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You searched for subject:(coupling reaction). Showing records 1 – 30 of 113 total matches.

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University of Saskatchewan

1. Bai, Qian. Nanoparticle catalysts for carbon-carbon coupling reactions.

Degree: 2010, University of Saskatchewan

 My research is focused on two main objectives, the study of catalytic efficiency and mechanism of palladium nanoparticles stabilized by poly(vinylpyrrolidone) (PVP) for carbon-carbon coupling(more)

Subjects/Keywords: nanoparticle; coupling reaction; catalyst

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APA (6th Edition):

Bai, Q. (2010). Nanoparticle catalysts for carbon-carbon coupling reactions. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-12212010-143820

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):

Bai, Qian. “Nanoparticle catalysts for carbon-carbon coupling reactions.” 2010. Thesis, University of Saskatchewan. Accessed March 23, 2019. http://hdl.handle.net/10388/etd-12212010-143820.

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

MLA Handbook (7th Edition):

Bai, Qian. “Nanoparticle catalysts for carbon-carbon coupling reactions.” 2010. Web. 23 Mar 2019.

Vancouver:

Bai Q. Nanoparticle catalysts for carbon-carbon coupling reactions. [Internet] [Thesis]. University of Saskatchewan; 2010. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10388/etd-12212010-143820.

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

Council of Science Editors:

Bai Q. Nanoparticle catalysts for carbon-carbon coupling reactions. [Thesis]. University of Saskatchewan; 2010. Available from: http://hdl.handle.net/10388/etd-12212010-143820

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


University of Illinois – Chicago

2. 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 March 23, 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. 23 Mar 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 Mar 23]. 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


University of South Africa

3. Oyeyiola, Felix Adetunji. Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .

Degree: 2011, University of South Africa

 The 2-aryl-2,3-dihydroquinolin-4(1H)-ones were prepared via acid-catalyzed cyclization of the corresponding 2-aminochalcones, which were in turn, prepared by base-promoted Claisen-Schmidt aldol condensation of 2-aminoacetophenone and benzaldehyde… (more)

Subjects/Keywords: 2-aminochalcones; Cross-coupling reaction; Suzuki-Miyaura

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APA (6th Edition):

Oyeyiola, F. A. (2011). Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/5842

Chicago Manual of Style (16th Edition):

Oyeyiola, Felix Adetunji. “Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .” 2011. Masters Thesis, University of South Africa. Accessed March 23, 2019. http://hdl.handle.net/10500/5842.

MLA Handbook (7th Edition):

Oyeyiola, Felix Adetunji. “Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .” 2011. Web. 23 Mar 2019.

Vancouver:

Oyeyiola FA. Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones . [Internet] [Masters thesis]. University of South Africa; 2011. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10500/5842.

Council of Science Editors:

Oyeyiola FA. Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones . [Masters Thesis]. University of South Africa; 2011. Available from: http://hdl.handle.net/10500/5842


University of South Africa

4. Makelane, Hlamulo Reply. Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .

Degree: 2010, University of South Africa

 Sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline derivatives with stoichiometric amount of terminal alkynes in the presence of bis(triphenylphosphine)palladium(II)chloride and copper iodide in triethylamine afforded the 3-(alkynyl)-2-aryl-4-chloroquinoline, exclusively.… (more)

Subjects/Keywords: 2-aryl-4-chloro-3-iodoquinoline; Sonogashira cross-coupling reaction; Suzuki cross-coupling reaction

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APA (6th Edition):

Makelane, H. R. (2010). Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/3838

Chicago Manual of Style (16th Edition):

Makelane, Hlamulo Reply. “Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .” 2010. Masters Thesis, University of South Africa. Accessed March 23, 2019. http://hdl.handle.net/10500/3838.

MLA Handbook (7th Edition):

Makelane, Hlamulo Reply. “Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .” 2010. Web. 23 Mar 2019.

Vancouver:

Makelane HR. Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes . [Internet] [Masters thesis]. University of South Africa; 2010. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10500/3838.

Council of Science Editors:

Makelane HR. Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes . [Masters Thesis]. University of South Africa; 2010. Available from: http://hdl.handle.net/10500/3838


University of Edinburgh

5. Geogheghan, Katherine Jayne. Boronic acid speciation in Suzuki-Miyaura cross-coupling.

Degree: PhD, 2018, University of Edinburgh

 Since its discovery in 1979, the Suzuki-Miyaura (SM) reaction has become one of the most widely utilised tools for carbon-carbon bond formation. The palladium catalysed… (more)

Subjects/Keywords: cross-coupling; Suzuki-Miyaura reaction; palladium catalysed coupling; boronic esters

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APA (6th Edition):

Geogheghan, K. J. (2018). Boronic acid speciation in Suzuki-Miyaura cross-coupling. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/33092

Chicago Manual of Style (16th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed March 23, 2019. http://hdl.handle.net/1842/33092.

MLA Handbook (7th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Web. 23 Mar 2019.

Vancouver:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/1842/33092.

