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You searched for subject:(trifluoromethylation). Showing records 1 – 27 of 27 total matches.

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University of Hawaii – Manoa

1. Ichioka, Hiromi. New nickel complexes for trifluoromethylation studies.

Degree: 2016, University of Hawaii – Manoa

M.S. University of Hawaii at Manoa 2012.

We decided to prepare bis-perfluoroalkyl nickel complexes bearing a bipyridine ligand for investigation of the fundamental nickel perfluoroalkyl… (more)

Subjects/Keywords: nickel; trifluoromethylation

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APA (6th Edition):

Ichioka, H. (2016). New nickel complexes for trifluoromethylation studies. (Thesis). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/100881

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):

Ichioka, Hiromi. “New nickel complexes for trifluoromethylation studies.” 2016. Thesis, University of Hawaii – Manoa. Accessed October 15, 2019. http://hdl.handle.net/10125/100881.

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

MLA Handbook (7th Edition):

Ichioka, Hiromi. “New nickel complexes for trifluoromethylation studies.” 2016. Web. 15 Oct 2019.

Vancouver:

Ichioka H. New nickel complexes for trifluoromethylation studies. [Internet] [Thesis]. University of Hawaii – Manoa; 2016. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/10125/100881.

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

Council of Science Editors:

Ichioka H. New nickel complexes for trifluoromethylation studies. [Thesis]. University of Hawaii – Manoa; 2016. Available from: http://hdl.handle.net/10125/100881

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


University of Kansas

2. Ambler, Brett R. Copper-Catalyzed Decarboxylative Trifluoromethylation Reactions.

Degree: PhD, Medicinal Chemistry, 2017, University of Kansas

 Trifluoromethanes play an important role in medicinal chemistry, and methods that enable the rapid synthesis of trifluoromethanes from common functional groups are essential for the… (more)

Subjects/Keywords: Chemistry; Organic chemistry; Chemistry; Copper; Fluorine; Medicinal Chemistry; Organic Chemistry; Trifluoromethylation

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APA (6th Edition):

Ambler, B. R. (2017). Copper-Catalyzed Decarboxylative Trifluoromethylation Reactions. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/26150

Chicago Manual of Style (16th Edition):

Ambler, Brett R. “Copper-Catalyzed Decarboxylative Trifluoromethylation Reactions.” 2017. Doctoral Dissertation, University of Kansas. Accessed October 15, 2019. http://hdl.handle.net/1808/26150.

MLA Handbook (7th Edition):

Ambler, Brett R. “Copper-Catalyzed Decarboxylative Trifluoromethylation Reactions.” 2017. Web. 15 Oct 2019.

Vancouver:

Ambler BR. Copper-Catalyzed Decarboxylative Trifluoromethylation Reactions. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/1808/26150.

Council of Science Editors:

Ambler BR. Copper-Catalyzed Decarboxylative Trifluoromethylation Reactions. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/26150


University of Oxford

3. Galicia Lopez, Oscar. Synthesis and trifluoromethylation of allylsilanes.

Degree: PhD, 2013, University of Oxford

 The first part of this thesis presents a novel approach for synthesising enantioenriched cyclic allylsilanes via asymmetric ring-closing metathesis (ARCM). The second part of this… (more)

Subjects/Keywords: 547; Organic synthesis; Catalysis; metal catalysis; organosilanes; trifluoromethylation

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APA (6th Edition):

Galicia Lopez, O. (2013). Synthesis and trifluoromethylation of allylsilanes. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:b1f58a1c-9213-4aac-9ece-9d9f944b5f9c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639950

Chicago Manual of Style (16th Edition):

Galicia Lopez, Oscar. “Synthesis and trifluoromethylation of allylsilanes.” 2013. Doctoral Dissertation, University of Oxford. Accessed October 15, 2019. http://ora.ox.ac.uk/objects/uuid:b1f58a1c-9213-4aac-9ece-9d9f944b5f9c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639950.

MLA Handbook (7th Edition):

Galicia Lopez, Oscar. “Synthesis and trifluoromethylation of allylsilanes.” 2013. Web. 15 Oct 2019.

Vancouver:

Galicia Lopez O. Synthesis and trifluoromethylation of allylsilanes. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Oct 15]. Available from: http://ora.ox.ac.uk/objects/uuid:b1f58a1c-9213-4aac-9ece-9d9f944b5f9c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639950.

Council of Science Editors:

Galicia Lopez O. Synthesis and trifluoromethylation of allylsilanes. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:b1f58a1c-9213-4aac-9ece-9d9f944b5f9c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639950

4. Clarke, Sarah L. Studies in asymmetric and heterocyclic synthesis: I. chiral ketones II. Quinolones III. Trifluoromethylated pyrones.

Degree: 2015, University College Cork

 This thesis is split into three sections based on three different areas of research. In the first section, investigations into the α-alkylation of ketones using… (more)

Subjects/Keywords: Asymmetric synthesis; Trifluoromethylation; Quinolones; Chiral auxiliary; Pyrone; Pyridone; Alpha alkylated ketone

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APA (6th Edition):

Clarke, S. L. (2015). Studies in asymmetric and heterocyclic synthesis: I. chiral ketones II. Quinolones III. Trifluoromethylated pyrones. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/3091

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):

Clarke, Sarah L. “Studies in asymmetric and heterocyclic synthesis: I. chiral ketones II. Quinolones III. Trifluoromethylated pyrones.” 2015. Thesis, University College Cork. Accessed October 15, 2019. http://hdl.handle.net/10468/3091.

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

MLA Handbook (7th Edition):

Clarke, Sarah L. “Studies in asymmetric and heterocyclic synthesis: I. chiral ketones II. Quinolones III. Trifluoromethylated pyrones.” 2015. Web. 15 Oct 2019.

Vancouver:

Clarke SL. Studies in asymmetric and heterocyclic synthesis: I. chiral ketones II. Quinolones III. Trifluoromethylated pyrones. [Internet] [Thesis]. University College Cork; 2015. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/10468/3091.

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

Council of Science Editors:

Clarke SL. Studies in asymmetric and heterocyclic synthesis: I. chiral ketones II. Quinolones III. Trifluoromethylated pyrones. [Thesis]. University College Cork; 2015. Available from: http://hdl.handle.net/10468/3091

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


ETH Zürich

5. Engl, Pascal Stephan. Development and Application of N-Trifluoromethyl NHC Ligands for Transition-Metal Catalysis.

Degree: 2017, ETH Zürich

 Starting from N-trifluoromethyl benzimidazole, a series of unsymmetrical N-trifluoromethyl benzimidazolium salts have been prepared and fully characterized as precursors for N-heterocyclic carbene (NHC) ligands. IR… (more)

Subjects/Keywords: ligand design; N-heterocyclic carbene; metathesis; trifluoromethylation; ethenolysis

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APA (6th Edition):

Engl, P. S. (2017). Development and Application of N-Trifluoromethyl NHC Ligands for Transition-Metal Catalysis. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/195781

Chicago Manual of Style (16th Edition):

Engl, Pascal Stephan. “Development and Application of N-Trifluoromethyl NHC Ligands for Transition-Metal Catalysis.” 2017. Doctoral Dissertation, ETH Zürich. Accessed October 15, 2019. http://hdl.handle.net/20.500.11850/195781.

