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You searched for subject:( C O bond activation). Showing records 1 – 30 of 19392 total matches.

[1] [2] [3] [4] [5] … [647]

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Princeton University

1. Nielsen, Daniel. Activation of Carbon-Heteroatom Bonds: Transition Metal-Catalyzed Coupling of Strained Rings .

Degree: PhD, 2013, Princeton University

 Epoxides and aziridines are invaluable substrates for complex molecule synthesis due to their accessibility and proclivity toward ring opening. Generally, C-C bond formation with these… (more)

Subjects/Keywords: aziridine; C-N bond activation; C-O bond activation; cross coupling; epoxide

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

APA (6th Edition):

Nielsen, D. (2013). Activation of Carbon-Heteroatom Bonds: Transition Metal-Catalyzed Coupling of Strained Rings . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01ww72bb577

Chicago Manual of Style (16th Edition):

Nielsen, Daniel. “Activation of Carbon-Heteroatom Bonds: Transition Metal-Catalyzed Coupling of Strained Rings .” 2013. Doctoral Dissertation, Princeton University. Accessed September 16, 2019. http://arks.princeton.edu/ark:/88435/dsp01ww72bb577.

MLA Handbook (7th Edition):

Nielsen, Daniel. “Activation of Carbon-Heteroatom Bonds: Transition Metal-Catalyzed Coupling of Strained Rings .” 2013. Web. 16 Sep 2019.

Vancouver:

Nielsen D. Activation of Carbon-Heteroatom Bonds: Transition Metal-Catalyzed Coupling of Strained Rings . [Internet] [Doctoral dissertation]. Princeton University; 2013. [cited 2019 Sep 16]. Available from: http://arks.princeton.edu/ark:/88435/dsp01ww72bb577.

Council of Science Editors:

Nielsen D. Activation of Carbon-Heteroatom Bonds: Transition Metal-Catalyzed Coupling of Strained Rings . [Doctoral Dissertation]. Princeton University; 2013. Available from: http://arks.princeton.edu/ark:/88435/dsp01ww72bb577


University of St. Andrews

2. Harkness, Gavin J. Sequential processes using catalytic C-O bond activation .

Degree: 2018, University of St. Andrews

 This thesis is centred around sequential C-C bond forming processes using oxygenated electrophiles. A major part of this research focuses on the constructive deoxygenation of… (more)

Subjects/Keywords: Catalysis; Cross-coupling; Constructive deoxygenation; C-O bond activation; Carbonylation; Flurbiprofen

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APA (6th Edition):

Harkness, G. J. (2018). Sequential processes using catalytic C-O bond activation . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/12809

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):

Harkness, Gavin J. “Sequential processes using catalytic C-O bond activation .” 2018. Thesis, University of St. Andrews. Accessed September 16, 2019. http://hdl.handle.net/10023/12809.

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

MLA Handbook (7th Edition):

Harkness, Gavin J. “Sequential processes using catalytic C-O bond activation .” 2018. Web. 16 Sep 2019.

Vancouver:

Harkness GJ. Sequential processes using catalytic C-O bond activation . [Internet] [Thesis]. University of St. Andrews; 2018. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/10023/12809.

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

Council of Science Editors:

Harkness GJ. Sequential processes using catalytic C-O bond activation . [Thesis]. University of St. Andrews; 2018. Available from: http://hdl.handle.net/10023/12809

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


UCLA

3. Fine Nathel, Noah Frederick. Reaction Discovery Using Nickel Catalysis and Total Syntheses of Indolactam Alkaloids.

Degree: Chemistry, 2015, UCLA

 Transition metal-catalyzed cross-coupling reactions are useful tools to assemble carbon–carbon (C–C) and carbon–heteroatom (C–X) bonds. Traditionally, electrophilic halides and pseudohalides have been cross-coupled to their… (more)

Subjects/Keywords: Organic chemistry; C–N Bond Activation; C–O Bond Activation; Cross-Coupling; Indolactam Alkaloids; Nickel Catalysis; Total Synthesis

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APA (6th Edition):

Fine Nathel, N. F. (2015). Reaction Discovery Using Nickel Catalysis and Total Syntheses of Indolactam Alkaloids. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/8qb6s7kz

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):

Fine Nathel, Noah Frederick. “Reaction Discovery Using Nickel Catalysis and Total Syntheses of Indolactam Alkaloids.” 2015. Thesis, UCLA. Accessed September 16, 2019. http://www.escholarship.org/uc/item/8qb6s7kz.

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

MLA Handbook (7th Edition):

Fine Nathel, Noah Frederick. “Reaction Discovery Using Nickel Catalysis and Total Syntheses of Indolactam Alkaloids.” 2015. Web. 16 Sep 2019.

Vancouver:

Fine Nathel NF. Reaction Discovery Using Nickel Catalysis and Total Syntheses of Indolactam Alkaloids. [Internet] [Thesis]. UCLA; 2015. [cited 2019 Sep 16]. Available from: http://www.escholarship.org/uc/item/8qb6s7kz.

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

Council of Science Editors:

Fine Nathel NF. Reaction Discovery Using Nickel Catalysis and Total Syntheses of Indolactam Alkaloids. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/8qb6s7kz

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


Texas A&M University

4. Zhu, Yanjun. Strong Bond Activation with Late Transition-Metal Pincer Complexes as a Foundation for Potential Catalysis.

Degree: 2012, Texas A&M University

 Strong bond activation mediated by pincer ligated transiton-metal complexes has been the subject of intense study in recent years, due to its potential involvement in… (more)

Subjects/Keywords: bond activation; transition-metal complxes; C-H activation; C-O activation; oxidative addition; reductive elimination; fluorocarbyne complex

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APA (6th Edition):

Zhu, Y. (2012). Strong Bond Activation with Late Transition-Metal Pincer Complexes as a Foundation for Potential Catalysis. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10965

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):

Zhu, Yanjun. “Strong Bond Activation with Late Transition-Metal Pincer Complexes as a Foundation for Potential Catalysis.” 2012. Thesis, Texas A&M University. Accessed September 16, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10965.

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

MLA Handbook (7th Edition):

Zhu, Yanjun. “Strong Bond Activation with Late Transition-Metal Pincer Complexes as a Foundation for Potential Catalysis.” 2012. Web. 16 Sep 2019.

Vancouver:

Zhu Y. Strong Bond Activation with Late Transition-Metal Pincer Complexes as a Foundation for Potential Catalysis. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10965.