Council of Science Editors:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/33092


NSYSU

6. Chiang, Meng-fan. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.

Degree: Master, Chemistry, 2015, NSYSU

 A direct ortho-aroylation of N-arylpyridin-2-amines with aldehydes to afford mono- and di-aroylated N-arylpyridin-2-amines in modest to good yields is presented. In the reaction, palladium(II) acetate,… (more)

Subjects/Keywords: palladium; C-C coupling; C-H activation; catalyzed reaction; ortho-aroylation

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APA (6th Edition):

Chiang, M. (2015). Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952

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):

Chiang, Meng-fan. “Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.” 2015. Thesis, NSYSU. Accessed March 23, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952.

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

MLA Handbook (7th Edition):

Chiang, Meng-fan. “Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.” 2015. Web. 23 Mar 2019.

Vancouver:

Chiang M. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. [Internet] [Thesis]. NSYSU; 2015. [cited 2019 Mar 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952.

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

Council of Science Editors:

Chiang M. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. [Thesis]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952

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


NSYSU

7. Chen, Jiun-hong. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.

Degree: Master, Chemistry, 2016, NSYSU

 A direct ortho-Arylation of 1-methyl-N-phenyl-1H-indole-3-carboxamide via Carbon-Hydride Bond Activation. In the reaction, Palladium(II) trifluoroacetate, Copper(II) acetate, Potassium phosphate, Pivalic acid, and DMF:1,4-Dioxane=1/9 were used as… (more)

Subjects/Keywords: palladium; ortho-aroylation; C-C coupling; catalyzed reaction; C-H activation

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APA (6th Edition):

Chen, J. (2016). Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826

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):

Chen, Jiun-hong. “Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.” 2016. Thesis, NSYSU. Accessed March 23, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826.

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

MLA Handbook (7th Edition):

Chen, Jiun-hong. “Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.” 2016. Web. 23 Mar 2019.

Vancouver:

Chen J. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. [Internet] [Thesis]. NSYSU; 2016. [cited 2019 Mar 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826.

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

Council of Science Editors:

Chen J. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826

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


NSYSU

8. Tsai, Mi-Ting. Synthesis of 3,3â-dihydroxy-2,2â-bipyridine Derivatives and Applications.

Degree: Master, Chemistry, 2012, NSYSU

 The thesis can be divided into two chapters: synthesis and application. The first chapter presents the basis of synthesis. Generally, electronic-deficient aromatic molecules require activation… (more)

Subjects/Keywords: calamitic; liquid crystal; iodine(III) reagents; bipyridine; coupling reaction

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APA (6th Edition):

Tsai, M. (2012). Synthesis of 3,3â-dihydroxy-2,2â-bipyridine Derivatives and Applications. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0815112-171440

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):

Tsai, Mi-Ting. “Synthesis of 3,3â-dihydroxy-2,2â-bipyridine Derivatives and Applications.” 2012. Thesis, NSYSU. Accessed March 23, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0815112-171440.

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

MLA Handbook (7th Edition):

Tsai, Mi-Ting. “Synthesis of 3,3â-dihydroxy-2,2â-bipyridine Derivatives and Applications.” 2012. Web. 23 Mar 2019.

Vancouver:

Tsai M. Synthesis of 3,3â-dihydroxy-2,2â-bipyridine Derivatives and Applications. [Internet] [Thesis]. NSYSU; 2012. [cited 2019 Mar 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0815112-171440.

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

Council of Science Editors:

Tsai M. Synthesis of 3,3â-dihydroxy-2,2â-bipyridine Derivatives and Applications. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0815112-171440

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


University of Edinburgh

9. Corrie, Thomas James Alexander. Intramolecular direct arylation.

Degree: PhD, 2017, University of Edinburgh

 The research conducted for this thesis has led to the development of an intramolecular gold-catalysed direct arylation protocol whereby tethered arenes and aryltrimethylsilanes are coupled… (more)

Subjects/Keywords: gold-catalysis; cross-coupling; intermolecular reaction; tethered arenes; aryltrimethylsilanes

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APA (6th Edition):

Corrie, T. J. A. (2017). Intramolecular direct arylation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28820

Chicago Manual of Style (16th Edition):

Corrie, Thomas James Alexander. “Intramolecular direct arylation.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed March 23, 2019. http://hdl.handle.net/1842/28820.

MLA Handbook (7th Edition):

Corrie, Thomas James Alexander. “Intramolecular direct arylation.” 2017. Web. 23 Mar 2019.

Vancouver:

Corrie TJA. Intramolecular direct arylation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/1842/28820.