MLA Handbook (7th Edition):

Engl, Pascal Stephan. “Development and Application of N-Trifluoromethyl NHC Ligands for Transition-Metal Catalysis.” 2017. Web. 15 Oct 2019.

Vancouver:

Engl PS. Development and Application of N-Trifluoromethyl NHC Ligands for Transition-Metal Catalysis. [Internet] [Doctoral dissertation]. ETH Zürich; 2017. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/20.500.11850/195781.

Council of Science Editors:

Engl PS. Development and Application of N-Trifluoromethyl NHC Ligands for Transition-Metal Catalysis. [Doctoral Dissertation]. ETH Zürich; 2017. Available from: http://hdl.handle.net/20.500.11850/195781


University of Minnesota

6. Ranade, Adwait. Library Synthesis Of Piperidinone Sulfonamides, Transition Metal-Free C-H Trifluoromethylation Of Cyclic Enaminones, And Elucidating The Binding Site Of Epothilones On Beta-Tubulin With Epothilone Photoaffinity Probes.

Degree: PhD, Medicinal Chemistry, 2014, University of Minnesota

 Chapter 1 focuses on synthesizing a library of piperidinone sulfonamides. The piperidinones serve as valuables intermediates for the synthesis of nitrogen-containing bioactive molecules, various alkaloids,… (more)

Subjects/Keywords: C-H trifluoromethylation; Epothilone; Medicinal Chemistry; Organic Chemistry; piperidone sulfonamides

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APA (6th Edition):

Ranade, A. (2014). Library Synthesis Of Piperidinone Sulfonamides, Transition Metal-Free C-H Trifluoromethylation Of Cyclic Enaminones, And Elucidating The Binding Site Of Epothilones On Beta-Tubulin With Epothilone Photoaffinity Probes. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/191462

Chicago Manual of Style (16th Edition):

Ranade, Adwait. “Library Synthesis Of Piperidinone Sulfonamides, Transition Metal-Free C-H Trifluoromethylation Of Cyclic Enaminones, And Elucidating The Binding Site Of Epothilones On Beta-Tubulin With Epothilone Photoaffinity Probes.” 2014. Doctoral Dissertation, University of Minnesota. Accessed October 15, 2019. http://hdl.handle.net/11299/191462.

MLA Handbook (7th Edition):

Ranade, Adwait. “Library Synthesis Of Piperidinone Sulfonamides, Transition Metal-Free C-H Trifluoromethylation Of Cyclic Enaminones, And Elucidating The Binding Site Of Epothilones On Beta-Tubulin With Epothilone Photoaffinity Probes.” 2014. Web. 15 Oct 2019.

Vancouver:

Ranade A. Library Synthesis Of Piperidinone Sulfonamides, Transition Metal-Free C-H Trifluoromethylation Of Cyclic Enaminones, And Elucidating The Binding Site Of Epothilones On Beta-Tubulin With Epothilone Photoaffinity Probes. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/11299/191462.

Council of Science Editors:

Ranade A. Library Synthesis Of Piperidinone Sulfonamides, Transition Metal-Free C-H Trifluoromethylation Of Cyclic Enaminones, And Elucidating The Binding Site Of Epothilones On Beta-Tubulin With Epothilone Photoaffinity Probes. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/191462

7. Ye, Yingda. Investigations into Transition Metal Catalyzed/Mediated Arene Trifluoromethylation and Fluorination Reactions.

Degree: PhD, Chemistry, 2013, University of Michigan

 Aryl–CF3 and aryl–F motifs are widely prevalent in pharmaceuticals and agrochemicals. As a result, the development of practical methods for the formation of these bonds… (more)

Subjects/Keywords: Fluorination; Trifluoromethylation; Chemistry; Science

…74 3. Ag-Mediated Aromatic Trifluoromethylation… …Scheme 1.8: First Cu-Catalyzed Trifluoromethylation of Aryl Iodides… …7 Scheme 1.12: Pd-Catalyzed Arene Trifluoromethylation via a Pd0/II Mechanistic Pathway… …9 Scheme 1.14: Pd-Catalyzed Trifluoromethylation of Aryl Chlorides… …15 CHAPTER 2 Cu-Based Trifluoromethylation of Arylboronic Acids with CF3 Radicals Scheme… 

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7

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APA (6th Edition):

Ye, Y. (2013). Investigations into Transition Metal Catalyzed/Mediated Arene Trifluoromethylation and Fluorination Reactions. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/99826

Chicago Manual of Style (16th Edition):

Ye, Yingda. “Investigations into Transition Metal Catalyzed/Mediated Arene Trifluoromethylation and Fluorination Reactions.” 2013. Doctoral Dissertation, University of Michigan. Accessed October 15, 2019. http://hdl.handle.net/2027.42/99826.

MLA Handbook (7th Edition):

Ye, Yingda. “Investigations into Transition Metal Catalyzed/Mediated Arene Trifluoromethylation and Fluorination Reactions.” 2013. Web. 15 Oct 2019.

Vancouver:

Ye Y. Investigations into Transition Metal Catalyzed/Mediated Arene Trifluoromethylation and Fluorination Reactions. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2027.42/99826.

Council of Science Editors:

Ye Y. Investigations into Transition Metal Catalyzed/Mediated Arene Trifluoromethylation and Fluorination Reactions. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/99826

8. Lafaye, Kévin. Métathèse croisée d'alcènes contenant des N-hétéroaryles. Trifluorométhylation d'ène-carbamates cycliques et dérivés : Cross-metathesis of aleknes containing N-heteroaryles. Trifluoromethylation of cyclic ene-carbamates and derivatives.

