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You searched for subject:(amination). Showing records 1 – 30 of 174 total matches.

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University of Illinois – Chicago

1. Kauser, Nabeelah I. Gamma-functionalization and Its Application Towards Total Synthesis.

Degree: 2018, University of Illinois – Chicago

 Synthetic efforts geared towards natural product synthesis highlight a clear deficiency in the synthetic technology directed at gamma-functionalization. The gamma-alkyl motif exists in numerous natural… (more)

Subjects/Keywords: alkylation; amination

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APA (6th Edition):

Kauser, N. I. (2018). Gamma-functionalization and Its Application Towards Total Synthesis. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22969

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):

Kauser, Nabeelah I. “Gamma-functionalization and Its Application Towards Total Synthesis.” 2018. Thesis, University of Illinois – Chicago. Accessed July 09, 2020. http://hdl.handle.net/10027/22969.

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

MLA Handbook (7th Edition):

Kauser, Nabeelah I. “Gamma-functionalization and Its Application Towards Total Synthesis.” 2018. Web. 09 Jul 2020.

Vancouver:

Kauser NI. Gamma-functionalization and Its Application Towards Total Synthesis. [Internet] [Thesis]. University of Illinois – Chicago; 2018. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10027/22969.

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

Council of Science Editors:

Kauser NI. Gamma-functionalization and Its Application Towards Total Synthesis. [Thesis]. University of Illinois – Chicago; 2018. Available from: http://hdl.handle.net/10027/22969

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


University of Arizona

2. Spanggord, Ronald Jay, 1942-. Aminomercuration of carbonyl-containing olefins .

Degree: 1971, University of Arizona

Subjects/Keywords: Amination.

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APA (6th Edition):

Spanggord, Ronald Jay, 1. (1971). Aminomercuration of carbonyl-containing olefins . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/565226

Chicago Manual of Style (16th Edition):

Spanggord, Ronald Jay, 1942-. “Aminomercuration of carbonyl-containing olefins .” 1971. Doctoral Dissertation, University of Arizona. Accessed July 09, 2020. http://hdl.handle.net/10150/565226.

MLA Handbook (7th Edition):

Spanggord, Ronald Jay, 1942-. “Aminomercuration of carbonyl-containing olefins .” 1971. Web. 09 Jul 2020.

Vancouver:

Spanggord, Ronald Jay 1. Aminomercuration of carbonyl-containing olefins . [Internet] [Doctoral dissertation]. University of Arizona; 1971. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10150/565226.

Council of Science Editors:

Spanggord, Ronald Jay 1. Aminomercuration of carbonyl-containing olefins . [Doctoral Dissertation]. University of Arizona; 1971. Available from: http://hdl.handle.net/10150/565226


University of California – Berkeley

3. Shunatona, Hunter Paul. Catalyzed Intramolecular Aminocyclization Reactions.

Degree: Chemistry, 2014, University of California – Berkeley

 The scope of my doctoral studies was intended to address the specific synthetic challenge of the construction of heterocycles. As a result, the synthesis of… (more)

Subjects/Keywords: Organic chemistry; Amination; Catalysis; Methodology

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APA (6th Edition):

Shunatona, H. P. (2014). Catalyzed Intramolecular Aminocyclization Reactions. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6n18t0hg

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):

Shunatona, Hunter Paul. “Catalyzed Intramolecular Aminocyclization Reactions.” 2014. Thesis, University of California – Berkeley. Accessed July 09, 2020. http://www.escholarship.org/uc/item/6n18t0hg.

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

MLA Handbook (7th Edition):

Shunatona, Hunter Paul. “Catalyzed Intramolecular Aminocyclization Reactions.” 2014. Web. 09 Jul 2020.

Vancouver:

Shunatona HP. Catalyzed Intramolecular Aminocyclization Reactions. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2020 Jul 09]. Available from: http://www.escholarship.org/uc/item/6n18t0hg.

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

Council of Science Editors:

Shunatona HP. Catalyzed Intramolecular Aminocyclization Reactions. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/6n18t0hg

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


Montana State University

4. Towey, Bradley David. Electronic structure determination of model complexes of [Mo-3Fe-4S] clusters and method development of in situ reductive amination using amine-boranes.

Degree: College of Letters & Science, 2014, Montana State University

 In nature, bacteria are able to convert inert nitrogen gas to ammonia using the iron molybdenum-cofactor of the nitrogenase enzyme. Even though the crystal structure… (more)

Subjects/Keywords: Electronic structure.; Molybdenum compounds.; Amination.

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APA (6th Edition):

Towey, B. D. (2014). Electronic structure determination of model complexes of [Mo-3Fe-4S] clusters and method development of in situ reductive amination using amine-boranes. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/9421

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):

Towey, Bradley David. “Electronic structure determination of model complexes of [Mo-3Fe-4S] clusters and method development of in situ reductive amination using amine-boranes.” 2014. Thesis, Montana State University. Accessed July 09, 2020. https://scholarworks.montana.edu/xmlui/handle/1/9421.

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

MLA Handbook (7th Edition):

Towey, Bradley David. “Electronic structure determination of model complexes of [Mo-3Fe-4S] clusters and method development of in situ reductive amination using amine-boranes.” 2014. Web. 09 Jul 2020.

Vancouver:

Towey BD. Electronic structure determination of model complexes of [Mo-3Fe-4S] clusters and method development of in situ reductive amination using amine-boranes. [Internet] [Thesis]. Montana State University; 2014. [cited 2020 Jul 09]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9421.

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

Council of Science Editors:

Towey BD. Electronic structure determination of model complexes of [Mo-3Fe-4S] clusters and method development of in situ reductive amination using amine-boranes. [Thesis]. Montana State University; 2014. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9421

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


NSYSU

5. Pan, Ming-kai. Copper-Catalyzed Amination of Indoles via C-H Bond Activation.

Degree: Master, Chemistry, 2012, NSYSU

 A new protocol for direct amination of N-Methyl-2-phenylindole catalyzed by copper(II) trifluoromethanesulfonate was presented. Both of (E)-N-(1,1'-Dimethyl-2,2' -diphenyl-2,3'-biindolin-3-ylidene)-4-methylbenzenesulfonamideï¼4ï¼and 4-methyl -N-(1-methyl-2-phenyl-1H-indol-3-yl)benzenesulfonamideï¼2ï¼were obtained under the optimal reaction… (more)

Subjects/Keywords: indole amination; copper catalyst; nitrene

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APA (6th Edition):

Pan, M. (2012). Copper-Catalyzed Amination of Indoles via C-H Bond Activation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907112-135201

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):

Pan, Ming-kai. “Copper-Catalyzed Amination of Indoles via C-H Bond Activation.” 2012. Thesis, NSYSU. Accessed July 09, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907112-135201.