Council of Science Editors:

Corrie TJA. Intramolecular direct arylation. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28820


University of Manchester

10. Zhang, Yuntong. Sulfoxide Directed Metal-free Cross Coupling: Propargylation of Aromatic and Heteroaromatic Systems.

Degree: 2015, University of Manchester

 This thesis describes the development of an interrupted Pummerer reaction and its application in aromatic and hereroaromatic carbon-hydrogen substitution. During the development of the approach,… (more)

Subjects/Keywords: sulfoxide; Pummerer reaction; carbon-carbon coupling; propargylation; metal-free

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APA (6th Edition):

Zhang, Y. (2015). Sulfoxide Directed Metal-free Cross Coupling: Propargylation of Aromatic and Heteroaromatic Systems. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:291306

Chicago Manual of Style (16th Edition):

Zhang, Yuntong. “Sulfoxide Directed Metal-free Cross Coupling: Propargylation of Aromatic and Heteroaromatic Systems.” 2015. Doctoral Dissertation, University of Manchester. Accessed March 23, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:291306.

MLA Handbook (7th Edition):

Zhang, Yuntong. “Sulfoxide Directed Metal-free Cross Coupling: Propargylation of Aromatic and Heteroaromatic Systems.” 2015. Web. 23 Mar 2019.

Vancouver:

Zhang Y. Sulfoxide Directed Metal-free Cross Coupling: Propargylation of Aromatic and Heteroaromatic Systems. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Mar 23]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:291306.

Council of Science Editors:

Zhang Y. Sulfoxide Directed Metal-free Cross Coupling: Propargylation of Aromatic and Heteroaromatic Systems. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:291306


Brandeis University

11. Litschel, Thomas. Microfluidic Networks of the Compartmentalized Belousov-Zhabotinsky Reaction.

Degree: 2016, Brandeis University

 The oscillating Belousov-Zhabotinsky reaction provides an experimental system with which to study networks of coupled oscillators. We developed a method that allows for creating highly… (more)

Subjects/Keywords: Microfluidics; Belousov-Zhabotinsky Reaction; Chemical Oscillations; Coupling; PDMS; Nonlinear Dynamics

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APA (6th Edition):

Litschel, T. (2016). Microfluidic Networks of the Compartmentalized Belousov-Zhabotinsky Reaction. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/32251

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):

Litschel, Thomas. “Microfluidic Networks of the Compartmentalized Belousov-Zhabotinsky Reaction.” 2016. Thesis, Brandeis University. Accessed March 23, 2019. http://hdl.handle.net/10192/32251.

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

MLA Handbook (7th Edition):

Litschel, Thomas. “Microfluidic Networks of the Compartmentalized Belousov-Zhabotinsky Reaction.” 2016. Web. 23 Mar 2019.

Vancouver:

Litschel T. Microfluidic Networks of the Compartmentalized Belousov-Zhabotinsky Reaction. [Internet] [Thesis]. Brandeis University; 2016. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10192/32251.

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

Council of Science Editors:

Litschel T. Microfluidic Networks of the Compartmentalized Belousov-Zhabotinsky Reaction. [Thesis]. Brandeis University; 2016. Available from: http://hdl.handle.net/10192/32251

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


University of Arizona

12. Bell, Christan Elizabeth. Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds .

Degree: 2012, University of Arizona

 This research focused on the synthesis of novel ogranoboron reagents in efforts to perform a variety of synthetic transformations, and additionally, the development of new… (more)

Subjects/Keywords: multicomponent reaction; Chemistry; cross-coupling; Frustrated Lewis pairs

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APA (6th Edition):

Bell, C. E. (2012). Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/265557

Chicago Manual of Style (16th Edition):

Bell, Christan Elizabeth. “Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds .” 2012. Doctoral Dissertation, University of Arizona. Accessed March 23, 2019. http://hdl.handle.net/10150/265557.

MLA Handbook (7th Edition):

Bell, Christan Elizabeth. “Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds .” 2012. Web. 23 Mar 2019.

Vancouver:

Bell CE. Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10150/265557.

Council of Science Editors:

Bell CE. Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/265557


Brigham Young University

13. Ma, Bing. Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C.

Degree: PhD, 2009, Brigham Young University

  Project I. Cinchona alkaloid-derived quaternary ammonium salts have been successfully used as phase-transfer catalysts, particularly in asymmetric alkylations. Our group applied this type of… (more)

Subjects/Keywords: Cinchona alkaloids; beta-Hydroxy alpha-amino acids; Sonogashira coupling; Heck reaction; Asymmetric aldol reaction; natural products; Celogentin C; oxidative coupling; peptides; radical reaction; total synthesis; Biochemistry; Chemistry

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APA (6th Edition):

Ma, B. (2009). Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3194&context=etd

Chicago Manual of Style (16th Edition):

Ma, Bing. “Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C.” 2009. Doctoral Dissertation, Brigham Young University. Accessed March 23, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3194&context=etd.

MLA Handbook (7th Edition):

Ma, Bing. “Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C.” 2009. Web. 23 Mar 2019.

Vancouver:

Ma B. Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C. [Internet] [Doctoral dissertation]. Brigham Young University; 2009. [cited 2019 Mar 23]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3194&context=etd.

