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You searched for subject:(C H activation). Showing records 1 – 30 of 202 total matches.

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University of Illinois – Urbana-Champaign

1. Liu, Wei. Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis.

Degree: PhD, Chemistry, 2018, University of Illinois – Urbana-Champaign

 Asymmetric C–H functionalization could deliver a highly efficient transformation by installing both oxidized functionality and absolute stereochemistry simultaneously. In this context, palladium(II)-catalyzed asymmetric allylic C–H(more)

Subjects/Keywords: C–H Activation; Asymmetric Catalysis

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APA (6th Edition):

Liu, W. (2018). Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/102431

Chicago Manual of Style (16th Edition):

Liu, Wei. “Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis.” 2018. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 21, 2019. http://hdl.handle.net/2142/102431.

MLA Handbook (7th Edition):

Liu, Wei. “Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis.” 2018. Web. 21 Oct 2019.

Vancouver:

Liu W. Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2018. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2142/102431.

Council of Science Editors:

Liu W. Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2018. Available from: http://hdl.handle.net/2142/102431


University of California – Berkeley

2. Bowring, Miriam Anna. Hydrocarbon Bond Activation with Platinum(II) Complexes.

Degree: Chemistry, 2013, University of California – Berkeley

 Chapter 1. The hydroarylation of unactivated olefins effected by Pt(II) precatalysts is found to proceed through the in situ production of protic acid followed by… (more)

Subjects/Keywords: Chemistry; catalysis; C-C activation; C-H activation; mechanism; organometallics; platinum

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APA (6th Edition):

Bowring, M. A. (2013). Hydrocarbon Bond Activation with Platinum(II) Complexes. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/93242966

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):

Bowring, Miriam Anna. “Hydrocarbon Bond Activation with Platinum(II) Complexes.” 2013. Thesis, University of California – Berkeley. Accessed October 21, 2019. http://www.escholarship.org/uc/item/93242966.

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

MLA Handbook (7th Edition):

Bowring, Miriam Anna. “Hydrocarbon Bond Activation with Platinum(II) Complexes.” 2013. Web. 21 Oct 2019.

Vancouver:

Bowring MA. Hydrocarbon Bond Activation with Platinum(II) Complexes. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Oct 21]. Available from: http://www.escholarship.org/uc/item/93242966.

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

Council of Science Editors:

Bowring MA. Hydrocarbon Bond Activation with Platinum(II) Complexes. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/93242966

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


University of Rochester

3. Wilklow-Marnell, Miles. Manipulation of carbon-element bonds by Pincer ligated iridium complexes.

Degree: PhD, 2017, University of Rochester

 Since the seminal contributions of Moulton and Shaw in the 1970’s, who synthesized the first “pincer” complexes, including tBuPCPIrHCl (tBuPCP = κ3-2,6-C6H3(CH2P(tBu)2)2), the chemistry of… (more)

Subjects/Keywords: C-C activation; C-H activation; Cyclometalation; Dehydrogenative coupling; Iridaindene; Quinones

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APA (6th Edition):

Wilklow-Marnell, M. (2017). Manipulation of carbon-element bonds by Pincer ligated iridium complexes. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/33156

Chicago Manual of Style (16th Edition):

Wilklow-Marnell, Miles. “Manipulation of carbon-element bonds by Pincer ligated iridium complexes.” 2017. Doctoral Dissertation, University of Rochester. Accessed October 21, 2019. http://hdl.handle.net/1802/33156.

MLA Handbook (7th Edition):

Wilklow-Marnell, Miles. “Manipulation of carbon-element bonds by Pincer ligated iridium complexes.” 2017. Web. 21 Oct 2019.

Vancouver:

Wilklow-Marnell M. Manipulation of carbon-element bonds by Pincer ligated iridium complexes. [Internet] [Doctoral dissertation]. University of Rochester; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1802/33156.

Council of Science Editors:

Wilklow-Marnell M. Manipulation of carbon-element bonds by Pincer ligated iridium complexes. [Doctoral Dissertation]. University of Rochester; 2017. Available from: http://hdl.handle.net/1802/33156


University of Texas – Austin

4. Ren, Zhi. Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy.

Degree: PhD, Chemistry, 2016, University of Texas – Austin

 Transition metal catalyzed functionalization of carbon-hydrogen bonds (C−H bonds) has become an exponentially growing field. Particularly, Pd-catalyzed methods with various directing groups (DGs) have been… (more)

Subjects/Keywords: C-H activation; C-H functionalization; Palladium catalysis

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APA (6th Edition):

Ren, Z. (2016). Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/39758

Chicago Manual of Style (16th Edition):

Ren, Zhi. “Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 21, 2019. http://hdl.handle.net/2152/39758.

MLA Handbook (7th Edition):

Ren, Zhi. “Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy.” 2016. Web. 21 Oct 2019.

Vancouver:

Ren Z. Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2152/39758.

Council of Science Editors:

Ren Z. Palladium-catalyzed carbon-hydrogen bond functionalization utilizing an exo-directing strategy. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/39758

5. Pierre, Cathleen. Synthèses de molécules polycycliques par arylation C(sp³)-H intramoléculaire catalysée par le palladium : synthesis of polycyclic molecules by intramolecular palladium-catalyzed C(sp³)-H arylation.