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

Council of Science Editors:

Zhu Y. Strong Bond Activation with Late Transition-Metal Pincer Complexes as a Foundation for Potential Catalysis. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10965

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


University of North Texas

5. Pahls, Dale R. Pathways for C—H Activation and Functionalization by Group 9 Metals.

Degree: 2015, University of North Texas

 As fossil fuel resources become more and more scarce, attention has been turned to alternative sources of fuels and energy. One promising prospect is the… (more)

Subjects/Keywords: reductive; functionalization; C-H activation; oxygen activation; M-O double bond; Methane.; Methanol.; Activation (Chemistry); Metal complexes.

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APA (6th Edition):

Pahls, D. R. (2015). Pathways for C—H Activation and Functionalization by Group 9 Metals. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc801909/

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):

Pahls, Dale R. “Pathways for C—H Activation and Functionalization by Group 9 Metals.” 2015. Thesis, University of North Texas. Accessed September 16, 2019. https://digital.library.unt.edu/ark:/67531/metadc801909/.

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

MLA Handbook (7th Edition):

Pahls, Dale R. “Pathways for C—H Activation and Functionalization by Group 9 Metals.” 2015. Web. 16 Sep 2019.

Vancouver:

Pahls DR. Pathways for C—H Activation and Functionalization by Group 9 Metals. [Internet] [Thesis]. University of North Texas; 2015. [cited 2019 Sep 16]. Available from: https://digital.library.unt.edu/ark:/67531/metadc801909/.

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

Council of Science Editors:

Pahls DR. Pathways for C—H Activation and Functionalization by Group 9 Metals. [Thesis]. University of North Texas; 2015. Available from: https://digital.library.unt.edu/ark:/67531/metadc801909/

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


University of Rochester

6. Evans, Meagan Elizabeth (1981 - ). I. Energetics of C–H bond activation of functionalized hydrocarbons. II. C–H and C–CN bond activation of acetonitrile and benzonitrile.

Degree: PhD, 2011, University of Rochester

 Several transition-metal systems have been used to establish correlations between metal-carbon and carbon-hydrogen bonds. In the following studies, the [Tp’RhL] fragment where Tp’ = tris(3,5-dimethylpyrazolyl)borate… (more)

Subjects/Keywords: Bond energies; Bond strength; C-H bond activation; Orthofluorine effect; C-C activation

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APA (6th Edition):

Evans, M. E. (. -. ). (2011). I. Energetics of C–H bond activation of functionalized hydrocarbons. II. C–H and C–CN bond activation of acetonitrile and benzonitrile. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/14773

Chicago Manual of Style (16th Edition):

Evans, Meagan Elizabeth (1981 - ). “I. Energetics of C–H bond activation of functionalized hydrocarbons. II. C–H and C–CN bond activation of acetonitrile and benzonitrile.” 2011. Doctoral Dissertation, University of Rochester. Accessed September 16, 2019. http://hdl.handle.net/1802/14773.

MLA Handbook (7th Edition):

Evans, Meagan Elizabeth (1981 - ). “I. Energetics of C–H bond activation of functionalized hydrocarbons. II. C–H and C–CN bond activation of acetonitrile and benzonitrile.” 2011. Web. 16 Sep 2019.

Vancouver:

Evans ME(-). I. Energetics of C–H bond activation of functionalized hydrocarbons. II. C–H and C–CN bond activation of acetonitrile and benzonitrile. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1802/14773.

Council of Science Editors:

Evans ME(-). I. Energetics of C–H bond activation of functionalized hydrocarbons. II. C–H and C–CN bond activation of acetonitrile and benzonitrile. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/14773


University of Rochester

7. Grochowski, Matthew Robert (1975 - ). Hydrodesulfurization modeling with iridium, rhodium, and nickel hydrides.

Degree: PhD, 2011, University of Rochester

 Reaction of (Cp*IrHCl)2 (Cp* = η5-C5Me5) with 2-methylthiophene and 2,5-dimethylthiophene at 120°C in the presence of H2 results in the cleavage of the thiophene carbon-sulfur… (more)

Subjects/Keywords: HDS; C-S bond activation; Substituted thiophenes

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APA (6th Edition):

Grochowski, M. R. (. -. ). (2011). Hydrodesulfurization modeling with iridium, rhodium, and nickel hydrides. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/14122

Chicago Manual of Style (16th Edition):

Grochowski, Matthew Robert (1975 - ). “Hydrodesulfurization modeling with iridium, rhodium, and nickel hydrides.” 2011. Doctoral Dissertation, University of Rochester. Accessed September 16, 2019. http://hdl.handle.net/1802/14122.

MLA Handbook (7th Edition):

Grochowski, Matthew Robert (1975 - ). “Hydrodesulfurization modeling with iridium, rhodium, and nickel hydrides.” 2011. Web. 16 Sep 2019.

Vancouver:

Grochowski MR(-). Hydrodesulfurization modeling with iridium, rhodium, and nickel hydrides. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1802/14122.

Council of Science Editors:

Grochowski MR(-). Hydrodesulfurization modeling with iridium, rhodium, and nickel hydrides. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/14122

8. Hamdaoui, Mustapha. Study and applications of the H-Si bond activation of silanes by iridacycles : a contribution to the design of multicompetent catalysts : Etude et applications de la réaction d'activation des silanes par les iridacycles : une contribution à l'élaboration de catalyseurs multicompétents.

Degree: Docteur es, Chimie, 2017, Université de Strasbourg

Une nouvelle famille de précatalyseurs à base d'lr(lll) a été découverte. La facilité de leur préparation, leur remarquable stabilité, et surtout leur excellente efficacité catalytique… (more)

Subjects/Keywords: Iridacycles ioniques; Catalyse homogène; O-silylation; Hydrosilylation; Activation C–F; Intermédiaires donneur-accepteur; [Ir(III)H]→[SiR3]; Ion silylium; Ligand Z; Ionic iridacycles; Homogeneous catalysis; O-silylation; Hydrosilylation; C–F bond activation; Donor-acceptor intermediates; [Ir(III)H]→[SiR3]; Silylium ion; Z ligand; 541.3

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APA (6th Edition):

Hamdaoui, M. (2017). Study and applications of the H-Si bond activation of silanes by iridacycles : a contribution to the design of multicompetent catalysts : Etude et applications de la réaction d'activation des silanes par les iridacycles : une contribution à l'élaboration de catalyseurs multicompétents. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2017STRAF007

Chicago Manual of Style (16th Edition):

Hamdaoui, Mustapha. “Study and applications of the H-Si bond activation of silanes by iridacycles : a contribution to the design of multicompetent catalysts : Etude et applications de la réaction d'activation des silanes par les iridacycles : une contribution à l'élaboration de catalyseurs multicompétents.” 2017. Doctoral Dissertation, Université de Strasbourg. Accessed September 16, 2019. http://www.theses.fr/2017STRAF007.

