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You searched for subject:(mechanistic organic chemistry). Showing records 1 – 13 of 13 total matches.

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Iowa State University

1. Goswami, Manibarsha. Thioglycoside activation using bismuth(V) chemistry.

Degree: 2014, Iowa State University

 Carbohydrates are considered important biomolecules and are the most efficient sources of energy, which is the reason they are known as the "fuel of life."… (more)

Subjects/Keywords: Chemistry (Organic Chemistry); Organic Chemistry; Chemistry; Bismuth; Carbohydrates; Glycosylation; Mechanistic studies; Vaccine adjuvants; Chemistry; Organic Chemistry

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APA (6th Edition):

Goswami, M. (2014). Thioglycoside activation using bismuth(V) chemistry. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/14139

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):

Goswami, Manibarsha. “Thioglycoside activation using bismuth(V) chemistry.” 2014. Thesis, Iowa State University. Accessed April 13, 2021. https://lib.dr.iastate.edu/etd/14139.

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

MLA Handbook (7th Edition):

Goswami, Manibarsha. “Thioglycoside activation using bismuth(V) chemistry.” 2014. Web. 13 Apr 2021.

Vancouver:

Goswami M. Thioglycoside activation using bismuth(V) chemistry. [Internet] [Thesis]. Iowa State University; 2014. [cited 2021 Apr 13]. Available from: https://lib.dr.iastate.edu/etd/14139.

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

Council of Science Editors:

Goswami M. Thioglycoside activation using bismuth(V) chemistry. [Thesis]. Iowa State University; 2014. Available from: https://lib.dr.iastate.edu/etd/14139

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


Penn State University

2. McCarthy, Sean M. Bond Activation by Geometrically Distorted P(III) Compounds.

Degree: 2017, Penn State University

 The activations of O-H and N-H bonds via oxidative addition are of significant importance as initiatory steps toward catalytic alcohol and amine functionalization. Such a… (more)

Subjects/Keywords: Bond Activation; Main group chemistry; Organophosphorus chemistry; Physical organic chemistry; Mechanistic chemistry

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APA (6th Edition):

McCarthy, S. M. (2017). Bond Activation by Geometrically Distorted P(III) Compounds. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/13678smm611

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):

McCarthy, Sean M. “Bond Activation by Geometrically Distorted P(III) Compounds.” 2017. Thesis, Penn State University. Accessed April 13, 2021. https://submit-etda.libraries.psu.edu/catalog/13678smm611.

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

MLA Handbook (7th Edition):

McCarthy, Sean M. “Bond Activation by Geometrically Distorted P(III) Compounds.” 2017. Web. 13 Apr 2021.

Vancouver:

McCarthy SM. Bond Activation by Geometrically Distorted P(III) Compounds. [Internet] [Thesis]. Penn State University; 2017. [cited 2021 Apr 13]. Available from: https://submit-etda.libraries.psu.edu/catalog/13678smm611.

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

Council of Science Editors:

McCarthy SM. Bond Activation by Geometrically Distorted P(III) Compounds. [Thesis]. Penn State University; 2017. Available from: https://submit-etda.libraries.psu.edu/catalog/13678smm611

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


University of California – Irvine

3. Camacho Fernandez, Miguel Angel. eta6-Arene Tethered Ruthenium (II) Complexes and Half-metallocene Dithiocarbamate Ruthenium (IV) Complex for Olefin Polymerization: Experimental, Mechanistic, and DFT Studies.

