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You searched for subject:(Coupling chemistry). Showing records 1 – 30 of 316 total matches.

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University of California – Irvine

1. Erickson, Lucas William. Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions.

Degree: Chemistry, 2017, University of California – Irvine

 In recent years, the Jarvo lab has developed the field of stereospecific nickel-catalyzed cross-coupling reactions of benzylic electrophiles. This chemistry allows for straightforward synthesis of… (more)

Subjects/Keywords: Chemistry; cross-coupling; cyclopropane; nickel; reductive coupling

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

APA (6th Edition):

Erickson, L. W. (2017). Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/3rr443q9

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):

Erickson, Lucas William. “Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions.” 2017. Thesis, University of California – Irvine. Accessed March 06, 2021. http://www.escholarship.org/uc/item/3rr443q9.

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

MLA Handbook (7th Edition):

Erickson, Lucas William. “Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions.” 2017. Web. 06 Mar 2021.

Vancouver:

Erickson LW. Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/3rr443q9.

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

Council of Science Editors:

Erickson LW. Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/3rr443q9

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


University of Gothenburg / Göteborgs Universitet

2. Hertzog, Manuel. Strong light-matter interaction and its consequences on molecular photophysics.

Degree: 2020, University of Gothenburg / Göteborgs Universitet

 Strong light-matter interaction offers the possibility to modify chemical and physical properties of molecules by modifying their photonic environment, resulting in the creation of hybrid… (more)

Subjects/Keywords: Strong coupling; Vibropolariton; Polaritonic Chemistry

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APA (6th Edition):

Hertzog, M. (2020). Strong light-matter interaction and its consequences on molecular photophysics. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/66473

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):

Hertzog, Manuel. “Strong light-matter interaction and its consequences on molecular photophysics.” 2020. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed March 06, 2021. http://hdl.handle.net/2077/66473.

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

MLA Handbook (7th Edition):

Hertzog, Manuel. “Strong light-matter interaction and its consequences on molecular photophysics.” 2020. Web. 06 Mar 2021.

Vancouver:

Hertzog M. Strong light-matter interaction and its consequences on molecular photophysics. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2020. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2077/66473.

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

Council of Science Editors:

Hertzog M. Strong light-matter interaction and its consequences on molecular photophysics. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2020. Available from: http://hdl.handle.net/2077/66473

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


University of California – San Diego

3. Lee, SangHyun. Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors.

Degree: Chemistry, 2018, University of California – San Diego

 Transition metal-catalyzed cross-coupling is a powerful methodology to strategically form carbon-carbon or carbon-heteroatom bonds. Advancements in cross-coupling strategies with diverse organometallic nucleophile reagents have been… (more)

Subjects/Keywords: Chemistry; cross-coupling; decarbonylative coupling; decarboxylative coupling; Hiyama-type; oxygenated precursors; radical-mediated coupling

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APA (6th Edition):

Lee, S. (2018). Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/5s81c8m1

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):

Lee, SangHyun. “Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors.” 2018. Thesis, University of California – San Diego. Accessed March 06, 2021. http://www.escholarship.org/uc/item/5s81c8m1.

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

MLA Handbook (7th Edition):

Lee, SangHyun. “Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors.” 2018. Web. 06 Mar 2021.

Vancouver:

Lee S. Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/5s81c8m1.

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

Council of Science Editors:

Lee S. Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/5s81c8m1

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


University of New Mexico

4. Shrestha, Bijay. Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel.

Degree: Department of Chemistry and Chemical Biology, 2018, University of New Mexico

  This thesis is divided into two parts. The first part focuses on the Cu-catalyzed cross-coupling of organoaluminum reagents with organohalides. One of the most… (more)

Subjects/Keywords: Cross-coupling; Dicarbofunctionalization; Chemistry; Organic Chemistry

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APA (6th Edition):

Shrestha, B. (2018). Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/chem_etds/99

Chicago Manual of Style (16th Edition):

Shrestha, Bijay. “Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel.” 2018. Doctoral Dissertation, University of New Mexico. Accessed March 06, 2021. https://digitalrepository.unm.edu/chem_etds/99.

MLA Handbook (7th Edition):

Shrestha, Bijay. “Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel.” 2018. Web. 06 Mar 2021.

Vancouver:

Shrestha B. Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel. [Internet] [Doctoral dissertation]. University of New Mexico; 2018. [cited 2021 Mar 06]. Available from: https://digitalrepository.unm.edu/chem_etds/99.

Council of Science Editors:

Shrestha B. Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel. [Doctoral Dissertation]. University of New Mexico; 2018. Available from: https://digitalrepository.unm.edu/chem_etds/99


University of Cincinnati

5. Rodrigo, Sanjeewa K. Nickel Catalyzed Regioselective Reductive Coupling Reactions.

Degree: PhD, Arts and Sciences: Chemistry, 2014, University of Cincinnati

Coupling or cycloaddition of two different p-components for the construction of more complex structural motifs is commonly used in organic synthesis. Most of these systems… (more)

Subjects/Keywords: Analytical Chemistry; Chemistry; reductive coupling reactions; cycloaddition

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APA (6th Edition):

Rodrigo, S. K. (2014). Nickel Catalyzed Regioselective Reductive Coupling Reactions. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622

Chicago Manual of Style (16th Edition):

Rodrigo, Sanjeewa K. “Nickel Catalyzed Regioselective Reductive Coupling Reactions.” 2014. Doctoral Dissertation, University of Cincinnati. Accessed March 06, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622.