Degree: Docteur es, Chimie organique, 2012, Université Claude Bernard – Lyon I

La synthèse de produits complexes se doit de prendre en compte de nouvelles méthodes desynthèse plus efficaces, dont la fonctionnalisation de liaisons carbone-hydrogène. Dans cecontexte,… (more)

Subjects/Keywords: Fonctionnalisation C-H; Activation C-H; Arylation C-H; Catalyse organométallique; Chloroarènes; Benzocyclobutènes; Activation C-H asymétrique; Palladium; C-H functionalization; C-H activation; C-H arylation; Organometallic catalysis; Chloroarenes; Benzocyclobutenes; Asymmetric C-H activation; Palladium; 541.395

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APA (6th Edition):

Pierre, C. (2012). Synthèses de molécules polycycliques par arylation C(sp³)-H intramoléculaire catalysée par le palladium : synthesis of polycyclic molecules by intramolecular palladium-catalyzed C(sp³)-H arylation. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2012LYO10207

Chicago Manual of Style (16th Edition):

Pierre, Cathleen. “Synthèses de molécules polycycliques par arylation C(sp³)-H intramoléculaire catalysée par le palladium : synthesis of polycyclic molecules by intramolecular palladium-catalyzed C(sp³)-H arylation.” 2012. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed October 21, 2019. http://www.theses.fr/2012LYO10207.

MLA Handbook (7th Edition):

Pierre, Cathleen. “Synthèses de molécules polycycliques par arylation C(sp³)-H intramoléculaire catalysée par le palladium : synthesis of polycyclic molecules by intramolecular palladium-catalyzed C(sp³)-H arylation.” 2012. Web. 21 Oct 2019.

Vancouver:

Pierre C. Synthèses de molécules polycycliques par arylation C(sp³)-H intramoléculaire catalysée par le palladium : synthesis of polycyclic molecules by intramolecular palladium-catalyzed C(sp³)-H arylation. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2012. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2012LYO10207.

Council of Science Editors:

Pierre C. Synthèses de molécules polycycliques par arylation C(sp³)-H intramoléculaire catalysée par le palladium : synthesis of polycyclic molecules by intramolecular palladium-catalyzed C(sp³)-H arylation. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2012. Available from: http://www.theses.fr/2012LYO10207


Penn State University

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

Degree: MS, Chemistry, 2012, Penn State University

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Lu, Chengxi. “Palladium-catalyzed Halogenation Of Ortho-c-h Bonds Of Benzylamine Picolinamides And Arylethylamine Picolinamides.” 2012. Masters Thesis, Penn State University. Accessed October 21, 2019. https://etda.libraries.psu.edu/catalog/21598.

MLA Handbook (7th Edition):

Lu, Chengxi. “Palladium-catalyzed Halogenation Of Ortho-c-h Bonds Of Benzylamine Picolinamides And Arylethylamine Picolinamides.” 2012. Web. 21 Oct 2019.

Vancouver:

Lu C. Palladium-catalyzed Halogenation Of Ortho-c-h Bonds Of Benzylamine Picolinamides And Arylethylamine Picolinamides. [Internet] [Masters thesis]. Penn State University; 2012. [cited 2019 Oct 21]. Available from: https://etda.libraries.psu.edu/catalog/21598.

Council of Science Editors:

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


University of California – Berkeley

7. Tsai, Andy Siu-Chun. Rhodium Catalyzed C-H Bond Functionalization: Development of Methods and Applications in Organic Synthesis.

Degree: Chemistry, 2011, University of California – Berkeley

 Chapter 1. A sequence of research projects beginning with studies in diastereoselective C-H bond functionalization applied to the synthesis of (-)-incarvaillateine to the Rh(III) catalyzed… (more)

Subjects/Keywords: Chemistry; catalysis; C-H activation; incarvillateine; rhodium

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APA (6th Edition):

Tsai, A. S. (2011). Rhodium Catalyzed C-H Bond Functionalization: Development of Methods and Applications in Organic Synthesis. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/23n227t9

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, Andy Siu-Chun. “Rhodium Catalyzed C-H Bond Functionalization: Development of Methods and Applications in Organic Synthesis.” 2011. Thesis, University of California – Berkeley. Accessed October 21, 2019. http://www.escholarship.org/uc/item/23n227t9.

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

MLA Handbook (7th Edition):

Tsai, Andy Siu-Chun. “Rhodium Catalyzed C-H Bond Functionalization: Development of Methods and Applications in Organic Synthesis.” 2011. Web. 21 Oct 2019.

Vancouver:

Tsai AS. Rhodium Catalyzed C-H Bond Functionalization: Development of Methods and Applications in Organic Synthesis. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2019 Oct 21]. Available from: http://www.escholarship.org/uc/item/23n227t9.

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

Council of Science Editors:

Tsai AS. Rhodium Catalyzed C-H Bond Functionalization: Development of Methods and Applications in Organic Synthesis. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/23n227t9

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


University of Manchester

8. Eichler, Anja. Investigations of Self-Sufficient P450cam Monooxygenases for Activity and Enantioselectivity.

Degree: 2016, University of Manchester

Catalytic, selective C-H bond activation for the oxidative hydroxylation RH → ROH of simple or complex compounds is of significant interest in synthetic organic chemistry.… (more)

Subjects/Keywords: C-H activation; P450 enzymes; Selectivity

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APA (6th Edition):

Eichler, A. (2016). Investigations of Self-Sufficient P450cam Monooxygenases for Activity and Enantioselectivity. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302167

Chicago Manual of Style (16th Edition):

Eichler, Anja. “Investigations of Self-Sufficient P450cam Monooxygenases for Activity and Enantioselectivity.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302167.