Degree: Chemistry, 2014, University of California – Irvine

 There are very few reports of ruthenium complexes for olefin polymerization and the active species are unknown. In this dissertation we explore a series of… (more)

Subjects/Keywords: Polymer chemistry; Inorganic chemistry; Organic chemistry; Catalysis; DFT; Mechanistic; Olefin Polymerization; Ruthenium

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APA (6th Edition):

Camacho Fernandez, M. A. (2014). eta6-Arene Tethered Ruthenium (II) Complexes and Half-metallocene Dithiocarbamate Ruthenium (IV) Complex for Olefin Polymerization: Experimental, Mechanistic, and DFT Studies. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/2w34r43b

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):

Camacho Fernandez, Miguel Angel. “eta6-Arene Tethered Ruthenium (II) Complexes and Half-metallocene Dithiocarbamate Ruthenium (IV) Complex for Olefin Polymerization: Experimental, Mechanistic, and DFT Studies.” 2014. Thesis, University of California – Irvine. Accessed April 13, 2021. http://www.escholarship.org/uc/item/2w34r43b.

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

MLA Handbook (7th Edition):

Camacho Fernandez, Miguel Angel. “eta6-Arene Tethered Ruthenium (II) Complexes and Half-metallocene Dithiocarbamate Ruthenium (IV) Complex for Olefin Polymerization: Experimental, Mechanistic, and DFT Studies.” 2014. Web. 13 Apr 2021.

Vancouver:

Camacho Fernandez MA. eta6-Arene Tethered Ruthenium (II) Complexes and Half-metallocene Dithiocarbamate Ruthenium (IV) Complex for Olefin Polymerization: Experimental, Mechanistic, and DFT Studies. [Internet] [Thesis]. University of California – Irvine; 2014. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/2w34r43b.

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

Council of Science Editors:

Camacho Fernandez MA. eta6-Arene Tethered Ruthenium (II) Complexes and Half-metallocene Dithiocarbamate Ruthenium (IV) Complex for Olefin Polymerization: Experimental, Mechanistic, and DFT Studies. [Thesis]. University of California – Irvine; 2014. Available from: http://www.escholarship.org/uc/item/2w34r43b

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


University of Colorado

4. Perkins, Russell James. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.

Degree: PhD, 2017, University of Colorado

  Many important chemical reactions from all branches of chemistry occur with water as a solvent. Furthermore, in environmental chemistry, biochemistry, and synthetic chemistry, key… (more)

Subjects/Keywords: aqueous interfaces; aromatic aggregation; mechanistic organic chemistry; membrane biophysics; preboitic chemistry; surfactants; Physical Chemistry

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APA (6th Edition):

Perkins, R. J. (2017). Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/219

Chicago Manual of Style (16th Edition):

Perkins, Russell James. “Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.” 2017. Doctoral Dissertation, University of Colorado. Accessed April 13, 2021. https://scholar.colorado.edu/chem_gradetds/219.

MLA Handbook (7th Edition):

Perkins, Russell James. “Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.” 2017. Web. 13 Apr 2021.

Vancouver:

Perkins RJ. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2021 Apr 13]. Available from: https://scholar.colorado.edu/chem_gradetds/219.

Council of Science Editors:

Perkins RJ. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/chem_gradetds/219


University of Colorado

5. Perkins, Russell James. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.

Degree: PhD, 2018, University of Colorado

  Many important chemical reactions from all branches of chemistry occur with water as a solvent. Furthermore, in environmental chemistry, biochemistry, and synthetic chemistry, key… (more)

Subjects/Keywords: aqueous interfaces; aromatic aggregation; mechanistic organic chemistry; membrane biophysics; preboitic chemistry; surfactants; Organic Chemistry; Physical Chemistry

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APA (6th Edition):

Perkins, R. J. (2018). Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/273

Chicago Manual of Style (16th Edition):

Perkins, Russell James. “Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 13, 2021. https://scholar.colorado.edu/chem_gradetds/273.

MLA Handbook (7th Edition):

Perkins, Russell James. “Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.” 2018. Web. 13 Apr 2021.

Vancouver:

Perkins RJ. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2021 Apr 13]. Available from: https://scholar.colorado.edu/chem_gradetds/273.