Council of Science Editors:

Ma B. Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C. [Doctoral Dissertation]. Brigham Young University; 2009. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3194&context=etd


Indian Institute of Science

14. Dhineshkumar, J. Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.

Degree: 2016, Indian Institute of Science

 Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions” is divided into two sections. Section-A, contains two chapters, describes the catalytic ability of iodine… (more)

Subjects/Keywords: Carbon-heteroatom Bond; Cross Dehydrogenative Coupling; Tetrabutylammonium Iodide; Cross-Hetero-Dehydrogenative Coupling Reaction; Phosphites; Quaternary Azides; Organic Chemistry

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APA (6th Edition):

Dhineshkumar, J. (2016). Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/3020

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):

Dhineshkumar, J. “Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.” 2016. Thesis, Indian Institute of Science. Accessed March 23, 2019. http://hdl.handle.net/2005/3020.

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

MLA Handbook (7th Edition):

Dhineshkumar, J. “Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.” 2016. Web. 23 Mar 2019.

Vancouver:

Dhineshkumar J. Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions. [Internet] [Thesis]. Indian Institute of Science; 2016. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2005/3020.

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

Council of Science Editors:

Dhineshkumar J. Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions. [Thesis]. Indian Institute of Science; 2016. Available from: http://hdl.handle.net/2005/3020

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

15. Schevciw, Evelyn Pucci. Reações de acoplamento-A3 visando a síntese da desoxicastanospermina e swainsonina.

Degree: Mestrado, Química, 2015, University of São Paulo

Esta dissertação de mestrado descreve os resultados obtidos acerca da aplicação de reações de acoplamento entre aldeídos, aminas e alquinos (A3) visando a síntese de… (more)

Subjects/Keywords: A3-Coupling reaction; Alcalóides; Alkaloids; Deoxycastanospermine; Desoxicastanospermina; Multicomponent reaction; Propargilaminas; Propargylamines; Reação de acoplamento-A3; Reação multicomponente; Swainsonina; Swainsonine

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APA (6th Edition):

Schevciw, E. P. (2015). Reações de acoplamento-A3 visando a síntese da desoxicastanospermina e swainsonina. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46136/tde-20072015-135552/ ;

Chicago Manual of Style (16th Edition):

Schevciw, Evelyn Pucci. “Reações de acoplamento-A3 visando a síntese da desoxicastanospermina e swainsonina.” 2015. Masters Thesis, University of São Paulo. Accessed March 23, 2019. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-20072015-135552/ ;.

MLA Handbook (7th Edition):

Schevciw, Evelyn Pucci. “Reações de acoplamento-A3 visando a síntese da desoxicastanospermina e swainsonina.” 2015. Web. 23 Mar 2019.

Vancouver:

Schevciw EP. Reações de acoplamento-A3 visando a síntese da desoxicastanospermina e swainsonina. [Internet] [Masters thesis]. University of São Paulo; 2015. [cited 2019 Mar 23]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-20072015-135552/ ;.

Council of Science Editors:

Schevciw EP. Reações de acoplamento-A3 visando a síntese da desoxicastanospermina e swainsonina. [Masters Thesis]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-20072015-135552/ ;

16. Carmona, Rafaela Costa. Estratégias assimétricas em reações de acoplamento A3.

Degree: Mestrado, Química, 2013, University of São Paulo

A presente dissertação de mestrado descreve estudos sobre as reações multicomponentes A3 na versão assimétrica. Diversas metodologias foram empregadas visando a obtenção de propargilaminas opticamente… (more)

Subjects/Keywords: A3-coupling reaction; Multicomponent reaction; Organic reactions; Propargilaminas; Propargylamines; Reação de acoplamento A3; Reação multicomponente; Reações orgânica

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APA (6th Edition):

Carmona, R. C. (2013). Estratégias assimétricas em reações de acoplamento A3. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46136/tde-23042013-082023/ ;

Chicago Manual of Style (16th Edition):

Carmona, Rafaela Costa. “Estratégias assimétricas em reações de acoplamento A3.” 2013. Masters Thesis, University of São Paulo. Accessed March 23, 2019. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-23042013-082023/ ;.

MLA Handbook (7th Edition):

Carmona, Rafaela Costa. “Estratégias assimétricas em reações de acoplamento A3.” 2013. Web. 23 Mar 2019.

Vancouver:

Carmona RC. Estratégias assimétricas em reações de acoplamento A3. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2019 Mar 23]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-23042013-082023/ ;.

Council of Science Editors:

Carmona RC. Estratégias assimétricas em reações de acoplamento A3. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-23042013-082023/ ;


NSYSU

17. 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 March 23, 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. 23 Mar 2019.