MLA Handbook (7th Edition):

Eichler, Anja. “Investigations of Self-Sufficient P450cam Monooxygenases for Activity and Enantioselectivity.” 2016. Web. 21 Oct 2019.

Vancouver:

Eichler A. Investigations of Self-Sufficient P450cam Monooxygenases for Activity and Enantioselectivity. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302167.

Council of Science Editors:

Eichler A. Investigations of Self-Sufficient P450cam Monooxygenases for Activity and Enantioselectivity. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302167


Mississippi State University

9. Reilly, Sean William. Synthesis and catalytic activity of CCC-NHC group 9 metal pincer complexes.

Degree: PhD, Chemistry, 2015, Mississippi State University

  <I>N</I>-Heterocyclic carbenes (NHCs) are one of the few ligand systems that can finely tune transition metal catalysts via sterics and electronics. The strong sigma-donating… (more)

Subjects/Keywords: C-H activation; pincer; NHC; carbene

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APA (6th Edition):

Reilly, S. W. (2015). Synthesis and catalytic activity of CCC-NHC group 9 metal pincer complexes. (Doctoral Dissertation). Mississippi State University. Retrieved from http://sun.library.msstate.edu/ETD-db/theses/available/etd-10222015-145433/ ;

Chicago Manual of Style (16th Edition):

Reilly, Sean William. “Synthesis and catalytic activity of CCC-NHC group 9 metal pincer complexes.” 2015. Doctoral Dissertation, Mississippi State University. Accessed October 21, 2019. http://sun.library.msstate.edu/ETD-db/theses/available/etd-10222015-145433/ ;.

MLA Handbook (7th Edition):

Reilly, Sean William. “Synthesis and catalytic activity of CCC-NHC group 9 metal pincer complexes.” 2015. Web. 21 Oct 2019.

Vancouver:

Reilly SW. Synthesis and catalytic activity of CCC-NHC group 9 metal pincer complexes. [Internet] [Doctoral dissertation]. Mississippi State University; 2015. [cited 2019 Oct 21]. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-10222015-145433/ ;.

Council of Science Editors:

Reilly SW. Synthesis and catalytic activity of CCC-NHC group 9 metal pincer complexes. [Doctoral Dissertation]. Mississippi State University; 2015. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-10222015-145433/ ;


North Carolina State University

10. Foley, Nicholas Adam. Synthesis and Comparative Studies of Ru(II) Complexes for Metal-mediated C-H Activation and Olefin Hydroarylation Catalysis.

Degree: PhD, Chemistry, 2009, North Carolina State University

 TpRu(CO)(NCMe)Ph catalyzes the addition of aromatic C-H bonds across double bonds (i.e., olefin hydroarylation). Second generation TpRu(L)(NCMe)R {L = PMe3, P(OCH2)3CEt or P(pyr)3; pyr =… (more)

Subjects/Keywords: Olefin Hydroarylation; C-H Activation; Ruthenium

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APA (6th Edition):

Foley, N. A. (2009). Synthesis and Comparative Studies of Ru(II) Complexes for Metal-mediated C-H Activation and Olefin Hydroarylation Catalysis. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/4976

Chicago Manual of Style (16th Edition):

Foley, Nicholas Adam. “Synthesis and Comparative Studies of Ru(II) Complexes for Metal-mediated C-H Activation and Olefin Hydroarylation Catalysis.” 2009. Doctoral Dissertation, North Carolina State University. Accessed October 21, 2019. http://www.lib.ncsu.edu/resolver/1840.16/4976.

MLA Handbook (7th Edition):

Foley, Nicholas Adam. “Synthesis and Comparative Studies of Ru(II) Complexes for Metal-mediated C-H Activation and Olefin Hydroarylation Catalysis.” 2009. Web. 21 Oct 2019.

Vancouver:

Foley NA. Synthesis and Comparative Studies of Ru(II) Complexes for Metal-mediated C-H Activation and Olefin Hydroarylation Catalysis. [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2019 Oct 21]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4976.

Council of Science Editors:

Foley NA. Synthesis and Comparative Studies of Ru(II) Complexes for Metal-mediated C-H Activation and Olefin Hydroarylation Catalysis. [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4976


University of Manchester

11. Eichler, Anja. Investigations of self-sufficient P450cam monooxygenases for activity and enantioselectivity.

Degree: PhD, 2016, University of Manchester

 Catalytic, selective C-H bond activation for the oxidative hydroxylation RH → ROH of simple or complex compounds is of significant interest in synthetic organic chemistry.… (more)

Subjects/Keywords: 572; C-H activation; P450 enzymes; Selectivity

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APA (6th Edition):

Eichler, A. (2016). Investigations of self-sufficient P450cam monooxygenases for activity and enantioselectivity. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/investigations-of-selfsufficient-p450cam-monooxygenases-for-activity-and-enantioselectivity(27df0fa8-b671-4593-8ec0-f993a31e120c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728108

Chicago Manual of Style (16th Edition):

Eichler, Anja. “Investigations of self-sufficient P450cam monooxygenases for activity and enantioselectivity.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. https://www.research.manchester.ac.uk/portal/en/theses/investigations-of-selfsufficient-p450cam-monooxygenases-for-activity-and-enantioselectivity(27df0fa8-b671-4593-8ec0-f993a31e120c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728108.