MLA Handbook (7th Edition):

Rodrigo, Sanjeewa K. “Nickel Catalyzed Regioselective Reductive Coupling Reactions.” 2014. Web. 06 Mar 2021.

Vancouver:

Rodrigo SK. Nickel Catalyzed Regioselective Reductive Coupling Reactions. [Internet] [Doctoral dissertation]. University of Cincinnati; 2014. [cited 2021 Mar 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622.

Council of Science Editors:

Rodrigo SK. Nickel Catalyzed Regioselective Reductive Coupling Reactions. [Doctoral Dissertation]. University of Cincinnati; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622


University of California – Irvine

6. Hanna, Luke Edward. Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes.

Degree: Chemistry, 2016, University of California – Irvine

 Cross-coupling technology has become an indispensable tool for the rapid and efficient synthesis of complex molecules. Over the past few decades a foundational understanding of… (more)

Subjects/Keywords: Chemistry; Catalysis; Cross-Coupling; Nickel; Organic

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APA (6th Edition):

Hanna, L. E. (2016). Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/83p514vc

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):

Hanna, Luke Edward. “Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes.” 2016. Thesis, University of California – Irvine. Accessed March 06, 2021. http://www.escholarship.org/uc/item/83p514vc.

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

MLA Handbook (7th Edition):

Hanna, Luke Edward. “Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes.” 2016. Web. 06 Mar 2021.

Vancouver:

Hanna LE. Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/83p514vc.

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

Council of Science Editors:

Hanna LE. Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/83p514vc

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

7. Tollefson, Emily Jean. Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions.

Degree: Chemistry, 2016, University of California – Irvine

 The development of asymmetric transition-metal-catalyzed reactions has emerged as an important area of research in the past decade. Advances in the field are transforming the… (more)

Subjects/Keywords: Organic chemistry; Catalysis; Cross-Coupling; Nickel; Stereospecific

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APA (6th Edition):

Tollefson, E. J. (2016). Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/9qh2x611

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):

Tollefson, Emily Jean. “Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions.” 2016. Thesis, University of California – Irvine. Accessed March 06, 2021. http://www.escholarship.org/uc/item/9qh2x611.

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

MLA Handbook (7th Edition):

Tollefson, Emily Jean. “Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions.” 2016. Web. 06 Mar 2021.

Vancouver:

Tollefson EJ. Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/9qh2x611.

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

Council of Science Editors:

Tollefson EJ. Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/9qh2x611

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


University of California – Irvine

8. Harris, Michael. Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives.

Degree: Chemistry, 2015, University of California – Irvine

 Transition metal catalyzed reactions are indispensable tools for the asymmetric construction of carbon–carbon bonds. Traditionally, cross-coupling reactions have relied on the use of aryl, vinyl… (more)

Subjects/Keywords: Organic chemistry; Catalysis; Cross-coupling; Nickel; Stereospecific

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APA (6th Edition):

Harris, M. (2015). Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/0c12t0wt

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):

Harris, Michael. “Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives.” 2015. Thesis, University of California – Irvine. Accessed March 06, 2021. http://www.escholarship.org/uc/item/0c12t0wt.

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

MLA Handbook (7th Edition):

Harris, Michael. “Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives.” 2015. Web. 06 Mar 2021.

Vancouver:

Harris M. Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/0c12t0wt.

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

Council of Science Editors:

Harris M. Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/0c12t0wt

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


Missouri University of Science and Technology

9. Wang, Xiaojiang. Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials.

Degree: M.S. in Chemistry, Chemistry, Missouri University of Science and Technology

 "Immobilization of catalysts is a promising approach to combine the advantages of heterogeneous and homogeneous catalysts. Pd(PPh₃)₂Cl₂ known as an extremely active homogeneous catalyst for… (more)

Subjects/Keywords: Sonogashira coupling; Chemistry

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APA (6th Edition):

Wang, X. (n.d.). Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials. (Masters Thesis). Missouri University of Science and Technology. Retrieved from https://scholarsmine.mst.edu/masters_theses/5905

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Chicago Manual of Style (16th Edition):

Wang, Xiaojiang. “Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials.” Masters Thesis, Missouri University of Science and Technology. Accessed March 06, 2021. https://scholarsmine.mst.edu/masters_theses/5905.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

MLA Handbook (7th Edition):

Wang, Xiaojiang. “Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials.” Web. 06 Mar 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Wang X. Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials. [Internet] [Masters thesis]. Missouri University of Science and Technology; [cited 2021 Mar 06]. Available from: https://scholarsmine.mst.edu/masters_theses/5905.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Council of Science Editors:

Wang X. Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials. [Masters Thesis]. Missouri University of Science and Technology; Available from: https://scholarsmine.mst.edu/masters_theses/5905

Note: this citation may be lacking information needed for this citation format:
No year of publication.


Princeton University

10. Twilton, Jack. NOVEL STRATEGIES FOR A-HYDROXY C–H ARYLATION AND OXIDATIVE C–N CROSS COUPLING VIA METALLAPHOTOREDOX CATALYSIS .