Vancouver:

Huang N. Development of New Synthesis of Sulfur-oxazoline Ligands. [Internet] [Thesis]. NSYSU; 2011. [cited 2019 Mar 23]. 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

18. Qu, Yangyang. Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives.

Degree: Docteur es, Chimie, 2018, Paris Saclay

Cette thèse porte sur la conception, la synthèse et la caractérisation de nouveaux dérivés accepteurs d'électrons. Elle se concentre sur l’étude des dérivés de la… (more)

Subjects/Keywords: Tétrazine; Benzonitrile; Thiatriazole; Fluorescence retardée; Réaction de couplage; Réaction Diels–Alder; Tetrazine; Benzonitrile; Thiatriazole; Delayed fluorescence; Coupling reaction; Diels–Alder reaction

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APA (6th Edition):

Qu, Y. (2018). Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLN051

Chicago Manual of Style (16th Edition):

Qu, Yangyang. “Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives.” 2018. Doctoral Dissertation, Paris Saclay. Accessed March 23, 2019. http://www.theses.fr/2018SACLN051.

MLA Handbook (7th Edition):

Qu, Yangyang. “Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives.” 2018. Web. 23 Mar 2019.

Vancouver:

Qu Y. Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Mar 23]. Available from: http://www.theses.fr/2018SACLN051.

Council of Science Editors:

Qu Y. Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLN051

19. Kwon, Ki Hyeok. Synthetic and Mechanistic Studies of Coupling Reactions Involving C-H Bond Activation.

Degree: 2011, Marquette University

 Transition metal-catalyzed C-C bond forming reactions involving C-H bond activation have been shown to be effective methods for functionalization of unreactive compounds. Since Murai's pioneering… (more)

Subjects/Keywords: Transition metal catalysts; Oxidative stress; Hydrocarbons; Activation (Chemistry); Organometallic compounds; Catalysis; Chemistry  – Dissertations C-H Bond Activation; Coupling Reaction; Oxidative Coupling Reaction; Tetrasubstituted Olefins; Chemistry; Inorganic Chemistry

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APA (6th Edition):

Kwon, K. H. (2011). Synthetic and Mechanistic Studies of Coupling Reactions Involving C-H Bond Activation. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/dissertations_mu/134

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):

Kwon, Ki Hyeok. “Synthetic and Mechanistic Studies of Coupling Reactions Involving C-H Bond Activation.” 2011. Thesis, Marquette University. Accessed March 23, 2019. https://epublications.marquette.edu/dissertations_mu/134.

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

MLA Handbook (7th Edition):

Kwon, Ki Hyeok. “Synthetic and Mechanistic Studies of Coupling Reactions Involving C-H Bond Activation.” 2011. Web. 23 Mar 2019.

Vancouver:

Kwon KH. Synthetic and Mechanistic Studies of Coupling Reactions Involving C-H Bond Activation. [Internet] [Thesis]. Marquette University; 2011. [cited 2019 Mar 23]. Available from: https://epublications.marquette.edu/dissertations_mu/134.

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

Council of Science Editors:

Kwon KH. Synthetic and Mechanistic Studies of Coupling Reactions Involving C-H Bond Activation. [Thesis]. Marquette University; 2011. Available from: https://epublications.marquette.edu/dissertations_mu/134

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


University of Alberta

20. Lee, Jack C. H. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.

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

 As Organic Chemistry evolves into the 21st Century, the goal of this discipline has altered dramatically from merely accessing target molecules to efficiently synthesizing these… (more)

Subjects/Keywords: Gold-catalyzed cycloisomerization; Suzuki-Miyaura cross-coupling; Chiral alkyl boronates; Heck reaction; Enantioselective conjugate addition

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APA (6th Edition):

Lee, J. C. H. (2013). Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/qn59q550n

Chicago Manual of Style (16th Edition):

Lee, Jack C H. “Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.” 2013. Doctoral Dissertation, University of Alberta. Accessed March 23, 2019. https://era.library.ualberta.ca/files/qn59q550n.

MLA Handbook (7th Edition):

Lee, Jack C H. “Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.” 2013. Web. 23 Mar 2019.

Vancouver:

Lee JCH. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2019 Mar 23]. Available from: https://era.library.ualberta.ca/files/qn59q550n.

Council of Science Editors:

Lee JCH. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/qn59q550n


NSYSU

21. Huang, Hao-ping. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.

Degree: Master, Chemistry, 2013, NSYSU

 The direct ortho arylation of 4-methyl-N-phenylpyridin-2-amines via palladium(II)-catalyzed C-H activation is described. Treatment of 4-methyl-N-phenylpyridin-2-amine with potassium aryltrifluoroborate using ten mol % of Pd(OAc)2 as… (more)

Subjects/Keywords: palladium; C-H bond activation; potassium aryltrifluoroborate; Suzuki-Miyaura cross-coupling reaction

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APA (6th Edition):

Huang, H. (2013). Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051

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, Hao-ping. “Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.” 2013. Thesis, NSYSU. Accessed March 23, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051.

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

MLA Handbook (7th Edition):

Huang, Hao-ping. “Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.” 2013. Web. 23 Mar 2019.

Vancouver:

Huang H. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. [Internet] [Thesis]. NSYSU; 2013. [cited 2019 Mar 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051.