MLA Handbook (7th Edition):

Eichler, Anja. “Investigations of self-sufficient P450cam monooxygenases for activity and enantioselectivity.” 2016. Web. 21 Oct 2019.

Vancouver:

Eichler A. Investigations of self-sufficient P450cam monooxygenases for activity and enantioselectivity. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigations-of-selfsufficient-p450cam-monooxygenases-for-activity-and-enantioselectivity(27df0fa8-b671-4593-8ec0-f993a31e120c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728108.

Council of Science Editors:

Eichler A. Investigations of self-sufficient P450cam monooxygenases for activity and enantioselectivity. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigations-of-selfsufficient-p450cam-monooxygenases-for-activity-and-enantioselectivity(27df0fa8-b671-4593-8ec0-f993a31e120c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728108


University of Michigan

12. Neufeldt, Sharon Rose. Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization.

Degree: PhD, Chemistry, 2013, University of Michigan

 Because of their abundance, C-H bonds are highly attractive starting materials for the elaboration of complex molecules. Transition metal catalysis can enable these typically inert… (more)

Subjects/Keywords: Palladium; C-H Activation; Radicals; Chemistry; Science

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APA (6th Edition):

Neufeldt, S. R. (2013). Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/98061

Chicago Manual of Style (16th Edition):

Neufeldt, Sharon Rose. “Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization.” 2013. Doctoral Dissertation, University of Michigan. Accessed October 21, 2019. http://hdl.handle.net/2027.42/98061.

MLA Handbook (7th Edition):

Neufeldt, Sharon Rose. “Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization.” 2013. Web. 21 Oct 2019.

Vancouver:

Neufeldt SR. Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2027.42/98061.

Council of Science Editors:

Neufeldt SR. Palladium-Catalyzed Ligand-Directed C-H and C=C Bond Functionalization. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/98061


University of Edinburgh

13. Cant, Alastair Alexander. Investigations into aryne chemistry.

Degree: PhD, 2012, University of Edinburgh

 The first project in this thesis describes our research reacting arynes with tertiary allyl amines to generate functionalised anilines via a benzyne induced aza-Claisen reaction.… (more)

Subjects/Keywords: 547.6; benzyne; arynes; C-H activation

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APA (6th Edition):

Cant, A. A. (2012). Investigations into aryne chemistry. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/6249

Chicago Manual of Style (16th Edition):

Cant, Alastair Alexander. “Investigations into aryne chemistry.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed October 21, 2019. http://hdl.handle.net/1842/6249.

MLA Handbook (7th Edition):

Cant, Alastair Alexander. “Investigations into aryne chemistry.” 2012. Web. 21 Oct 2019.

Vancouver:

Cant AA. Investigations into aryne chemistry. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1842/6249.

Council of Science Editors:

Cant AA. Investigations into aryne chemistry. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/6249


Princeton University

14. Boaz, Nicholas Charles. The Development and Study of Practical C-H Functionalization Reactions Using Mechanistic Tools .

Degree: PhD, 2015, Princeton University

 The unactivated C-H bonds of hydrocarbons are some of the most common chemical functionalities in organic molecules. Despite their ubiquity, they are some of the… (more)

Subjects/Keywords: C-H Activation; Heme; Iodine; Iron; Methane

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APA (6th Edition):

Boaz, N. C. (2015). The Development and Study of Practical C-H Functionalization Reactions Using Mechanistic Tools . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01ks65hf52g

Chicago Manual of Style (16th Edition):

Boaz, Nicholas Charles. “The Development and Study of Practical C-H Functionalization Reactions Using Mechanistic Tools .” 2015. Doctoral Dissertation, Princeton University. Accessed October 21, 2019. http://arks.princeton.edu/ark:/88435/dsp01ks65hf52g.

MLA Handbook (7th Edition):

Boaz, Nicholas Charles. “The Development and Study of Practical C-H Functionalization Reactions Using Mechanistic Tools .” 2015. Web. 21 Oct 2019.

Vancouver:

Boaz NC. The Development and Study of Practical C-H Functionalization Reactions Using Mechanistic Tools . [Internet] [Doctoral dissertation]. Princeton University; 2015. [cited 2019 Oct 21]. Available from: http://arks.princeton.edu/ark:/88435/dsp01ks65hf52g.

Council of Science Editors:

Boaz NC. The Development and Study of Practical C-H Functionalization Reactions Using Mechanistic Tools . [Doctoral Dissertation]. Princeton University; 2015. Available from: http://arks.princeton.edu/ark:/88435/dsp01ks65hf52g


Universitat de Girona

15. Planas Fàbrega, Oriol. Cobalt-catalyzed C-H functionalization: from mechanistic studies to synthetic methodologies.

Degree: Departament de Química, 2018, Universitat de Girona

 L’objectiu principal d’aquesta tesi doctoral és la síntesis i la caracterització d’espècies organometàl•liques i estables aril-Co(III), fent ús de salts de cobalt(II) i d’un lligand… (more)

Subjects/Keywords: Cobalt; Cobalto; C-H functionalization; C-H activation; Activació d'enllaços C-H; Activación de enlaces C-H; Catalysis; Catàlisi; Catálisis; 546

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APA (6th Edition):

Planas Fàbrega, O. (2018). Cobalt-catalyzed C-H functionalization: from mechanistic studies to synthetic methodologies. (Thesis). Universitat de Girona. Retrieved from http://hdl.handle.net/10803/482111

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):

Planas Fàbrega, Oriol. “Cobalt-catalyzed C-H functionalization: from mechanistic studies to synthetic methodologies.” 2018. Thesis, Universitat de Girona. Accessed October 21, 2019. http://hdl.handle.net/10803/482111.

