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You searched for subject:( catalyzed). Showing records 1 – 30 of 235 total matches.

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University of Georgia

1. Luo, Qi. Degradation of perfluoroalkyl acids by enzyme catalyzed oxidative humification reactions.

Degree: PhD, Toxicology, 2015, University of Georgia

 The historical mass production, long term utilization and direct disposal of perfluoroalkyl acids (PFAAs) resulted in the wide distribution of such chemicals in the environment.… (more)

Subjects/Keywords: Enzyme catalyzed oxidative humificaiton reactions

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APA (6th Edition):

Luo, Q. (2015). Degradation of perfluoroalkyl acids by enzyme catalyzed oxidative humification reactions. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/luo_qi_201512_phd

Chicago Manual of Style (16th Edition):

Luo, Qi. “Degradation of perfluoroalkyl acids by enzyme catalyzed oxidative humification reactions.” 2015. Doctoral Dissertation, University of Georgia. Accessed October 17, 2019. http://purl.galileo.usg.edu/uga_etd/luo_qi_201512_phd.

MLA Handbook (7th Edition):

Luo, Qi. “Degradation of perfluoroalkyl acids by enzyme catalyzed oxidative humification reactions.” 2015. Web. 17 Oct 2019.

Vancouver:

Luo Q. Degradation of perfluoroalkyl acids by enzyme catalyzed oxidative humification reactions. [Internet] [Doctoral dissertation]. University of Georgia; 2015. [cited 2019 Oct 17]. Available from: http://purl.galileo.usg.edu/uga_etd/luo_qi_201512_phd.

Council of Science Editors:

Luo Q. Degradation of perfluoroalkyl acids by enzyme catalyzed oxidative humification reactions. [Doctoral Dissertation]. University of Georgia; 2015. Available from: http://purl.galileo.usg.edu/uga_etd/luo_qi_201512_phd


University of Illinois – Chicago

2. Shi, Yi. Development of Transition-Metal-Catalyzed Transformations of Triazoles.

Degree: 2017, University of Illinois – Chicago

 This thesis defense presentation describes the development of transition-metal-catalyzed transformations of fused pyridotriazoles, as well as monocyclic N-sulfonyl-1,2,3-triazoles, which allows efficient synthesis of various valuable… (more)

Subjects/Keywords: Triazoles; Transition-Metal-Catalyzed

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APA (6th Edition):

Shi, Y. (2017). Development of Transition-Metal-Catalyzed Transformations of Triazoles. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21887

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):

Shi, Yi. “Development of Transition-Metal-Catalyzed Transformations of Triazoles.” 2017. Thesis, University of Illinois – Chicago. Accessed October 17, 2019. http://hdl.handle.net/10027/21887.

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

MLA Handbook (7th Edition):

Shi, Yi. “Development of Transition-Metal-Catalyzed Transformations of Triazoles.” 2017. Web. 17 Oct 2019.

Vancouver:

Shi Y. Development of Transition-Metal-Catalyzed Transformations of Triazoles. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10027/21887.

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

Council of Science Editors:

Shi Y. Development of Transition-Metal-Catalyzed Transformations of Triazoles. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/21887

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


University of Illinois – Chicago

3. Mamidipalli, Phani Raja P. Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes.

Degree: 2015, University of Illinois – Chicago

 This thesis has two main parts. Part I is composed of two chapters which describes mechanistic investigation of copper catalyzed reactions of diazo compounds followed… (more)

Subjects/Keywords: Copper catalyzed coupling; HDDA reaction

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APA (6th Edition):

Mamidipalli, P. R. P. (2015). Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19456

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):

Mamidipalli, Phani Raja P. “Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes.” 2015. Thesis, University of Illinois – Chicago. Accessed October 17, 2019. http://hdl.handle.net/10027/19456.

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

MLA Handbook (7th Edition):

Mamidipalli, Phani Raja P. “Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes.” 2015. Web. 17 Oct 2019.

Vancouver:

Mamidipalli PRP. Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10027/19456.

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

Council of Science Editors:

Mamidipalli PRP. Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19456

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

4. Bartlett, Mark J. Transition Metal Catalyzed Linchpin-Based Strategies in Natural Product Synthesis: Synthesis of Asteriscunolide D, Aspergillide B and the Core of Labillarides E-H.

Degree: 2013, Victoria University of Wellington

 The construction of complex molecular architectures in a facile and efficient manner remains an overarching goal for the chemical sciences. The development of synthetic linchpins,… (more)

Subjects/Keywords: Synthesis; Natural products; Catalyzed

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APA (6th Edition):

Bartlett, M. J. (2013). Transition Metal Catalyzed Linchpin-Based Strategies in Natural Product Synthesis: Synthesis of Asteriscunolide D, Aspergillide B and the Core of Labillarides E-H. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/2656

Chicago Manual of Style (16th Edition):

Bartlett, Mark J. “Transition Metal Catalyzed Linchpin-Based Strategies in Natural Product Synthesis: Synthesis of Asteriscunolide D, Aspergillide B and the Core of Labillarides E-H.” 2013. Doctoral Dissertation, Victoria University of Wellington. Accessed October 17, 2019. http://hdl.handle.net/10063/2656.

MLA Handbook (7th Edition):

Bartlett, Mark J. “Transition Metal Catalyzed Linchpin-Based Strategies in Natural Product Synthesis: Synthesis of Asteriscunolide D, Aspergillide B and the Core of Labillarides E-H.” 2013. Web. 17 Oct 2019.

Vancouver:

Bartlett MJ. Transition Metal Catalyzed Linchpin-Based Strategies in Natural Product Synthesis: Synthesis of Asteriscunolide D, Aspergillide B and the Core of Labillarides E-H. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2013. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10063/2656.