MLA Handbook (7th Edition):

Hamdaoui, Mustapha. “Study and applications of the H-Si bond activation of silanes by iridacycles : a contribution to the design of multicompetent catalysts : Etude et applications de la réaction d'activation des silanes par les iridacycles : une contribution à l'élaboration de catalyseurs multicompétents.” 2017. Web. 16 Sep 2019.

Vancouver:

Hamdaoui M. Study and applications of the H-Si bond activation of silanes by iridacycles : a contribution to the design of multicompetent catalysts : Etude et applications de la réaction d'activation des silanes par les iridacycles : une contribution à l'élaboration de catalyseurs multicompétents. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2017. [cited 2019 Sep 16]. Available from: http://www.theses.fr/2017STRAF007.

Council of Science Editors:

Hamdaoui M. Study and applications of the H-Si bond activation of silanes by iridacycles : a contribution to the design of multicompetent catalysts : Etude et applications de la réaction d'activation des silanes par les iridacycles : une contribution à l'élaboration de catalyseurs multicompétents. [Doctoral Dissertation]. Université de Strasbourg; 2017. Available from: http://www.theses.fr/2017STRAF007


University of Rochester

9. Li, Ting (1982 - ); Jones, William D.; Ateşin, Tülay Aygan (1976 - ). Experimental and theoretical investigations of C-C, C-H and C-S bond activations of nitriles using zerovalent nickel.

Degree: PhD, 2011, University of Rochester

 [Ni(dippe)H]2 complex has been reacted with a variety of carbon nitriles. Upon mixing with substrates, it releases H2 to generate the 14-electron fragment [Ni(dippe)], which… (more)

Subjects/Keywords: C-C bond activation; DFT calculation; Nickel; Bisphosphine ligands

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APA (6th Edition):

Li, Ting (1982 - ); Jones, William D.; Ateşin, T. A. (. -. ). (2011). Experimental and theoretical investigations of C-C, C-H and C-S bond activations of nitriles using zerovalent nickel. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/14156

Chicago Manual of Style (16th Edition):

Li, Ting (1982 - ); Jones, William D.; Ateşin, Tülay Aygan (1976 - ). “Experimental and theoretical investigations of C-C, C-H and C-S bond activations of nitriles using zerovalent nickel.” 2011. Doctoral Dissertation, University of Rochester. Accessed September 16, 2019. http://hdl.handle.net/1802/14156.

MLA Handbook (7th Edition):

Li, Ting (1982 - ); Jones, William D.; Ateşin, Tülay Aygan (1976 - ). “Experimental and theoretical investigations of C-C, C-H and C-S bond activations of nitriles using zerovalent nickel.” 2011. Web. 16 Sep 2019.

Vancouver:

Li, Ting (1982 - ); Jones, William D.; Ateşin TA(-). Experimental and theoretical investigations of C-C, C-H and C-S bond activations of nitriles using zerovalent nickel. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1802/14156.

Council of Science Editors:

Li, Ting (1982 - ); Jones, William D.; Ateşin TA(-). Experimental and theoretical investigations of C-C, C-H and C-S bond activations of nitriles using zerovalent nickel. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/14156


Queens University

10. Zhao, Yigang. Reduction of Tertiary Benzamides to Benzaldehydes by an in situ-Generated Schwartz Reagent (Cp2Zr(H)Cl); Formal Synthesis of Lysergic Acid 2. Ru-Catalyzed Amide-Directed Aryl C-H, C-N and C-O Bond Functionalizations: C-B Formation, C-C Suzuki Cross Coupling and Hydrodemethoxylation .

Degree: Chemistry, 2011, Queens University

 Chapter 2 of the thesis describes a highly efficient in situ method for the reduction of amides to aldehydes and aryl O-carbamates to phenols and… (more)

Subjects/Keywords: reduction; Schwartz reagent; amide; aldehyde;

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APA (6th Edition):

Zhao, Y. (2011). Reduction of Tertiary Benzamides to Benzaldehydes by an in situ-Generated Schwartz Reagent (Cp2Zr(H)Cl); Formal Synthesis of Lysergic Acid 2. Ru-Catalyzed Amide-Directed Aryl C-H, C-N and C-O Bond Functionalizations: C-B Formation, C-C Suzuki Cross Coupling and Hydrodemethoxylation . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6671

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):

Zhao, Yigang. “Reduction of Tertiary Benzamides to Benzaldehydes by an in situ-Generated Schwartz Reagent (Cp2Zr(H)Cl); Formal Synthesis of Lysergic Acid 2. Ru-Catalyzed Amide-Directed Aryl C-H, C-N and C-O Bond Functionalizations: C-B Formation, C-C Suzuki Cross Coupling and Hydrodemethoxylation .” 2011. Thesis, Queens University. Accessed September 16, 2019. http://hdl.handle.net/1974/6671.

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

MLA Handbook (7th Edition):

Zhao, Yigang. “Reduction of Tertiary Benzamides to Benzaldehydes by an in situ-Generated Schwartz Reagent (Cp2Zr(H)Cl); Formal Synthesis of Lysergic Acid 2. Ru-Catalyzed Amide-Directed Aryl C-H, C-N and C-O Bond Functionalizations: C-B Formation, C-C Suzuki Cross Coupling and Hydrodemethoxylation .” 2011. Web. 16 Sep 2019.

Vancouver:

Zhao Y. Reduction of Tertiary Benzamides to Benzaldehydes by an in situ-Generated Schwartz Reagent (Cp2Zr(H)Cl); Formal Synthesis of Lysergic Acid 2. Ru-Catalyzed Amide-Directed Aryl C-H, C-N and C-O Bond Functionalizations: C-B Formation, C-C Suzuki Cross Coupling and Hydrodemethoxylation . [Internet] [Thesis]. Queens University; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1974/6671.

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

Council of Science Editors:

Zhao Y. Reduction of Tertiary Benzamides to Benzaldehydes by an in situ-Generated Schwartz Reagent (Cp2Zr(H)Cl); Formal Synthesis of Lysergic Acid 2. Ru-Catalyzed Amide-Directed Aryl C-H, C-N and C-O Bond Functionalizations: C-B Formation, C-C Suzuki Cross Coupling and Hydrodemethoxylation . [Thesis]. Queens University; 2011. Available from: http://hdl.handle.net/1974/6671

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


Texas A&M University

11. Vastine, Benjamin Alan. Understanding mechanisms for C-H bond activation.

Degree: 2009, Texas A&M University

 The results from density functional theory (DFT) studies into C?H bond activation, hydrogen transfer, and alkyne?to?vinylidene isomerization are presented in this work. The reaction mechanism… (more)

Subjects/Keywords: Density functional theory; C-H bond activation; hydrogen transfer; Bader's analysis

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APA (6th Edition):

Vastine, B. A. (2009). Understanding mechanisms for C-H bond activation. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2679

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):

Vastine, Benjamin Alan. “Understanding mechanisms for C-H bond activation.” 2009. Thesis, Texas A&M University. Accessed September 16, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2679.