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

MLA Handbook (7th Edition):

Planas Fàbrega, Oriol. “Cobalt-catalyzed C-H functionalization: from mechanistic studies to synthetic methodologies.” 2018. Web. 21 Oct 2019.

Vancouver:

Planas Fàbrega O. Cobalt-catalyzed C-H functionalization: from mechanistic studies to synthetic methodologies. [Internet] [Thesis]. Universitat de Girona; 2018. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/10803/482111.

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

Council of Science Editors:

Planas Fàbrega O. Cobalt-catalyzed C-H functionalization: from mechanistic studies to synthetic methodologies. [Thesis]. Universitat de Girona; 2018. Available from: http://hdl.handle.net/10803/482111

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


NSYSU

16. 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 October 21, 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. 21 Oct 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 Oct 21]. 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

17. 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 October 21, 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. 21 Oct 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 Oct 21]. 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


University of Rochester

18. 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 October 21, 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. 21 Oct 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 Oct 21]. 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

19. Rhinehart, Jennifer Lee (1984 - ). Development of novel rhodium and iridium complexes with a fac-chelating ligand for electrophilic C-H activation.

Degree: PhD, 2012, University of Rochester

 Several new bis-3,5(dimethylpyrazol-1-yl)acetate rhodium and iridium complexes were synthesized from MCl3•H2O. [Rh(bdmpza)Cl3]- was isolated with three different cations, lithium, sodium and tetraethylamonium, to obtain a… (more)

Subjects/Keywords: Electrophilic C-H activation; H/D exchange; Iridium; Rhodium

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APA (6th Edition):

Rhinehart, J. L. (. -. ). (2012). Development of novel rhodium and iridium complexes with a fac-chelating ligand for electrophilic C-H activation. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/19453

Chicago Manual of Style (16th Edition):

Rhinehart, Jennifer Lee (1984 - ). “Development of novel rhodium and iridium complexes with a fac-chelating ligand for electrophilic C-H activation.” 2012. Doctoral Dissertation, University of Rochester. Accessed October 21, 2019. http://hdl.handle.net/1802/19453.

MLA Handbook (7th Edition):

Rhinehart, Jennifer Lee (1984 - ). “Development of novel rhodium and iridium complexes with a fac-chelating ligand for electrophilic C-H activation.” 2012. Web. 21 Oct 2019.

Vancouver:

Rhinehart JL(-). Development of novel rhodium and iridium complexes with a fac-chelating ligand for electrophilic C-H activation. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1802/19453.

Council of Science Editors:

Rhinehart JL(-). Development of novel rhodium and iridium complexes with a fac-chelating ligand for electrophilic C-H activation. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/19453


Queens University

20. 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 October 21, 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. 21 Oct 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 Oct 21]. 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

21. Press, Loren Paul. High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes.

Degree: PhD, Chemistry, 2016, Texas A&M University

 Over the last century, transition metal-catalyzed C-H functionalization has emerged as one of the most important topics in synthetic chemistry. One type of C-H functionalization,… (more)

Subjects/Keywords: C-H functionalization; C-H activation; borylation; POCOP; iridium; POCS; triflyloxy; carboranes; weakly coordinating anions

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APA (6th Edition):

Press, L. P. (2016). High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158080

Chicago Manual of Style (16th Edition):

Press, Loren Paul. “High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes.” 2016. Doctoral Dissertation, Texas A&M University. Accessed October 21, 2019. http://hdl.handle.net/1969.1/158080.

MLA Handbook (7th Edition):

Press, Loren Paul. “High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes.” 2016. Web. 21 Oct 2019.

Vancouver:

Press LP. High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1969.1/158080.

Council of Science Editors:

Press LP. High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158080


Queens University

22. Cosman, Jennifer. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .

Degree: Chemistry, 2015, Queens University

 Chapter one of this thesis describes the iridium-catalyzed ortho-selective C–H borylation reaction of tertiary benzamides. An iridium(I) complex paired with an electron-deficient phosphine ligand allows… (more)

Subjects/Keywords: multicomponent reactions; C-H activation; allylic substitution; Mizoroki-Heck reaction; iridium-catalyzed C-H borylation

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APA (6th Edition):

Cosman, J. (2015). Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13534

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):

Cosman, Jennifer. “Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .” 2015. Thesis, Queens University. Accessed October 21, 2019. http://hdl.handle.net/1974/13534.

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

MLA Handbook (7th Edition):

Cosman, Jennifer. “Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .” 2015. Web. 21 Oct 2019.

Vancouver:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1974/13534.

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

Council of Science Editors:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13534

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

23. Fallon, Brendan. Cobalt-catalyzed bond activation : C-H functionalization, hydrosilylation and coupling reactions : Activation de liaisons catalysée par le cobalt : fonctionnalisation de liaisons C-H, hydrosilylation et réactions de couplage.