Council of Science Editors:

Bartlett MJ. Transition Metal Catalyzed Linchpin-Based Strategies in Natural Product Synthesis: Synthesis of Asteriscunolide D, Aspergillide B and the Core of Labillarides E-H. [Doctoral Dissertation]. Victoria University of Wellington; 2013. Available from: http://hdl.handle.net/10063/2656


Queens University

5. Negru, Elena Daniela. Rhodium-Catalyzed Carbocyclizations of Alkylidenecyclopropanes with Allenes and Carbon Monoxide: Stereoselective Construction of Six- and Seven-Membered Rings .

Degree: Chemistry, 2015, Queens University

 This thesis is divided in the following manner: Chapter 1 offers a short introduction, Chapter 2 describes the higher-order rhodium-catalyzed semi-intermolecular [(3+2)+2] carbocyclizations of alkylidenecyclopropanes… (more)

Subjects/Keywords: rhodium-catalyzed carbocyclizations; alkylidenecyclopropanes

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APA (6th Edition):

Negru, E. D. (2015). Rhodium-Catalyzed Carbocyclizations of Alkylidenecyclopropanes with Allenes and Carbon Monoxide: Stereoselective Construction of Six- and Seven-Membered Rings . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13839

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):

Negru, Elena Daniela. “Rhodium-Catalyzed Carbocyclizations of Alkylidenecyclopropanes with Allenes and Carbon Monoxide: Stereoselective Construction of Six- and Seven-Membered Rings .” 2015. Thesis, Queens University. Accessed October 17, 2019. http://hdl.handle.net/1974/13839.

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

MLA Handbook (7th Edition):

Negru, Elena Daniela. “Rhodium-Catalyzed Carbocyclizations of Alkylidenecyclopropanes with Allenes and Carbon Monoxide: Stereoselective Construction of Six- and Seven-Membered Rings .” 2015. Web. 17 Oct 2019.

Vancouver:

Negru ED. Rhodium-Catalyzed Carbocyclizations of Alkylidenecyclopropanes with Allenes and Carbon Monoxide: Stereoselective Construction of Six- and Seven-Membered Rings . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1974/13839.

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

Council of Science Editors:

Negru ED. Rhodium-Catalyzed Carbocyclizations of Alkylidenecyclopropanes with Allenes and Carbon Monoxide: Stereoselective Construction of Six- and Seven-Membered Rings . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13839

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


University of Guelph

6. Petko, Dina. Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition .

Degree: 2018, University of Guelph

 Synthetic organic chemistry is an integral part of pharmaceutical design and development, which builds upon past literature to create molecules that mimic nature. The synthesis… (more)

Subjects/Keywords: Ruthenium; catalyzed; cycloaddition; Diels-Alder

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APA (6th Edition):

Petko, D. (2018). Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14094

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):

Petko, Dina. “Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition .” 2018. Thesis, University of Guelph. Accessed October 17, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14094.

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

MLA Handbook (7th Edition):

Petko, Dina. “Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition .” 2018. Web. 17 Oct 2019.

Vancouver:

Petko D. Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition . [Internet] [Thesis]. University of Guelph; 2018. [cited 2019 Oct 17]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14094.

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

Council of Science Editors:

Petko D. Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition . [Thesis]. University of Guelph; 2018. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14094

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


Anna University

7. Raja M. Meso Tetraphenylporphyriniron Iii Chloride Catalyzed Oxidation Of Aniline And Its Substituents;.

Degree: chemistry, 2013, Anna University

Chemists have shown a great deal of attention towards modeling newlineof cytochrome P450 monooxygenase using synthetic metalloporphyrins as newlinethey have a strapping resemblance to heme… (more)

Subjects/Keywords: Aniline; Catalyzed; Meso; Oxidation; Substituents; Tetraphenylporphyriniron

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APA (6th Edition):

M, R. (2013). Meso Tetraphenylporphyriniron Iii Chloride Catalyzed Oxidation Of Aniline And Its Substituents;. (Thesis). Anna University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/27784

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):

M, Raja. “Meso Tetraphenylporphyriniron Iii Chloride Catalyzed Oxidation Of Aniline And Its Substituents;.” 2013. Thesis, Anna University. Accessed October 17, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/27784.

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

MLA Handbook (7th Edition):

M, Raja. “Meso Tetraphenylporphyriniron Iii Chloride Catalyzed Oxidation Of Aniline And Its Substituents;.” 2013. Web. 17 Oct 2019.

Vancouver:

M R. Meso Tetraphenylporphyriniron Iii Chloride Catalyzed Oxidation Of Aniline And Its Substituents;. [Internet] [Thesis]. Anna University; 2013. [cited 2019 Oct 17]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/27784.

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

Council of Science Editors:

M R. Meso Tetraphenylporphyriniron Iii Chloride Catalyzed Oxidation Of Aniline And Its Substituents;. [Thesis]. Anna University; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/27784

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


Texas A&M University

8. Matla, Andrea Slava. Expanding the scope of the nucleophile catalyzed aldol lactonization (NCALl) process and transformations of the resulting beta-lactones.

Degree: 2009, Texas A&M University

 Expanding the uses of the NCAL and finding the spectrum of substrates best suited for such a transformation has been the main effort of my… (more)

Subjects/Keywords: nucleophile catalyzed aldol lactonization (NCAL); beta-lactones

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APA (6th Edition):

Matla, A. S. (2009). Expanding the scope of the nucleophile catalyzed aldol lactonization (NCALl) process and transformations of the resulting beta-lactones. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2676

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):

Matla, Andrea Slava. “Expanding the scope of the nucleophile catalyzed aldol lactonization (NCALl) process and transformations of the resulting beta-lactones.” 2009. Thesis, Texas A&M University. Accessed October 17, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2676.