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

Council of Science Editors:

Huang H. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051

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


NSYSU

22. Liao, Jia-Shiang. Chemical ligation at methionine via acyl transfer of homocysteine thiolactone.

Degree: Master, Chemistry, 2016, NSYSU

 Peptide synthesis had been developed for more than 30 years. For the moment, there have been many methods for peptide synthesis. During the development of… (more)

Subjects/Keywords: acyl transfer; peptide synthesis; ring-opening reaction; peptide coupling; native chemical ligation

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APA (6th Edition):

Liao, J. (2016). Chemical ligation at methionine via acyl transfer of homocysteine thiolactone. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708116-113037

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):

Liao, Jia-Shiang. “Chemical ligation at methionine via acyl transfer of homocysteine thiolactone.” 2016. Thesis, NSYSU. Accessed March 23, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708116-113037.

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

MLA Handbook (7th Edition):

Liao, Jia-Shiang. “Chemical ligation at methionine via acyl transfer of homocysteine thiolactone.” 2016. Web. 23 Mar 2019.

Vancouver:

Liao J. Chemical ligation at methionine via acyl transfer of homocysteine thiolactone. [Internet] [Thesis]. NSYSU; 2016. [cited 2019 Mar 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708116-113037.

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

Council of Science Editors:

Liao J. Chemical ligation at methionine via acyl transfer of homocysteine thiolactone. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708116-113037

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


NSYSU

23. Wu, Chung-chiu. Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation.

Degree: Master, Chemistry, 2012, NSYSU

 A one-pot synthesis of ortho-arylated 9-(pyridin-2-yl)-9H-carbazoles via C-H bond activation, in which palladium(II)-catalyzed cross-coupling of 9-(pyridin-2-yl)-9H-carbazoles with potassium aryltrifluoroborates is presented. Silver nitrate and tert-butanol… (more)

Subjects/Keywords: potassium aryltrifluoroborate; palladium catalysis; C-H bond activation; carbazole; Suzuki-Miyaura coupling reaction

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APA (6th Edition):

Wu, C. (2012). Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941

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):

Wu, Chung-chiu. “Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation.” 2012. Thesis, NSYSU. Accessed March 23, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941.

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

MLA Handbook (7th Edition):

Wu, Chung-chiu. “Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation.” 2012. Web. 23 Mar 2019.

Vancouver:

Wu C. Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation. [Internet] [Thesis]. NSYSU; 2012. [cited 2019 Mar 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941.

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

Council of Science Editors:

Wu C. Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941

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

24. Takaishi, Takeshi. Numerical Simulations of Bifurcation Phenomena in Reaction Diffusion Systems : 反応拡散系における分岐現象の数値シミュレーション.

Degree: 博士(理学), 2010, Hiroshima University / 広島大学

 The bifurcation structures of two types of reaction diffusion systems are investigated.A phase field model for anti-plane shear crack growth in two dimensional isotropic elastic… (more)

Subjects/Keywords: reaction-diffusion system; crack growth; phase field model; Turing pattern; diffusive coupling; numerical simulation

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APA (6th Edition):

Takaishi, T. (2010). Numerical Simulations of Bifurcation Phenomena in Reaction Diffusion Systems : 反応拡散系における分岐現象の数値シミュレーション. (Thesis). Hiroshima University / 広島大学. Retrieved from http://ir.lib.hiroshima-u.ac.jp/00031669

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):

Takaishi, Takeshi. “Numerical Simulations of Bifurcation Phenomena in Reaction Diffusion Systems : 反応拡散系における分岐現象の数値シミュレーション.” 2010. Thesis, Hiroshima University / 広島大学. Accessed March 23, 2019. http://ir.lib.hiroshima-u.ac.jp/00031669.

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

MLA Handbook (7th Edition):

Takaishi, Takeshi. “Numerical Simulations of Bifurcation Phenomena in Reaction Diffusion Systems : 反応拡散系における分岐現象の数値シミュレーション.” 2010. Web. 23 Mar 2019.

Vancouver:

Takaishi T. Numerical Simulations of Bifurcation Phenomena in Reaction Diffusion Systems : 反応拡散系における分岐現象の数値シミュレーション. [Internet] [Thesis]. Hiroshima University / 広島大学; 2010. [cited 2019 Mar 23]. Available from: http://ir.lib.hiroshima-u.ac.jp/00031669.

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

Council of Science Editors:

Takaishi T. Numerical Simulations of Bifurcation Phenomena in Reaction Diffusion Systems : 反応拡散系における分岐現象の数値シミュレーション. [Thesis]. Hiroshima University / 広島大学; 2010. Available from: http://ir.lib.hiroshima-u.ac.jp/00031669

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


NSYSU

25. Tsai, Yan-Ting. Synthesis and design of vanadium catalysts for harvesting chemical feedstocks from lignin degradation and biomimicking bromoperoxidase to brominate organic substrates.