Degree: Docteur es, Chimie Organique, 2015, Université Pierre et Marie Curie – Paris VI

La métathèse d'oléfines est une des réactions les plus efficaces pour former des liaisons carbone-carbone et elle est maintenant utilisée pour synthétiser une large gamme… (more)

Subjects/Keywords: Métathèse croisée; N-Hétérocycles; Pyridines; Trifluorométhylation; Ene-Carbamates; Pipéridines; Cross-metathesis; Trifluoromethylation; 540

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APA (6th Edition):

Lafaye, K. (2015). Métathèse croisée d'alcènes contenant des N-hétéroaryles. Trifluorométhylation d'ène-carbamates cycliques et dérivés : Cross-metathesis of aleknes containing N-heteroaryles. Trifluoromethylation of cyclic ene-carbamates and derivatives. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2015PA066488

Chicago Manual of Style (16th Edition):

Lafaye, Kévin. “Métathèse croisée d'alcènes contenant des N-hétéroaryles. Trifluorométhylation d'ène-carbamates cycliques et dérivés : Cross-metathesis of aleknes containing N-heteroaryles. Trifluoromethylation of cyclic ene-carbamates and derivatives.” 2015. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 15, 2019. http://www.theses.fr/2015PA066488.

MLA Handbook (7th Edition):

Lafaye, Kévin. “Métathèse croisée d'alcènes contenant des N-hétéroaryles. Trifluorométhylation d'ène-carbamates cycliques et dérivés : Cross-metathesis of aleknes containing N-heteroaryles. Trifluoromethylation of cyclic ene-carbamates and derivatives.” 2015. Web. 15 Oct 2019.

Vancouver:

Lafaye K. Métathèse croisée d'alcènes contenant des N-hétéroaryles. Trifluorométhylation d'ène-carbamates cycliques et dérivés : Cross-metathesis of aleknes containing N-heteroaryles. Trifluoromethylation of cyclic ene-carbamates and derivatives. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. [cited 2019 Oct 15]. Available from: http://www.theses.fr/2015PA066488.

Council of Science Editors:

Lafaye K. Métathèse croisée d'alcènes contenant des N-hétéroaryles. Trifluorométhylation d'ène-carbamates cycliques et dérivés : Cross-metathesis of aleknes containing N-heteroaryles. Trifluoromethylation of cyclic ene-carbamates and derivatives. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. Available from: http://www.theses.fr/2015PA066488


University of Oxford

9. Ó Dúill, Miriam Leslie. Late-stage fluorination and perfluoroalkylation.

Degree: PhD, 2015, University of Oxford

 In this thesis new synthetic routes towards perfluorinated compounds are described, as well as their radiolabelling with fluorine-18, with the aim of application in pharmaceutically… (more)

Subjects/Keywords: 547; Chemistry, Organic; Fluorine; Photocatalysis; Trifluoromethylation; 18F Radiochemistry; Transition Metal Catalysis; Perfluoroalkylation; Fluorination

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APA (6th Edition):

Ó Dúill, M. L. (2015). Late-stage fluorination and perfluoroalkylation. (Doctoral Dissertation). University of Oxford. Retrieved from https://ora.ox.ac.uk/objects/uuid:25373cc9-ae25-45c4-aafc-a1706e289ea3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.712045

Chicago Manual of Style (16th Edition):

Ó Dúill, Miriam Leslie. “Late-stage fluorination and perfluoroalkylation.” 2015. Doctoral Dissertation, University of Oxford. Accessed October 15, 2019. https://ora.ox.ac.uk/objects/uuid:25373cc9-ae25-45c4-aafc-a1706e289ea3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.712045.

MLA Handbook (7th Edition):

Ó Dúill, Miriam Leslie. “Late-stage fluorination and perfluoroalkylation.” 2015. Web. 15 Oct 2019.

Vancouver:

Ó Dúill ML. Late-stage fluorination and perfluoroalkylation. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2019 Oct 15]. Available from: https://ora.ox.ac.uk/objects/uuid:25373cc9-ae25-45c4-aafc-a1706e289ea3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.712045.

Council of Science Editors:

Ó Dúill ML. Late-stage fluorination and perfluoroalkylation. [Doctoral Dissertation]. University of Oxford; 2015. Available from: https://ora.ox.ac.uk/objects/uuid:25373cc9-ae25-45c4-aafc-a1706e289ea3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.712045

10. Guieu, Benjamin. Synthèse de pyrroles polysubstitués par cyclisation à l'or : évaluation de l'activité de 3-arylpyrroles sur les microtubules : Polysubstituted pyrroles synthesis via gold-catalysed cyclisation : evaluation of the activity of 3-arylpyrroles on microtubules.

Degree: Docteur es, Chimie, 2017, Rennes 1

Des composés de type 3-arylpyrroles appelés pyakols ont montré une activité antimitotique sur des cellules tumorales murines, avec en particulier un effet sur les microtubules.… (more)

Subjects/Keywords: Pyrrole; Cyclisation; Catalyse à l’or; Cancer; Microtubules; Mitose; Marquage fluorescent; Trifluorométhylation; Pyrrole; Gold-Catalysed cyclisation; Cancer; Microtubules; Mitosis; Fluorescent labeling; Trifluoromethylation

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APA (6th Edition):

Guieu, B. (2017). Synthèse de pyrroles polysubstitués par cyclisation à l'or : évaluation de l'activité de 3-arylpyrroles sur les microtubules : Polysubstituted pyrroles synthesis via gold-catalysed cyclisation : evaluation of the activity of 3-arylpyrroles on microtubules. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2017REN1S084

Chicago Manual of Style (16th Edition):

Guieu, Benjamin. “Synthèse de pyrroles polysubstitués par cyclisation à l'or : évaluation de l'activité de 3-arylpyrroles sur les microtubules : Polysubstituted pyrroles synthesis via gold-catalysed cyclisation : evaluation of the activity of 3-arylpyrroles on microtubules.” 2017. Doctoral Dissertation, Rennes 1. Accessed October 15, 2019. http://www.theses.fr/2017REN1S084.

MLA Handbook (7th Edition):

Guieu, Benjamin. “Synthèse de pyrroles polysubstitués par cyclisation à l'or : évaluation de l'activité de 3-arylpyrroles sur les microtubules : Polysubstituted pyrroles synthesis via gold-catalysed cyclisation : evaluation of the activity of 3-arylpyrroles on microtubules.” 2017. Web. 15 Oct 2019.

Vancouver:

Guieu B. Synthèse de pyrroles polysubstitués par cyclisation à l'or : évaluation de l'activité de 3-arylpyrroles sur les microtubules : Polysubstituted pyrroles synthesis via gold-catalysed cyclisation : evaluation of the activity of 3-arylpyrroles on microtubules. [Internet] [Doctoral dissertation]. Rennes 1; 2017. [cited 2019 Oct 15]. Available from: http://www.theses.fr/2017REN1S084.