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

MLA Handbook (7th Edition):

Matla, Andrea Slava. “Expanding the scope of the nucleophile catalyzed aldol lactonization (NCALl) process and transformations of the resulting beta-lactones.” 2009. Web. 17 Oct 2019.

Vancouver:

Matla AS. Expanding the scope of the nucleophile catalyzed aldol lactonization (NCALl) process and transformations of the resulting beta-lactones. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2676.

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

Council of Science Editors:

Matla AS. Expanding the scope of the nucleophile catalyzed aldol lactonization (NCALl) process and transformations of the resulting beta-lactones. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2676

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


Penn State University

9. Lu, Chengxi. Palladium-catalyzed Halogenation Of Ortho-c-h Bonds Of Benzylamine Picolinamides And Arylethylamine Picolinamides.

Degree: MS, Chemistry, 2012, Penn State University

 A new Pd-catalyzed picolinamide-directed halogenation reaction of ortho-C(sp2)-H bonds is discussed. The usage of inexpensive inorganic salt (KBrO3, NaClO3/NaClO2 and KIO3) as halide source and… (more)

Subjects/Keywords: Pd-catalyzed; C-H activation; Halogenation

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APA (6th Edition):

Lu, C. (2012). Palladium-catalyzed Halogenation Of Ortho-c-h Bonds Of Benzylamine Picolinamides And Arylethylamine Picolinamides. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/21598

Chicago Manual of Style (16th Edition):

Lu, Chengxi. “Palladium-catalyzed Halogenation Of Ortho-c-h Bonds Of Benzylamine Picolinamides And Arylethylamine Picolinamides.” 2012. Masters Thesis, Penn State University. Accessed October 17, 2019. https://etda.libraries.psu.edu/catalog/21598.

MLA Handbook (7th Edition):

Lu, Chengxi. “Palladium-catalyzed Halogenation Of Ortho-c-h Bonds Of Benzylamine Picolinamides And Arylethylamine Picolinamides.” 2012. Web. 17 Oct 2019.

Vancouver:

Lu C. Palladium-catalyzed Halogenation Of Ortho-c-h Bonds Of Benzylamine Picolinamides And Arylethylamine Picolinamides. [Internet] [Masters thesis]. Penn State University; 2012. [cited 2019 Oct 17]. Available from: https://etda.libraries.psu.edu/catalog/21598.

Council of Science Editors:

Lu C. Palladium-catalyzed Halogenation Of Ortho-c-h Bonds Of Benzylamine Picolinamides And Arylethylamine Picolinamides. [Masters Thesis]. Penn State University; 2012. Available from: https://etda.libraries.psu.edu/catalog/21598


University of California – Berkeley

10. Sethofer, Steven Gregory. The Development and Application of Gold(I)-Catalyzed Cyclization Cascades.

Degree: Chemistry, 2011, University of California – Berkeley

 The formation of saturated carbon-carbon bonds in a precise andcontrolled manner is arguably the principal objective of organic synthesis.Carbocyclic ring systems comprise the underlying structure… (more)

Subjects/Keywords: Chemistry; Carbocyclization; Catalyzed; Cycloisomerization; Enyne; Gold; Polycyclization

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APA (6th Edition):

Sethofer, S. G. (2011). The Development and Application of Gold(I)-Catalyzed Cyclization Cascades. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/48j418nx

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):

Sethofer, Steven Gregory. “The Development and Application of Gold(I)-Catalyzed Cyclization Cascades.” 2011. Thesis, University of California – Berkeley. Accessed October 17, 2019. http://www.escholarship.org/uc/item/48j418nx.

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

MLA Handbook (7th Edition):

Sethofer, Steven Gregory. “The Development and Application of Gold(I)-Catalyzed Cyclization Cascades.” 2011. Web. 17 Oct 2019.

Vancouver:

Sethofer SG. The Development and Application of Gold(I)-Catalyzed Cyclization Cascades. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2019 Oct 17]. Available from: http://www.escholarship.org/uc/item/48j418nx.

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

Council of Science Editors:

Sethofer SG. The Development and Application of Gold(I)-Catalyzed Cyclization Cascades. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/48j418nx

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


Duke University

11. Duncan, Alethea. Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles .

Degree: 2011, Duke University

  The importance of nitrogen-containing compounds in human life has drawn us to focus on the preparation of amine derivatives, combined with the limitations associated… (more)

Subjects/Keywords: Chemistry; allenes; Gold-catalyzed; hydroalkoxylation; hydroamination; Hydrofunctionilzation

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APA (6th Edition):

Duncan, A. (2011). Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/5654

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):

Duncan, Alethea. “Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles .” 2011. Thesis, Duke University. Accessed October 17, 2019. http://hdl.handle.net/10161/5654.

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

MLA Handbook (7th Edition):

Duncan, Alethea. “Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles .” 2011. Web. 17 Oct 2019.

Vancouver:

Duncan A. Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles . [Internet] [Thesis]. Duke University; 2011. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10161/5654.

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

Council of Science Editors:

Duncan A. Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles . [Thesis]. Duke University; 2011. Available from: http://hdl.handle.net/10161/5654

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


Wayne State University

12. Ariyasena, Thiloka Chandima. (i)chromatographic Methods For Solute Descriptor Determinations (ii)ruthenium Substrate-Catalyzed Growth Of Nickel Nitride Thin Films By Atomic Layer Deposition.