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

MLA Handbook (7th Edition):

Pan, Ming-kai. “Copper-Catalyzed Amination of Indoles via C-H Bond Activation.” 2012. Web. 09 Jul 2020.

Vancouver:

Pan M. Copper-Catalyzed Amination of Indoles via C-H Bond Activation. [Internet] [Thesis]. NSYSU; 2012. [cited 2020 Jul 09]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907112-135201.

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

Council of Science Editors:

Pan M. Copper-Catalyzed Amination of Indoles via C-H Bond Activation. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907112-135201

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


Queens University

6. Borjian Borojeni, Sogol. Studies on the Optimization of Buchwald-Hartwig Amination of Aryl Halides .

Degree: Chemistry, 2014, Queens University

 Developing new catalyst systems for cross-coupling reactions such as Buchwald-Hartwig aminations has been one of the remarkable topics in the palladium-catalyzed, cross-coupling reaction research area.… (more)

Subjects/Keywords: Buchwald-Hartwig Amination; Catalysis; Organometallics

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APA (6th Edition):

Borjian Borojeni, S. (2014). Studies on the Optimization of Buchwald-Hartwig Amination of Aryl Halides . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/12519

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):

Borjian Borojeni, Sogol. “Studies on the Optimization of Buchwald-Hartwig Amination of Aryl Halides .” 2014. Thesis, Queens University. Accessed July 09, 2020. http://hdl.handle.net/1974/12519.

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

MLA Handbook (7th Edition):

Borjian Borojeni, Sogol. “Studies on the Optimization of Buchwald-Hartwig Amination of Aryl Halides .” 2014. Web. 09 Jul 2020.

Vancouver:

Borjian Borojeni S. Studies on the Optimization of Buchwald-Hartwig Amination of Aryl Halides . [Internet] [Thesis]. Queens University; 2014. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/1974/12519.

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

Council of Science Editors:

Borjian Borojeni S. Studies on the Optimization of Buchwald-Hartwig Amination of Aryl Halides . [Thesis]. Queens University; 2014. Available from: http://hdl.handle.net/1974/12519

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


University of Michigan

7. Mantell, Mark. Developing Strategies to Control Reactivity and Selectivity in Catalytic Transformations.

Degree: PhD, Chemistry, 2020, University of Michigan

 This thesis focuses on: (1) the development of catalysts for the C–H borylation of methane (Chapter 2); (2) the development of new methods for C(sp2)–N… (more)

Subjects/Keywords: Chemistry; Amination; Borylation; Chemistry; Science

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APA (6th Edition):

Mantell, M. (2020). Developing Strategies to Control Reactivity and Selectivity in Catalytic Transformations. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/155112

Chicago Manual of Style (16th Edition):

Mantell, Mark. “Developing Strategies to Control Reactivity and Selectivity in Catalytic Transformations.” 2020. Doctoral Dissertation, University of Michigan. Accessed July 09, 2020. http://hdl.handle.net/2027.42/155112.

MLA Handbook (7th Edition):

Mantell, Mark. “Developing Strategies to Control Reactivity and Selectivity in Catalytic Transformations.” 2020. Web. 09 Jul 2020.

Vancouver:

Mantell M. Developing Strategies to Control Reactivity and Selectivity in Catalytic Transformations. [Internet] [Doctoral dissertation]. University of Michigan; 2020. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2027.42/155112.

Council of Science Editors:

Mantell M. Developing Strategies to Control Reactivity and Selectivity in Catalytic Transformations. [Doctoral Dissertation]. University of Michigan; 2020. Available from: http://hdl.handle.net/2027.42/155112


Duke University

8. Hemric, Brett Nathaniel. Copper-Catalyzed Amino Oxygenation of Alkenes and Dienes: A Novel Amino-Initiation Pathway Using O-Benzoylhydroxylamines .

Degree: 2018, Duke University

  Nitrogen-containing compounds, specifically the 1,2-oxyamino moiety, are of vital importance to modern pharmaceuticals, natural products, and agrochemicals. 1,2-Difunctionalization of alkenes offers an efficient approach… (more)

Subjects/Keywords: Organic chemistry; alkene; amination; copper

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APA (6th Edition):

Hemric, B. N. (2018). Copper-Catalyzed Amino Oxygenation of Alkenes and Dienes: A Novel Amino-Initiation Pathway Using O-Benzoylhydroxylamines . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/18286

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):

Hemric, Brett Nathaniel. “Copper-Catalyzed Amino Oxygenation of Alkenes and Dienes: A Novel Amino-Initiation Pathway Using O-Benzoylhydroxylamines .” 2018. Thesis, Duke University. Accessed July 09, 2020. http://hdl.handle.net/10161/18286.

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

MLA Handbook (7th Edition):

Hemric, Brett Nathaniel. “Copper-Catalyzed Amino Oxygenation of Alkenes and Dienes: A Novel Amino-Initiation Pathway Using O-Benzoylhydroxylamines .” 2018. Web. 09 Jul 2020.

Vancouver:

Hemric BN. Copper-Catalyzed Amino Oxygenation of Alkenes and Dienes: A Novel Amino-Initiation Pathway Using O-Benzoylhydroxylamines . [Internet] [Thesis]. Duke University; 2018. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10161/18286.

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

Council of Science Editors:

Hemric BN. Copper-Catalyzed Amino Oxygenation of Alkenes and Dienes: A Novel Amino-Initiation Pathway Using O-Benzoylhydroxylamines . [Thesis]. Duke University; 2018. Available from: http://hdl.handle.net/10161/18286

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

9. Lombardi, Christopher Daniel. Synthesis of Primary Arylamines Using Bulky Palladium N-heterocyclic Carbene Precatalysts.