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

Dans cette thèse, nous nous concentrerons principalement sur l’utilisation de complexes basse-valence de cobalt bien définis de la famille des RCo(PMe3)4 pour l’activation de divers… (more)

Subjects/Keywords: Cobalt; Activation de liaisons C-H; LLHT; Hydrosilylation; Homocouplage; Diméthylzinc; Cobalt; C-H activation; Hydroarylation; 547.2

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APA (6th Edition):

Fallon, B. (2016). Cobalt-catalyzed bond activation : C-H functionalization, hydrosilylation and coupling reactions : Activation de liaisons catalysée par le cobalt : fonctionnalisation de liaisons C-H, hydrosilylation et réactions de couplage. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066411

Chicago Manual of Style (16th Edition):

Fallon, Brendan. “Cobalt-catalyzed bond activation : C-H functionalization, hydrosilylation and coupling reactions : Activation de liaisons catalysée par le cobalt : fonctionnalisation de liaisons C-H, hydrosilylation et réactions de couplage.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 21, 2019. http://www.theses.fr/2016PA066411.

MLA Handbook (7th Edition):

Fallon, Brendan. “Cobalt-catalyzed bond activation : C-H functionalization, hydrosilylation and coupling reactions : Activation de liaisons catalysée par le cobalt : fonctionnalisation de liaisons C-H, hydrosilylation et réactions de couplage.” 2016. Web. 21 Oct 2019.

Vancouver:

Fallon B. Cobalt-catalyzed bond activation : C-H functionalization, hydrosilylation and coupling reactions : Activation de liaisons catalysée par le cobalt : fonctionnalisation de liaisons C-H, hydrosilylation et réactions de couplage. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2016PA066411.

Council of Science Editors:

Fallon B. Cobalt-catalyzed bond activation : C-H functionalization, hydrosilylation and coupling reactions : Activation de liaisons catalysée par le cobalt : fonctionnalisation de liaisons C-H, hydrosilylation et réactions de couplage. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066411

24. Quint, Valentin. Formation de liaison C-P par fonctionnalisation de liaison C-H sans métal de transition : aspects snthétiques et mécanistiques : C-P Bond Formation through C-H activation without any transition metal : synthetic and mecanistic aspects.

Degree: Docteur es, Chimie, 2017, Normandie

Cette thèse décrit le développement de trois méthodes de formation de liaison C-P par fonctionnalisation de liaison C-H avec l’utilisation d’aucun métal de transition.Tout d’abord,… (more)

Subjects/Keywords: C-H activation; Organophotocatalyse; Complexes à transfert de charge; Phosphorus, C-H activation; Organophotocatalysis; Charge-transfert complex

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APA (6th Edition):

Quint, V. (2017). Formation de liaison C-P par fonctionnalisation de liaison C-H sans métal de transition : aspects snthétiques et mécanistiques : C-P Bond Formation through C-H activation without any transition metal : synthetic and mecanistic aspects. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2017NORMC219

Chicago Manual of Style (16th Edition):

Quint, Valentin. “Formation de liaison C-P par fonctionnalisation de liaison C-H sans métal de transition : aspects snthétiques et mécanistiques : C-P Bond Formation through C-H activation without any transition metal : synthetic and mecanistic aspects.” 2017. Doctoral Dissertation, Normandie. Accessed October 21, 2019. http://www.theses.fr/2017NORMC219.

MLA Handbook (7th Edition):

Quint, Valentin. “Formation de liaison C-P par fonctionnalisation de liaison C-H sans métal de transition : aspects snthétiques et mécanistiques : C-P Bond Formation through C-H activation without any transition metal : synthetic and mecanistic aspects.” 2017. Web. 21 Oct 2019.

Vancouver:

Quint V. Formation de liaison C-P par fonctionnalisation de liaison C-H sans métal de transition : aspects snthétiques et mécanistiques : C-P Bond Formation through C-H activation without any transition metal : synthetic and mecanistic aspects. [Internet] [Doctoral dissertation]. Normandie; 2017. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2017NORMC219.

Council of Science Editors:

Quint V. Formation de liaison C-P par fonctionnalisation de liaison C-H sans métal de transition : aspects snthétiques et mécanistiques : C-P Bond Formation through C-H activation without any transition metal : synthetic and mecanistic aspects. [Doctoral Dissertation]. Normandie; 2017. Available from: http://www.theses.fr/2017NORMC219


Université de Montréal

25. Régnier, Sophie. Synthèse efficace d'hétérocycles azotés par activation d'amides engendrée par l'anhydride trifluorométhanesulfonique .

Degree: 2017, Université de Montréal

 Les hétérocycles azotés sont d’une importance considérable dans le domaine pharmaceutique. En effet, ces composés se retrouvent dans de nombreuses structures bioactives brevetées dans les… (more)

Subjects/Keywords: amides; hétérocycles; anhydride trifluorométhanesulfonique; 3-aminoindazoles; 3-aminoimidazo[1,2-a]pyridines; activation C-H; Heterocycles; Trifluoromethanesulfonic; Anhydride; C-H activation

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

APA (6th Edition):

Régnier, S. (2017). Synthèse efficace d'hétérocycles azotés par activation d'amides engendrée par l'anhydride trifluorométhanesulfonique . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/18658

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):

Régnier, Sophie. “Synthèse efficace d'hétérocycles azotés par activation d'amides engendrée par l'anhydride trifluorométhanesulfonique .” 2017. Thesis, Université de Montréal. Accessed October 21, 2019. http://hdl.handle.net/1866/18658.