Degree: PhD, Chemistry, 2015, Wayne State University

  Determination of distribution levels of environmentally important compounds in various environmental compartments is a major procedure in many fields including environmental risk assessment, food… (more)

Subjects/Keywords: ALD; Catalyzed; Chromatographic; Descriptor; Ruthenium; Substrate; Chemistry

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APA (6th Edition):

Ariyasena, T. C. (2015). (i)chromatographic Methods For Solute Descriptor Determinations (ii)ruthenium Substrate-Catalyzed Growth Of Nickel Nitride Thin Films By Atomic Layer Deposition. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1114

Chicago Manual of Style (16th Edition):

Ariyasena, Thiloka Chandima. “(i)chromatographic Methods For Solute Descriptor Determinations (ii)ruthenium Substrate-Catalyzed Growth Of Nickel Nitride Thin Films By Atomic Layer Deposition.” 2015. Doctoral Dissertation, Wayne State University. Accessed October 17, 2019. https://digitalcommons.wayne.edu/oa_dissertations/1114.

MLA Handbook (7th Edition):

Ariyasena, Thiloka Chandima. “(i)chromatographic Methods For Solute Descriptor Determinations (ii)ruthenium Substrate-Catalyzed Growth Of Nickel Nitride Thin Films By Atomic Layer Deposition.” 2015. Web. 17 Oct 2019.

Vancouver:

Ariyasena TC. (i)chromatographic Methods For Solute Descriptor Determinations (ii)ruthenium Substrate-Catalyzed Growth Of Nickel Nitride Thin Films By Atomic Layer Deposition. [Internet] [Doctoral dissertation]. Wayne State University; 2015. [cited 2019 Oct 17]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1114.

Council of Science Editors:

Ariyasena TC. (i)chromatographic Methods For Solute Descriptor Determinations (ii)ruthenium Substrate-Catalyzed Growth Of Nickel Nitride Thin Films By Atomic Layer Deposition. [Doctoral Dissertation]. Wayne State University; 2015. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1114


University of Illinois – Urbana-Champaign

13. Madrahimov, Sherzod. Mechanistic studies on iridium catalyzed allylic substitution.

Degree: PhD, 0335, 2012, University of Illinois – Urbana-Champaign

 Mechanistic studies on iridium catalyzed allylic substitution reactions catalyzed by iridium phosphoramidite complexes revealed that the active catalyst is generated through a base assisted cyclometalation… (more)

Subjects/Keywords: allylic substitution; mechanistic studies; iridium catalyzed

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APA (6th Edition):

Madrahimov, S. (2012). Mechanistic studies on iridium catalyzed allylic substitution. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/34371

Chicago Manual of Style (16th Edition):

Madrahimov, Sherzod. “Mechanistic studies on iridium catalyzed allylic substitution.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 17, 2019. http://hdl.handle.net/2142/34371.

MLA Handbook (7th Edition):

Madrahimov, Sherzod. “Mechanistic studies on iridium catalyzed allylic substitution.” 2012. Web. 17 Oct 2019.

Vancouver:

Madrahimov S. Mechanistic studies on iridium catalyzed allylic substitution. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2142/34371.

Council of Science Editors:

Madrahimov S. Mechanistic studies on iridium catalyzed allylic substitution. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/34371


Boston College

14. Hong, Kai. Platinum-Catalyzed Enantioselective Diboration of 1,3-Dienes and Imines and Functionalization of 1,2- and Geminal Bis(boronic) Esters.

Degree: PhD, Chemistry, 2015, Boston College

 Platinum-catalyzed enantioselective 1,4-diboration of cyclic 1,3-dienes is reported, providing enantioenriched 1,4-bis(boronic) esters in good yield and up to 96:4 er. The analogous diboration reaction of… (more)

Subjects/Keywords: Alkylation; Allylboration; Diboration; Diene; Imine; Pt-catalyzed

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APA (6th Edition):

Hong, K. (2015). Platinum-Catalyzed Enantioselective Diboration of 1,3-Dienes and Imines and Functionalization of 1,2- and Geminal Bis(boronic) Esters. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104130

Chicago Manual of Style (16th Edition):

Hong, Kai. “Platinum-Catalyzed Enantioselective Diboration of 1,3-Dienes and Imines and Functionalization of 1,2- and Geminal Bis(boronic) Esters.” 2015. Doctoral Dissertation, Boston College. Accessed October 17, 2019. http://dlib.bc.edu/islandora/object/bc-ir:104130.

MLA Handbook (7th Edition):

Hong, Kai. “Platinum-Catalyzed Enantioselective Diboration of 1,3-Dienes and Imines and Functionalization of 1,2- and Geminal Bis(boronic) Esters.” 2015. Web. 17 Oct 2019.

Vancouver:

Hong K. Platinum-Catalyzed Enantioselective Diboration of 1,3-Dienes and Imines and Functionalization of 1,2- and Geminal Bis(boronic) Esters. [Internet] [Doctoral dissertation]. Boston College; 2015. [cited 2019 Oct 17]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104130.

Council of Science Editors:

Hong K. Platinum-Catalyzed Enantioselective Diboration of 1,3-Dienes and Imines and Functionalization of 1,2- and Geminal Bis(boronic) Esters. [Doctoral Dissertation]. Boston College; 2015. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104130


Boston College

15. Stephani, Carolynn Kay. Artificial Photosynthesis: An Investigation of Silicon Nanowires in Nickel Catalyzed Carboxylation.

Degree: MS, Chemistry, 2014, Boston College

 Silicon nanowires are utilized to harvest the energy from visible light. The introduction of a nickel pre-catalyst, 1, allows for this energy to be stored… (more)

Subjects/Keywords: artificial photosynthesis; carboxylation; catalyzed; nickel; silicon nanowires

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APA (6th Edition):

Stephani, C. K. (2014). Artificial Photosynthesis: An Investigation of Silicon Nanowires in Nickel Catalyzed Carboxylation. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101266

Chicago Manual of Style (16th Edition):

Stephani, Carolynn Kay. “Artificial Photosynthesis: An Investigation of Silicon Nanowires in Nickel Catalyzed Carboxylation.” 2014. Masters Thesis, Boston College. Accessed October 17, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101266.