Degree: PhD, 2019, Princeton University

 Transition metal catalyzed cross-coupling is an incredibly powerful platform for the construction of organic architectures, since the advent of these technologies their impact has been… (more)

Subjects/Keywords: Cross Coupling; Organic Chemistry; Photoredox Catalysis

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APA (6th Edition):

Twilton, J. (2019). NOVEL STRATEGIES FOR A-HYDROXY C–H ARYLATION AND OXIDATIVE C–N CROSS COUPLING VIA METALLAPHOTOREDOX CATALYSIS . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01st74ct389

Chicago Manual of Style (16th Edition):

Twilton, Jack. “NOVEL STRATEGIES FOR A-HYDROXY C–H ARYLATION AND OXIDATIVE C–N CROSS COUPLING VIA METALLAPHOTOREDOX CATALYSIS .” 2019. Doctoral Dissertation, Princeton University. Accessed March 06, 2021. http://arks.princeton.edu/ark:/88435/dsp01st74ct389.

MLA Handbook (7th Edition):

Twilton, Jack. “NOVEL STRATEGIES FOR A-HYDROXY C–H ARYLATION AND OXIDATIVE C–N CROSS COUPLING VIA METALLAPHOTOREDOX CATALYSIS .” 2019. Web. 06 Mar 2021.

Vancouver:

Twilton J. NOVEL STRATEGIES FOR A-HYDROXY C–H ARYLATION AND OXIDATIVE C–N CROSS COUPLING VIA METALLAPHOTOREDOX CATALYSIS . [Internet] [Doctoral dissertation]. Princeton University; 2019. [cited 2021 Mar 06]. Available from: http://arks.princeton.edu/ark:/88435/dsp01st74ct389.

Council of Science Editors:

Twilton J. NOVEL STRATEGIES FOR A-HYDROXY C–H ARYLATION AND OXIDATIVE C–N CROSS COUPLING VIA METALLAPHOTOREDOX CATALYSIS . [Doctoral Dissertation]. Princeton University; 2019. Available from: http://arks.princeton.edu/ark:/88435/dsp01st74ct389


Queens University

11. Fraser, Andrew. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .

Degree: Chemistry, 2013, Queens University

 Little attention has been given to the formation of the putative PdL2 species required for Pd-catalyzed cross-coupling reactions. Active species are generally difficult to store… (more)

Subjects/Keywords: Catalysis ; Palladium ; Cross-Coupling ; Organometallic Chemistry

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APA (6th Edition):

Fraser, A. (2013). Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8094

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):

Fraser, Andrew. “Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .” 2013. Thesis, Queens University. Accessed March 06, 2021. http://hdl.handle.net/1974/8094.

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

MLA Handbook (7th Edition):

Fraser, Andrew. “Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .” 2013. Web. 06 Mar 2021.

Vancouver:

Fraser A. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . [Internet] [Thesis]. Queens University; 2013. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1974/8094.

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

Council of Science Editors:

Fraser A. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/8094

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


UCLA

12. Silberstein, Amanda Leanne. Base Metal-Catalyzed Cross-Couplings of Unconventional Oxygen-Based Electrophiles and Total Synthesis of Tubingensin A.

Degree: Chemistry, 2014, UCLA

 Transition metal-catalyzed cross-couplings provide a powerful means to assemble carbon-carbon (C-C) and carbon-heteroatom (C-X) bonds. Although halides are the most commonly employed electrophilic partner, phenolic… (more)

Subjects/Keywords: Chemistry; Organic chemistry; carbamate; carbazolyne; cross-coupling; sulfamate; tubingensin A

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APA (6th Edition):

Silberstein, A. L. (2014). Base Metal-Catalyzed Cross-Couplings of Unconventional Oxygen-Based Electrophiles and Total Synthesis of Tubingensin A. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/3qn610nf

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):

Silberstein, Amanda Leanne. “Base Metal-Catalyzed Cross-Couplings of Unconventional Oxygen-Based Electrophiles and Total Synthesis of Tubingensin A.” 2014. Thesis, UCLA. Accessed March 06, 2021. http://www.escholarship.org/uc/item/3qn610nf.

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

MLA Handbook (7th Edition):

Silberstein, Amanda Leanne. “Base Metal-Catalyzed Cross-Couplings of Unconventional Oxygen-Based Electrophiles and Total Synthesis of Tubingensin A.” 2014. Web. 06 Mar 2021.

Vancouver:

Silberstein AL. Base Metal-Catalyzed Cross-Couplings of Unconventional Oxygen-Based Electrophiles and Total Synthesis of Tubingensin A. [Internet] [Thesis]. UCLA; 2014. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/3qn610nf.

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

Council of Science Editors:

Silberstein AL. Base Metal-Catalyzed Cross-Couplings of Unconventional Oxygen-Based Electrophiles and Total Synthesis of Tubingensin A. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/3qn610nf

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

13. Roberts, Gina M. Greener and renewable methods for Pd-catalyzed cross-coupling and alkoxycarbonylation reactions.

Degree: 2014, Iowa State University

 In response to current environmental issues and concerns, an abundance of chemical literature focuses upon green, benign methodologies. Considering these issues, work presented within this… (more)

Subjects/Keywords: Biorenewable; Carbonylation; Catalysis; Cross Coupling; Green Chemistry; Palladium; Chemistry

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APA (6th Edition):

Roberts, G. M. (2014). Greener and renewable methods for Pd-catalyzed cross-coupling and alkoxycarbonylation reactions. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/13808

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):

Roberts, Gina M. “Greener and renewable methods for Pd-catalyzed cross-coupling and alkoxycarbonylation reactions.” 2014. Thesis, Iowa State University. Accessed March 06, 2021. https://lib.dr.iastate.edu/etd/13808.