Degree: MSc -MS, Chemistry, 2017, York University

 The reaction between aryl halides and ammonia was investigated using N-heterocyclic carbene (NHC) ligated palladium pre-catalysts. The use of NHCs is well documented for coupling… (more)

Subjects/Keywords: Chemistry; Palladium; Catalysis; NHC; Amination; Buchwald-Hartwig amination; Ammonia; Aminotriphenysilane

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APA (6th Edition):

Lombardi, C. D. (2017). Synthesis of Primary Arylamines Using Bulky Palladium N-heterocyclic Carbene Precatalysts. (Masters Thesis). York University. Retrieved from http://hdl.handle.net/10315/33513

Chicago Manual of Style (16th Edition):

Lombardi, Christopher Daniel. “Synthesis of Primary Arylamines Using Bulky Palladium N-heterocyclic Carbene Precatalysts.” 2017. Masters Thesis, York University. Accessed July 09, 2020. http://hdl.handle.net/10315/33513.

MLA Handbook (7th Edition):

Lombardi, Christopher Daniel. “Synthesis of Primary Arylamines Using Bulky Palladium N-heterocyclic Carbene Precatalysts.” 2017. Web. 09 Jul 2020.

Vancouver:

Lombardi CD. Synthesis of Primary Arylamines Using Bulky Palladium N-heterocyclic Carbene Precatalysts. [Internet] [Masters thesis]. York University; 2017. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10315/33513.

Council of Science Editors:

Lombardi CD. Synthesis of Primary Arylamines Using Bulky Palladium N-heterocyclic Carbene Precatalysts. [Masters Thesis]. York University; 2017. Available from: http://hdl.handle.net/10315/33513


Montana State University

10. Huynh, Khoi Quang. Part 1: study toward the total synthesis of acutumine ; : Part 2: asymmetric intramolecular hydroamination catalyzed by group 3 metal complexes.

Degree: College of Letters & Science, 2014, Montana State University

 Acutumine 1 is a tetracylic alkaloid isolated from Menispermum daurcum, which exhibits selective T-Cell cytotoxicity. It is potentially useful for specific therapy T-Cell related Leukemia… (more)

Subjects/Keywords: Alkaloids Synthesis.; Menispermaceae.; Amination.; Metal complexes.

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APA (6th Edition):

Huynh, K. Q. (2014). Part 1: study toward the total synthesis of acutumine ; : Part 2: asymmetric intramolecular hydroamination catalyzed by group 3 metal complexes. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/8780

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):

Huynh, Khoi Quang. “Part 1: study toward the total synthesis of acutumine ; : Part 2: asymmetric intramolecular hydroamination catalyzed by group 3 metal complexes.” 2014. Thesis, Montana State University. Accessed July 09, 2020. https://scholarworks.montana.edu/xmlui/handle/1/8780.

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

MLA Handbook (7th Edition):

Huynh, Khoi Quang. “Part 1: study toward the total synthesis of acutumine ; : Part 2: asymmetric intramolecular hydroamination catalyzed by group 3 metal complexes.” 2014. Web. 09 Jul 2020.

Vancouver:

Huynh KQ. Part 1: study toward the total synthesis of acutumine ; : Part 2: asymmetric intramolecular hydroamination catalyzed by group 3 metal complexes. [Internet] [Thesis]. Montana State University; 2014. [cited 2020 Jul 09]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/8780.

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

Council of Science Editors:

Huynh KQ. Part 1: study toward the total synthesis of acutumine ; : Part 2: asymmetric intramolecular hydroamination catalyzed by group 3 metal complexes. [Thesis]. Montana State University; 2014. Available from: https://scholarworks.montana.edu/xmlui/handle/1/8780

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


Montana State University

11. Sunsdahl, Bryce Gregory. Diethyl zinc mediated metalloamination : development and its application to the synthesis of functionalized pyrrolidines and piperidines.

Degree: College of Letters & Science, 2015, Montana State University

 The ability to synthesize nitrogen heterocycles of industrial and academic significance remains a central goal of organic synthesis. Substantial effort has been made to develop… (more)

Subjects/Keywords: Organozinc compounds.; Amination.; Pyrrolidine Synthesis.; Piperidine Synthesis.

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APA (6th Edition):

Sunsdahl, B. G. (2015). Diethyl zinc mediated metalloamination : development and its application to the synthesis of functionalized pyrrolidines and piperidines. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/9081

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):

Sunsdahl, Bryce Gregory. “Diethyl zinc mediated metalloamination : development and its application to the synthesis of functionalized pyrrolidines and piperidines.” 2015. Thesis, Montana State University. Accessed July 09, 2020. https://scholarworks.montana.edu/xmlui/handle/1/9081.

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

MLA Handbook (7th Edition):

Sunsdahl, Bryce Gregory. “Diethyl zinc mediated metalloamination : development and its application to the synthesis of functionalized pyrrolidines and piperidines.” 2015. Web. 09 Jul 2020.

Vancouver:

Sunsdahl BG. Diethyl zinc mediated metalloamination : development and its application to the synthesis of functionalized pyrrolidines and piperidines. [Internet] [Thesis]. Montana State University; 2015. [cited 2020 Jul 09]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9081.

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

Council of Science Editors:

Sunsdahl BG. Diethyl zinc mediated metalloamination : development and its application to the synthesis of functionalized pyrrolidines and piperidines. [Thesis]. Montana State University; 2015. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9081

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


Montana State University

12. Smith, Adrian Robert. Synthesis of nitrogenous heterocycles via group 3 metal-catalyzed hydroamination and zinc (II) mediated metalloamination.

Degree: College of Letters & Science, 2015, Montana State University

 Pyrrolidines and piperidines respresent a motif found in a wide array of bioactive compounds. Hydroamination, or the insertion of a carbon-nitrogen bond into a site… (more)

Subjects/Keywords: Heterocyclic compounds Synthesis.; Amination.; Organometallic compounds.

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APA (6th Edition):

Smith, A. R. (2015). Synthesis of nitrogenous heterocycles via group 3 metal-catalyzed hydroamination and zinc (II) mediated metalloamination. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/9079

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):

Smith, Adrian Robert. “Synthesis of nitrogenous heterocycles via group 3 metal-catalyzed hydroamination and zinc (II) mediated metalloamination.” 2015. Thesis, Montana State University. Accessed July 09, 2020. https://scholarworks.montana.edu/xmlui/handle/1/9079.

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

MLA Handbook (7th Edition):

Smith, Adrian Robert. “Synthesis of nitrogenous heterocycles via group 3 metal-catalyzed hydroamination and zinc (II) mediated metalloamination.” 2015. Web. 09 Jul 2020.