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

MLA Handbook (7th Edition):

Vastine, Benjamin Alan. “Understanding mechanisms for C-H bond activation.” 2009. Web. 16 Sep 2019.

Vancouver:

Vastine BA. Understanding mechanisms for C-H bond activation. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2679.

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

Council of Science Editors:

Vastine BA. Understanding mechanisms for C-H bond activation. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2679

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


NSYSU

12. Li, Ya-Ming. Synthesis and Mechanistic Studies on the Reaction of N-phenylpyridin-2-Amine Palladacycle with Aryltrifluoroboratess to 9-(pryidin-2yl)-9H-carbazole.

Degree: Master, Chemistry, 2010, NSYSU

 An effiecient stoichiometric amount system has been developed for the synthesis of N-phenylpyridin-2-amine Palladacycle, and then reation with aryl trifluoroborate to 9-(pyridine-2-yl)-9H-carbazoles by C-H bond(more)

Subjects/Keywords: kinetic isotope effect; C-H bond activation; carbazole

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APA (6th Edition):

Li, Y. (2010). Synthesis and Mechanistic Studies on the Reaction of N-phenylpyridin-2-Amine Palladacycle with Aryltrifluoroboratess to 9-(pryidin-2yl)-9H-carbazole. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809110-201045

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):

Li, Ya-Ming. “Synthesis and Mechanistic Studies on the Reaction of N-phenylpyridin-2-Amine Palladacycle with Aryltrifluoroboratess to 9-(pryidin-2yl)-9H-carbazole.” 2010. Thesis, NSYSU. Accessed September 16, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809110-201045.

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

MLA Handbook (7th Edition):

Li, Ya-Ming. “Synthesis and Mechanistic Studies on the Reaction of N-phenylpyridin-2-Amine Palladacycle with Aryltrifluoroboratess to 9-(pryidin-2yl)-9H-carbazole.” 2010. Web. 16 Sep 2019.

Vancouver:

Li Y. Synthesis and Mechanistic Studies on the Reaction of N-phenylpyridin-2-Amine Palladacycle with Aryltrifluoroboratess to 9-(pryidin-2yl)-9H-carbazole. [Internet] [Thesis]. NSYSU; 2010. [cited 2019 Sep 16]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809110-201045.

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

Council of Science Editors:

Li Y. Synthesis and Mechanistic Studies on the Reaction of N-phenylpyridin-2-Amine Palladacycle with Aryltrifluoroboratess to 9-(pryidin-2yl)-9H-carbazole. [Thesis]. NSYSU; 2010. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809110-201045

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


NSYSU

13. Hsu, Wen-Ting. Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect.

Degree: Master, Chemistry, 2013, NSYSU

 An intramolecular cyclization of N-([1,1'-biphenyl]-2-yl)pyridin-2-amines catalyzed by hypervalent iodine(III) via C-H activation / C-N formation was investigated. The influence of electronic effect regarding the cyclization… (more)

Subjects/Keywords: electronic effect; benzimidazole; C-H bond activation; carbazole; hypervalent iodine(III)

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APA (6th Edition):

Hsu, W. (2013). Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0616113-135655

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):

Hsu, Wen-Ting. “Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect.” 2013. Thesis, NSYSU. Accessed September 16, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0616113-135655.

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

MLA Handbook (7th Edition):

Hsu, Wen-Ting. “Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect.” 2013. Web. 16 Sep 2019.

Vancouver:

Hsu W. Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect. [Internet] [Thesis]. NSYSU; 2013. [cited 2019 Sep 16]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0616113-135655.

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

Council of Science Editors:

Hsu W. Intramolecular Cyclization of N-([1,1'-Biphenyl]-2-yl)pyridin-2-amines via Hypervalent Iodine(III)-Induced C-H Activation/C-N Formation: The Influence of Electronic Effect. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0616113-135655

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


NSYSU

14. Wu, Yi-hua. I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation.

Degree: Master, Chemistry, 2014, NSYSU

 The first chapter summaries present that the hypervalent iodine(III) reagents induced the direct intramolecular C-N cyclization of N-(biphenyl)pyridin-2-amines to establisha variety of 6-arylbenzimidazoles and N-pyridinyl-9H-carbazoles.We… (more)

Subjects/Keywords: carbazole; C-H bond activation; benzimidazol; Hypervalent Iodine(III)

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APA (6th Edition):

Wu, Y. (2014). I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0526114-094415

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, Yi-hua. “I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation.” 2014. Thesis, NSYSU. Accessed September 16, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0526114-094415.

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

MLA Handbook (7th Edition):

Wu, Yi-hua. “I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation.” 2014. Web. 16 Sep 2019.

Vancouver:

Wu Y. I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation. [Internet] [Thesis]. NSYSU; 2014. [cited 2019 Sep 16]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0526114-094415.

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

Council of Science Editors:

Wu Y. I.Electronic Effects on the Selective Intramolecular C-N Cyclization of N-(Biphenyl)pyridin-2-amines Induced by Hypervalent Iodine(III) Reagents II.Palladium(II)-Catalyzed Ortho Aroylation of 3,5-Diphenylisoxazoles via C-H Activation. [Thesis]. NSYSU; 2014. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0526114-094415

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


University of Rochester

15. Yuan, Hongmei. Synthesis and characterization of group VIII & IX transition metal complexes and their application in C-H bond activation and hydrogen transformation.

Degree: PhD, 2018, University of Rochester

 A cobalt analogue of Cp*Co(PMe3)Me(OTf) (Cp* = 1, 2, 3, 4, 5 - pentamethylcyclopenta-dienyl, OTf = OSO2CF3), in Chapter 2, was attempted to be synthesized… (more)

Subjects/Keywords: C-H bond activation; Group VIII & IX transition metal; Hydrogen transformation

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APA (6th Edition):

Yuan, H. (2018). Synthesis and characterization of group VIII & IX transition metal complexes and their application in C-H bond activation and hydrogen transformation. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/33863

Chicago Manual of Style (16th Edition):

Yuan, Hongmei. “Synthesis and characterization of group VIII & IX transition metal complexes and their application in C-H bond activation and hydrogen transformation.” 2018. Doctoral Dissertation, University of Rochester. Accessed September 16, 2019. http://hdl.handle.net/1802/33863.

MLA Handbook (7th Edition):

Yuan, Hongmei. “Synthesis and characterization of group VIII & IX transition metal complexes and their application in C-H bond activation and hydrogen transformation.” 2018. Web. 16 Sep 2019.