Council of Science Editors:

Guieu B. Synthèse de pyrroles polysubstitués par cyclisation à l'or : évaluation de l'activité de 3-arylpyrroles sur les microtubules : Polysubstituted pyrroles synthesis via gold-catalysed cyclisation : evaluation of the activity of 3-arylpyrroles on microtubules. [Doctoral Dissertation]. Rennes 1; 2017. Available from: http://www.theses.fr/2017REN1S084

11. Carboni, Aude. Développement de nouvelles réactions de trifluorométhylation photocatalysées : difonctionnalisation vicinale d'alcènes : Development of photocatalytic trifluoromethylated reactions : Vicinal Difunctionalization of Alkenes.

Degree: Docteur es, Chimie, 2015, Paris Saclay

La chimie du fluor a connu un essor considérable ces dernières années en raison des caractéristiques remarquables de cet halogène et de l'influence qu'il exerce… (more)

Subjects/Keywords: Trifluorométhylation; Catalyse photoredox; Difonctionnalisation; Styrène; Ènecarbamates; 1; 3-dihydroisobenzofurane; Trifluoromethylation; Photoredox catalysis; Difunctionalization; Styrene; Enecarbamates; 1; 3-dihydroisobenzofuran

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APA (6th Edition):

Carboni, A. (2015). Développement de nouvelles réactions de trifluorométhylation photocatalysées : difonctionnalisation vicinale d'alcènes : Development of photocatalytic trifluoromethylated reactions : Vicinal Difunctionalization of Alkenes. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2015SACLS110

Chicago Manual of Style (16th Edition):

Carboni, Aude. “Développement de nouvelles réactions de trifluorométhylation photocatalysées : difonctionnalisation vicinale d'alcènes : Development of photocatalytic trifluoromethylated reactions : Vicinal Difunctionalization of Alkenes.” 2015. Doctoral Dissertation, Paris Saclay. Accessed October 15, 2019. http://www.theses.fr/2015SACLS110.

MLA Handbook (7th Edition):

Carboni, Aude. “Développement de nouvelles réactions de trifluorométhylation photocatalysées : difonctionnalisation vicinale d'alcènes : Development of photocatalytic trifluoromethylated reactions : Vicinal Difunctionalization of Alkenes.” 2015. Web. 15 Oct 2019.

Vancouver:

Carboni A. Développement de nouvelles réactions de trifluorométhylation photocatalysées : difonctionnalisation vicinale d'alcènes : Development of photocatalytic trifluoromethylated reactions : Vicinal Difunctionalization of Alkenes. [Internet] [Doctoral dissertation]. Paris Saclay; 2015. [cited 2019 Oct 15]. Available from: http://www.theses.fr/2015SACLS110.

Council of Science Editors:

Carboni A. Développement de nouvelles réactions de trifluorométhylation photocatalysées : difonctionnalisation vicinale d'alcènes : Development of photocatalytic trifluoromethylated reactions : Vicinal Difunctionalization of Alkenes. [Doctoral Dissertation]. Paris Saclay; 2015. Available from: http://www.theses.fr/2015SACLS110


University of Connecticut

12. Rudzinski, DiAndra M. Preparation of Organofluorine Compounds: Exploring Mono-, Di-, and Tri-fluorination.

Degree: MS, Chemistry, 2013, University of Connecticut

  Organofluorine compounds exhibit biological activity and have advantageous properties for drug design. Natural occurring fluorinated molecules are rare, demanding new synthetic methods for their… (more)

Subjects/Keywords: Organofluorine Compounds; Trifluoromethyl Ketone; Mono-trifluoromethylation; Weinreb Amide; (Trifluoromethyl)trimethylsilane; Aryl Fluorides; Tetrahedral Intermediate; Difluoromethyl Ketone; Fluoride Initiator; Silylated Intermediate

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APA (6th Edition):

Rudzinski, D. M. (2013). Preparation of Organofluorine Compounds: Exploring Mono-, Di-, and Tri-fluorination. (Masters Thesis). University of Connecticut. Retrieved from https://opencommons.uconn.edu/gs_theses/380

Chicago Manual of Style (16th Edition):

Rudzinski, DiAndra M. “Preparation of Organofluorine Compounds: Exploring Mono-, Di-, and Tri-fluorination.” 2013. Masters Thesis, University of Connecticut. Accessed October 15, 2019. https://opencommons.uconn.edu/gs_theses/380.

MLA Handbook (7th Edition):

Rudzinski, DiAndra M. “Preparation of Organofluorine Compounds: Exploring Mono-, Di-, and Tri-fluorination.” 2013. Web. 15 Oct 2019.

Vancouver:

Rudzinski DM. Preparation of Organofluorine Compounds: Exploring Mono-, Di-, and Tri-fluorination. [Internet] [Masters thesis]. University of Connecticut; 2013. [cited 2019 Oct 15]. Available from: https://opencommons.uconn.edu/gs_theses/380.

Council of Science Editors:

Rudzinski DM. Preparation of Organofluorine Compounds: Exploring Mono-, Di-, and Tri-fluorination. [Masters Thesis]. University of Connecticut; 2013. Available from: https://opencommons.uconn.edu/gs_theses/380


University of Southern California

13. Upton, Thomas George. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.

Degree: PhD, Chemistry, 2009, University of Southern California

 A stereoelectronically varied series of alpha-substituted methylenebisphosphonic acids (X,Y = H, F, Cl, Br, CH3) was synthesized and used to prepare corresponding dNTP beta,y-CXY and… (more)

Subjects/Keywords: DNA polymerase beta; bisphosphonates; titrations; fluorination; trifluoromethylation; halogenation; nucleotide analogues; stereoselectivity; autodock; docking; inhibitor design; HIV reverse transcriptase; polymerase kinetics

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APA (6th Edition):

Upton, T. G. (2009). Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859

Chicago Manual of Style (16th Edition):

Upton, Thomas George. “Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.” 2009. Doctoral Dissertation, University of Southern California. Accessed October 15, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859.

MLA Handbook (7th Edition):

Upton, Thomas George. “Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.” 2009. Web. 15 Oct 2019.

Vancouver:

Upton TG. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Oct 15]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859.

Council of Science Editors:

Upton TG. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859

14. Jarrige, Lucie. Nouvelles méthodes de synthèse et de fonctionnalisation d'hétérocycles par catalyse photorédox et organocatalyse : New methods for the synthesis and the functionalization of heterocyclic compunds.