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

MLA Handbook (7th Edition):

Roberts, Gina M. “Greener and renewable methods for Pd-catalyzed cross-coupling and alkoxycarbonylation reactions.” 2014. Web. 06 Mar 2021.

Vancouver:

Roberts GM. Greener and renewable methods for Pd-catalyzed cross-coupling and alkoxycarbonylation reactions. [Internet] [Thesis]. Iowa State University; 2014. [cited 2021 Mar 06]. Available from: https://lib.dr.iastate.edu/etd/13808.

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

Council of Science Editors:

Roberts GM. Greener and renewable methods for Pd-catalyzed cross-coupling and alkoxycarbonylation reactions. [Thesis]. Iowa State University; 2014. Available from: https://lib.dr.iastate.edu/etd/13808

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


University of New Mexico

14. Basnet, Prakash. DEVELOPMENT OF COPPER-CATALYZED SUZUKI-MIYAURA COUPLING USING ALKYLBORON REAGENTS AND NICKEL-CATALYZED ALKENE DICARBOFUNCTIONALIZATION REACTIONS.

Degree: Department of Chemistry and Chemical Biology, 2018, University of New Mexico

  This thesis is divided into two parts. The first part deals with the development of copper-catalyzed Suzuki-Miyaura coupling of alkylboron reagents for the first… (more)

Subjects/Keywords: copper; cross-coupling; nickel; dicarbofunctionalization; cationic; catalysis; Chemistry; Organic Chemistry

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APA (6th Edition):

Basnet, P. (2018). DEVELOPMENT OF COPPER-CATALYZED SUZUKI-MIYAURA COUPLING USING ALKYLBORON REAGENTS AND NICKEL-CATALYZED ALKENE DICARBOFUNCTIONALIZATION REACTIONS. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/chem_etds/146

Chicago Manual of Style (16th Edition):

Basnet, Prakash. “DEVELOPMENT OF COPPER-CATALYZED SUZUKI-MIYAURA COUPLING USING ALKYLBORON REAGENTS AND NICKEL-CATALYZED ALKENE DICARBOFUNCTIONALIZATION REACTIONS.” 2018. Doctoral Dissertation, University of New Mexico. Accessed March 06, 2021. https://digitalrepository.unm.edu/chem_etds/146.

MLA Handbook (7th Edition):

Basnet, Prakash. “DEVELOPMENT OF COPPER-CATALYZED SUZUKI-MIYAURA COUPLING USING ALKYLBORON REAGENTS AND NICKEL-CATALYZED ALKENE DICARBOFUNCTIONALIZATION REACTIONS.” 2018. Web. 06 Mar 2021.

Vancouver:

Basnet P. DEVELOPMENT OF COPPER-CATALYZED SUZUKI-MIYAURA COUPLING USING ALKYLBORON REAGENTS AND NICKEL-CATALYZED ALKENE DICARBOFUNCTIONALIZATION REACTIONS. [Internet] [Doctoral dissertation]. University of New Mexico; 2018. [cited 2021 Mar 06]. Available from: https://digitalrepository.unm.edu/chem_etds/146.

Council of Science Editors:

Basnet P. DEVELOPMENT OF COPPER-CATALYZED SUZUKI-MIYAURA COUPLING USING ALKYLBORON REAGENTS AND NICKEL-CATALYZED ALKENE DICARBOFUNCTIONALIZATION REACTIONS. [Doctoral Dissertation]. University of New Mexico; 2018. Available from: https://digitalrepository.unm.edu/chem_etds/146


University of Arkansas

15. Ngebichie Njabon, Roland. An Investigation of the Electronic Coupling in Some Dimeric Ruthenium (II) Polypyridine Complexes.

Degree: PhD, 2013, University of Arkansas

  A detailed understanding of respiration at the molecular level requires an understanding of the many electron transfer steps involved in the process. These electron… (more)

Subjects/Keywords: Pure sciences; Electronic coupling; Polypyridines; Ruthenium; Inorganic Chemistry; Materials Chemistry

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APA (6th Edition):

Ngebichie Njabon, R. (2013). An Investigation of the Electronic Coupling in Some Dimeric Ruthenium (II) Polypyridine Complexes. (Doctoral Dissertation). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/678

Chicago Manual of Style (16th Edition):

Ngebichie Njabon, Roland. “An Investigation of the Electronic Coupling in Some Dimeric Ruthenium (II) Polypyridine Complexes.” 2013. Doctoral Dissertation, University of Arkansas. Accessed March 06, 2021. https://scholarworks.uark.edu/etd/678.

MLA Handbook (7th Edition):

Ngebichie Njabon, Roland. “An Investigation of the Electronic Coupling in Some Dimeric Ruthenium (II) Polypyridine Complexes.” 2013. Web. 06 Mar 2021.

Vancouver:

Ngebichie Njabon R. An Investigation of the Electronic Coupling in Some Dimeric Ruthenium (II) Polypyridine Complexes. [Internet] [Doctoral dissertation]. University of Arkansas; 2013. [cited 2021 Mar 06]. Available from: https://scholarworks.uark.edu/etd/678.

Council of Science Editors:

Ngebichie Njabon R. An Investigation of the Electronic Coupling in Some Dimeric Ruthenium (II) Polypyridine Complexes. [Doctoral Dissertation]. University of Arkansas; 2013. Available from: https://scholarworks.uark.edu/etd/678


University of Maryland

16. Nytko, III, Frederick Emil. ADVANCES IN SILOXANE-BASED COUPLING TECHNOLOGIES: APPROACHES TOWARD PANCRATISTATIN AND STREPTONIGRIN.