Vancouver:

Smith AR. Synthesis of nitrogenous heterocycles via group 3 metal-catalyzed hydroamination and zinc (II) mediated metalloamination. [Internet] [Thesis]. Montana State University; 2015. [cited 2020 Jul 09]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9079.

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

Council of Science Editors:

Smith AR. Synthesis of nitrogenous heterocycles via group 3 metal-catalyzed hydroamination and zinc (II) mediated metalloamination. [Thesis]. Montana State University; 2015. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9079

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


University of Kansas

13. Lang, Simon Bouyea. Discovery and Evaluation of Catalytic Allylation and Amination Reactions.

Degree: PhD, Chemistry, 2016, University of Kansas

 Presented herein is the development and evaluation of several palladium-catalyzed allylic alkylation reactions and a method for visible light-mediated radical decarboxylative amination. These atom economical,… (more)

Subjects/Keywords: Organic chemistry; Allylation; Amination; Palladium catalysis; Photocatalysis

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APA (6th Edition):

Lang, S. B. (2016). Discovery and Evaluation of Catalytic Allylation and Amination Reactions. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/22469

Chicago Manual of Style (16th Edition):

Lang, Simon Bouyea. “Discovery and Evaluation of Catalytic Allylation and Amination Reactions.” 2016. Doctoral Dissertation, University of Kansas. Accessed July 09, 2020. http://hdl.handle.net/1808/22469.

MLA Handbook (7th Edition):

Lang, Simon Bouyea. “Discovery and Evaluation of Catalytic Allylation and Amination Reactions.” 2016. Web. 09 Jul 2020.

Vancouver:

Lang SB. Discovery and Evaluation of Catalytic Allylation and Amination Reactions. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/1808/22469.

Council of Science Editors:

Lang SB. Discovery and Evaluation of Catalytic Allylation and Amination Reactions. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/22469


Harvard University

14. Hennessy, Elisabeth Therese. C-H Amination Catalysis from High-Spin Ferrous Complexes.

Degree: PhD, Chemistry and Chemical Biology, 2013, Harvard University

The C-H amination and olefin aziridination chemistry of iron supported by dipyrromethene ligands (RLAr, L=1,9-R2-5-aryldipyrromethene, R = Mes, 2,4,6-Ph3C6H2, tBu, Ad, 10-camphoryl, Ar = Mes,… (more)

Subjects/Keywords: Chemistry; Amination; Catalysis; C-H Functionalization; Iron

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APA (6th Edition):

Hennessy, E. T. (2013). C-H Amination Catalysis from High-Spin Ferrous Complexes. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:11169787

Chicago Manual of Style (16th Edition):

Hennessy, Elisabeth Therese. “C-H Amination Catalysis from High-Spin Ferrous Complexes.” 2013. Doctoral Dissertation, Harvard University. Accessed July 09, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:11169787.

MLA Handbook (7th Edition):

Hennessy, Elisabeth Therese. “C-H Amination Catalysis from High-Spin Ferrous Complexes.” 2013. Web. 09 Jul 2020.

Vancouver:

Hennessy ET. C-H Amination Catalysis from High-Spin Ferrous Complexes. [Internet] [Doctoral dissertation]. Harvard University; 2013. [cited 2020 Jul 09]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11169787.

Council of Science Editors:

Hennessy ET. C-H Amination Catalysis from High-Spin Ferrous Complexes. [Doctoral Dissertation]. Harvard University; 2013. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11169787


University of California – Berkeley

15. Strom, Alexandra Eve. Synthetic and Mechanistic Studies of Transition Metal-Mediated Carbon-Nitrogen Bond Forming Reactions.

Degree: Chemistry, 2015, University of California – Berkeley

 The following dissertation discusses reactions for the formation of carbon-nitrogen bonds mediated by organotransition metal reagents and catalysts. Chapter 1 presents a synthetic method for… (more)

Subjects/Keywords: Chemistry; Amination; Aminocarbonylation; Hydroamination; Hydrozirconation; Organometallic Chemistry

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APA (6th Edition):

Strom, A. E. (2015). Synthetic and Mechanistic Studies of Transition Metal-Mediated Carbon-Nitrogen Bond Forming Reactions. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/5403h5m9

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):

Strom, Alexandra Eve. “Synthetic and Mechanistic Studies of Transition Metal-Mediated Carbon-Nitrogen Bond Forming Reactions.” 2015. Thesis, University of California – Berkeley. Accessed July 09, 2020. http://www.escholarship.org/uc/item/5403h5m9.

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

MLA Handbook (7th Edition):

Strom, Alexandra Eve. “Synthetic and Mechanistic Studies of Transition Metal-Mediated Carbon-Nitrogen Bond Forming Reactions.” 2015. Web. 09 Jul 2020.

Vancouver:

Strom AE. Synthetic and Mechanistic Studies of Transition Metal-Mediated Carbon-Nitrogen Bond Forming Reactions. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2020 Jul 09]. Available from: http://www.escholarship.org/uc/item/5403h5m9.

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

Council of Science Editors:

Strom AE. Synthetic and Mechanistic Studies of Transition Metal-Mediated Carbon-Nitrogen Bond Forming Reactions. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/5403h5m9

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


Mississippi State University

16. Box, Hannah Killian. The development of next generation, unsymmetrical CCC-NHC pincer ligand architectures and metalation to form unsymmetrical CCCNHC pincer Ta complexes.

Degree: PhD, Chemistry, 2015, Mississippi State University

  The impact of <i>N</i>-heterocyclic carbenes (NHC) as ligands for transition metal catalysis has been rigorously investigated since their isolation by Arduengo in 1991. NHCs… (more)

Subjects/Keywords: Unsymmetrical CCCNHC; Ta complexes; Oxidative Amination

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APA (6th Edition):

Box, H. K. (2015). The development of next generation, unsymmetrical CCC-NHC pincer ligand architectures and metalation to form unsymmetrical CCCNHC pincer Ta complexes. (Doctoral Dissertation). Mississippi State University. Retrieved from http://sun.library.msstate.edu/ETD-db/theses/available/etd-04282015-140641/ ;

Chicago Manual of Style (16th Edition):

Box, Hannah Killian. “The development of next generation, unsymmetrical CCC-NHC pincer ligand architectures and metalation to form unsymmetrical CCCNHC pincer Ta complexes.” 2015. Doctoral Dissertation, Mississippi State University. Accessed July 09, 2020. http://sun.library.msstate.edu/ETD-db/theses/available/etd-04282015-140641/ ;.