Degree: Docteur es, Chimie, 2018, Paris Saclay

Les hétérocycles constituent une des classes les plus importantes de composés chimiques. Ces motifs structuraux sont les éléments clés d’une large gamme de produits naturels… (more)

Subjects/Keywords: Organocatalyse; Catalyse Photorédox; Hétérocycles; Synthèse asymétrique; Trifluorométhylation; Cycloadditions [4+2]; Organocatalysis; Photoredox Catalysis; Heterocycles; Asymmetric synthesis; Trifluoromethylation; [4+2] Cycloadditions

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APA (6th Edition):

Jarrige, L. (2018). Nouvelles méthodes de synthèse et de fonctionnalisation d'hétérocycles par catalyse photorédox et organocatalyse : New methods for the synthesis and the functionalization of heterocyclic compunds. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS215

Chicago Manual of Style (16th Edition):

Jarrige, Lucie. “Nouvelles méthodes de synthèse et de fonctionnalisation d'hétérocycles par catalyse photorédox et organocatalyse : New methods for the synthesis and the functionalization of heterocyclic compunds.” 2018. Doctoral Dissertation, Paris Saclay. Accessed October 15, 2019. http://www.theses.fr/2018SACLS215.

MLA Handbook (7th Edition):

Jarrige, Lucie. “Nouvelles méthodes de synthèse et de fonctionnalisation d'hétérocycles par catalyse photorédox et organocatalyse : New methods for the synthesis and the functionalization of heterocyclic compunds.” 2018. Web. 15 Oct 2019.

Vancouver:

Jarrige L. Nouvelles méthodes de synthèse et de fonctionnalisation d'hétérocycles par catalyse photorédox et organocatalyse : New methods for the synthesis and the functionalization of heterocyclic compunds. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Oct 15]. Available from: http://www.theses.fr/2018SACLS215.

Council of Science Editors:

Jarrige L. Nouvelles méthodes de synthèse et de fonctionnalisation d'hétérocycles par catalyse photorédox et organocatalyse : New methods for the synthesis and the functionalization of heterocyclic compunds. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS215

15. Allen, Anna Elizabeth. The Productive Merger of Transition Metal and Enamine Catalysis for the Enantioselective Functionalization of Aldehydes .

Degree: PhD, 2012, Princeton University

 Enamine catalysis is a branch of organocatalysis that enables the stereoselective construction of carbon-carbon and carbon-heteroatom bonds at the α-position of aldehydes and ketones using… (more)

Subjects/Keywords: Arylation; Copper; Enamine; Hypervalent Iodine; Organocatalysis; Trifluoromethylation

…5 Chapter 2: Development of an Enantioselective α-Trifluoromethylation of Aldehydes Using… …10 xi Chapter 2: Development of an Enantioselective α-Trifluoromethylation of Aldehydes… …trifluoromethylation of enamines using trifluoromethyl radicals… …18 2. Asymmetric triethylborane-mediated radical trifluoromethylation of carbonyl… …19 3. The direct α-trifluoromethylation aldehydes via photoredox catalysis… 

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APA (6th Edition):

Allen, A. E. (2012). The Productive Merger of Transition Metal and Enamine Catalysis for the Enantioselective Functionalization of Aldehydes . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01p8418n242

Chicago Manual of Style (16th Edition):

Allen, Anna Elizabeth. “The Productive Merger of Transition Metal and Enamine Catalysis for the Enantioselective Functionalization of Aldehydes .” 2012. Doctoral Dissertation, Princeton University. Accessed October 15, 2019. http://arks.princeton.edu/ark:/88435/dsp01p8418n242.

MLA Handbook (7th Edition):

Allen, Anna Elizabeth. “The Productive Merger of Transition Metal and Enamine Catalysis for the Enantioselective Functionalization of Aldehydes .” 2012. Web. 15 Oct 2019.

Vancouver:

Allen AE. The Productive Merger of Transition Metal and Enamine Catalysis for the Enantioselective Functionalization of Aldehydes . [Internet] [Doctoral dissertation]. Princeton University; 2012. [cited 2019 Oct 15]. Available from: http://arks.princeton.edu/ark:/88435/dsp01p8418n242.

Council of Science Editors:

Allen AE. The Productive Merger of Transition Metal and Enamine Catalysis for the Enantioselective Functionalization of Aldehydes . [Doctoral Dissertation]. Princeton University; 2012. Available from: http://arks.princeton.edu/ark:/88435/dsp01p8418n242

16. Wang, Kung-Pern. Enyne Metathesis (Part I) and Development of New Methods for Functionalized Arenes (Part II).

Degree: 2013, University of Illinois – Chicago

 This thesis has two main parts. Part I is composed of two chapters which describe the structure and reactivity of alkyne-chelated ruthenium alkylidene complexes and… (more)

Subjects/Keywords: enyne metathesis Aryne fluorination trifluoromethylation trifluoromethylthiolation Grubbs catalyst alkylidene carbene

…167 Table 6.6. Optimal conditions for trifluoromethylation and trifluoromethylthiolation… …170 Table 6.7. Reaction scope of trifluoromethylation… 

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APA (6th Edition):

Wang, K. (2013). Enyne Metathesis (Part I) and Development of New Methods for Functionalized Arenes (Part II). (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10347

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):

Wang, Kung-Pern. “Enyne Metathesis (Part I) and Development of New Methods for Functionalized Arenes (Part II).” 2013. Thesis, University of Illinois – Chicago. Accessed October 15, 2019. http://hdl.handle.net/10027/10347.

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

MLA Handbook (7th Edition):

Wang, Kung-Pern. “Enyne Metathesis (Part I) and Development of New Methods for Functionalized Arenes (Part II).” 2013. Web. 15 Oct 2019.

Vancouver:

Wang K. Enyne Metathesis (Part I) and Development of New Methods for Functionalized Arenes (Part II). [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/10027/10347.

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

Council of Science Editors:

Wang K. Enyne Metathesis (Part I) and Development of New Methods for Functionalized Arenes (Part II). [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10347

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

17. Fier, Patrick Scott. Transition-Metal Mediated Fluorination and Fluoroalkylation Reactions.

Degree: Chemistry, 2014, University of California – Berkeley

 The following dissertation discusses the development, study, and applications ofmethods to prepare perfluoroalkyl arenes, difluoromethyl arenes, aryl difluoromethylethers, and aryl fluorides. The final section discusses… (more)

Subjects/Keywords: Chemistry; Organic chemistry; Copper; Difluoromethylation; Fluorination; Fluoroalkylation; Silver; Trifluoromethylation

…in the development of these trifluoromethylation reactions, which are shown schematically… …coppermediate trifluoromethylation reactions mostly revolve around the unstable CF3 anion. Most… …the trifluoromethylation of an aryl electrophile and challenges associated with each step… …As mentioned above, most trifluoromethylation reactions have used Cu instead of Pd. Besides… …trifluoromethylation reaction with Pd is the slow reductive elimination step that forms the Ar-CF3 bond from… 

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APA (6th Edition):

Fier, P. S. (2014). Transition-Metal Mediated Fluorination and Fluoroalkylation Reactions. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/2nh4j82g

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):

Fier, Patrick Scott. “Transition-Metal Mediated Fluorination and Fluoroalkylation Reactions.” 2014. Thesis, University of California – Berkeley. Accessed October 15, 2019. http://www.escholarship.org/uc/item/2nh4j82g.

