude de la réaction de désaromatisation oxydante à l’aide d’iode hypervalent (III) ou (V) : Synthetic approach toward the total synthesis of epicocconone, studies of oxydative dearomatization mediated by I(III) or I(V).” 2014. Web. 03 Apr 2020.

Vancouver:

Soulard M. Approche synthétique vers la synthèse totale de l’epicocconone, étude de la réaction de désaromatisation oxydante à l’aide d’iode hypervalent (III) ou (V) : Synthetic approach toward the total synthesis of epicocconone, studies of oxydative dearomatization mediated by I(III) or I(V). [Internet] [Doctoral dissertation]. Rouen, INSA; 2014. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2014ISAM0005.

Council of Science Editors:

Soulard M. Approche synthétique vers la synthèse totale de l’epicocconone, étude de la réaction de désaromatisation oxydante à l’aide d’iode hypervalent (III) ou (V) : Synthetic approach toward the total synthesis of epicocconone, studies of oxydative dearomatization mediated by I(III) or I(V). [Doctoral Dissertation]. Rouen, INSA; 2014. Available from: http://www.theses.fr/2014ISAM0005

24. Nasrallah, Ali. Complexe de Rhodium(II) et iode hypervalent en catalyse : époxydation d’alcènes et amination de liaisons C(sp³)-H : Complex of Rhodium(II) and hypervalent iodine in catalysis : epoxidation of alkenes and amination of C(sp³)–H bonds.

Degree: Docteur es, Chimie, 2019, Université Paris-Saclay (ComUE)

Cette thèse a pour but de développer de nouveaux procédés catalytiques en combinant de réactifs de l’iode hypervalent avec des complexes de rhodium(II).Le premier chapitre… (more)

Subjects/Keywords: Nitrène; Fonctionnalisation C–H; Amination énantiosélective; Iode hypervalent; Epoxydation; Alcane; Nitrene; C–H Functionnalization; Enantioselective Amination; Hypervalent Iodine; Epoxidation; Alkane

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APA (6th Edition):

Nasrallah, A. (2019). Complexe de Rhodium(II) et iode hypervalent en catalyse : époxydation d’alcènes et amination de liaisons C(sp³)-H : Complex of Rhodium(II) and hypervalent iodine in catalysis : epoxidation of alkenes and amination of C(sp³)–H bonds. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS427

Chicago Manual of Style (16th Edition):

Nasrallah, Ali. “Complexe de Rhodium(II) et iode hypervalent en catalyse : époxydation d’alcènes et amination de liaisons C(sp³)-H : Complex of Rhodium(II) and hypervalent iodine in catalysis : epoxidation of alkenes and amination of C(sp³)–H bonds.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 03, 2020. http://www.theses.fr/2019SACLS427.

MLA Handbook (7th Edition):

Nasrallah, Ali. “Complexe de Rhodium(II) et iode hypervalent en catalyse : époxydation d’alcènes et amination de liaisons C(sp³)-H : Complex of Rhodium(II) and hypervalent iodine in catalysis : epoxidation of alkenes and amination of C(sp³)–H bonds.” 2019. Web. 03 Apr 2020.

Vancouver:

Nasrallah A. Complexe de Rhodium(II) et iode hypervalent en catalyse : époxydation d’alcènes et amination de liaisons C(sp³)-H : Complex of Rhodium(II) and hypervalent iodine in catalysis : epoxidation of alkenes and amination of C(sp³)–H bonds. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2019SACLS427.

Council of Science Editors:

Nasrallah A. Complexe de Rhodium(II) et iode hypervalent en catalyse : époxydation d’alcènes et amination de liaisons C(sp³)-H : Complex of Rhodium(II) and hypervalent iodine in catalysis : epoxidation of alkenes and amination of C(sp³)–H bonds. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS427

25. Dumoulin, Audrey. Synthèse asymétrique de 1,2-diamines et développement de nouveaux organoiodanes chiraux pour des réactions d'oxygénation : Asymmetric synthesis of 1,2-diamines and development of new chiral organoiodanes for oxygenation reactions.