MLA Handbook (7th Edition):

Box, Hannah Killian. “The development of next generation, unsymmetrical CCC-NHC pincer ligand architectures and metalation to form unsymmetrical CCCNHC pincer Ta complexes.” 2015. Web. 09 Jul 2020.

Vancouver:

Box HK. The development of next generation, unsymmetrical CCC-NHC pincer ligand architectures and metalation to form unsymmetrical CCCNHC pincer Ta complexes. [Internet] [Doctoral dissertation]. Mississippi State University; 2015. [cited 2020 Jul 09]. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-04282015-140641/ ;.

Council of Science Editors:

Box HK. The development of next generation, unsymmetrical CCC-NHC pincer ligand architectures and metalation to form unsymmetrical CCCNHC pincer Ta complexes. [Doctoral Dissertation]. Mississippi State University; 2015. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-04282015-140641/ ;


University of Oklahoma

17. Lamar, Angus Andrew. Nitrogenation of Hydrocarbons via Transition-Metal and Non-Metal Catalysis.

Degree: PhD, 2010, University of Oklahoma

hydrocarbons under remarkably mild conditions. Advisors/Committee Members: Nicholas, Kenneth M (advisor).

Subjects/Keywords: Amination; Hydrocarbons; Nitrogen

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APA (6th Edition):

Lamar, A. A. (2010). Nitrogenation of Hydrocarbons via Transition-Metal and Non-Metal Catalysis. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/319133

Chicago Manual of Style (16th Edition):

Lamar, Angus Andrew. “Nitrogenation of Hydrocarbons via Transition-Metal and Non-Metal Catalysis.” 2010. Doctoral Dissertation, University of Oklahoma. Accessed July 09, 2020. http://hdl.handle.net/11244/319133.

MLA Handbook (7th Edition):

Lamar, Angus Andrew. “Nitrogenation of Hydrocarbons via Transition-Metal and Non-Metal Catalysis.” 2010. Web. 09 Jul 2020.

Vancouver:

Lamar AA. Nitrogenation of Hydrocarbons via Transition-Metal and Non-Metal Catalysis. [Internet] [Doctoral dissertation]. University of Oklahoma; 2010. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/11244/319133.

Council of Science Editors:

Lamar AA. Nitrogenation of Hydrocarbons via Transition-Metal and Non-Metal Catalysis. [Doctoral Dissertation]. University of Oklahoma; 2010. Available from: http://hdl.handle.net/11244/319133

18. Sharif, Sepideh. Application of Pd-NHC Complexes in Challenging Amination Reactions.

Degree: PhD, Chemistry, 2019, York University

 Among Pd-catalyzed carbon-heteroatom cross-coupling reactions, C-N bond formation, known as Buchwald-Hartwig amination (BHA), is by far the most studied reaction owing to the prevalence of… (more)

Subjects/Keywords: Chemistry; Buchwald-Hartwig amination; Pd-NHC complexes; C-N challenging amination reactions

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APA (6th Edition):

Sharif, S. (2019). Application of Pd-NHC Complexes in Challenging Amination Reactions. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/36279

Chicago Manual of Style (16th Edition):

Sharif, Sepideh. “Application of Pd-NHC Complexes in Challenging Amination Reactions.” 2019. Doctoral Dissertation, York University. Accessed July 09, 2020. http://hdl.handle.net/10315/36279.

MLA Handbook (7th Edition):

Sharif, Sepideh. “Application of Pd-NHC Complexes in Challenging Amination Reactions.” 2019. Web. 09 Jul 2020.

Vancouver:

Sharif S. Application of Pd-NHC Complexes in Challenging Amination Reactions. [Internet] [Doctoral dissertation]. York University; 2019. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10315/36279.

Council of Science Editors:

Sharif S. Application of Pd-NHC Complexes in Challenging Amination Reactions. [Doctoral Dissertation]. York University; 2019. Available from: http://hdl.handle.net/10315/36279

19. Mora, Anne-Sophie. Élaboration de revêtements époxy pour contact alimentaire à empreinte environnementale réduite : Development of epoxy coatings for food contact with reduced environmental footprint.

Degree: Docteur es, Chimie et Physico-Chimie des Matériaux, 2019, Montpellier, Ecole nationale supérieure de chimie

Les travaux de thèse présentés sont issus d’une collaboration industrielle avec la société Nouvelle Sogatra, spécialisée dans la conception, la fabrication et la commercialisation de… (more)

Subjects/Keywords: Époxy; Amine; Biosourcé; Amination; Matériaux thermodurcissables; Epoxy; Amine; Bio-Based; Amination; Thermoset materials; 540

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APA (6th Edition):

Mora, A. (2019). Élaboration de revêtements époxy pour contact alimentaire à empreinte environnementale réduite : Development of epoxy coatings for food contact with reduced environmental footprint. (Doctoral Dissertation). Montpellier, Ecole nationale supérieure de chimie. Retrieved from http://www.theses.fr/2019ENCM0012

Chicago Manual of Style (16th Edition):

Mora, Anne-Sophie. “Élaboration de revêtements époxy pour contact alimentaire à empreinte environnementale réduite : Development of epoxy coatings for food contact with reduced environmental footprint.” 2019. Doctoral Dissertation, Montpellier, Ecole nationale supérieure de chimie. Accessed July 09, 2020. http://www.theses.fr/2019ENCM0012.

MLA Handbook (7th Edition):

Mora, Anne-Sophie. “Élaboration de revêtements époxy pour contact alimentaire à empreinte environnementale réduite : Development of epoxy coatings for food contact with reduced environmental footprint.” 2019. Web. 09 Jul 2020.

Vancouver:

Mora A. Élaboration de revêtements époxy pour contact alimentaire à empreinte environnementale réduite : Development of epoxy coatings for food contact with reduced environmental footprint. [Internet] [Doctoral dissertation]. Montpellier, Ecole nationale supérieure de chimie; 2019. [cited 2020 Jul 09]. Available from: http://www.theses.fr/2019ENCM0012.