MLA Handbook (7th Edition):

Stephani, Carolynn Kay. “Artificial Photosynthesis: An Investigation of Silicon Nanowires in Nickel Catalyzed Carboxylation.” 2014. Web. 17 Oct 2019.

Vancouver:

Stephani CK. Artificial Photosynthesis: An Investigation of Silicon Nanowires in Nickel Catalyzed Carboxylation. [Internet] [Masters thesis]. Boston College; 2014. [cited 2019 Oct 17]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101266.

Council of Science Editors:

Stephani CK. Artificial Photosynthesis: An Investigation of Silicon Nanowires in Nickel Catalyzed Carboxylation. [Masters Thesis]. Boston College; 2014. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101266


University of Michigan

16. Todd, David. Development of Nickel-Catalyzed Methods for Deoxygenation Processes.

Degree: PhD, Chemistry, 2017, University of Michigan

 A new method for the reductive coupling of enals or enones and alkynes has been developed. The method results in a unique net four-electron reduction… (more)

Subjects/Keywords: Nickel-Catalyzed Methods; Deoxygenation Processes; Chemistry; Science

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APA (6th Edition):

Todd, D. (2017). Development of Nickel-Catalyzed Methods for Deoxygenation Processes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/137174

Chicago Manual of Style (16th Edition):

Todd, David. “Development of Nickel-Catalyzed Methods for Deoxygenation Processes.” 2017. Doctoral Dissertation, University of Michigan. Accessed October 17, 2019. http://hdl.handle.net/2027.42/137174.

MLA Handbook (7th Edition):

Todd, David. “Development of Nickel-Catalyzed Methods for Deoxygenation Processes.” 2017. Web. 17 Oct 2019.

Vancouver:

Todd D. Development of Nickel-Catalyzed Methods for Deoxygenation Processes. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2027.42/137174.

Council of Science Editors:

Todd D. Development of Nickel-Catalyzed Methods for Deoxygenation Processes. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/137174


University of Michigan

17. Jackson, Evan P. Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes.

Degree: PhD, Chemistry, 2015, University of Michigan

 Advances in nickel catalyzed reactions have been achieved that allow for alteration and control of the rate- and regioselectivity determining step in nickel-catalyzed aldehyde-alkyne reductive… (more)

Subjects/Keywords: Ni-Catalyzed Reductive Couplings; Chemistry; Science

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APA (6th Edition):

Jackson, E. P. (2015). Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113425

Chicago Manual of Style (16th Edition):

Jackson, Evan P. “Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes.” 2015. Doctoral Dissertation, University of Michigan. Accessed October 17, 2019. http://hdl.handle.net/2027.42/113425.

MLA Handbook (7th Edition):

Jackson, Evan P. “Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes.” 2015. Web. 17 Oct 2019.

Vancouver:

Jackson EP. Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2027.42/113425.

Council of Science Editors:

Jackson EP. Advances in Regiocontrol and Bench Stability in Nickel Catalyzed Reductive Couplings of Aldehydes and Alkynes. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113425


University of Michigan

18. Kubota, Asako. Pd-Catalyzed Oxidative Functionalizations.

Degree: PhD, Chemistry, 2012, University of Michigan

 A traditional Pd(0/II) mechanism is commonly evoked for a number of well-known cross-coupling reactions (i.e. Heck, Suzuki, Negishi, etc). In recent years, there has been… (more)

Subjects/Keywords: Pd-catalyzed Olefin Difunctionalization; Chemistry; Science

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APA (6th Edition):

Kubota, A. (2012). Pd-Catalyzed Oxidative Functionalizations. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/94086

Chicago Manual of Style (16th Edition):

Kubota, Asako. “Pd-Catalyzed Oxidative Functionalizations.” 2012. Doctoral Dissertation, University of Michigan. Accessed October 17, 2019. http://hdl.handle.net/2027.42/94086.

MLA Handbook (7th Edition):

Kubota, Asako. “Pd-Catalyzed Oxidative Functionalizations.” 2012. Web. 17 Oct 2019.

Vancouver:

Kubota A. Pd-Catalyzed Oxidative Functionalizations. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2027.42/94086.

Council of Science Editors:

Kubota A. Pd-Catalyzed Oxidative Functionalizations. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/94086


University of Michigan

19. Baxter, Ryan David. Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes.

Degree: PhD, Chemistry, 2010, University of Michigan

 Many classes of standard organic transformations involve the coupling or cycloaddition of two different π-components to assemble a more functionalized product. Many such processes are… (more)

Subjects/Keywords: Nickel Catalyzed Reductive Coupling; Chemistry; Science

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APA (6th Edition):

Baxter, R. D. (2010). Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/78979

Chicago Manual of Style (16th Edition):

Baxter, Ryan David. “Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes.” 2010. Doctoral Dissertation, University of Michigan. Accessed October 17, 2019. http://hdl.handle.net/2027.42/78979.

MLA Handbook (7th Edition):

Baxter, Ryan David. “Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes.” 2010. Web. 17 Oct 2019.

Vancouver:

Baxter RD. Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2027.42/78979.

Council of Science Editors:

Baxter RD. Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/78979


University of Michigan

20. Malik, Hasnain A. Strategies for Regio- and Enantiocontrol in Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes.