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

MLA Handbook (7th Edition):

Fier, Patrick Scott. “Transition-Metal Mediated Fluorination and Fluoroalkylation Reactions.” 2014. Web. 15 Oct 2019.

Vancouver:

Fier PS. Transition-Metal Mediated Fluorination and Fluoroalkylation Reactions. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2019 Oct 15]. Available from: http://www.escholarship.org/uc/item/2nh4j82g.

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

Council of Science Editors:

Fier PS. Transition-Metal Mediated Fluorination and Fluoroalkylation Reactions. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/2nh4j82g

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

18. Seo, Sangwon. Decarboxylative and direct functionalisations of aromatic compounds.

Degree: 2014, University of Manchester

 Aromatic rings are privileged structures found in a diverse range of natural and synthetic compounds, thus synthetic methods for their functionalisations are important in organic… (more)

Subjects/Keywords: Decarboxylative arylation; Protodecarboxylation; Trifluoromethylation; Radical substitution reaction; Silver-catalysed reaction

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7

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APA (6th Edition):

Seo, S. (2014). Decarboxylative and direct functionalisations of aromatic compounds. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:226619

Chicago Manual of Style (16th Edition):

Seo, Sangwon. “Decarboxylative and direct functionalisations of aromatic compounds.” 2014. Doctoral Dissertation, University of Manchester. Accessed October 15, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:226619.

MLA Handbook (7th Edition):

Seo, Sangwon. “Decarboxylative and direct functionalisations of aromatic compounds.” 2014. Web. 15 Oct 2019.

Vancouver:

Seo S. Decarboxylative and direct functionalisations of aromatic compounds. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2019 Oct 15]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:226619.

Council of Science Editors:

Seo S. Decarboxylative and direct functionalisations of aromatic compounds. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:226619


University of Delaware

19. Devannah, Vijayarajan. Transition metal-catalyzed enantioselective C-alkylation of nitroalkanes and trifluoromethylation of nitroalkanes .

Degree: 2018, University of Delaware

 This dissertation focused on the development of new methods to synthesize enantioenriched complex nitroalkanes using transition metal catalysis. Nitroalkanes are useful intermediates in several C–C… (more)

Subjects/Keywords: Pure sciences; 2 diamines; Asymmetric nitroalkane alkylation; Enantioenriched beta nitroamides; Enantioselective nickel catalysis; Nickel catalysis for synthesis of complex nitroalkanes; Novel chiral 1; Trifluoromethylation

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APA (6th Edition):

Devannah, V. (2018). Transition metal-catalyzed enantioselective C-alkylation of nitroalkanes and trifluoromethylation of nitroalkanes . (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/23911

Chicago Manual of Style (16th Edition):

Devannah, Vijayarajan. “Transition metal-catalyzed enantioselective C-alkylation of nitroalkanes and trifluoromethylation of nitroalkanes .” 2018. Doctoral Dissertation, University of Delaware. Accessed October 15, 2019. http://udspace.udel.edu/handle/19716/23911.

MLA Handbook (7th Edition):

Devannah, Vijayarajan. “Transition metal-catalyzed enantioselective C-alkylation of nitroalkanes and trifluoromethylation of nitroalkanes .” 2018. Web. 15 Oct 2019.

Vancouver:

Devannah V. Transition metal-catalyzed enantioselective C-alkylation of nitroalkanes and trifluoromethylation of nitroalkanes . [Internet] [Doctoral dissertation]. University of Delaware; 2018. [cited 2019 Oct 15]. Available from: http://udspace.udel.edu/handle/19716/23911.

Council of Science Editors:

Devannah V. Transition metal-catalyzed enantioselective C-alkylation of nitroalkanes and trifluoromethylation of nitroalkanes . [Doctoral Dissertation]. University of Delaware; 2018. Available from: http://udspace.udel.edu/handle/19716/23911

20. Rey-Rodriguez, Romain. Fonctionnalisation directe métallo-catalysée de liaison C-H d’énamides : Metal-Catalysed direct C-H Functionalization of enamides.

Degree: Docteur es, Chimie organique, 2016, Université d'Orléans

L’objectif de cette thèse de doctorat a été la mise au point de nouvelles méthodes de synthèse pour la fonctionnalisation directe de liaison C-H d’énamide… (more)

Subjects/Keywords: Enamide; Liaison C-H; Métallo-catalysée; Trifluorométhylation; Azidation; Nitrènes; Oxyamidation; C-H amination; Enamide; Direct C-H functionalization; Metal-catalyzed; Trifluoromethylation; Azidation; Nitrenes; Oxyamidation; C-H amination; 547

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APA (6th Edition):

Rey-Rodriguez, R. (2016). Fonctionnalisation directe métallo-catalysée de liaison C-H d’énamides : Metal-Catalysed direct C-H Functionalization of enamides. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2016ORLE2005

Chicago Manual of Style (16th Edition):

Rey-Rodriguez, Romain. “Fonctionnalisation directe métallo-catalysée de liaison C-H d’énamides : Metal-Catalysed direct C-H Functionalization of enamides.” 2016. Doctoral Dissertation, Université d'Orléans. Accessed October 15, 2019. http://www.theses.fr/2016ORLE2005.

MLA Handbook (7th Edition):

Rey-Rodriguez, Romain. “Fonctionnalisation directe métallo-catalysée de liaison C-H d’énamides : Metal-Catalysed direct C-H Functionalization of enamides.” 2016. Web. 15 Oct 2019.

Vancouver:

Rey-Rodriguez R. Fonctionnalisation directe métallo-catalysée de liaison C-H d’énamides : Metal-Catalysed direct C-H Functionalization of enamides. [Internet] [Doctoral dissertation]. Université d'Orléans; 2016. [cited 2019 Oct 15]. Available from: http://www.theses.fr/2016ORLE2005.

Council of Science Editors:

Rey-Rodriguez R. Fonctionnalisation directe métallo-catalysée de liaison C-H d’énamides : Metal-Catalysed direct C-H Functionalization of enamides. [Doctoral Dissertation]. Université d'Orléans; 2016. Available from: http://www.theses.fr/2016ORLE2005


Freie Universität Berlin

21. Schmidt, Bernd M. Fluorierte und trifluormethylierte schalenförmige Aromaten.

Degree: 2013, Freie Universität Berlin

 In dieser Arbeit wurde der Einfluss elektronenziehender Gruppen auf nicht- planare, polyzyklische, aromatische Kohlenwasserstoffe untersucht. Das schalenförmige Molekül Corannulen (C20H10) wurde dargestellt, durch direkte Methoden… (more)

Subjects/Keywords: buckybowls; corannulene; sumanene; trifluoromethylation; electrochemistry; 500 Naturwissenschaften und Mathematik; 500 Naturwissenschaften und Mathematik::540 Chemie; 500 Naturwissenschaften und Mathematik::540 Chemie::547 Organische Chemie

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APA (6th Edition):

Schmidt, B. M. (2013). Fluorierte und trifluormethylierte schalenförmige Aromaten. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-7963

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):

Schmidt, Bernd M. “Fluorierte und trifluormethylierte schalenförmige Aromaten.” 2013. Thesis, Freie Universität Berlin. Accessed October 15, 2019. http://dx.doi.org/10.17169/refubium-7963.