Degree: Chemistry, 2014, University of Maryland

 The ability to form carbon-carbon bonds, arguably the most important transformation in synthetic chemistry, has been critically facilitated via the implementation of transition metal catalysts… (more)

Subjects/Keywords: Organic chemistry; Pancratistatin; Pyridone Chemistry; Siloxane-Based Coupling; Streptonigrin

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APA (6th Edition):

Nytko, III, F. E. (2014). ADVANCES IN SILOXANE-BASED COUPLING TECHNOLOGIES: APPROACHES TOWARD PANCRATISTATIN AND STREPTONIGRIN. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/16482

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):

Nytko, III, Frederick Emil. “ADVANCES IN SILOXANE-BASED COUPLING TECHNOLOGIES: APPROACHES TOWARD PANCRATISTATIN AND STREPTONIGRIN.” 2014. Thesis, University of Maryland. Accessed March 06, 2021. http://hdl.handle.net/1903/16482.

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

MLA Handbook (7th Edition):

Nytko, III, Frederick Emil. “ADVANCES IN SILOXANE-BASED COUPLING TECHNOLOGIES: APPROACHES TOWARD PANCRATISTATIN AND STREPTONIGRIN.” 2014. Web. 06 Mar 2021.

Vancouver:

Nytko, III FE. ADVANCES IN SILOXANE-BASED COUPLING TECHNOLOGIES: APPROACHES TOWARD PANCRATISTATIN AND STREPTONIGRIN. [Internet] [Thesis]. University of Maryland; 2014. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1903/16482.

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

Council of Science Editors:

Nytko, III FE. ADVANCES IN SILOXANE-BASED COUPLING TECHNOLOGIES: APPROACHES TOWARD PANCRATISTATIN AND STREPTONIGRIN. [Thesis]. University of Maryland; 2014. Available from: http://hdl.handle.net/1903/16482

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


The Ohio State University

17. Okumu, Antony A. Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34.

Degree: PhD, Chemistry, 2016, The Ohio State University

 Azaspiracids are a class of marine natural products that accumulate in shellfish. Azaspiracid 1 was first reported in 1995 in the Netherlands after a poisoning… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Azaspiracid; Natural Product Synthesis; NHK Coupling

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APA (6th Edition):

Okumu, A. A. (2016). Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1461282755

Chicago Manual of Style (16th Edition):

Okumu, Antony A. “Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34.” 2016. Doctoral Dissertation, The Ohio State University. Accessed March 06, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1461282755.

MLA Handbook (7th Edition):

Okumu, Antony A. “Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34.” 2016. Web. 06 Mar 2021.

Vancouver:

Okumu AA. Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2021 Mar 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1461282755.

Council of Science Editors:

Okumu AA. Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1461282755


Johannes Gutenberg Universität Mainz

18. Zöphel, Lukas Julian. Chemical transformations of the pyrene K-region for functional materials.

Degree: 2012, Johannes Gutenberg Universität Mainz

In dieser Arbeit wurde eine neue Methode zur asymmetrischen Substitution der K-Regionen von Pyren entwickelt, auf welcher das Design und die Synthese von neuartigen, Pyren-basierten… (more)

Subjects/Keywords: Organische Synthese; organische Elektronik; Pyren-Chemie; Suzuki Kupplung; Nichtplanar; organic synthesis; organic electronics; pyrene chemistry; Suzuki coupling; non-planar; Chemistry and allied sciences

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APA (6th Edition):

Zöphel, L. J. (2012). Chemical transformations of the pyrene K-region for functional materials. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2012/3228/

Chicago Manual of Style (16th Edition):

Zöphel, Lukas Julian. “Chemical transformations of the pyrene K-region for functional materials.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed March 06, 2021. http://ubm.opus.hbz-nrw.de/volltexte/2012/3228/.

MLA Handbook (7th Edition):

Zöphel, Lukas Julian. “Chemical transformations of the pyrene K-region for functional materials.” 2012. Web. 06 Mar 2021.

Vancouver:

Zöphel LJ. Chemical transformations of the pyrene K-region for functional materials. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2021 Mar 06]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3228/.

Council of Science Editors:

Zöphel LJ. Chemical transformations of the pyrene K-region for functional materials. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3228/


University of Washington

19. Lesniak, Valerie Ann. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.

Degree: 2016, University of Washington

 A new method to synthesize substituted homoallylic amines is reported. Homoallylic amines are important structural moieties in natural products and pharmaceutical agents. The reaction couples… (more)

Subjects/Keywords: alkenylboronic acid; aziridine; boronic acid; cross-coupling; homoallylic amine; Palladium-catalyzed; Chemistry; Organic chemistry; chemistry

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APA (6th Edition):

Lesniak, V. A. (2016). Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/37060

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):

Lesniak, Valerie Ann. “Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.” 2016. Thesis, University of Washington. Accessed March 06, 2021. http://hdl.handle.net/1773/37060.

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

MLA Handbook (7th Edition):

Lesniak, Valerie Ann. “Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.” 2016. Web. 06 Mar 2021.

Vancouver:

Lesniak VA. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. [Internet] [Thesis]. University of Washington; 2016. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1773/37060.