Degree: PhD, Chemistry, 2011, University of Michigan

 A highly regioselective nickel-catalyzed reductive couplings of propargyl alcohol derivatives and aldehydes have been developed. Consideration of the interplay of sterics and electronics between reactive… (more)

Subjects/Keywords: Nickel-Catalyzed Reductive Couplings; Chemistry; Science

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APA (6th Edition):

Malik, H. A. (2011). Strategies for Regio- and Enantiocontrol in Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/84656

Chicago Manual of Style (16th Edition):

Malik, Hasnain A. “Strategies for Regio- and Enantiocontrol in Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes.” 2011. Doctoral Dissertation, University of Michigan. Accessed October 17, 2019. http://hdl.handle.net/2027.42/84656.

MLA Handbook (7th Edition):

Malik, Hasnain A. “Strategies for Regio- and Enantiocontrol in Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes.” 2011. Web. 17 Oct 2019.

Vancouver:

Malik HA. Strategies for Regio- and Enantiocontrol in Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2027.42/84656.

Council of Science Editors:

Malik HA. Strategies for Regio- and Enantiocontrol in Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/84656

21. Shukla, Satya Prakash. Iodine mediated and metal catalyzed synthesis of heterocycles via electrophilic 6 endo dig ring closure of alkynes; -.

Degree: Chemistry, 2012, University of Delhi

Available

-

Advisors/Committee Members: Verma, Akhilesh Kumar and Chauhan, S M S.

Subjects/Keywords: catalyzed synthesis; heterocycles; Iodine mediated; metal catalyzed

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APA (6th Edition):

Shukla, S. P. (2012). Iodine mediated and metal catalyzed synthesis of heterocycles via electrophilic 6 endo dig ring closure of alkynes; -. (Thesis). University of Delhi. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/31471

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):

Shukla, Satya Prakash. “Iodine mediated and metal catalyzed synthesis of heterocycles via electrophilic 6 endo dig ring closure of alkynes; -.” 2012. Thesis, University of Delhi. Accessed October 17, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/31471.

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

MLA Handbook (7th Edition):

Shukla, Satya Prakash. “Iodine mediated and metal catalyzed synthesis of heterocycles via electrophilic 6 endo dig ring closure of alkynes; -.” 2012. Web. 17 Oct 2019.

Vancouver:

Shukla SP. Iodine mediated and metal catalyzed synthesis of heterocycles via electrophilic 6 endo dig ring closure of alkynes; -. [Internet] [Thesis]. University of Delhi; 2012. [cited 2019 Oct 17]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/31471.

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

Council of Science Editors:

Shukla SP. Iodine mediated and metal catalyzed synthesis of heterocycles via electrophilic 6 endo dig ring closure of alkynes; -. [Thesis]. University of Delhi; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/31471

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


NSYSU

22. Huang, Nan-Yuan. Development of New Synthesis of Sulfur-oxazoline Ligands.

Degree: Master, Chemistry, 2011, NSYSU

 This thesis is the use of commercially available methyl 2-iodobenzoate as the starting material and was prepared into iodine - oxazoline compound 118. Then, we… (more)

Subjects/Keywords: CuI-catalyzed reaction; Iodooxazoline; Pd-catalyzed asymmetric alkylation; Carbon-sulfur coupling reaction; Chiral sulfur-oxazoline ligands

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APA (6th Edition):

Huang, N. (2011). Development of New Synthesis of Sulfur-oxazoline Ligands. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108

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):

Huang, Nan-Yuan. “Development of New Synthesis of Sulfur-oxazoline Ligands.” 2011. Thesis, NSYSU. Accessed October 17, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108.

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

MLA Handbook (7th Edition):

Huang, Nan-Yuan. “Development of New Synthesis of Sulfur-oxazoline Ligands.” 2011. Web. 17 Oct 2019.

Vancouver:

Huang N. Development of New Synthesis of Sulfur-oxazoline Ligands. [Internet] [Thesis]. NSYSU; 2011. [cited 2019 Oct 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108.

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

Council of Science Editors:

Huang N. Development of New Synthesis of Sulfur-oxazoline Ligands. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108

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


Queens University

23. Dalziel, Michael. Advances in Directed Ortho Metalation: Copper- and Rhodium-Catalyzed Allylic Substitution and the DMG Dance .

Degree: Chemistry, 2015, Queens University

 Chapter one of this thesis describes preliminary efforts towards the development of the rhodium-catalyzed allylic arylation reaction employing nucleophiles containing ortho-DMGs (directed metalation groups). Unfortunately,… (more)

Subjects/Keywords: Copper-Catalyzed Allylic Substitution; DMG Dance; 7-Azaindole; Directed Ortho Metalation; Rhodium-Catalyzed Allylic Substitution; Hard Nucleophiles

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APA (6th Edition):

Dalziel, M. (2015). Advances in Directed Ortho Metalation: Copper- and Rhodium-Catalyzed Allylic Substitution and the DMG Dance . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13501

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):

Dalziel, Michael. “Advances in Directed Ortho Metalation: Copper- and Rhodium-Catalyzed Allylic Substitution and the DMG Dance .” 2015. Thesis, Queens University. Accessed October 17, 2019. http://hdl.handle.net/1974/13501.

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

MLA Handbook (7th Edition):

Dalziel, Michael. “Advances in Directed Ortho Metalation: Copper- and Rhodium-Catalyzed Allylic Substitution and the DMG Dance .” 2015. Web. 17 Oct 2019.

Vancouver:

Dalziel M. Advances in Directed Ortho Metalation: Copper- and Rhodium-Catalyzed Allylic Substitution and the DMG Dance . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1974/13501.

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

Council of Science Editors:

Dalziel M. Advances in Directed Ortho Metalation: Copper- and Rhodium-Catalyzed Allylic Substitution and the DMG Dance . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13501

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

24. Xu, Lusha. Development of Palladium Catalyzed Alkene Difunctionalization on Vinyl-Quinoline Type Substrate and Isolation of Pd-Alkyl Intermediate.