Degree: Docteur es, Chimie, 2016, Université Paris-Saclay (ComUE)

Les 1,2-diamines sont présentes dans de nombreux produits biologiquement actifs, ce qui a poussé les chimistes organiciens à développer de nouvelles voies d’accès à ces… (more)

Subjects/Keywords: Chimie organique; Catalyse; Acide phosphorique; 1.2-Diamine; Iode hypervalent; Asymétrique; Organic chemistry; Catalysis; Phosphoric acid; 1.2-Diamine; Hypervalent iodine; Asymmetric

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APA (6th Edition):

Dumoulin, A. (2016). Synthèse asymétrique de 1,2-diamines et développement de nouveaux organoiodanes chiraux pour des réactions d'oxygénation : Asymmetric synthesis of 1,2-diamines and development of new chiral organoiodanes for oxygenation reactions. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2016SACLS364

Chicago Manual of Style (16th Edition):

Dumoulin, Audrey. “Synthèse asymétrique de 1,2-diamines et développement de nouveaux organoiodanes chiraux pour des réactions d'oxygénation : Asymmetric synthesis of 1,2-diamines and development of new chiral organoiodanes for oxygenation reactions.” 2016. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 03, 2020. http://www.theses.fr/2016SACLS364.

MLA Handbook (7th Edition):

Dumoulin, Audrey. “Synthèse asymétrique de 1,2-diamines et développement de nouveaux organoiodanes chiraux pour des réactions d'oxygénation : Asymmetric synthesis of 1,2-diamines and development of new chiral organoiodanes for oxygenation reactions.” 2016. Web. 03 Apr 2020.

Vancouver:

Dumoulin A. Synthèse asymétrique de 1,2-diamines et développement de nouveaux organoiodanes chiraux pour des réactions d'oxygénation : Asymmetric synthesis of 1,2-diamines and development of new chiral organoiodanes for oxygenation reactions. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2016. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2016SACLS364.

Council of Science Editors:

Dumoulin A. Synthèse asymétrique de 1,2-diamines et développement de nouveaux organoiodanes chiraux pour des réactions d'oxygénation : Asymmetric synthesis of 1,2-diamines and development of new chiral organoiodanes for oxygenation reactions. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2016. Available from: http://www.theses.fr/2016SACLS364

26. Grayfer, Tatyana. Synthèse totale de la mallotojaponine C et bromofonctionnalisations de polyprénoïdes initiées par l'iode(III) hypervalent : Total synthesis of mallotojaponin C and hypervalent iodine(III)-mediated bromofunctionalisations of polyprenoids.

Degree: Docteur es, Chimie, 2017, Université Paris-Saclay (ComUE)

Le paludisme est une maladie parasitaire qui présente une problématique de santé majeure, touchant actuellement plus de 200 millions de personnes dans le monde. Le… (more)

Subjects/Keywords: Paludisme; Terpènes; Iode hypervalent; Bromation; Synthèse totale; Produits naturels; Malaria; Terpenes; Hypervalent iodine; Bromination; Total synthesis; Natural products

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APA (6th Edition):

Grayfer, T. (2017). Synthèse totale de la mallotojaponine C et bromofonctionnalisations de polyprénoïdes initiées par l'iode(III) hypervalent : Total synthesis of mallotojaponin C and hypervalent iodine(III)-mediated bromofunctionalisations of polyprenoids. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2017SACLS349

Chicago Manual of Style (16th Edition):

Grayfer, Tatyana. “Synthèse totale de la mallotojaponine C et bromofonctionnalisations de polyprénoïdes initiées par l'iode(III) hypervalent : Total synthesis of mallotojaponin C and hypervalent iodine(III)-mediated bromofunctionalisations of polyprenoids.” 2017. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 03, 2020. http://www.theses.fr/2017SACLS349.

MLA Handbook (7th Edition):

Grayfer, Tatyana. “Synthèse totale de la mallotojaponine C et bromofonctionnalisations de polyprénoïdes initiées par l'iode(III) hypervalent : Total synthesis of mallotojaponin C and hypervalent iodine(III)-mediated bromofunctionalisations of polyprenoids.” 2017. Web. 03 Apr 2020.

Vancouver:

Grayfer T. Synthèse totale de la mallotojaponine C et bromofonctionnalisations de polyprénoïdes initiées par l'iode(III) hypervalent : Total synthesis of mallotojaponin C and hypervalent iodine(III)-mediated bromofunctionalisations of polyprenoids. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2017. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2017SACLS349.

Council of Science Editors:

Grayfer T. Synthèse totale de la mallotojaponine C et bromofonctionnalisations de polyprénoïdes initiées par l'iode(III) hypervalent : Total synthesis of mallotojaponin C and hypervalent iodine(III)-mediated bromofunctionalisations of polyprenoids. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2017. Available from: http://www.theses.fr/2017SACLS349

27. Antien, Kevin. Développement de nouveaux réactifs iodés hypervalents chiraux hélicéniques. Synthèse collective stéréodivergente d’alcaloïdes de Securinega. : Development of new chiral helicenic hypervalent iodine reagents. Stereodivergent collective synthesis of Securinega alkaloids.