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

MLA Handbook (7th Edition):

Régnier, Sophie. “Synthèse efficace d'hétérocycles azotés par activation d'amides engendrée par l'anhydride trifluorométhanesulfonique .” 2017. Web. 21 Oct 2019.

Vancouver:

Régnier S. Synthèse efficace d'hétérocycles azotés par activation d'amides engendrée par l'anhydride trifluorométhanesulfonique . [Internet] [Thesis]. Université de Montréal; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1866/18658.

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

Council of Science Editors:

Régnier S. Synthèse efficace d'hétérocycles azotés par activation d'amides engendrée par l'anhydride trifluorométhanesulfonique . [Thesis]. Université de Montréal; 2017. Available from: http://hdl.handle.net/1866/18658

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


EPFL

26. Vechorkin, Oleg. A Well-Defined Ni Pincer Catalyst for Cross Coupling of Non-Activated Alkyl Halides and Direct C-H Alkylation.

Degree: 2011, EPFL

 Carbon-carbon bond forming reactions are among the most important and useful methods for organic synthesis. During the last years, significant progress has been made in… (more)

Subjects/Keywords: pincer complex; catalysis; cross coupling; C-H activation; alkyl halides; complexe pincer; catalyse; couplage croisé; C-H activation; halogénures d'alkyle

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

APA (6th Edition):

Vechorkin, O. (2011). A Well-Defined Ni Pincer Catalyst for Cross Coupling of Non-Activated Alkyl Halides and Direct C-H Alkylation. (Thesis). EPFL. Retrieved from http://infoscience.epfl.ch/record/165384

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):

Vechorkin, Oleg. “A Well-Defined Ni Pincer Catalyst for Cross Coupling of Non-Activated Alkyl Halides and Direct C-H Alkylation.” 2011. Thesis, EPFL. Accessed October 21, 2019. http://infoscience.epfl.ch/record/165384.

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

MLA Handbook (7th Edition):

Vechorkin, Oleg. “A Well-Defined Ni Pincer Catalyst for Cross Coupling of Non-Activated Alkyl Halides and Direct C-H Alkylation.” 2011. Web. 21 Oct 2019.

Vancouver:

Vechorkin O. A Well-Defined Ni Pincer Catalyst for Cross Coupling of Non-Activated Alkyl Halides and Direct C-H Alkylation. [Internet] [Thesis]. EPFL; 2011. [cited 2019 Oct 21]. Available from: http://infoscience.epfl.ch/record/165384.

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

Council of Science Editors:

Vechorkin O. A Well-Defined Ni Pincer Catalyst for Cross Coupling of Non-Activated Alkyl Halides and Direct C-H Alkylation. [Thesis]. EPFL; 2011. Available from: http://infoscience.epfl.ch/record/165384

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

27. 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 October 21, 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. 21 Oct 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 Oct 21]. 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

28. Babin, Victor. Conception de nouveaux agents iodés pour l'imagerie TEMP des récepteurs 5-HT4 : Design of new iodinated ligands for the SPECT imaging of 5-HT4 receptors.

Degree: Docteur es, Chimie, 2018, Normandie

La maladie d’Alzheimer est une maladie neurodégénérative touchant près d’un million de personnes en France et dont les perspectives actuelles laissent suggérer une forte augmentation… (more)

Subjects/Keywords: Récepteur sérotoninergique 5-HT4; Lipophilie; Activation C-H; Radioiodation; Serotoninergic receptor 5-HT4; Radioligand; Lipophilicity; C-H activation

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

APA (6th Edition):

Babin, V. (2018). Conception de nouveaux agents iodés pour l'imagerie TEMP des récepteurs 5-HT4 : Design of new iodinated ligands for the SPECT imaging of 5-HT4 receptors. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2018NORMC244

Chicago Manual of Style (16th Edition):

Babin, Victor. “Conception de nouveaux agents iodés pour l'imagerie TEMP des récepteurs 5-HT4 : Design of new iodinated ligands for the SPECT imaging of 5-HT4 receptors.” 2018. Doctoral Dissertation, Normandie. Accessed October 21, 2019. http://www.theses.fr/2018NORMC244.

MLA Handbook (7th Edition):

Babin, Victor. “Conception de nouveaux agents iodés pour l'imagerie TEMP des récepteurs 5-HT4 : Design of new iodinated ligands for the SPECT imaging of 5-HT4 receptors.” 2018. Web. 21 Oct 2019.

Vancouver:

Babin V. Conception de nouveaux agents iodés pour l'imagerie TEMP des récepteurs 5-HT4 : Design of new iodinated ligands for the SPECT imaging of 5-HT4 receptors. [Internet] [Doctoral dissertation]. Normandie; 2018. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2018NORMC244.

Council of Science Editors:

Babin V. Conception de nouveaux agents iodés pour l'imagerie TEMP des récepteurs 5-HT4 : Design of new iodinated ligands for the SPECT imaging of 5-HT4 receptors. [Doctoral Dissertation]. Normandie; 2018. Available from: http://www.theses.fr/2018NORMC244

29. Lebedeva, Anastasia. Nanomatériaux à base de ruthénium et de manganèse pour l'oxydation catalytique d'hydrocarbures dans l'eau : Nanomaterials based on ruthenium and manganese for the catalytic oxidation of hydrocarbons in water.