Degree: MS, Chemistry and Biochemistry, 2016, U of Denver

  The synthesis of quinoline derivatives is a continuing issue facing organic chemists in both academia and industry. To address this problem, palladium-catalyzed alkene difunctionalization… (more)

Subjects/Keywords: 8-Vinylquinoline; Alkene; Catalyzed; Difunctionalization; Oxidation; Palladium; Chemistry

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APA (6th Edition):

Xu, L. (2016). Development of Palladium Catalyzed Alkene Difunctionalization on Vinyl-Quinoline Type Substrate and Isolation of Pd-Alkyl Intermediate. (Thesis). U of Denver. Retrieved from https://digitalcommons.du.edu/etd/1185

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):

Xu, Lusha. “Development of Palladium Catalyzed Alkene Difunctionalization on Vinyl-Quinoline Type Substrate and Isolation of Pd-Alkyl Intermediate.” 2016. Thesis, U of Denver. Accessed October 17, 2019. https://digitalcommons.du.edu/etd/1185.

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

MLA Handbook (7th Edition):

Xu, Lusha. “Development of Palladium Catalyzed Alkene Difunctionalization on Vinyl-Quinoline Type Substrate and Isolation of Pd-Alkyl Intermediate.” 2016. Web. 17 Oct 2019.

Vancouver:

Xu L. Development of Palladium Catalyzed Alkene Difunctionalization on Vinyl-Quinoline Type Substrate and Isolation of Pd-Alkyl Intermediate. [Internet] [Thesis]. U of Denver; 2016. [cited 2019 Oct 17]. Available from: https://digitalcommons.du.edu/etd/1185.

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

Council of Science Editors:

Xu L. Development of Palladium Catalyzed Alkene Difunctionalization on Vinyl-Quinoline Type Substrate and Isolation of Pd-Alkyl Intermediate. [Thesis]. U of Denver; 2016. Available from: https://digitalcommons.du.edu/etd/1185

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


University of Utah

25. Liao, Longyan. Development of palladium-catalyzed difunctionalization reactions of 1,3-dienes and alkenes.

Degree: PhD, Chemistry, 2012, University of Utah

 Palladium (Pd)-catalyzed alkene difunctionalization reactions have been an active area of research in recent years. Expanding the diversity of alkene functionalization reactions to strategically impact… (more)

Subjects/Keywords: 1,3-dienes; Difunctionalization; Palladium-catalyzed; Allylpalladium; Benzylpalladium; Terminal alkenes

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APA (6th Edition):

Liao, L. (2012). Development of palladium-catalyzed difunctionalization reactions of 1,3-dienes and alkenes. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3453/rec/715

Chicago Manual of Style (16th Edition):

Liao, Longyan. “Development of palladium-catalyzed difunctionalization reactions of 1,3-dienes and alkenes.” 2012. Doctoral Dissertation, University of Utah. Accessed October 17, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3453/rec/715.

MLA Handbook (7th Edition):

Liao, Longyan. “Development of palladium-catalyzed difunctionalization reactions of 1,3-dienes and alkenes.” 2012. Web. 17 Oct 2019.

Vancouver:

Liao L. Development of palladium-catalyzed difunctionalization reactions of 1,3-dienes and alkenes. [Internet] [Doctoral dissertation]. University of Utah; 2012. [cited 2019 Oct 17]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3453/rec/715.

Council of Science Editors:

Liao L. Development of palladium-catalyzed difunctionalization reactions of 1,3-dienes and alkenes. [Doctoral Dissertation]. University of Utah; 2012. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3453/rec/715


University of Alberta

26. Fatemi, Solmaz. Improved Gram-Scale Procedure for MIBA-Catalyzed Direct Amidation and Its Application to the Preparation of alpha and beta Peptides.

Degree: MS, Department of Chemistry, 2015, University of Alberta

 Direct condensation between a carboxylic acid and amine must overcome the initial formation of a thermodynamically stable and unreactive carboxylate-ammonium salt, providing the amide product… (more)

Subjects/Keywords: MIBA-Catalyzed; Direct Amidation; alpha and beta Peptides

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APA (6th Edition):

Fatemi, S. (2015). Improved Gram-Scale Procedure for MIBA-Catalyzed Direct Amidation and Its Application to the Preparation of alpha and beta Peptides. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/chx11xf25b

Chicago Manual of Style (16th Edition):

Fatemi, Solmaz. “Improved Gram-Scale Procedure for MIBA-Catalyzed Direct Amidation and Its Application to the Preparation of alpha and beta Peptides.” 2015. Masters Thesis, University of Alberta. Accessed October 17, 2019. https://era.library.ualberta.ca/files/chx11xf25b.

MLA Handbook (7th Edition):

Fatemi, Solmaz. “Improved Gram-Scale Procedure for MIBA-Catalyzed Direct Amidation and Its Application to the Preparation of alpha and beta Peptides.” 2015. Web. 17 Oct 2019.

Vancouver:

Fatemi S. Improved Gram-Scale Procedure for MIBA-Catalyzed Direct Amidation and Its Application to the Preparation of alpha and beta Peptides. [Internet] [Masters thesis]. University of Alberta; 2015. [cited 2019 Oct 17]. Available from: https://era.library.ualberta.ca/files/chx11xf25b.