Degree: Master, Chemistry, 2018, NSYSU

 Lignin is a major component of plant cell wall consisted of poly-phenol with diverse linkage modes. In order to obtain chemical feedstock from renewable biomass,… (more)

Subjects/Keywords: vanadium bromoperoxidase; organobromide; coupling reaction; biomass; selective oxidation; catalysis; lignin; selective bromination

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APA (6th Edition):

Tsai, Y. (2018). Synthesis and design of vanadium catalysts for harvesting chemical feedstocks from lignin degradation and biomimicking bromoperoxidase to brominate organic substrates. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0109118-145742

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):

Tsai, Yan-Ting. “Synthesis and design of vanadium catalysts for harvesting chemical feedstocks from lignin degradation and biomimicking bromoperoxidase to brominate organic substrates.” 2018. Thesis, NSYSU. Accessed March 23, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0109118-145742.

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

MLA Handbook (7th Edition):

Tsai, Yan-Ting. “Synthesis and design of vanadium catalysts for harvesting chemical feedstocks from lignin degradation and biomimicking bromoperoxidase to brominate organic substrates.” 2018. Web. 23 Mar 2019.

Vancouver:

Tsai Y. Synthesis and design of vanadium catalysts for harvesting chemical feedstocks from lignin degradation and biomimicking bromoperoxidase to brominate organic substrates. [Internet] [Thesis]. NSYSU; 2018. [cited 2019 Mar 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0109118-145742.

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

Council of Science Editors:

Tsai Y. Synthesis and design of vanadium catalysts for harvesting chemical feedstocks from lignin degradation and biomimicking bromoperoxidase to brominate organic substrates. [Thesis]. NSYSU; 2018. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0109118-145742

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


University of California – Berkeley

26. Lee, Hohjai. Two-color Three-pulse Photon Echo Studies on the Photosynthetic Bacterial Reaction Center.

Degree: Chemistry, 2009, University of California – Berkeley

 Photosynthesis begins with absorbing the sun light by the light harvesting complexes. The solar energy is then funneled into the reaction center (RC) via the… (more)

Subjects/Keywords: Chemistry, Physical; Bacterial Reaction Center; Excitonic Coupling; Photon Echo; Photosynthesis; Pigment-protein complex; Quantum Coherence

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APA (6th Edition):

Lee, H. (2009). Two-color Three-pulse Photon Echo Studies on the Photosynthetic Bacterial Reaction Center. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/1d23j386

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, Hohjai. “Two-color Three-pulse Photon Echo Studies on the Photosynthetic Bacterial Reaction Center.” 2009. Thesis, University of California – Berkeley. Accessed March 23, 2019. http://www.escholarship.org/uc/item/1d23j386.

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

MLA Handbook (7th Edition):

Lee, Hohjai. “Two-color Three-pulse Photon Echo Studies on the Photosynthetic Bacterial Reaction Center.” 2009. Web. 23 Mar 2019.

Vancouver:

Lee H. Two-color Three-pulse Photon Echo Studies on the Photosynthetic Bacterial Reaction Center. [Internet] [Thesis]. University of California – Berkeley; 2009. [cited 2019 Mar 23]. Available from: http://www.escholarship.org/uc/item/1d23j386.

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

Council of Science Editors:

Lee H. Two-color Three-pulse Photon Echo Studies on the Photosynthetic Bacterial Reaction Center. [Thesis]. University of California – Berkeley; 2009. Available from: http://www.escholarship.org/uc/item/1d23j386

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

27. Urgin, Karene. Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2010, Université Paris-Est

Les hétérocycles aromatiques sont des motifs structuraux rencontrés dans un grand nombre de substances d'intérêts biologiques ou pharmacologiques. Plus particulièrement, les pyridazines substituées font l'objet… (more)

Subjects/Keywords: Pyridazine; Couplage; Electrosynthèse; Organozinciques; Triarylbismuths; Palladium; Pyridazine; Cross-coupling reaction; Electrosynthesis; Organozinc compounds; Triarylbismuths; Palladium

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APA (6th Edition):

Urgin, K. (2010). Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic. (Doctoral Dissertation). Université Paris-Est. Retrieved from http://www.theses.fr/2010PEST1094

Chicago Manual of Style (16th Edition):

Urgin, Karene. “Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic.” 2010. Doctoral Dissertation, Université Paris-Est. Accessed March 23, 2019. http://www.theses.fr/2010PEST1094.

MLA Handbook (7th Edition):

Urgin, Karene. “Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic.” 2010. Web. 23 Mar 2019.

Vancouver:

Urgin K. Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic. [Internet] [Doctoral dissertation]. Université Paris-Est; 2010. [cited 2019 Mar 23]. Available from: http://www.theses.fr/2010PEST1094.