Degree: Docteur es, Chimie, 2017, Rennes 1; Université de Rennes1

L'activation de la liaison Csp3-H peu réactive et sa fonctionnalisation en liaison carbone-hétéroatome constituent un défi pour les chimistes de synthèse. Un exemple d'intérêt industriel… (more)

Subjects/Keywords: Activation C-H; Oxydation sélective; Nanomatériaux; Hydrocarbures; Cyclohexane; Ruthénium; Manganèse; C-H activation; Selective oxidation; Nanomaterials; Hydrocarbons; Cyclohexane; Ruthenium; Manganese

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

APA (6th Edition):

Lebedeva, A. (2017). Nanomatériaux à base de ruthénium et de manganèse pour l'oxydation catalytique d'hydrocarbures dans l'eau : Nanomaterials based on ruthenium and manganese for the catalytic oxidation of hydrocarbons in water. (Doctoral Dissertation). Rennes 1; Université de Rennes1. Retrieved from http://www.theses.fr/2017REN1S099

Chicago Manual of Style (16th Edition):

Lebedeva, Anastasia. “Nanomatériaux à base de ruthénium et de manganèse pour l'oxydation catalytique d'hydrocarbures dans l'eau : Nanomaterials based on ruthenium and manganese for the catalytic oxidation of hydrocarbons in water.” 2017. Doctoral Dissertation, Rennes 1; Université de Rennes1. Accessed October 21, 2019. http://www.theses.fr/2017REN1S099.

MLA Handbook (7th Edition):

Lebedeva, Anastasia. “Nanomatériaux à base de ruthénium et de manganèse pour l'oxydation catalytique d'hydrocarbures dans l'eau : Nanomaterials based on ruthenium and manganese for the catalytic oxidation of hydrocarbons in water.” 2017. Web. 21 Oct 2019.

Vancouver:

Lebedeva A. Nanomatériaux à base de ruthénium et de manganèse pour l'oxydation catalytique d'hydrocarbures dans l'eau : Nanomaterials based on ruthenium and manganese for the catalytic oxidation of hydrocarbons in water. [Internet] [Doctoral dissertation]. Rennes 1; Université de Rennes1; 2017. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2017REN1S099.

Council of Science Editors:

Lebedeva A. Nanomatériaux à base de ruthénium et de manganèse pour l'oxydation catalytique d'hydrocarbures dans l'eau : Nanomaterials based on ruthenium and manganese for the catalytic oxidation of hydrocarbons in water. [Doctoral Dissertation]. Rennes 1; Université de Rennes1; 2017. Available from: http://www.theses.fr/2017REN1S099

30. Baladi, Tom. Autour du noyau imidazo[4,5-b]pyridine : inhibiteurs potentiels de la protéine kinase Tyro3 et fonctionnalisation directe de liaisons CH. : The imidazo[4,5-b]pyridine scaffold : inhibitors of protein kinase Tyro3 and direct C - H functionalization.

Degree: Docteur es, Chimie, 2016, Paris Saclay

Etant au quatrième rang des cancers les plus fréquents chez l'homme, le cancer de la vessie représente un enjeu médical important. Pourtant, à ce jour,… (more)

Subjects/Keywords: Chimie thérapeutique; Activation de liaisons C-H; Protéines kinases; Fonctionnalisation directe; Medicinal chemistry; C-H activation; Protein kinases; Direct functionalization

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

APA (6th Edition):

Baladi, T. (2016). Autour du noyau imidazo[4,5-b]pyridine : inhibiteurs potentiels de la protéine kinase Tyro3 et fonctionnalisation directe de liaisons C – H. : The imidazo[4,5-b]pyridine scaffold : inhibitors of protein kinase Tyro3 and direct C - H functionalization. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2016SACLS386

Chicago Manual of Style (16th Edition):

Baladi, Tom. “Autour du noyau imidazo[4,5-b]pyridine : inhibiteurs potentiels de la protéine kinase Tyro3 et fonctionnalisation directe de liaisons C – H. : The imidazo[4,5-b]pyridine scaffold : inhibitors of protein kinase Tyro3 and direct C - H functionalization.” 2016. Doctoral Dissertation, Paris Saclay. Accessed October 21, 2019. http://www.theses.fr/2016SACLS386.

MLA Handbook (7th Edition):

Baladi, Tom. “Autour du noyau imidazo[4,5-b]pyridine : inhibiteurs potentiels de la protéine kinase Tyro3 et fonctionnalisation directe de liaisons C – H. : The imidazo[4,5-b]pyridine scaffold : inhibitors of protein kinase Tyro3 and direct C - H functionalization.” 2016. Web. 21 Oct 2019.

Vancouver:

Baladi T. Autour du noyau imidazo[4,5-b]pyridine : inhibiteurs potentiels de la protéine kinase Tyro3 et fonctionnalisation directe de liaisons C – H. : The imidazo[4,5-b]pyridine scaffold : inhibitors of protein kinase Tyro3 and direct C - H functionalization. [Internet] [Doctoral dissertation]. Paris Saclay; 2016. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2016SACLS386.

Council of Science Editors:

Baladi T. Autour du noyau imidazo[4,5-b]pyridine : inhibiteurs potentiels de la protéine kinase Tyro3 et fonctionnalisation directe de liaisons C – H. : The imidazo[4,5-b]pyridine scaffold : inhibitors of protein kinase Tyro3 and direct C - H functionalization. [Doctoral Dissertation]. Paris Saclay; 2016. Available from: http://www.theses.fr/2016SACLS386

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