Council of Science Editors:

Fatemi S. Improved Gram-Scale Procedure for MIBA-Catalyzed Direct Amidation and Its Application to the Preparation of alpha and beta Peptides. [Masters Thesis]. University of Alberta; 2015. Available from: https://era.library.ualberta.ca/files/chx11xf25b


NSYSU

27. Su, Yung-yu. Solid-phase Cyclic Tetrapeptide Synthesis via Cu(I)-catalyzed Denitrogenative Annulation.

Degree: Master, Chemistry, 2017, NSYSU

 In this research, a Cu(I)-catalyzed denitrogenative reaction has been used in the solid-phase synthesis of cyclic tetrapeptide. First, the hydrolysis of a linear tripeptide has… (more)

Subjects/Keywords: tosyl-amidine; hydrolysis; SPPS; cyclic tetrapeptide; Cu-catalyzed

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APA (6th Edition):

Su, Y. (2017). Solid-phase Cyclic Tetrapeptide Synthesis via Cu(I)-catalyzed Denitrogenative Annulation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0702117-014153

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):

Su, Yung-yu. “Solid-phase Cyclic Tetrapeptide Synthesis via Cu(I)-catalyzed Denitrogenative Annulation.” 2017. Thesis, NSYSU. Accessed October 17, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0702117-014153.

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

MLA Handbook (7th Edition):

Su, Yung-yu. “Solid-phase Cyclic Tetrapeptide Synthesis via Cu(I)-catalyzed Denitrogenative Annulation.” 2017. Web. 17 Oct 2019.

Vancouver:

Su Y. Solid-phase Cyclic Tetrapeptide Synthesis via Cu(I)-catalyzed Denitrogenative Annulation. [Internet] [Thesis]. NSYSU; 2017. [cited 2019 Oct 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0702117-014153.

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

Council of Science Editors:

Su Y. Solid-phase Cyclic Tetrapeptide Synthesis via Cu(I)-catalyzed Denitrogenative Annulation. [Thesis]. NSYSU; 2017. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0702117-014153

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


Texas A&M University

28. Shirley, Morgan. ?-Lactones as Key Building Blocks: Synthetic Applications to Diverse Natural Products.

Degree: 2014, Texas A&M University

 A history and detailed account of the applications of ?-lactones towards natural products and bioactive compounds in the last ten years is discussed as these… (more)

Subjects/Keywords: NCMAL; Beta-lactones; NCAL; nucleophile catalyzed aldol-lactonization; caulolactone A

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

APA (6th Edition):

Shirley, M. (2014). ?-Lactones as Key Building Blocks: Synthetic Applications to Diverse Natural Products. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152839

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):

Shirley, Morgan. “?-Lactones as Key Building Blocks: Synthetic Applications to Diverse Natural Products.” 2014. Thesis, Texas A&M University. Accessed October 17, 2019. http://hdl.handle.net/1969.1/152839.

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

MLA Handbook (7th Edition):

Shirley, Morgan. “?-Lactones as Key Building Blocks: Synthetic Applications to Diverse Natural Products.” 2014. Web. 17 Oct 2019.

Vancouver:

Shirley M. ?-Lactones as Key Building Blocks: Synthetic Applications to Diverse Natural Products. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1969.1/152839.

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

Council of Science Editors:

Shirley M. ?-Lactones as Key Building Blocks: Synthetic Applications to Diverse Natural Products. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152839

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


NSYSU

29. Jhang, You-min. Synthesis of Bicyclic Tetrahydrothiophene Derivatives.

Degree: Master, Chemistry, 2017, NSYSU

 Tetrahydrothiophene derivatives are commonly found in the structures of natural products, these biologically active tetrahydrothiophene derivatives can be used as medicinal drugs. Tetrahydrothiophene derivatives also… (more)

Subjects/Keywords: cyclopenta[c]thiophene; Ruthenium catalyzed ring-closing metathesis; Claisen / Overman rearrangement

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

APA (6th Edition):

Jhang, Y. (2017). Synthesis of Bicyclic Tetrahydrothiophene Derivatives. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-174815

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):

Jhang, You-min. “Synthesis of Bicyclic Tetrahydrothiophene Derivatives.” 2017. Thesis, NSYSU. Accessed October 17, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-174815.

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

MLA Handbook (7th Edition):

Jhang, You-min. “Synthesis of Bicyclic Tetrahydrothiophene Derivatives.” 2017. Web. 17 Oct 2019.

Vancouver:

Jhang Y. Synthesis of Bicyclic Tetrahydrothiophene Derivatives. [Internet] [Thesis]. NSYSU; 2017. [cited 2019 Oct 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-174815.

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

Council of Science Editors:

Jhang Y. Synthesis of Bicyclic Tetrahydrothiophene Derivatives. [Thesis]. NSYSU; 2017. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-174815

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

30. Singh, Ritu. Kinetics of micelle catalyzed oxidation of toluidine;.

Degree: Chemistry, 2003, Aligarh Muslim University

Abstract not available newline newline newline

-

Advisors/Committee Members: Ahmad, Firoz.

Subjects/Keywords: Kinetics; Micelle; Catalyzed; Oxidation; Toluidine

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

APA (6th Edition):

Singh, R. (2003). Kinetics of micelle catalyzed oxidation of toluidine;. (Thesis). Aligarh Muslim University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/53669

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):

Singh, Ritu. “Kinetics of micelle catalyzed oxidation of toluidine;.” 2003. Thesis, Aligarh Muslim University. Accessed October 17, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/53669.

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

MLA Handbook (7th Edition):

Singh, Ritu. “Kinetics of micelle catalyzed oxidation of toluidine;.” 2003. Web. 17 Oct 2019.

Vancouver:

Singh R. Kinetics of micelle catalyzed oxidation of toluidine;. [Internet] [Thesis]. Aligarh Muslim University; 2003. [cited 2019 Oct 17]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/53669.

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

Council of Science Editors:

Singh R. Kinetics of micelle catalyzed oxidation of toluidine;. [Thesis]. Aligarh Muslim University; 2003. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/53669

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

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