Council of Science Editors:

Urgin K. Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic. [Doctoral Dissertation]. Université Paris-Est; 2010. Available from: http://www.theses.fr/2010PEST1094


Boston College

28. Zhang, Liang. Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions.

Degree: PhD, Chemistry, 2017, Boston College

 This dissertation will present four main projects focused on stereoselective construction of borylated compounds as well as their applications in asymmetric syntheses. The first two… (more)

Subjects/Keywords: boron-Wittig reaction; catalytic conjunctive cross-coupling; catalytic diboration; enantioselective synthesis; organoboronates

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APA (6th Edition):

Zhang, L. (2017). Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107561

Chicago Manual of Style (16th Edition):

Zhang, Liang. “Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions.” 2017. Doctoral Dissertation, Boston College. Accessed March 23, 2019. http://dlib.bc.edu/islandora/object/bc-ir:107561.

MLA Handbook (7th Edition):

Zhang, Liang. “Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions.” 2017. Web. 23 Mar 2019.

Vancouver:

Zhang L. Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions. [Internet] [Doctoral dissertation]. Boston College; 2017. [cited 2019 Mar 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107561.

Council of Science Editors:

Zhang L. Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions. [Doctoral Dissertation]. Boston College; 2017. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107561


University of Lund

29. Sisodiya, Sheetal. Supported Mono- and Bimetallic Gold Nanoparticle Catalysts for Different Organic Transformations.

Degree: 2017, University of Lund

 Supported gold nanoparticles are emerging as an important class of catalysts for various organic transformations due to their tunable properties. This thesis embraces the fundamental… (more)

Subjects/Keywords: Naturvetenskap; Gold nanoparticles; coupling reaction; styrene epoxidation; bimetallic nanoparticle; supported gold nanoparticle

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APA (6th Edition):

Sisodiya, S. (2017). Supported Mono- and Bimetallic Gold Nanoparticle Catalysts for Different Organic Transformations. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/c25319ec-d5a2-49a7-997b-b3b06a8ec9de ; http://portal.research.lu.se/ws/files/25700601/PhD_thesis_Sheetal_Sisodiya.pdf

Chicago Manual of Style (16th Edition):

Sisodiya, Sheetal. “Supported Mono- and Bimetallic Gold Nanoparticle Catalysts for Different Organic Transformations.” 2017. Doctoral Dissertation, University of Lund. Accessed March 23, 2019. http://lup.lub.lu.se/record/c25319ec-d5a2-49a7-997b-b3b06a8ec9de ; http://portal.research.lu.se/ws/files/25700601/PhD_thesis_Sheetal_Sisodiya.pdf.

MLA Handbook (7th Edition):

Sisodiya, Sheetal. “Supported Mono- and Bimetallic Gold Nanoparticle Catalysts for Different Organic Transformations.” 2017. Web. 23 Mar 2019.

Vancouver:

Sisodiya S. Supported Mono- and Bimetallic Gold Nanoparticle Catalysts for Different Organic Transformations. [Internet] [Doctoral dissertation]. University of Lund; 2017. [cited 2019 Mar 23]. Available from: http://lup.lub.lu.se/record/c25319ec-d5a2-49a7-997b-b3b06a8ec9de ; http://portal.research.lu.se/ws/files/25700601/PhD_thesis_Sheetal_Sisodiya.pdf.

Council of Science Editors:

Sisodiya S. Supported Mono- and Bimetallic Gold Nanoparticle Catalysts for Different Organic Transformations. [Doctoral Dissertation]. University of Lund; 2017. Available from: http://lup.lub.lu.se/record/c25319ec-d5a2-49a7-997b-b3b06a8ec9de ; http://portal.research.lu.se/ws/files/25700601/PhD_thesis_Sheetal_Sisodiya.pdf


University of South Africa

30. Lesenyeho, Lehlogonolo Godfrey. Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines .

Degree: 2010, University of South Africa

 The previously described 2-aryl-4-chloro-3-iodoquinolines were prepared following literature procedure and in turn converted to the corresponding hitherto unknown 2-aryl-3-iodo-4-(phenylamino)quinoline derivatives using aniline in refluxing ethanol.… (more)

Subjects/Keywords: 2-Aryl-3-iodo-4-(phenylamino)quinoline; Sonogashira cross-coupling reaction; Intramolecular Heck reaction; 2-Aryl-3-iodo-4-(phenylamino)quinoline; 4-(N,N-allylphenylamino)-2-aryl-3-iodoquinolines; Sonogashira cross-coupling reaction; intramolecular Heck reaction; 1H-pyrrolo[3,2-c]quinolines

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APA (6th Edition):

Lesenyeho, L. G. (2010). Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/3970

Chicago Manual of Style (16th Edition):

Lesenyeho, Lehlogonolo Godfrey. “Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines .” 2010. Masters Thesis, University of South Africa. Accessed March 23, 2019. http://hdl.handle.net/10500/3970.

MLA Handbook (7th Edition):

Lesenyeho, Lehlogonolo Godfrey. “Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines .” 2010. Web. 23 Mar 2019.

Vancouver:

Lesenyeho LG. Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines . [Internet] [Masters thesis]. University of South Africa; 2010. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10500/3970.

Council of Science Editors:

Lesenyeho LG. Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines . [Masters Thesis]. University of South Africa; 2010. Available from: http://hdl.handle.net/10500/3970

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