Council of Science Editors:

Mora A. Élaboration de revêtements époxy pour contact alimentaire à empreinte environnementale réduite : Development of epoxy coatings for food contact with reduced environmental footprint. [Doctoral Dissertation]. Montpellier, Ecole nationale supérieure de chimie; 2019. Available from: http://www.theses.fr/2019ENCM0012

20. Zhang, Yin. Backbone decoration of imidazol-2-ylidene ligands with amino groups and their application in palladium catalyzed arylative amination reaction : Carbènes N-hétérocycliques de type imidazol-2-ylidène à squelette aminé et leur application en amination arylique au palladium.

Degree: Docteur es, Chimie moléculaire, 2015, Université Toulouse III – Paul Sabatier

 Ce travail s'inscrit dans le cadre de la chimie des carbènes N-hétérocycliques (NHC) et s'articule autour de la fonctionnalisation directe de l'hétérocycle des l'imidazol-2-ylidènes par… (more)

Subjects/Keywords: Catalyse homogène; Chimie organométallique; Carbènes; Palladium; Amination; Carbenes; Homogeneous catalysis; Organometallic chemistry; Palladium; Amination

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APA (6th Edition):

Zhang, Y. (2015). Backbone decoration of imidazol-2-ylidene ligands with amino groups and their application in palladium catalyzed arylative amination reaction : Carbènes N-hétérocycliques de type imidazol-2-ylidène à squelette aminé et leur application en amination arylique au palladium. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2015TOU30109

Chicago Manual of Style (16th Edition):

Zhang, Yin. “Backbone decoration of imidazol-2-ylidene ligands with amino groups and their application in palladium catalyzed arylative amination reaction : Carbènes N-hétérocycliques de type imidazol-2-ylidène à squelette aminé et leur application en amination arylique au palladium.” 2015. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed July 09, 2020. http://www.theses.fr/2015TOU30109.

MLA Handbook (7th Edition):

Zhang, Yin. “Backbone decoration of imidazol-2-ylidene ligands with amino groups and their application in palladium catalyzed arylative amination reaction : Carbènes N-hétérocycliques de type imidazol-2-ylidène à squelette aminé et leur application en amination arylique au palladium.” 2015. Web. 09 Jul 2020.

Vancouver:

Zhang Y. Backbone decoration of imidazol-2-ylidene ligands with amino groups and their application in palladium catalyzed arylative amination reaction : Carbènes N-hétérocycliques de type imidazol-2-ylidène à squelette aminé et leur application en amination arylique au palladium. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2015. [cited 2020 Jul 09]. Available from: http://www.theses.fr/2015TOU30109.

Council of Science Editors:

Zhang Y. Backbone decoration of imidazol-2-ylidene ligands with amino groups and their application in palladium catalyzed arylative amination reaction : Carbènes N-hétérocycliques de type imidazol-2-ylidène à squelette aminé et leur application en amination arylique au palladium. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2015. Available from: http://www.theses.fr/2015TOU30109

21. Colin, Olivier. Plateforme pyridylalkylamine modulable : un outil pour la catalyse : Flexible pyridylalkylamine plateform : a tool for catalysis.

Degree: Docteur es, Chimie organique, 2015, Versailles-St Quentin en Yvelines

Les travaux exposés dans ce manuscrit s’articulent autour de l’élaboration de nouvelles plateformes pyridylalkylamines polyfonctionelles et chirales afin de permettre le développement d’un nouveau processus… (more)

Subjects/Keywords: Métallocatalyse; Organocatalyse; Cascade; Pyridylalkylamine; Urées; Imidazolidine; Amination; Réaction de Prins; Metallocatalysis; Organocatalysis; Cascade; Pyridylalkylamine; Ureas; Imidazolidine; Amination; Prins reaction; 547

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APA (6th Edition):

Colin, O. (2015). Plateforme pyridylalkylamine modulable : un outil pour la catalyse : Flexible pyridylalkylamine plateform : a tool for catalysis. (Doctoral Dissertation). Versailles-St Quentin en Yvelines. Retrieved from http://www.theses.fr/2015VERS023V

Chicago Manual of Style (16th Edition):

Colin, Olivier. “Plateforme pyridylalkylamine modulable : un outil pour la catalyse : Flexible pyridylalkylamine plateform : a tool for catalysis.” 2015. Doctoral Dissertation, Versailles-St Quentin en Yvelines. Accessed July 09, 2020. http://www.theses.fr/2015VERS023V.

MLA Handbook (7th Edition):

Colin, Olivier. “Plateforme pyridylalkylamine modulable : un outil pour la catalyse : Flexible pyridylalkylamine plateform : a tool for catalysis.” 2015. Web. 09 Jul 2020.

Vancouver:

Colin O. Plateforme pyridylalkylamine modulable : un outil pour la catalyse : Flexible pyridylalkylamine plateform : a tool for catalysis. [Internet] [Doctoral dissertation]. Versailles-St Quentin en Yvelines; 2015. [cited 2020 Jul 09]. Available from: http://www.theses.fr/2015VERS023V.

Council of Science Editors:

Colin O. Plateforme pyridylalkylamine modulable : un outil pour la catalyse : Flexible pyridylalkylamine plateform : a tool for catalysis. [Doctoral Dissertation]. Versailles-St Quentin en Yvelines; 2015. Available from: http://www.theses.fr/2015VERS023V

22. Dumon, Alexandre. Selective Alcohol Amination : theoretical Study for the Design of Innovative Heterogenerous Catalysts : Amination sélective d'alcools : une étude théorique pour le design de catalyseurs hétérogènes innovants.

Degree: Docteur es, Chimie, 2016, Lyon

Les polyamines sont des intermédiaires industriels très importants, cependant leur production dépend du pétrole, d’un apport en hydrogène et de produits toxiques (HCN, HCl). Il… (more)

Subjects/Keywords: Amination; Hétérogène; Catalyse; DFT; H-borrowing; Alcools; Environnement chimique; Amination; Heterogeneous; Catalysis; DFT; H-Borrowing; Alcohols; Chemical environment

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APA (6th Edition):

Dumon, A. (2016). Selective Alcohol Amination : theoretical Study for the Design of Innovative Heterogenerous Catalysts : Amination sélective d'alcools : une étude théorique pour le design de catalyseurs hétérogènes innovants. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2016LYSEN020

Chicago Manual of Style (16th Edition):

Dumon, Alexandre. “Selective Alcohol Amination : theoretical Study for the Design of Innovative Heterogenerous Catalysts : Amination sélective d'alcools : une étude théorique pour le design de catalyseurs hétérogènes innovants.” 2016. Doctoral Dissertation, Lyon. Accessed July 09, 2020. http://www.theses.fr/2016LYSEN020.