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

Council of Science Editors:

Lesniak VA. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. [Thesis]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/37060

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

20. Zhang, Na. Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles.

Degree: 2015, University of Pennsylvania

 The Suzuki-Miyaura cross-coupling is widely used in the synthesis of pharmaceuticals, agrochemicals, and organic light-emitting materials. Utilization of phenol derivatives in Suzuki-Miyaura coupling is economically,… (more)

Subjects/Keywords: Borylation; C-O Electrophile; Cross-Coupling; Nickel; Suzuki-Miyaura; Chemistry; Inorganic Chemistry; Organic Chemistry

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APA (6th Edition):

Zhang, N. (2015). Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1170

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):

Zhang, Na. “Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles.” 2015. Thesis, University of Pennsylvania. Accessed March 06, 2021. https://repository.upenn.edu/edissertations/1170.

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

MLA Handbook (7th Edition):

Zhang, Na. “Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles.” 2015. Web. 06 Mar 2021.

Vancouver:

Zhang N. Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2021 Mar 06]. Available from: https://repository.upenn.edu/edissertations/1170.

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

Council of Science Editors:

Zhang N. Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/1170

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


UCLA

21. Hie, Liana. Development of Nickel-Catalyzed Cross-Coupling Reactions.

Degree: Chemistry, 2016, UCLA

 Transition metal-catalyzed cross-couplings provide a powerful means to assemble carbon–carbon (C–C) and carbon–heteroatom (C–X) bonds. Although Pd catalysis is most commonly used in these transformations,… (more)

Subjects/Keywords: Chemistry; catalysis; cross-coupling; nickel; non-precious metal

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APA (6th Edition):

Hie, L. (2016). Development of Nickel-Catalyzed Cross-Coupling Reactions. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/9zg7z83s

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):

Hie, Liana. “Development of Nickel-Catalyzed Cross-Coupling Reactions.” 2016. Thesis, UCLA. Accessed March 06, 2021. http://www.escholarship.org/uc/item/9zg7z83s.

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

MLA Handbook (7th Edition):

Hie, Liana. “Development of Nickel-Catalyzed Cross-Coupling Reactions.” 2016. Web. 06 Mar 2021.

Vancouver:

Hie L. Development of Nickel-Catalyzed Cross-Coupling Reactions. [Internet] [Thesis]. UCLA; 2016. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/9zg7z83s.

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

Council of Science Editors:

Hie L. Development of Nickel-Catalyzed Cross-Coupling Reactions. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/9zg7z83s

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


University of California – Irvine

22. Agee, Christopher. Palladium-Catalyzed Carbenylative Cross-Coupling and Carbenylative Amination Utilizing Vinylcarbenes.

Degree: Chemistry, 2017, University of California – Irvine

 This work focuses on the use of N-tosylhydrazones derived from α,β-unsaturated aldehydes – precursors to vinylcarbene ligands – in palladium-catalyzed carbenylative cross-coupling and carbenylative amination… (more)

Subjects/Keywords: Organic chemistry; Carbene; carbenylative; cross-coupling; Insertion; Palladium

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APA (6th Edition):

Agee, C. (2017). Palladium-Catalyzed Carbenylative Cross-Coupling and Carbenylative Amination Utilizing Vinylcarbenes. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/9c21b7jd

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):

Agee, Christopher. “Palladium-Catalyzed Carbenylative Cross-Coupling and Carbenylative Amination Utilizing Vinylcarbenes.” 2017. Thesis, University of California – Irvine. Accessed March 06, 2021. http://www.escholarship.org/uc/item/9c21b7jd.

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

MLA Handbook (7th Edition):

Agee, Christopher. “Palladium-Catalyzed Carbenylative Cross-Coupling and Carbenylative Amination Utilizing Vinylcarbenes.” 2017. Web. 06 Mar 2021.

Vancouver:

Agee C. Palladium-Catalyzed Carbenylative Cross-Coupling and Carbenylative Amination Utilizing Vinylcarbenes. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/9c21b7jd.

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

Council of Science Editors:

Agee C. Palladium-Catalyzed Carbenylative Cross-Coupling and Carbenylative Amination Utilizing Vinylcarbenes. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/9c21b7jd

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


University of California – Irvine

23. Johnson, Aaron George. Stereospecific Nickel-Catalyzed Cross-Coupling Reactions.

Degree: Chemistry, 2015, University of California – Irvine

 Transition metal catalyzed cross-coupling reactions have become a staple of organic synthesis and are frequently the most practical strategy for the preparation of medicinal agents… (more)

Subjects/Keywords: Chemistry; anti-cancer; catalysis; cross-coupling; enantioenriched; nickel; stereospecific

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APA (6th Edition):

Johnson, A. G. (2015). Stereospecific Nickel-Catalyzed Cross-Coupling Reactions. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/5fc2p3ps

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):

Johnson, Aaron George. “Stereospecific Nickel-Catalyzed Cross-Coupling Reactions.” 2015. Thesis, University of California – Irvine. Accessed March 06, 2021. http://www.escholarship.org/uc/item/5fc2p3ps.

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

MLA Handbook (7th Edition):

Johnson, Aaron George. “Stereospecific Nickel-Catalyzed Cross-Coupling Reactions.” 2015. Web. 06 Mar 2021.

Vancouver:

Johnson AG. Stereospecific Nickel-Catalyzed Cross-Coupling Reactions. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/5fc2p3ps.

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

Council of Science Editors:

Johnson AG. Stereospecific Nickel-Catalyzed Cross-Coupling Reactions. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/5fc2p3ps

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


University of California – Irvine

24. Endean, Thomas. Investigation of Silver-Catalyzed Propargylation Reactions and Nickel-Catalyzed Cross-Electrophile Couplings.