Vancouver:

Yuan H. Synthesis and characterization of group VIII & IX transition metal complexes and their application in C-H bond activation and hydrogen transformation. [Internet] [Doctoral dissertation]. University of Rochester; 2018. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1802/33863.

Council of Science Editors:

Yuan H. Synthesis and characterization of group VIII & IX transition metal complexes and their application in C-H bond activation and hydrogen transformation. [Doctoral Dissertation]. University of Rochester; 2018. Available from: http://hdl.handle.net/1802/33863


University of Manitoba

16. Taleb Sereshki, Farzaneh. Rh-catalyzed asymmetric C-H bond activation by chiral primary amine.

Degree: Chemistry, 2017, University of Manitoba

 Developing asymmetric C-H bond activation methods in order to achieve enantiopure products is crucial for the advancement of the field and for the production of… (more)

Subjects/Keywords: Rh catalyzed; Asymmetric synthesis; C-H Bond activation; Chiral amine

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APA (6th Edition):

Taleb Sereshki, F. (2017). Rh-catalyzed asymmetric C-H bond activation by chiral primary amine. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/32091

Chicago Manual of Style (16th Edition):

Taleb Sereshki, Farzaneh. “Rh-catalyzed asymmetric C-H bond activation by chiral primary amine.” 2017. Masters Thesis, University of Manitoba. Accessed September 16, 2019. http://hdl.handle.net/1993/32091.

MLA Handbook (7th Edition):

Taleb Sereshki, Farzaneh. “Rh-catalyzed asymmetric C-H bond activation by chiral primary amine.” 2017. Web. 16 Sep 2019.

Vancouver:

Taleb Sereshki F. Rh-catalyzed asymmetric C-H bond activation by chiral primary amine. [Internet] [Masters thesis]. University of Manitoba; 2017. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1993/32091.

Council of Science Editors:

Taleb Sereshki F. Rh-catalyzed asymmetric C-H bond activation by chiral primary amine. [Masters Thesis]. University of Manitoba; 2017. Available from: http://hdl.handle.net/1993/32091


Rutgers University

17. Li, Bo. Catalytic C-C (C-N) bond formation and C-O bond cleavage by pincer-ligated iridium complexes.

Degree: PhD, Chemistry and Chemical Biology, 2019, Rutgers University

Since the initial reports of catalytic alkane dehydrogenation by (tBuPCP)Ir (tBuPCP = κ3-2,6-C6H3(CH2tBu2)2) in 1996, pincer-iridium complexes have grown rapidly to include a family of… (more)

Subjects/Keywords: C-C bond formation; C-O bond cleavage; Dehydrogenation; Dehydrogenative coupling; Hydrogenolysis; Pincer-ligated iridium complex

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APA (6th Edition):

Li, B. (2019). Catalytic C-C (C-N) bond formation and C-O bond cleavage by pincer-ligated iridium complexes. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/60829/

Chicago Manual of Style (16th Edition):

Li, Bo. “Catalytic C-C (C-N) bond formation and C-O bond cleavage by pincer-ligated iridium complexes.” 2019. Doctoral Dissertation, Rutgers University. Accessed September 16, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/60829/.

MLA Handbook (7th Edition):

Li, Bo. “Catalytic C-C (C-N) bond formation and C-O bond cleavage by pincer-ligated iridium complexes.” 2019. Web. 16 Sep 2019.

Vancouver:

Li B. Catalytic C-C (C-N) bond formation and C-O bond cleavage by pincer-ligated iridium complexes. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2019 Sep 16]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60829/.

Council of Science Editors:

Li B. Catalytic C-C (C-N) bond formation and C-O bond cleavage by pincer-ligated iridium complexes. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60829/


University of Michigan

18. 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 September 16, 2019. 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. 16 Sep 2019.

Vancouver:

Wiensch E. Silyloxyarenes as C-O Electrophilic Coupling Partners Enabled by Nickel Catalysis. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Sep 16]. 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

19. Li, Bin. Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II).

Degree: Docteur es, Chimie, 2013, Rennes 1

Dans ce travail de recherche, la synthèse de complexes de ruthénium cyclometallés a été effectuée à partir d'imines, 2-phénylpyridine, 2-phényloxazoline, phénylpyrazole, et benzo[h]quinoline par réaction… (more)

Subjects/Keywords: Ruthénium; Catalyse; Activation C-H; Couplages mixtes; Hydrosilylation; Ruthenium; Catalysis; C-H bond activation; Cross-couplings; Hydrosilylation

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APA (6th Edition):

Li, B. (2013). Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II). (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2013REN1S114

Chicago Manual of Style (16th Edition):

Li, Bin. “Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II).” 2013. Doctoral Dissertation, Rennes 1. Accessed September 16, 2019. http://www.theses.fr/2013REN1S114.

MLA Handbook (7th Edition):

Li, Bin. “Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II).” 2013. Web. 16 Sep 2019.

Vancouver:

Li B. Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II). [Internet] [Doctoral dissertation]. Rennes 1; 2013. [cited 2019 Sep 16]. Available from: http://www.theses.fr/2013REN1S114.

Council of Science Editors:

Li B. Ruthenium(II) catalyzed C-H bond functionalization and hydrosilylation reactions : Réactions de fonctionnalisation de liaisons C-H et d'hydrosilylation catalysée par le Ruthénium(II). [Doctoral Dissertation]. Rennes 1; 2013. Available from: http://www.theses.fr/2013REN1S114

20. MAK KAR HANG, GARVIN. Bond activation studies with pentacyclopentadienyl iridium complexes.

Degree: 2012, National University of Singapore

Subjects/Keywords: C-F bond activation; C-C bond activation; Cp* iridium; reaction pathways; alkyne

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APA (6th Edition):

MAK KAR HANG, G. (2012). Bond activation studies with pentacyclopentadienyl iridium complexes. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/37908

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):

MAK KAR HANG, GARVIN. “Bond activation studies with pentacyclopentadienyl iridium complexes.” 2012. Thesis, National University of Singapore. Accessed September 16, 2019. http://scholarbank.nus.edu.sg/handle/10635/37908.

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

MLA Handbook (7th Edition):

MAK KAR HANG, GARVIN. “Bond activation studies with pentacyclopentadienyl iridium complexes.” 2012. Web. 16 Sep 2019.

Vancouver:

MAK KAR HANG G. Bond activation studies with pentacyclopentadienyl iridium complexes. [Internet] [Thesis]. National University of Singapore; 2012. [cited 2019 Sep 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/37908.