MLA Handbook (7th Edition):

Dumon, Alexandre. “Selective Alcohol Amination : theoretical Study for the Design of Innovative Heterogenerous Catalysts : Amination sélective d'alcools : une étude théorique pour le design de catalyseurs hétérogènes innovants.” 2016. Web. 09 Jul 2020.

Vancouver:

Dumon A. Selective Alcohol Amination : theoretical Study for the Design of Innovative Heterogenerous Catalysts : Amination sélective d'alcools : une étude théorique pour le design de catalyseurs hétérogènes innovants. [Internet] [Doctoral dissertation]. Lyon; 2016. [cited 2020 Jul 09]. Available from: http://www.theses.fr/2016LYSEN020.

Council of Science Editors:

Dumon A. Selective Alcohol Amination : theoretical Study for the Design of Innovative Heterogenerous Catalysts : Amination sélective d'alcools : une étude théorique pour le design de catalyseurs hétérogènes innovants. [Doctoral Dissertation]. Lyon; 2016. Available from: http://www.theses.fr/2016LYSEN020


Université Paris-Sud – Paris XI

23. Mazurais, Marie. Nitrènes et amination de liaisons C(sp³)-H : applications en synthèse et développement de nouvelles conditions oxydantes : Nitrene and C(sp³)-H amination : applications in synthesis and development of new oxidizing conditions.

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

Les transferts de nitrène représentent un outil synthétique très intéressant pour former simplement une liaison C-N à partir d’une liaison C-H. Notre laboratoire a développé… (more)

Subjects/Keywords: Nitrène; Amination C-H; Sulfonimidamide; Perhydroindole; Iode catalytique; Haloamine; Dibromophakellstatine; Nitrene; C-H amination; Sulfonimidamide; Perhydroindole; Iode catalytique; Haloamine; Dibromophakellstatin

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APA (6th Edition):

Mazurais, M. (2014). Nitrènes et amination de liaisons C(sp³)-H : applications en synthèse et développement de nouvelles conditions oxydantes : Nitrene and C(sp³)-H amination : applications in synthesis and development of new oxidizing conditions. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA112257

Chicago Manual of Style (16th Edition):

Mazurais, Marie. “Nitrènes et amination de liaisons C(sp³)-H : applications en synthèse et développement de nouvelles conditions oxydantes : Nitrene and C(sp³)-H amination : applications in synthesis and development of new oxidizing conditions.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed July 09, 2020. http://www.theses.fr/2014PA112257.

MLA Handbook (7th Edition):

Mazurais, Marie. “Nitrènes et amination de liaisons C(sp³)-H : applications en synthèse et développement de nouvelles conditions oxydantes : Nitrene and C(sp³)-H amination : applications in synthesis and development of new oxidizing conditions.” 2014. Web. 09 Jul 2020.

Vancouver:

Mazurais M. Nitrènes et amination de liaisons C(sp³)-H : applications en synthèse et développement de nouvelles conditions oxydantes : Nitrene and C(sp³)-H amination : applications in synthesis and development of new oxidizing conditions. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2020 Jul 09]. Available from: http://www.theses.fr/2014PA112257.

Council of Science Editors:

Mazurais M. Nitrènes et amination de liaisons C(sp³)-H : applications en synthèse et développement de nouvelles conditions oxydantes : Nitrene and C(sp³)-H amination : applications in synthesis and development of new oxidizing conditions. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA112257


University of Illinois – Chicago

24. Sun, Chunrui. New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions.

Degree: 2013, University of Illinois – Chicago

 This thesis contains two parts. Part I is about the development of novel α-amination of carbonyl compounds using lithium trimethylsilyldiazomethane and its application to the… (more)

Subjects/Keywords: lithium trimethylsilyldiazomethane; [3+2] cycloaddition; N–N bond cleavage; α-amination; amathaspiramide; massadine; cyclopropene; C–H amination

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APA (6th Edition):

Sun, C. (2013). New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10062

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):

Sun, Chunrui. “New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions.” 2013. Thesis, University of Illinois – Chicago. Accessed July 09, 2020. http://hdl.handle.net/10027/10062.

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

MLA Handbook (7th Edition):

Sun, Chunrui. “New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions.” 2013. Web. 09 Jul 2020.

Vancouver:

Sun C. New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10027/10062.

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

Council of Science Editors:

Sun C. New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10062

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

25. Bedier, Matthieu. Synthèse et Réactivité des Fluorures Allyliques Fonctionnalisés (alpha-Fluoroénamides) et Applications Synthétiques. : Synthesis and reactivity of functionalized allylic fluorides (alpha-fluoroenamides) and synthetic applications.

Degree: Docteur es, Chimie, 2018, Normandie

Le fluor a gagné un intérêt croissant dans de nombreux domaines de la chimie organique. De nombreuses méthodes de fluoration ont vu le jour afin… (more)

Subjects/Keywords: Fluorure allylique; Fluoration électrophile; Métathèse croisée; Amination; Catalyse au platine; Allylic fluorides; Electrophilic fluorination; Cross-metathesis; Amination; Platinum catalysis; 541.39

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APA (6th Edition):

Bedier, M. (2018). Synthèse et Réactivité des Fluorures Allyliques Fonctionnalisés (alpha-Fluoroénamides) et Applications Synthétiques. : Synthesis and reactivity of functionalized allylic fluorides (alpha-fluoroenamides) and synthetic applications. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2018NORMR033

Chicago Manual of Style (16th Edition):

Bedier, Matthieu. “Synthèse et Réactivité des Fluorures Allyliques Fonctionnalisés (alpha-Fluoroénamides) et Applications Synthétiques. : Synthesis and reactivity of functionalized allylic fluorides (alpha-fluoroenamides) and synthetic applications.” 2018. Doctoral Dissertation, Normandie. Accessed July 09, 2020. http://www.theses.fr/2018NORMR033.

MLA Handbook (7th Edition):

Bedier, Matthieu. “Synthèse et Réactivité des Fluorures Allyliques Fonctionnalisés (alpha-Fluoroénamides) et Applications Synthétiques. : Synthesis and reactivity of functionalized allylic fluorides (alpha-fluoroenamides) and synthetic applications.” 2018. Web. 09 Jul 2020.