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

MLA Handbook (7th Edition):

Schmidt, Bernd M. “Fluorierte und trifluormethylierte schalenförmige Aromaten.” 2013. Web. 15 Oct 2019.

Vancouver:

Schmidt BM. Fluorierte und trifluormethylierte schalenförmige Aromaten. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2019 Oct 15]. Available from: http://dx.doi.org/10.17169/refubium-7963.

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

Council of Science Editors:

Schmidt BM. Fluorierte und trifluormethylierte schalenförmige Aromaten. [Thesis]. Freie Universität Berlin; 2013. Available from: http://dx.doi.org/10.17169/refubium-7963

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


Tokyo Institute of Technology / 東京工業大学

22. 安, 祐輔. Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究.

Degree: 博士(工学), 2014, Tokyo Institute of Technology / 東京工業大学

Subjects/Keywords: photoredox catalysis; フォトレドックス触媒; radical reactions; ラジカル反応; photochemistry; 光化学; trifluoromethylation; トリフルオロメチル化

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APA (6th Edition):

安, . (2014). Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究. (Thesis). Tokyo Institute of Technology / 東京工業大学. Retrieved from http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100667480

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):

安, 祐輔. “Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究.” 2014. Thesis, Tokyo Institute of Technology / 東京工業大学. Accessed October 15, 2019. http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100667480.

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

MLA Handbook (7th Edition):

安, 祐輔. “Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究.” 2014. Web. 15 Oct 2019.

Vancouver:

安 . Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究. [Internet] [Thesis]. Tokyo Institute of Technology / 東京工業大学; 2014. [cited 2019 Oct 15]. Available from: http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100667480.

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

Council of Science Editors:

安 . Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究. [Thesis]. Tokyo Institute of Technology / 東京工業大学; 2014. Available from: http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100667480

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


Tokyo Institute of Technology / 東京工業大学

23. 安, 祐輔. Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究.

Degree: 博士(工学), 2015, Tokyo Institute of Technology / 東京工業大学

Subjects/Keywords: photoredox catalysis; フォトレドックス触媒; radical reactions; ラジカル反応; photochemistry; 光化学; trifluoromethylation; トリフルオロメチル化

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APA (6th Edition):

安, . (2015). Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究. (Thesis). Tokyo Institute of Technology / 東京工業大学. Retrieved from http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100691040

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):

安, 祐輔. “Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究.” 2015. Thesis, Tokyo Institute of Technology / 東京工業大学. Accessed October 15, 2019. http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100691040.

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

MLA Handbook (7th Edition):

安, 祐輔. “Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究.” 2015. Web. 15 Oct 2019.

Vancouver:

安 . Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究. [Internet] [Thesis]. Tokyo Institute of Technology / 東京工業大学; 2015. [cited 2019 Oct 15]. Available from: http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100691040.

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

Council of Science Editors:

安 . Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis : Study on New Methodology for Radical Functionalization of Olefins by Photoredox Catalysis; フォトレドックス触媒によるオレフィン類の新規なラジカル的官能基化法に関する研究. [Thesis]. Tokyo Institute of Technology / 東京工業大学; 2015. Available from: http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100691040

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

24. Harris, Caleb Frank. Novel redox non-innocent bis(phenoxide) pincer complexes of cobalt: Connecting electronic structures and reactivity.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

 In this thesis, I describe the synthesis, characterization, and reactivity of a variety of new cobalt complexes containing redox-active, pincer-type ligands based on an N-heterocyclic… (more)

Subjects/Keywords: Redox-active; Non-innocent; Electron transfer; Trifluoromethylation; C-H activation; Cobalt

…iso surface set at 80.0. 103 Table 4.1 Radical trifluoromethylation of silyl enol ethers… …description of the 5- and 6coordinate complexes. 108 Figure 3.19 Radical trifluoromethylation of… …Figure 3.22 Substrates evaluated trifluoromethylation by 4. 115 for ligand directed C-H… …118 Figure 4.1 Commonly used electrophilic trifluoromethylation reagents. 137 Figure 4.2… …Proposed reaction mechanism for trifluoromethylation of silyl enol ethers. the catalytic 154… 

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Harris, C. F. (2017). Novel redox non-innocent bis(phenoxide) pincer complexes of cobalt: Connecting electronic structures and reactivity. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58738

Chicago Manual of Style (16th Edition):

Harris, Caleb Frank. “Novel redox non-innocent bis(phenoxide) pincer complexes of cobalt: Connecting electronic structures and reactivity.” 2017. Doctoral Dissertation, Georgia Tech. Accessed October 15, 2019. http://hdl.handle.net/1853/58738.

MLA Handbook (7th Edition):

Harris, Caleb Frank. “Novel redox non-innocent bis(phenoxide) pincer complexes of cobalt: Connecting electronic structures and reactivity.” 2017. Web. 15 Oct 2019.

Vancouver:

Harris CF. Novel redox non-innocent bis(phenoxide) pincer complexes of cobalt: Connecting electronic structures and reactivity. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/1853/58738.

Council of Science Editors:

Harris CF. Novel redox non-innocent bis(phenoxide) pincer complexes of cobalt: Connecting electronic structures and reactivity. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/58738

25. Seo, Sangwon. Decarboxylative and direct functionalisations of aromatic compounds.

Degree: PhD, 2014, University of Manchester

 Aromatic rings are privileged structures found in a diverse range of natural and synthetic compounds, thus synthetic methods for their functionalisations are important in organic… (more)

Subjects/Keywords: 547; Decarboxylative arylation; Protodecarboxylation; Trifluoromethylation; Radical substitution reaction; Silver-catalysed reaction

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7

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APA (6th Edition):

Seo, S. (2014). Decarboxylative and direct functionalisations of aromatic compounds. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/decarboxylative-and-direct-functionalisations-of-aromatic-compounds(a9ddab1b-86a0-491e-a95b-d6b40c8bd7ab).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618007

Chicago Manual of Style (16th Edition):

Seo, Sangwon. “Decarboxylative and direct functionalisations of aromatic compounds.” 2014. Doctoral Dissertation, University of Manchester. Accessed October 15, 2019. https://www.research.manchester.ac.uk/portal/en/theses/decarboxylative-and-direct-functionalisations-of-aromatic-compounds(a9ddab1b-86a0-491e-a95b-d6b40c8bd7ab).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618007.