Council of Science Editors:

Perkins RJ. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/273


Lehigh University

6. Choquette, Kimberly Ann. Mechanistic Studies on the Effect of Additives in SmI2-Mediated Reactions.

Degree: PhD, Chemistry, 2013, Lehigh University

 Samarium diiodide (SmI2) was first introduced to synthetic chemists in 1980. Although initially considered an esoteric compound, SmI2 is now a standard reductant in organic(more)

Subjects/Keywords: Mechanistic Studies; Physical Organic Chemistry; Samarium diiodide; SmI2; Chemistry; Physical Sciences and Mathematics

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APA (6th Edition):

Choquette, K. A. (2013). Mechanistic Studies on the Effect of Additives in SmI2-Mediated Reactions. (Doctoral Dissertation). Lehigh University. Retrieved from https://preserve.lehigh.edu/etd/1457

Chicago Manual of Style (16th Edition):

Choquette, Kimberly Ann. “Mechanistic Studies on the Effect of Additives in SmI2-Mediated Reactions.” 2013. Doctoral Dissertation, Lehigh University. Accessed April 13, 2021. https://preserve.lehigh.edu/etd/1457.

MLA Handbook (7th Edition):

Choquette, Kimberly Ann. “Mechanistic Studies on the Effect of Additives in SmI2-Mediated Reactions.” 2013. Web. 13 Apr 2021.

Vancouver:

Choquette KA. Mechanistic Studies on the Effect of Additives in SmI2-Mediated Reactions. [Internet] [Doctoral dissertation]. Lehigh University; 2013. [cited 2021 Apr 13]. Available from: https://preserve.lehigh.edu/etd/1457.

Council of Science Editors:

Choquette KA. Mechanistic Studies on the Effect of Additives in SmI2-Mediated Reactions. [Doctoral Dissertation]. Lehigh University; 2013. Available from: https://preserve.lehigh.edu/etd/1457


University of Minnesota

7. Frost, Grant. Organic Reaction Selectivity via Metal-Catalysis: Discovery, Development, and Mechanistic Analysis of Nitrile, Ester, Arene, Azide, and Alkene Transformations.

Degree: PhD, Chemistry, 2019, University of Minnesota

 The focus of my doctoral dissertation is the discovery, development, and mechanistic analysis of metal-catalyzed organic reactions. My work highlights organometallic catalysis as a strategy… (more)

Subjects/Keywords: Mechanistic Analysis; Organic Chemistry; Organometallic Catalysis; Reaction Development; Reaction Discovery; Reaction Selectivity

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APA (6th Edition):

Frost, G. (2019). Organic Reaction Selectivity via Metal-Catalysis: Discovery, Development, and Mechanistic Analysis of Nitrile, Ester, Arene, Azide, and Alkene Transformations. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/202909

Chicago Manual of Style (16th Edition):

Frost, Grant. “Organic Reaction Selectivity via Metal-Catalysis: Discovery, Development, and Mechanistic Analysis of Nitrile, Ester, Arene, Azide, and Alkene Transformations.” 2019. Doctoral Dissertation, University of Minnesota. Accessed April 13, 2021. http://hdl.handle.net/11299/202909.

MLA Handbook (7th Edition):

Frost, Grant. “Organic Reaction Selectivity via Metal-Catalysis: Discovery, Development, and Mechanistic Analysis of Nitrile, Ester, Arene, Azide, and Alkene Transformations.” 2019. Web. 13 Apr 2021.

Vancouver:

Frost G. Organic Reaction Selectivity via Metal-Catalysis: Discovery, Development, and Mechanistic Analysis of Nitrile, Ester, Arene, Azide, and Alkene Transformations. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/11299/202909.

Council of Science Editors:

Frost G. Organic Reaction Selectivity via Metal-Catalysis: Discovery, Development, and Mechanistic Analysis of Nitrile, Ester, Arene, Azide, and Alkene Transformations. [Doctoral Dissertation]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/202909

8. Perego, Luca Alessandro. Transition metal-catalyzed reactions : mechanistic studies and methodology developments : Réactions catalysées par des complexes métalliques : études mécanistiques et développements méthodologiques.