Vancouver:

Bedier M. Synthèse et Réactivité des Fluorures Allyliques Fonctionnalisés (alpha-Fluoroénamides) et Applications Synthétiques. : Synthesis and reactivity of functionalized allylic fluorides (alpha-fluoroenamides) and synthetic applications. [Internet] [Doctoral dissertation]. Normandie; 2018. [cited 2020 Jul 09]. Available from: http://www.theses.fr/2018NORMR033.

Council of Science Editors:

Bedier M. Synthèse et Réactivité des Fluorures Allyliques Fonctionnalisés (alpha-Fluoroénamides) et Applications Synthétiques. : Synthesis and reactivity of functionalized allylic fluorides (alpha-fluoroenamides) and synthetic applications. [Doctoral Dissertation]. Normandie; 2018. Available from: http://www.theses.fr/2018NORMR033

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

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 July 09, 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. 09 Jul 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 Jul 09]. 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


Dalhousie University

27. Alsabeh, Pamela G. The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions.

Degree: PhD, Department of Chemistry, 2013, Dalhousie University

 The use of homogeneous organometallic catalysis for otherwise challenging chemical transformations is a concept that has gained significant interest in recent decades, providing access to… (more)

Subjects/Keywords: catalysis; cross-coupling; palladium; ammonia; amination; carbonylation; indole synthesis

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

APA (6th Edition):

Alsabeh, P. G. (2013). The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/39740

Chicago Manual of Style (16th Edition):

Alsabeh, Pamela G. “The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions.” 2013. Doctoral Dissertation, Dalhousie University. Accessed July 09, 2020. http://hdl.handle.net/10222/39740.

MLA Handbook (7th Edition):

Alsabeh, Pamela G. “The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions.” 2013. Web. 09 Jul 2020.

Vancouver:

Alsabeh PG. The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions. [Internet] [Doctoral dissertation]. Dalhousie University; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10222/39740.

Council of Science Editors:

Alsabeh PG. The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions. [Doctoral Dissertation]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/39740


Penn State University

28. Ai, Zhaoyan. fast copper-catalyzed aryl c(sp2)-h amination with n-(2-pyridyl)sulfonyl directing group at ambient temperature.

Degree: MS, Chemistry, 2014, Penn State University

 The ubiquity of aryl amines makes them a crucial part in various organic syntheses. An immense effort has been made, therefore, to develop efficient methods… (more)

Subjects/Keywords: c-h activation; cu catalysis; aryl amination; room temperature

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APA (6th Edition):

Ai, Z. (2014). fast copper-catalyzed aryl c(sp2)-h amination with n-(2-pyridyl)sulfonyl directing group at ambient temperature. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/21536

Chicago Manual of Style (16th Edition):

Ai, Zhaoyan. “fast copper-catalyzed aryl c(sp2)-h amination with n-(2-pyridyl)sulfonyl directing group at ambient temperature.” 2014. Masters Thesis, Penn State University. Accessed July 09, 2020. https://etda.libraries.psu.edu/catalog/21536.

MLA Handbook (7th Edition):

Ai, Zhaoyan. “fast copper-catalyzed aryl c(sp2)-h amination with n-(2-pyridyl)sulfonyl directing group at ambient temperature.” 2014. Web. 09 Jul 2020.

Vancouver:

Ai Z. fast copper-catalyzed aryl c(sp2)-h amination with n-(2-pyridyl)sulfonyl directing group at ambient temperature. [Internet] [Masters thesis]. Penn State University; 2014. [cited 2020 Jul 09]. Available from: https://etda.libraries.psu.edu/catalog/21536.

Council of Science Editors:

Ai Z. fast copper-catalyzed aryl c(sp2)-h amination with n-(2-pyridyl)sulfonyl directing group at ambient temperature. [Masters Thesis]. Penn State University; 2014. Available from: https://etda.libraries.psu.edu/catalog/21536


UCLA

29. Ramgren, Stephen David. Catalytic Methods for Carbon-Carbon and Carbon-Nitrogen Bond Formation.

Degree: Chemistry, 2014, UCLA

 This dissertation describes the study of metal-catalyzed cross-coupling reactions to construct carbon-carbon and carbon-heteroatom bonds. The key feature of much of this work is the… (more)

Subjects/Keywords: Chemistry; Amination; carbamate; Iron; Nickel; sulfamate; Suzuki-Miyaura

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APA (6th Edition):

Ramgren, S. D. (2014). Catalytic Methods for Carbon-Carbon and Carbon-Nitrogen Bond Formation. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1jn4h6wj

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):

Ramgren, Stephen David. “Catalytic Methods for Carbon-Carbon and Carbon-Nitrogen Bond Formation.” 2014. Thesis, UCLA. Accessed July 09, 2020. http://www.escholarship.org/uc/item/1jn4h6wj.

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

MLA Handbook (7th Edition):

Ramgren, Stephen David. “Catalytic Methods for Carbon-Carbon and Carbon-Nitrogen Bond Formation.” 2014. Web. 09 Jul 2020.

Vancouver:

Ramgren SD. Catalytic Methods for Carbon-Carbon and Carbon-Nitrogen Bond Formation. [Internet] [Thesis]. UCLA; 2014. [cited 2020 Jul 09]. Available from: http://www.escholarship.org/uc/item/1jn4h6wj.

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

Council of Science Editors:

Ramgren SD. Catalytic Methods for Carbon-Carbon and Carbon-Nitrogen Bond Formation. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/1jn4h6wj

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


Texas A&M University

30. Huehls, Christopher Bryan. Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes.

Degree: 2014, Texas A&M University

 Indole-containing structures and their generation still draw much attention because of their ubiquity in natural products, medicinal compounds, and organic materials. Given this prevalence, synthetic… (more)

Subjects/Keywords: indole; indolenine; nitrone; pyrroloindoline; hydrocarbazole; conjugate addition; iron; amination; hydroamination

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

APA (6th Edition):

Huehls, C. B. (2014). Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152597

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):

Huehls, Christopher Bryan. “Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes.” 2014. Thesis, Texas A&M University. Accessed July 09, 2020. http://hdl.handle.net/1969.1/152597.

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

MLA Handbook (7th Edition):

Huehls, Christopher Bryan. “Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes.” 2014. Web. 09 Jul 2020.

Vancouver:

Huehls CB. Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/1969.1/152597.

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

Council of Science Editors:

Huehls CB. Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152597

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

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