Degree: Chemistry, 2018, University of California – Irvine

 Metal-catalyzed reactions often allow access to reactivity that would be otherwise unavailable to researchers using more conventional synthetic methods. The Jarvo lab has worked to… (more)

Subjects/Keywords: Organic chemistry; Cross-coupling; Enantioselective; Nickel; Propargylation; Silver; Stereospecific

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APA (6th Edition):

Endean, T. (2018). Investigation of Silver-Catalyzed Propargylation Reactions and Nickel-Catalyzed Cross-Electrophile Couplings. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/2801z280

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):

Endean, Thomas. “Investigation of Silver-Catalyzed Propargylation Reactions and Nickel-Catalyzed Cross-Electrophile Couplings.” 2018. Thesis, University of California – Irvine. Accessed March 06, 2021. http://www.escholarship.org/uc/item/2801z280.

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

MLA Handbook (7th Edition):

Endean, Thomas. “Investigation of Silver-Catalyzed Propargylation Reactions and Nickel-Catalyzed Cross-Electrophile Couplings.” 2018. Web. 06 Mar 2021.

Vancouver:

Endean T. Investigation of Silver-Catalyzed Propargylation Reactions and Nickel-Catalyzed Cross-Electrophile Couplings. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/2801z280.

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

Council of Science Editors:

Endean T. Investigation of Silver-Catalyzed Propargylation Reactions and Nickel-Catalyzed Cross-Electrophile Couplings. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/2801z280

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


University of California – San Diego

25. Wang, Zhao. Artificial Melanin: From Synthesis to Chemical Properties and Applications.

Degree: Chemistry, 2018, University of California – San Diego

 Melanins are a class of naturally occurring pigments found throughout nature. They have gained great attention because it has a unique combination of properties functions… (more)

Subjects/Keywords: Chemistry; antiferromagnetic coupling; Melanin; Metal Coordination; MRI; Polydopamine; Relaxivity

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APA (6th Edition):

Wang, Z. (2018). Artificial Melanin: From Synthesis to Chemical Properties and Applications. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/0w56j817

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

Chicago Manual of Style (16th Edition):

Wang, Zhao. “Artificial Melanin: From Synthesis to Chemical Properties and Applications.” 2018. Thesis, University of California – San Diego. Accessed March 06, 2021. http://www.escholarship.org/uc/item/0w56j817.

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

MLA Handbook (7th Edition):

Wang, Zhao. “Artificial Melanin: From Synthesis to Chemical Properties and Applications.” 2018. Web. 06 Mar 2021.

Vancouver:

Wang Z. Artificial Melanin: From Synthesis to Chemical Properties and Applications. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/0w56j817.

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

Council of Science Editors:

Wang Z. Artificial Melanin: From Synthesis to Chemical Properties and Applications. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/0w56j817

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


University of Michigan

26. Wiensch, Eric. Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis.

Degree: PhD, Chemistry, 2018, University of Michigan

 Silane protecting groups are traditionally only viewed as inert protecting groups to mask an alcohol functionality, allowing for orthogonal reactivity compared with other protecting groups… (more)

Subjects/Keywords: Silyloxyarene; C-O Bond Coupling; Nickel Catalysis; Chemistry; Science

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APA (6th Edition):

Wiensch, E. (2018). Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/146110

Chicago Manual of Style (16th Edition):

Wiensch, Eric. “Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis.” 2018. Doctoral Dissertation, University of Michigan. Accessed March 06, 2021. http://hdl.handle.net/2027.42/146110.

MLA Handbook (7th Edition):

Wiensch, Eric. “Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis.” 2018. Web. 06 Mar 2021.

Vancouver:

Wiensch E. Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2027.42/146110.

Council of Science Editors:

Wiensch E. Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/146110


Penn State University

27. Christensen, Caroline Marie. Synthesis and Cross-linking of Anthracene-based Polymers and Optimization of Single-phase Suzuki Polycondensation.

Degree: 2015, Penn State University

 Conjugated alternating copolymers containing cross-linkable 9,10-bis(hexyloxy)anthracene moieties were synthesized via Suzuki cross-coupling polymerization. Uncross-linked polymers fluoresced due to conjugation in the backbone from 9,10-dihexocyanthracene and… (more)

Subjects/Keywords: Chemistry; polymers; conjugated polymers; Suzuki coupling; Suzuki Polycondensation; anthracene; organic synthesis

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APA (6th Edition):

Christensen, C. M. (2015). Synthesis and Cross-linking of Anthracene-based Polymers and Optimization of Single-phase Suzuki Polycondensation. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/27147

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):

Christensen, Caroline Marie. “Synthesis and Cross-linking of Anthracene-based Polymers and Optimization of Single-phase Suzuki Polycondensation.” 2015. Thesis, Penn State University. Accessed March 06, 2021. https://submit-etda.libraries.psu.edu/catalog/27147.

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

MLA Handbook (7th Edition):

Christensen, Caroline Marie. “Synthesis and Cross-linking of Anthracene-based Polymers and Optimization of Single-phase Suzuki Polycondensation.” 2015. Web. 06 Mar 2021.

Vancouver:

Christensen CM. Synthesis and Cross-linking of Anthracene-based Polymers and Optimization of Single-phase Suzuki Polycondensation. [Internet] [Thesis]. Penn State University; 2015. [cited 2021 Mar 06]. Available from: https://submit-etda.libraries.psu.edu/catalog/27147.