Degree: Docteur es, Chimie théorique, physique, analytique, 2018, Paris Sciences et Lettres (ComUE)

Dans cette thèse les mécanismes de trois réactions catalysées par des complexes de palladium et de cuivre ont été étudiés en utilisant des méthodes expérimentales… (more)

Subjects/Keywords: Catalyse; Études mécanistiques; Chimie organique; Synthèse organique; Chimie organométallique; DFT; Catalysis; Mechanistic studies; Organic chemistry; Organic synthesis; Organometallic chemistry; DFT; 541.3

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APA (6th Edition):

Perego, L. A. (2018). Transition metal-catalyzed reactions : mechanistic studies and methodology developments : Réactions catalysées par des complexes métalliques : études mécanistiques et développements méthodologiques. (Doctoral Dissertation). Paris Sciences et Lettres (ComUE). Retrieved from http://www.theses.fr/2018PSLEE003

Chicago Manual of Style (16th Edition):

Perego, Luca Alessandro. “Transition metal-catalyzed reactions : mechanistic studies and methodology developments : Réactions catalysées par des complexes métalliques : études mécanistiques et développements méthodologiques.” 2018. Doctoral Dissertation, Paris Sciences et Lettres (ComUE). Accessed April 13, 2021. http://www.theses.fr/2018PSLEE003.

MLA Handbook (7th Edition):

Perego, Luca Alessandro. “Transition metal-catalyzed reactions : mechanistic studies and methodology developments : Réactions catalysées par des complexes métalliques : études mécanistiques et développements méthodologiques.” 2018. Web. 13 Apr 2021.

Vancouver:

Perego LA. Transition metal-catalyzed reactions : mechanistic studies and methodology developments : Réactions catalysées par des complexes métalliques : études mécanistiques et développements méthodologiques. [Internet] [Doctoral dissertation]. Paris Sciences et Lettres (ComUE); 2018. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2018PSLEE003.

Council of Science Editors:

Perego LA. Transition metal-catalyzed reactions : mechanistic studies and methodology developments : Réactions catalysées par des complexes métalliques : études mécanistiques et développements méthodologiques. [Doctoral Dissertation]. Paris Sciences et Lettres (ComUE); 2018. Available from: http://www.theses.fr/2018PSLEE003

9. Tiwari, Swapna. mechanistic studies on pyridinium chlorochromate oxidation of some organic compounds; -.

Degree: -, 1989, INFLIBNET

Abstract is available

Bibliography p. 143 - 154

Advisors/Committee Members: Agarwal.

Subjects/Keywords: chemistry; mechanistic studies; organic compounds; pyridinium chlorochromate

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APA (6th Edition):

Tiwari, S. (1989). mechanistic studies on pyridinium chlorochromate oxidation of some organic compounds; -. (Thesis). INFLIBNET. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/34100

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):

Tiwari, Swapna. “mechanistic studies on pyridinium chlorochromate oxidation of some organic compounds; -.” 1989. Thesis, INFLIBNET. Accessed April 13, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/34100.

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

MLA Handbook (7th Edition):

Tiwari, Swapna. “mechanistic studies on pyridinium chlorochromate oxidation of some organic compounds; -.” 1989. Web. 13 Apr 2021.

Vancouver:

Tiwari S. mechanistic studies on pyridinium chlorochromate oxidation of some organic compounds; -. [Internet] [Thesis]. INFLIBNET; 1989. [cited 2021 Apr 13]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/34100.

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

Council of Science Editors:

Tiwari S. mechanistic studies on pyridinium chlorochromate oxidation of some organic compounds; -. [Thesis]. INFLIBNET; 1989. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/34100

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


University of Maryland

10. Ma, Da. Acyclic Congeners of Cucurbit[n]uril and a Related Mechanistic Study on the Cucurbit[n]uril Forming Reaction.