Degree: Docteur es, Chimie organique, 2018, Bordeaux

La chimie des composés iodés hypervalents, ou organoiodanes, suscite un engouement croissant de la part de la communauté scientifique depuis maintenant près de 30 ans.… (more)

Subjects/Keywords: Iodane; Iode hypervalent; Hélicène; Alcaloïde de Securinega; Synthèse totale; Synthèse stéréodivergente; Iodane; Hypervalent iodine; Helicene; Securinega alkaloid; Total synthesis; Stereodivergent synthesis

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APA (6th Edition):

Antien, K. (2018). Développement de nouveaux réactifs iodés hypervalents chiraux hélicéniques. Synthèse collective stéréodivergente d’alcaloïdes de Securinega. : Development of new chiral helicenic hypervalent iodine reagents. Stereodivergent collective synthesis of Securinega alkaloids. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2018BORD0349

Chicago Manual of Style (16th Edition):

Antien, Kevin. “Développement de nouveaux réactifs iodés hypervalents chiraux hélicéniques. Synthèse collective stéréodivergente d’alcaloïdes de Securinega. : Development of new chiral helicenic hypervalent iodine reagents. Stereodivergent collective synthesis of Securinega alkaloids.” 2018. Doctoral Dissertation, Bordeaux. Accessed April 03, 2020. http://www.theses.fr/2018BORD0349.

MLA Handbook (7th Edition):

Antien, Kevin. “Développement de nouveaux réactifs iodés hypervalents chiraux hélicéniques. Synthèse collective stéréodivergente d’alcaloïdes de Securinega. : Development of new chiral helicenic hypervalent iodine reagents. Stereodivergent collective synthesis of Securinega alkaloids.” 2018. Web. 03 Apr 2020.

Vancouver:

Antien K. Développement de nouveaux réactifs iodés hypervalents chiraux hélicéniques. Synthèse collective stéréodivergente d’alcaloïdes de Securinega. : Development of new chiral helicenic hypervalent iodine reagents. Stereodivergent collective synthesis of Securinega alkaloids. [Internet] [Doctoral dissertation]. Bordeaux; 2018. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2018BORD0349.

Council of Science Editors:

Antien K. Développement de nouveaux réactifs iodés hypervalents chiraux hélicéniques. Synthèse collective stéréodivergente d’alcaloïdes de Securinega. : Development of new chiral helicenic hypervalent iodine reagents. Stereodivergent collective synthesis of Securinega alkaloids. [Doctoral Dissertation]. Bordeaux; 2018. Available from: http://www.theses.fr/2018BORD0349

28. Aubineau, Thomas. Synthèse d'hétérocycles azotés : tétrahydropyrazines et morpholines : Synthesis of nitrogen-containing heterocycles : tetrahydropyrazines and morpholines.

Degree: Docteur es, Chimie organique, 2018, Sorbonne université

Les tétrahydropyrazines et les morpholines sont des hétérocycles à six chaînons comportant deux hétéroatomes en position 1,4. Les objectifs de cette thèse ont été la… (more)

Subjects/Keywords: Tétrahydropyrazine; Morpholine; Monotope; Iode hypervalent; Palladium; Fer; Tetrahydropyrazines; Morpholines; One-pot; Hypervalent iodine; Palladium; Iron; 547.04

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APA (6th Edition):

Aubineau, T. (2018). Synthèse d'hétérocycles azotés : tétrahydropyrazines et morpholines : Synthesis of nitrogen-containing heterocycles : tetrahydropyrazines and morpholines. (Doctoral Dissertation). Sorbonne université. Retrieved from http://www.theses.fr/2018SORUS144

Chicago Manual of Style (16th Edition):

Aubineau, Thomas. “Synthèse d'hétérocycles azotés : tétrahydropyrazines et morpholines : Synthesis of nitrogen-containing heterocycles : tetrahydropyrazines and morpholines.” 2018. Doctoral Dissertation, Sorbonne université. Accessed April 03, 2020. http://www.theses.fr/2018SORUS144.

MLA Handbook (7th Edition):

Aubineau, Thomas. “Synthèse d'hétérocycles azotés : tétrahydropyrazines et morpholines : Synthesis of nitrogen-containing heterocycles : tetrahydropyrazines and morpholines.” 2018. Web. 03 Apr 2020.

Vancouver:

Aubineau T. Synthèse d'hétérocycles azotés : tétrahydropyrazines et morpholines : Synthesis of nitrogen-containing heterocycles : tetrahydropyrazines and morpholines. [Internet] [Doctoral dissertation]. Sorbonne université; 2018. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2018SORUS144.