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

Council of Science Editors:

Christensen CM. Synthesis and Cross-linking of Anthracene-based Polymers and Optimization of Single-phase Suzuki Polycondensation. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/27147

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


University of Vermont

28. Sadlowski, Corinne Marie. Studies Toward The Total Synthesis Of Subincanadine E.

Degree: PhD, Chemistry, 2015, University of Vermont

  Progress towards a concise total synthesis of subincanadine E is reported. This natural product was first isolated from the Picralima nitida cell suspension culture… (more)

Subjects/Keywords: Beckmann; carvone; cross-coupling; palladium; pericine; subincanadine E; Chemistry

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

APA (6th Edition):

Sadlowski, C. M. (2015). Studies Toward The Total Synthesis Of Subincanadine E. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/343

Chicago Manual of Style (16th Edition):

Sadlowski, Corinne Marie. “Studies Toward The Total Synthesis Of Subincanadine E.” 2015. Doctoral Dissertation, University of Vermont. Accessed March 06, 2021. https://scholarworks.uvm.edu/graddis/343.

MLA Handbook (7th Edition):

Sadlowski, Corinne Marie. “Studies Toward The Total Synthesis Of Subincanadine E.” 2015. Web. 06 Mar 2021.

Vancouver:

Sadlowski CM. Studies Toward The Total Synthesis Of Subincanadine E. [Internet] [Doctoral dissertation]. University of Vermont; 2015. [cited 2021 Mar 06]. Available from: https://scholarworks.uvm.edu/graddis/343.

Council of Science Editors:

Sadlowski CM. Studies Toward The Total Synthesis Of Subincanadine E. [Doctoral Dissertation]. University of Vermont; 2015. Available from: https://scholarworks.uvm.edu/graddis/343


University of Houston

29. Truong, Thanh V. 1984-. CARBON–CARBON AND CARBON–HETEROATOM BOND FORMATION THROUGH C–H BOND FUNCTIONALIZATION.

Degree: PhD, Chemistry, 2013, University of Houston

 Direct C–H bond functionalization provides an efficient route by allowing the construction of C – C bonds directly from C–H bonds. In this dissertation, methods… (more)

Subjects/Keywords: Benzyne; C-H functionalization; Coupling reactions; Arylation; Chemistry

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APA (6th Edition):

Truong, T. V. 1. (2013). CARBON–CARBON AND CARBON–HETEROATOM BOND FORMATION THROUGH C–H BOND FUNCTIONALIZATION. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/1049

Chicago Manual of Style (16th Edition):

Truong, Thanh V 1984-. “CARBON–CARBON AND CARBON–HETEROATOM BOND FORMATION THROUGH C–H BOND FUNCTIONALIZATION.” 2013. Doctoral Dissertation, University of Houston. Accessed March 06, 2021. http://hdl.handle.net/10657/1049.

MLA Handbook (7th Edition):

Truong, Thanh V 1984-. “CARBON–CARBON AND CARBON–HETEROATOM BOND FORMATION THROUGH C–H BOND FUNCTIONALIZATION.” 2013. Web. 06 Mar 2021.

Vancouver:

Truong TV1. CARBON–CARBON AND CARBON–HETEROATOM BOND FORMATION THROUGH C–H BOND FUNCTIONALIZATION. [Internet] [Doctoral dissertation]. University of Houston; 2013. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10657/1049.

Council of Science Editors:

Truong TV1. CARBON–CARBON AND CARBON–HETEROATOM BOND FORMATION THROUGH C–H BOND FUNCTIONALIZATION. [Doctoral Dissertation]. University of Houston; 2013. Available from: http://hdl.handle.net/10657/1049


Boston University

30. Lerch, Sarah. Effects of biomolecular linkers and interstitial nanocrystals on plasmon coupling in nanoparticle dimers.

Degree: PhD, Chemistry, 2018, Boston University

 Plasmon coupling is known to cause distance dependent red-shifts of the characteristic plasmon resonance and localize strong electric fields to the gap between individual nanoparticles.… (more)

Subjects/Keywords: Physical chemistry; DNA; Nanoparticle; Plasmonics; Charge transfer; Molecular linker; Plasmon coupling

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

APA (6th Edition):

Lerch, S. (2018). Effects of biomolecular linkers and interstitial nanocrystals on plasmon coupling in nanoparticle dimers. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/33090

Chicago Manual of Style (16th Edition):

Lerch, Sarah. “Effects of biomolecular linkers and interstitial nanocrystals on plasmon coupling in nanoparticle dimers.” 2018. Doctoral Dissertation, Boston University. Accessed March 06, 2021. http://hdl.handle.net/2144/33090.

MLA Handbook (7th Edition):

Lerch, Sarah. “Effects of biomolecular linkers and interstitial nanocrystals on plasmon coupling in nanoparticle dimers.” 2018. Web. 06 Mar 2021.

Vancouver:

Lerch S. Effects of biomolecular linkers and interstitial nanocrystals on plasmon coupling in nanoparticle dimers. [Internet] [Doctoral dissertation]. Boston University; 2018. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2144/33090.

Council of Science Editors:

Lerch S. Effects of biomolecular linkers and interstitial nanocrystals on plasmon coupling in nanoparticle dimers. [Doctoral Dissertation]. Boston University; 2018. Available from: http://hdl.handle.net/2144/33090

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