Degree: Chemistry, 2010, University of Maryland

 Supramolecular chemistry has been a very important research area in the past several decades. In this research field, molecular containers, such as cyclodextrin, attracts special… (more)

Subjects/Keywords: Organic Chemistry; Aclyclic; Cucurbituril; Mechanistic Study; Synthesis

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APA (6th Edition):

Ma, D. (2010). Acyclic Congeners of Cucurbit[n]uril and a Related Mechanistic Study on the Cucurbit[n]uril Forming Reaction. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/11122

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):

Ma, Da. “Acyclic Congeners of Cucurbit[n]uril and a Related Mechanistic Study on the Cucurbit[n]uril Forming Reaction.” 2010. Thesis, University of Maryland. Accessed April 13, 2021. http://hdl.handle.net/1903/11122.

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

MLA Handbook (7th Edition):

Ma, Da. “Acyclic Congeners of Cucurbit[n]uril and a Related Mechanistic Study on the Cucurbit[n]uril Forming Reaction.” 2010. Web. 13 Apr 2021.

Vancouver:

Ma D. Acyclic Congeners of Cucurbit[n]uril and a Related Mechanistic Study on the Cucurbit[n]uril Forming Reaction. [Internet] [Thesis]. University of Maryland; 2010. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1903/11122.

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

Council of Science Editors:

Ma D. Acyclic Congeners of Cucurbit[n]uril and a Related Mechanistic Study on the Cucurbit[n]uril Forming Reaction. [Thesis]. University of Maryland; 2010. Available from: http://hdl.handle.net/1903/11122

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


University of Lund

11. Johnsson, Richard. Synthetic studies on naphthoxylosides - labeled compounds and mechanistic studies on acetals.

Degree: 2008, University of Lund

 Labeled analogs to an antiproliferative naphthoxyloside have been synthesized and evaluated. Our investigations have shown that the fluorescently labeled analogs are poor structural analogs, and… (more)

Subjects/Keywords: Organic Chemistry; Fluorescent xylosides; Carbohydrates; Naphthoxylosides; Cancer; Mechanistic studies; Radioactive xylosides; Acetals

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APA (6th Edition):

Johnsson, R. (2008). Synthetic studies on naphthoxylosides - labeled compounds and mechanistic studies on acetals. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/1051679 ; https://portal.research.lu.se/ws/files/5721633/1051680.pdf

Chicago Manual of Style (16th Edition):

Johnsson, Richard. “Synthetic studies on naphthoxylosides - labeled compounds and mechanistic studies on acetals.” 2008. Doctoral Dissertation, University of Lund. Accessed April 13, 2021. https://lup.lub.lu.se/record/1051679 ; https://portal.research.lu.se/ws/files/5721633/1051680.pdf.

MLA Handbook (7th Edition):

Johnsson, Richard. “Synthetic studies on naphthoxylosides - labeled compounds and mechanistic studies on acetals.” 2008. Web. 13 Apr 2021.

Vancouver:

Johnsson R. Synthetic studies on naphthoxylosides - labeled compounds and mechanistic studies on acetals. [Internet] [Doctoral dissertation]. University of Lund; 2008. [cited 2021 Apr 13]. Available from: https://lup.lub.lu.se/record/1051679 ; https://portal.research.lu.se/ws/files/5721633/1051680.pdf.