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

Council of Science Editors:

MAK KAR HANG G. Bond activation studies with pentacyclopentadienyl iridium complexes. [Thesis]. National University of Singapore; 2012. Available from: http://scholarbank.nus.edu.sg/handle/10635/37908

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


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 September 16, 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. 16 Sep 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 Sep 16]. 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. 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 September 16, 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. 16 Sep 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 Sep 16]. 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


East Carolina University

23. Ravindranathan, Deepak. SYNTHESIS AND PHOTOPHYSICAL CHARACTERIZATION OF TRIDENTATE C^N*N PLATINUM (II) COMPLEXES and, INVESTIGATION OF SELECTIVITY IN C-H BOND ACTIVATION BY PLATINUM.

Degree: 2012, East Carolina University

 The synthesis, structure, and photophysical properties of a series of novel, highly luminescent tridentate platinum complexes with general coordination geometry of (C^N*N)-PtL are reported, where… (more)

Subjects/Keywords: Chemistry; C-H bond activation; Complexes; Cyclometalation; Phosphorescence; Organoplatinum compounds; Platinum; Chemical bonds

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APA (6th Edition):

Ravindranathan, D. (2012). SYNTHESIS AND PHOTOPHYSICAL CHARACTERIZATION OF TRIDENTATE C^N*N PLATINUM (II) COMPLEXES and, INVESTIGATION OF SELECTIVITY IN C-H BOND ACTIVATION BY PLATINUM. (Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4007

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):

Ravindranathan, Deepak. “SYNTHESIS AND PHOTOPHYSICAL CHARACTERIZATION OF TRIDENTATE C^N*N PLATINUM (II) COMPLEXES and, INVESTIGATION OF SELECTIVITY IN C-H BOND ACTIVATION BY PLATINUM.” 2012. Thesis, East Carolina University. Accessed September 16, 2019. http://hdl.handle.net/10342/4007.

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

MLA Handbook (7th Edition):

Ravindranathan, Deepak. “SYNTHESIS AND PHOTOPHYSICAL CHARACTERIZATION OF TRIDENTATE C^N*N PLATINUM (II) COMPLEXES and, INVESTIGATION OF SELECTIVITY IN C-H BOND ACTIVATION BY PLATINUM.” 2012. Web. 16 Sep 2019.

Vancouver:

Ravindranathan D. SYNTHESIS AND PHOTOPHYSICAL CHARACTERIZATION OF TRIDENTATE C^N*N PLATINUM (II) COMPLEXES and, INVESTIGATION OF SELECTIVITY IN C-H BOND ACTIVATION BY PLATINUM. [Internet] [Thesis]. East Carolina University; 2012. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/10342/4007.

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

Council of Science Editors:

Ravindranathan D. SYNTHESIS AND PHOTOPHYSICAL CHARACTERIZATION OF TRIDENTATE C^N*N PLATINUM (II) COMPLEXES and, INVESTIGATION OF SELECTIVITY IN C-H BOND ACTIVATION BY PLATINUM. [Thesis]. East Carolina University; 2012. Available from: http://hdl.handle.net/10342/4007

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

24. Kalutharage, Nishantha Kumara. Synthetic and Mechanistic Studies of Ruthenium Catalyzed C-C, C-N and C-O Bond Activation Reactions.

Degree: 2015, Marquette University

 Transition metal catalyzed selective C-C, C-N and C-O bond activation reactions are fundamentally important in organometallic chemistry and organic synthesis. Catalytic C-C, C-N and C-O(more)

Subjects/Keywords: amine coupling; C-N bond activation; deamination; deoxygenation; etherification; Ru catalyst; Inorganic Chemistry

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APA (6th Edition):

Kalutharage, N. K. (2015). Synthetic and Mechanistic Studies of Ruthenium Catalyzed C-C, C-N and C-O Bond Activation Reactions. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/dissertations_mu/506

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):

Kalutharage, Nishantha Kumara. “Synthetic and Mechanistic Studies of Ruthenium Catalyzed C-C, C-N and C-O Bond Activation Reactions.” 2015. Thesis, Marquette University. Accessed September 16, 2019. https://epublications.marquette.edu/dissertations_mu/506.

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

MLA Handbook (7th Edition):

Kalutharage, Nishantha Kumara. “Synthetic and Mechanistic Studies of Ruthenium Catalyzed C-C, C-N and C-O Bond Activation Reactions.” 2015. Web. 16 Sep 2019.

Vancouver:

Kalutharage NK. Synthetic and Mechanistic Studies of Ruthenium Catalyzed C-C, C-N and C-O Bond Activation Reactions. [Internet] [Thesis]. Marquette University; 2015. [cited 2019 Sep 16]. Available from: https://epublications.marquette.edu/dissertations_mu/506.

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

Council of Science Editors:

Kalutharage NK. Synthetic and Mechanistic Studies of Ruthenium Catalyzed C-C, C-N and C-O Bond Activation Reactions. [Thesis]. Marquette University; 2015. Available from: https://epublications.marquette.edu/dissertations_mu/506

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


University of the Western Cape

25. Mungwe, Nothando Wandile. The synthesis of the cyclometallated palladium complexes and their applications in olefin oligomerization and in phenylacetylene oligomerization/polymerization .

Degree: 2007, University of the Western Cape

This thesis reports the synthesis of the imine ligands from Schiff base condensation reaction of aldehyde derivatives and equimolar quantities of aniline derivatives. The imine ligands spectrometry. Advisors/Committee Members: Mapolie, S.F (advisor).

Subjects/Keywords: C-H bond activation; Cyclometallated; Metallocycles

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APA (6th Edition):

Mungwe, N. W. (2007). The synthesis of the cyclometallated palladium complexes and their applications in olefin oligomerization and in phenylacetylene oligomerization/polymerization . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/3690

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):

Mungwe, Nothando Wandile. “The synthesis of the cyclometallated palladium complexes and their applications in olefin oligomerization and in phenylacetylene oligomerization/polymerization .” 2007. Thesis, University of the Western Cape. Accessed September 16, 2019. http://hdl.handle.net/11394/3690.

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

MLA Handbook (7th Edition):

Mungwe, Nothando Wandile. “The synthesis of the cyclometallated palladium complexes and their applications in olefin oligomerization and in phenylacetylene oligomerization/polymerization .” 2007. Web. 16 Sep 2019.

Vancouver:

Mungwe NW. The synthesis of the cyclometallated palladium complexes and their applications in olefin oligomerization and in phenylacetylene oligomerization/polymerization . [Internet] [Thesis]. University of the Western Cape; 2007. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/11394/3690.

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

Council of Science Editors:

Mungwe NW. The synthesis of the cyclometallated palladium complexes and their applications in olefin oligomerization and in phenylacetylene oligomerization/polymerization . [Thesis]. University of the Western Cape; 2007. Available from: http://hdl.handle.net/11394/3690

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


North Carolina State University

26. Lail, Marty A. Synthesis and Reactivity of Ruthenium Alkyl and Aryl Complexes and Their Application towards Aromatic C-H Bond Activation and Olefin Hydroarylation.