Council of Science Editors:

Aubineau T. Synthèse d'hétérocycles azotés : tétrahydropyrazines et morpholines : Synthesis of nitrogen-containing heterocycles : tetrahydropyrazines and morpholines. [Doctoral Dissertation]. Sorbonne université; 2018. Available from: http://www.theses.fr/2018SORUS144


University of Florida

29. Shelton, Phillip. Investigations of Heterobimetallic Catalysis of Various Organic Reactions and Metal-Free Carbonylation of Amines to Ureas Using the Hypervalent Iodine Species Sodium Periodate.

Degree: PhD, Chemistry, 2010, University of Florida

 The homogeneous heterobimetallic catalysts CpRu(PPh3)Cl(mu-dppm)AuCl, CpRu(PPh3)I(mu-dppm)AuI, CpRu(PPh3)(mu-Cl)(mu-dppm)PdCl2, CpRu(PPh3)(mu-I)(mu-dppm)PdI2, and CpRu(PPh3)2SnCl3, were used in the cyclization of enyne starting materials. The reaction required high temperatures (90… (more)

Subjects/Keywords: Amines; ATMs; Catalysis; Catalysts; Iodine; Oxidation; Quinolines; Selenium; Solvents; Sulfur; bimetallic, carbonylation, homogeneous, hypervalent, iodine, oxidative, urea

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APA (6th Edition):

Shelton, P. (2010). Investigations of Heterobimetallic Catalysis of Various Organic Reactions and Metal-Free Carbonylation of Amines to Ureas Using the Hypervalent Iodine Species Sodium Periodate. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0025126

Chicago Manual of Style (16th Edition):

Shelton, Phillip. “Investigations of Heterobimetallic Catalysis of Various Organic Reactions and Metal-Free Carbonylation of Amines to Ureas Using the Hypervalent Iodine Species Sodium Periodate.” 2010. Doctoral Dissertation, University of Florida. Accessed April 03, 2020. http://ufdc.ufl.edu/UFE0025126.

MLA Handbook (7th Edition):

Shelton, Phillip. “Investigations of Heterobimetallic Catalysis of Various Organic Reactions and Metal-Free Carbonylation of Amines to Ureas Using the Hypervalent Iodine Species Sodium Periodate.” 2010. Web. 03 Apr 2020.

Vancouver:

Shelton P. Investigations of Heterobimetallic Catalysis of Various Organic Reactions and Metal-Free Carbonylation of Amines to Ureas Using the Hypervalent Iodine Species Sodium Periodate. [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2020 Apr 03]. Available from: http://ufdc.ufl.edu/UFE0025126.

Council of Science Editors:

Shelton P. Investigations of Heterobimetallic Catalysis of Various Organic Reactions and Metal-Free Carbonylation of Amines to Ureas Using the Hypervalent Iodine Species Sodium Periodate. [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0025126


Universitat Rovira i Virgili

30. Bosnidou, Alexandra Eleni. New Methodology for C-N Bond Formation within Iodine Redox Manifolds.

Degree: Departament de Química Física i Inorgànica, 2019, Universitat Rovira i Virgili

 The latest developments in the field of oxidative carbon-nitrogen bond construction are represented in this Doctoral Thesis. Greener alternatives to established synthetic methodologies have been… (more)

Subjects/Keywords: Aminació; Iodo hipervalente; Catálisi de iode; Aminación; Yodo Hipervalente; Catálisis de yodo; Amination; Hypervalent Iodine; Iodine Catalysis; Ciències; 54; 547

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APA (6th Edition):

Bosnidou, A. E. (2019). New Methodology for C-N Bond Formation within Iodine Redox Manifolds. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/668478

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bosnidou, Alexandra Eleni. “New Methodology for C-N Bond Formation within Iodine Redox Manifolds.” 2019. Thesis, Universitat Rovira i Virgili. Accessed April 03, 2020. http://hdl.handle.net/10803/668478.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bosnidou, Alexandra Eleni. “New Methodology for C-N Bond Formation within Iodine Redox Manifolds.” 2019. Web. 03 Apr 2020.

Vancouver:

Bosnidou AE. New Methodology for C-N Bond Formation within Iodine Redox Manifolds. [Internet] [Thesis]. Universitat Rovira i Virgili; 2019. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10803/668478.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bosnidou AE. New Methodology for C-N Bond Formation within Iodine Redox Manifolds. [Thesis]. Universitat Rovira i Virgili; 2019. Available from: http://hdl.handle.net/10803/668478

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2] [3]

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