Council of Science Editors:

Johnsson R. Synthetic studies on naphthoxylosides - labeled compounds and mechanistic studies on acetals. [Doctoral Dissertation]. University of Lund; 2008. Available from: https://lup.lub.lu.se/record/1051679 ; https://portal.research.lu.se/ws/files/5721633/1051680.pdf


York University

12. McCann, Lucas Charles. Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline.

Degree: PhD, Chemistry, 2016, York University

 Part I: An efficient method for alkyl-alkyl Negishi cross-coupling reaction of unactivated primary alkyl halides with higher-order zincate species (synthesized from dialkylzinc and a non-coordinating… (more)

Subjects/Keywords: Inorganic chemistry; Cross-coupling; Palladium; Zincate; Zinc; Chemistry; Organic chemistry; Methodology; Industrial chemistry; Pd-PEPPSI; PEPPSI; PEPPSI catalyst; Synthesis; Organometallic chemistry; Organometallic; Inorganic; Inorganic chemistry; Scale-up; Process chemistry; Optimization; Negishi; Negishi Cross-coupling; Alkyl-alkyl; Bond formation; NHC; N-heterocyclic carbene; Carbene; Mechanistic determination; Reaction mechanism; Aryl-aryl; Pd-PEPPSI-IPent; Pd-PEPPSI-IHept; Pd-PEPPSI-IPr; Pd-PEPPSI-IPentCl; Pd-PEPPSI-IHeptCl; 2; 6-DI(4-HEPTYL)ANILINE; 6-DI(3-PENTYL)ANILINE; Large-scale

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APA (6th Edition):

McCann, L. C. (2016). Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/32194

Chicago Manual of Style (16th Edition):

McCann, Lucas Charles. “Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline.” 2016. Doctoral Dissertation, York University. Accessed April 13, 2021. http://hdl.handle.net/10315/32194.

MLA Handbook (7th Edition):

McCann, Lucas Charles. “Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline.” 2016. Web. 13 Apr 2021.

Vancouver:

McCann LC. Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline. [Internet] [Doctoral dissertation]. York University; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10315/32194.

Council of Science Editors:

McCann LC. Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline. [Doctoral Dissertation]. York University; 2016. Available from: http://hdl.handle.net/10315/32194

13. Hardouin Duparc, Valérie. Complexes de cuivre (II) portant des ligands sulfonés ou carboxylates et leur application en catalyse.

Degree: 2019, Université de Montréal

Subjects/Keywords: Couplage Chan-Evans-Lam; Polymérisation lactide; Complexes de cuivre; Ligands sulfonés; Ligand carboxylate; Catalyse; Études mécanistiques; Chan-Evans-Lam coupling; Lactide polymerization; Copper complexes; Sulfonated ligands; Carboxylate ligand; Catalysis; Mechanistic studies; Chemistry - Organic / Chimie organique (UMI : 0490)

Chemistry" pour décrire les réactions spécifiques, simples et hauts rendement, fonctionnant… …n’entre pas dans les réactions dites de "Click Chemistry". Figure 1.8 : Réaction de… …de type « Click chemistry ». Figure 1.9 : Réaction de Sharpless-Meldal. Malgré ces… 

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APA (6th Edition):

Hardouin Duparc, V. (2019). Complexes de cuivre (II) portant des ligands sulfonés ou carboxylates et leur application en catalyse. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/21696

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):

Hardouin Duparc, Valérie. “Complexes de cuivre (II) portant des ligands sulfonés ou carboxylates et leur application en catalyse.” 2019. Thesis, Université de Montréal. Accessed April 13, 2021. http://hdl.handle.net/1866/21696.

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

MLA Handbook (7th Edition):

Hardouin Duparc, Valérie. “Complexes de cuivre (II) portant des ligands sulfonés ou carboxylates et leur application en catalyse.” 2019. Web. 13 Apr 2021.

Vancouver:

Hardouin Duparc V. Complexes de cuivre (II) portant des ligands sulfonés ou carboxylates et leur application en catalyse. [Internet] [Thesis]. Université de Montréal; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1866/21696.

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

Council of Science Editors:

Hardouin Duparc V. Complexes de cuivre (II) portant des ligands sulfonés ou carboxylates et leur application en catalyse. [Thesis]. Université de Montréal; 2019. Available from: http://hdl.handle.net/1866/21696

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

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