Degree: PhD, Chemistry, 2007, North Carolina State University

Subjects/Keywords: ruthenium; bond homolysis; catalysis; C-H bond activation; hydroarylation

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APA (6th Edition):

Lail, M. A. (2007). Synthesis and Reactivity of Ruthenium Alkyl and Aryl Complexes and Their Application towards Aromatic C-H Bond Activation and Olefin Hydroarylation. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/5776

Chicago Manual of Style (16th Edition):

Lail, Marty A. “Synthesis and Reactivity of Ruthenium Alkyl and Aryl Complexes and Their Application towards Aromatic C-H Bond Activation and Olefin Hydroarylation.” 2007. Doctoral Dissertation, North Carolina State University. Accessed September 16, 2019. http://www.lib.ncsu.edu/resolver/1840.16/5776.

MLA Handbook (7th Edition):

Lail, Marty A. “Synthesis and Reactivity of Ruthenium Alkyl and Aryl Complexes and Their Application towards Aromatic C-H Bond Activation and Olefin Hydroarylation.” 2007. Web. 16 Sep 2019.

Vancouver:

Lail MA. Synthesis and Reactivity of Ruthenium Alkyl and Aryl Complexes and Their Application towards Aromatic C-H Bond Activation and Olefin Hydroarylation. [Internet] [Doctoral dissertation]. North Carolina State University; 2007. [cited 2019 Sep 16]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5776.

Council of Science Editors:

Lail MA. Synthesis and Reactivity of Ruthenium Alkyl and Aryl Complexes and Their Application towards Aromatic C-H Bond Activation and Olefin Hydroarylation. [Doctoral Dissertation]. North Carolina State University; 2007. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5776

27. Τζουμανίκας, Χρήστος-Ευάγγελος. Σύνθεση υποκατάστατων χαλκού και χρήση των αντίστοιχων οργανομεταλλικών συμπλόκων ως μιμητές της μονοξυγονάσης του μεθανίου στην καταλυτική ενεργοποίηση-οξείδωση δεσμών Csp3-H.

Degree: 2015, University of Patras

Η εργασία αυτή αποτελεί τη διπλωματική εργασία που εκπονήθηκε στα πλαίσια του διατμηματικού μεταπτυχιακού προγράμματος “Ιατρική Χηµεία: Σχεδιασμός και Ανάπτυξη Φαρμακευτικών Προϊόντων” του Πανεπιστημίου Πατρών.… (more)

Subjects/Keywords: Ενεργοποίηση δεσμών C-H; Σύμπλοκα χαλκού; Υποκαταστάτες χαλκού; Καταλυτική οξείδωση; 572.518; C-H bond activation; Copper complexes; Copper ligands; Catalytic oxidation

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APA (6th Edition):

Τζουμανίκας, . (2015). Σύνθεση υποκατάστατων χαλκού και χρήση των αντίστοιχων οργανομεταλλικών συμπλόκων ως μιμητές της μονοξυγονάσης του μεθανίου στην καταλυτική ενεργοποίηση-οξείδωση δεσμών Csp3-H. (Masters Thesis). University of Patras. Retrieved from http://hdl.handle.net/10889/8798

Chicago Manual of Style (16th Edition):

Τζουμανίκας, Χρήστος-Ευάγγελος. “Σύνθεση υποκατάστατων χαλκού και χρήση των αντίστοιχων οργανομεταλλικών συμπλόκων ως μιμητές της μονοξυγονάσης του μεθανίου στην καταλυτική ενεργοποίηση-οξείδωση δεσμών Csp3-H.” 2015. Masters Thesis, University of Patras. Accessed September 16, 2019. http://hdl.handle.net/10889/8798.

MLA Handbook (7th Edition):

Τζουμανίκας, Χρήστος-Ευάγγελος. “Σύνθεση υποκατάστατων χαλκού και χρήση των αντίστοιχων οργανομεταλλικών συμπλόκων ως μιμητές της μονοξυγονάσης του μεθανίου στην καταλυτική ενεργοποίηση-οξείδωση δεσμών Csp3-H.” 2015. Web. 16 Sep 2019.

Vancouver:

Τζουμανίκας . Σύνθεση υποκατάστατων χαλκού και χρήση των αντίστοιχων οργανομεταλλικών συμπλόκων ως μιμητές της μονοξυγονάσης του μεθανίου στην καταλυτική ενεργοποίηση-οξείδωση δεσμών Csp3-H. [Internet] [Masters thesis]. University of Patras; 2015. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/10889/8798.

Council of Science Editors:

Τζουμανίκας . Σύνθεση υποκατάστατων χαλκού και χρήση των αντίστοιχων οργανομεταλλικών συμπλόκων ως μιμητές της μονοξυγονάσης του μεθανίου στην καταλυτική ενεργοποίηση-οξείδωση δεσμών Csp3-H. [Masters Thesis]. University of Patras; 2015. Available from: http://hdl.handle.net/10889/8798

28. Hostier, Thomas. Activation de liaisons C-O catalysée par le nickel et sulfénylation de liaisons C-H : Nickel-catalyzed C-O bond activation and sulfenylation of C-H bonds.

Degree: Docteur es, Chimie organique, 2016, Université Pierre et Marie Curie – Paris VI

La mise au point de nouvelles méthodes de synthèse flexibles, robustes et polyvalentes pour la formation régiosélective de liaisons carbone-carbone ou carbone-hétéroatome représente un défi… (more)

Subjects/Keywords: Couplage de Kumada; Activation C-O; Nickel; Éther d'énol méthylique; Sulfénylation électrophile; Indole; C-O activation; Electrophilic sulfenylation; Electron-rich aromatics; 541.2

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APA (6th Edition):

Hostier, T. (2016). Activation de liaisons C-O catalysée par le nickel et sulfénylation de liaisons C-H : Nickel-catalyzed C-O bond activation and sulfenylation of C-H bonds. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066587

Chicago Manual of Style (16th Edition):

Hostier, Thomas. “Activation de liaisons C-O catalysée par le nickel et sulfénylation de liaisons C-H : Nickel-catalyzed C-O bond activation and sulfenylation of C-H bonds.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed September 16, 2019. http://www.theses.fr/2016PA066587.

MLA Handbook (7th Edition):

Hostier, Thomas. “Activation de liaisons C-O catalysée par le nickel et sulfénylation de liaisons C-H : Nickel-catalyzed C-O bond activation and sulfenylation of C-H bonds.” 2016. Web. 16 Sep 2019.