MLA Handbook (7th Edition):

Seo, Sangwon. “Decarboxylative and direct functionalisations of aromatic compounds.” 2014. Web. 15 Oct 2019.

Vancouver:

Seo S. Decarboxylative and direct functionalisations of aromatic compounds. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2019 Oct 15]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/decarboxylative-and-direct-functionalisations-of-aromatic-compounds(a9ddab1b-86a0-491e-a95b-d6b40c8bd7ab).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618007.

Council of Science Editors:

Seo S. Decarboxylative and direct functionalisations of aromatic compounds. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/decarboxylative-and-direct-functionalisations-of-aromatic-compounds(a9ddab1b-86a0-491e-a95b-d6b40c8bd7ab).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618007

26. Savvopoulou, Ioanna. Ανάπτυξη καταλυτικών ασύμμετρων μεθοδολογιών με εφαρμογή στη σύνθεση φαρμακευτικά δραστικών ουσιών.

Degree: 2018, University of Patras; Πανεπιστήμιο Πατρών

Asymmetric organocatalysis has been established as one of the most effective tools for asymmetric synthesis, nevertheless its implementation in industrial syntheses remains limited and certainly… (more)

Subjects/Keywords: Οργανοκατάλυση; Χειρόμορφοι οργανοκαταλύτες; Ασύμμετρη αλογονοκυκλοποίηση; Εναντιοεκλεκτικότητα; Αλογονωτικά μέσα; Αμίνες; Φωσφίνες; Θειοφωσφινοξείδια; Ιμινοφωσφοράνια; Ουρίες; Σκουαραμίδια; Χειρόμορφες μέθοδοι HPLC; Τριφθορομεθυλίωση; Αντιδραστήριο rupperts; Σουλφιναμίδια; Ν-οξείδια; Φαινόλες; Φωσφονικά άλατα; Organocatalysis; Chiral organocatalysts; Asymmetric halocyclisation; Enantioselectivity; Halogenating agents; Amines; Phosphines; Thiophosphinoxides; Iminophoshoranes; Ureas; Squaramides; Chiral HPLC methods; Trifluoromethylation; Rupperts reagent; Sulfinamides; N-oxides; Phenols; Phosphonium salts

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Savvopoulou, I. (2018). Ανάπτυξη καταλυτικών ασύμμετρων μεθοδολογιών με εφαρμογή στη σύνθεση φαρμακευτικά δραστικών ουσιών. (Thesis). University of Patras; Πανεπιστήμιο Πατρών. Retrieved from http://hdl.handle.net/10442/hedi/44655

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):

Savvopoulou, Ioanna. “Ανάπτυξη καταλυτικών ασύμμετρων μεθοδολογιών με εφαρμογή στη σύνθεση φαρμακευτικά δραστικών ουσιών.” 2018. Thesis, University of Patras; Πανεπιστήμιο Πατρών. Accessed October 15, 2019. http://hdl.handle.net/10442/hedi/44655.

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

MLA Handbook (7th Edition):

Savvopoulou, Ioanna. “Ανάπτυξη καταλυτικών ασύμμετρων μεθοδολογιών με εφαρμογή στη σύνθεση φαρμακευτικά δραστικών ουσιών.” 2018. Web. 15 Oct 2019.

Vancouver:

Savvopoulou I. Ανάπτυξη καταλυτικών ασύμμετρων μεθοδολογιών με εφαρμογή στη σύνθεση φαρμακευτικά δραστικών ουσιών. [Internet] [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2018. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/10442/hedi/44655.

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

Council of Science Editors:

Savvopoulou I. Ανάπτυξη καταλυτικών ασύμμετρων μεθοδολογιών με εφαρμογή στη σύνθεση φαρμακευτικά δραστικών ουσιών. [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2018. Available from: http://hdl.handle.net/10442/hedi/44655

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

27. Konovalov, Andrey I. Reaction Mechanisms on the Way from CHF3 to ArCF3. The Nature of the Ortho-Effect and Electronic Properties of the CF3 Group.

Degree: Departament de Química Analítica i Química Orgànica, 2015, Universitat Rovira i Virgili

 Organic compounds bearing a CF3 substituent, especially on an aromatic ring are in exceedingly high demand as building blocks for the needs of the agrochemical,… (more)

Subjects/Keywords: trifluorometilación; mecanisme de reacció; fluoroform; trifluorometilación; mecanismo de reacción; fluoroformo; trifluoromethylation; reaction mechanism; flouroform; 54; 542; 544

…studies on the mechanism of trifluoromethylation of UNIVERSITAT ROVIRA I VIRGILI REACTION… …Int. Ed. 2013, 52, 11637.  Mechanism of Trifluoromethylation of Aryl Halides with CuCF3… …12 General Introduction. Mechanisms of Cu-Mediated Aromatic Trifluoromethylation… …69 Chapter 2. Mechanism of Trifluoromethylation of Haloarenes with CuCF3 ............. 77… …107 Chapter 3. Ortho-Effect in Trifluoromethylation of Haloarenes… 

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Konovalov, A. I. (2015). Reaction Mechanisms on the Way from CHF3 to ArCF3. The Nature of the Ortho-Effect and Electronic Properties of the CF3 Group. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/318807

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):

Konovalov, Andrey I. “Reaction Mechanisms on the Way from CHF3 to ArCF3. The Nature of the Ortho-Effect and Electronic Properties of the CF3 Group.” 2015. Thesis, Universitat Rovira i Virgili. Accessed October 15, 2019. http://hdl.handle.net/10803/318807.

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

MLA Handbook (7th Edition):

Konovalov, Andrey I. “Reaction Mechanisms on the Way from CHF3 to ArCF3. The Nature of the Ortho-Effect and Electronic Properties of the CF3 Group.” 2015. Web. 15 Oct 2019.

Vancouver:

Konovalov AI. Reaction Mechanisms on the Way from CHF3 to ArCF3. The Nature of the Ortho-Effect and Electronic Properties of the CF3 Group. [Internet] [Thesis]. Universitat Rovira i Virgili; 2015. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/10803/318807.

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

Council of Science Editors:

Konovalov AI. Reaction Mechanisms on the Way from CHF3 to ArCF3. The Nature of the Ortho-Effect and Electronic Properties of the CF3 Group. [Thesis]. Universitat Rovira i Virgili; 2015. Available from: http://hdl.handle.net/10803/318807

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

.