Vancouver:

Hostier T. Activation de liaisons C-O catalysée par le nickel et sulfénylation de liaisons C-H : Nickel-catalyzed C-O bond activation and sulfenylation of C-H bonds. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2019 Sep 16]. Available from: http://www.theses.fr/2016PA066587.

Council of Science Editors:

Hostier T. Activation de liaisons C-O catalysée par le nickel et sulfénylation de liaisons C-H : Nickel-catalyzed C-O bond activation and sulfenylation of C-H bonds. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066587

29. Sofack-Kreutzer, Julien. Synthèses de carbocycles et d'hétérocycles à cinq chaînons par activation de liaisons c(sp3)-h non activées : Intramolecular Palladium-Catalyzed C(sp3)-H Arylation of aryl and alkenyl halides : synthesis of fused five-membered rings.

Degree: Docteur es, Chimie organique, 2011, Université Claude Bernard – Lyon I

La fonctionnalisation de liaisons C-H réputées peu réactives ouvre de nouvelles perspectives en synthèse organique. La catalyse par un métal de transition comme le palladium… (more)

Subjects/Keywords: Fonctionnalisation C-H; Activation C-H; Indanes; Indolines; Catalyse organométallique; Chloroarènes; Formation de liaisons C-C; Palladium; Bromoalcènes; Hexahydroindoles; Aéruginosines; C-H functionalization; C-H activation; Indanes; Indoles; Organometallic catalysis; C-C bond formation; Palladium; Hexahydroindoles; Aeruginosins; 547

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APA (6th Edition):

Sofack-Kreutzer, J. (2011). Synthèses de carbocycles et d'hétérocycles à cinq chaînons par activation de liaisons c(sp3)-h non activées : Intramolecular Palladium-Catalyzed C(sp3)-H Arylation of aryl and alkenyl halides : synthesis of fused five-membered rings. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2011LYO10302

Chicago Manual of Style (16th Edition):

Sofack-Kreutzer, Julien. “Synthèses de carbocycles et d'hétérocycles à cinq chaînons par activation de liaisons c(sp3)-h non activées : Intramolecular Palladium-Catalyzed C(sp3)-H Arylation of aryl and alkenyl halides : synthesis of fused five-membered rings.” 2011. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed September 16, 2019. http://www.theses.fr/2011LYO10302.

MLA Handbook (7th Edition):

Sofack-Kreutzer, Julien. “Synthèses de carbocycles et d'hétérocycles à cinq chaînons par activation de liaisons c(sp3)-h non activées : Intramolecular Palladium-Catalyzed C(sp3)-H Arylation of aryl and alkenyl halides : synthesis of fused five-membered rings.” 2011. Web. 16 Sep 2019.

Vancouver:

Sofack-Kreutzer J. Synthèses de carbocycles et d'hétérocycles à cinq chaînons par activation de liaisons c(sp3)-h non activées : Intramolecular Palladium-Catalyzed C(sp3)-H Arylation of aryl and alkenyl halides : synthesis of fused five-membered rings. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2011. [cited 2019 Sep 16]. Available from: http://www.theses.fr/2011LYO10302.

Council of Science Editors:

Sofack-Kreutzer J. Synthèses de carbocycles et d'hétérocycles à cinq chaînons par activation de liaisons c(sp3)-h non activées : Intramolecular Palladium-Catalyzed C(sp3)-H Arylation of aryl and alkenyl halides : synthesis of fused five-membered rings. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2011. Available from: http://www.theses.fr/2011LYO10302

30. Zhao, Liqin. Palladium-catalyzed direct arylation via sp² and sp³ C-H activation of hetero(aromatics) and hydrocarbons for C-C bond formation : Arylations directe catalysées au palladium via activation de liaisons C-H de type sp² et sp³ d'hétéro(aromatiques) et d'hydrocarbures pour la formation de liaisons C-C.

Degree: Docteur es, Chimie, 2014, Rennes 1

Au cours de cette thèse, nous nous sommes intéressés à l'activation de liaisons sp² et sp³ C-H catalysée par le palladium pour la préparation d'(hétéro)aryl-aryles… (more)

Subjects/Keywords: Arylation; Hétéroaromatiques; Palladium; Activation de liaison C-H; Economie d'atomes; Biaryls; Activation de liaison sp3 et sp2 C-H; Halogénures d'aryle; Catalyse Homogène.; Arylation; Heteroaromatics; Palladium; C-H activation; Atom-Economy; Biaryls; Sp3 and sp2 C-H bond activation; Aryl halides; Homogeneous catalysis.

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APA (6th Edition):

Zhao, L. (2014). Palladium-catalyzed direct arylation via sp² and sp³ C-H activation of hetero(aromatics) and hydrocarbons for C-C bond formation : Arylations directe catalysées au palladium via activation de liaisons C-H de type sp² et sp³ d'hétéro(aromatiques) et d'hydrocarbures pour la formation de liaisons C-C. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2014REN1S038

Chicago Manual of Style (16th Edition):

Zhao, Liqin. “Palladium-catalyzed direct arylation via sp² and sp³ C-H activation of hetero(aromatics) and hydrocarbons for C-C bond formation : Arylations directe catalysées au palladium via activation de liaisons C-H de type sp² et sp³ d'hétéro(aromatiques) et d'hydrocarbures pour la formation de liaisons C-C.” 2014. Doctoral Dissertation, Rennes 1. Accessed September 16, 2019. http://www.theses.fr/2014REN1S038.

MLA Handbook (7th Edition):

Zhao, Liqin. “Palladium-catalyzed direct arylation via sp² and sp³ C-H activation of hetero(aromatics) and hydrocarbons for C-C bond formation : Arylations directe catalysées au palladium via activation de liaisons C-H de type sp² et sp³ d'hétéro(aromatiques) et d'hydrocarbures pour la formation de liaisons C-C.” 2014. Web. 16 Sep 2019.

Vancouver:

Zhao L. Palladium-catalyzed direct arylation via sp² and sp³ C-H activation of hetero(aromatics) and hydrocarbons for C-C bond formation : Arylations directe catalysées au palladium via activation de liaisons C-H de type sp² et sp³ d'hétéro(aromatiques) et d'hydrocarbures pour la formation de liaisons C-C. [Internet] [Doctoral dissertation]. Rennes 1; 2014. [cited 2019 Sep 16]. Available from: http://www.theses.fr/2014REN1S038.

Council of Science Editors:

Zhao L. Palladium-catalyzed direct arylation via sp² and sp³ C-H activation of hetero(aromatics) and hydrocarbons for C-C bond formation : Arylations directe catalysées au palladium via activation de liaisons C-H de type sp² et sp³ d'hétéro(aromatiques) et d'hydrocarbures pour la formation de liaisons C-C. [Doctoral Dissertation]. Rennes 1; 2014. Available from: http://www.theses.fr/2014REN1S038

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