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You searched for subject:(Cross Dehydrogenative Coupling Reactions). Showing records 1 – 30 of 15166 total matches.

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Indian Institute of Science

1. Yogesh, S. Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds.

Degree: 2017, Indian Institute of Science

 The thesis entitled “Design and Development of Metal-Free Cross Dehydrogenative Coupling Reactions for the construction of C-S, C-O and C-C bonds” is divided into three… (more)

Subjects/Keywords: Cross Dehydrogenative Coupling Reactions; Chemoselective α-Aminoxylation; Acylation Quinolines; Transition Metal Free Minisci Reaction; CDC Reactions; Dimethyl Sulfoxide; Carbonyl Compounds; Ketones; Pyrazolones; Orcanic Chemistry

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APA (6th Edition):

Yogesh, S. (2017). Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3698 ; http://etd.iisc.ernet.in/abstracts/4568/G28588-Abs.pdf

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):

Yogesh, S. “Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds.” 2017. Thesis, Indian Institute of Science. Accessed October 14, 2019. http://etd.iisc.ernet.in/2005/3698 ; http://etd.iisc.ernet.in/abstracts/4568/G28588-Abs.pdf.

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

MLA Handbook (7th Edition):

Yogesh, S. “Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds.” 2017. Web. 14 Oct 2019.

Vancouver:

Yogesh S. Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds. [Internet] [Thesis]. Indian Institute of Science; 2017. [cited 2019 Oct 14]. Available from: http://etd.iisc.ernet.in/2005/3698 ; http://etd.iisc.ernet.in/abstracts/4568/G28588-Abs.pdf.

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

Council of Science Editors:

Yogesh S. Design and Development of Metal-free Cross Dehydrogenative Coupling Reactions for the Construction of C-S, C-O and C-C bonds. [Thesis]. Indian Institute of Science; 2017. Available from: http://etd.iisc.ernet.in/2005/3698 ; http://etd.iisc.ernet.in/abstracts/4568/G28588-Abs.pdf

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


Indian Institute of Science

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

Degree: 2016, Indian Institute of Science

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Dhineshkumar, J. “Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.” 2016. Thesis, Indian Institute of Science. Accessed October 14, 2019. http://hdl.handle.net/2005/3020.

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

MLA Handbook (7th Edition):

Dhineshkumar, J. “Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.” 2016. Web. 14 Oct 2019.

Vancouver:

Dhineshkumar J. Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions. [Internet] [Thesis]. Indian Institute of Science; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2005/3020.

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

Council of Science Editors:

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

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


Australian National University

3. Saglam, Mehmet Fatih. Investigation into Higher Dendralenes .

Degree: 2016, Australian National University

 As synthetic organic chemists, one of our most important desires is to synthesize complex target molecules efficiently in the shortest time and lowest step count,… (more)

Subjects/Keywords: Hydrocarbons; Dendralenes; Diels-Alder reactions; Metal Catalysed Cross-Coupling reactions

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APA (6th Edition):

Saglam, M. F. (2016). Investigation into Higher Dendralenes . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/107105

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):

Saglam, Mehmet Fatih. “Investigation into Higher Dendralenes .” 2016. Thesis, Australian National University. Accessed October 14, 2019. http://hdl.handle.net/1885/107105.

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

MLA Handbook (7th Edition):

Saglam, Mehmet Fatih. “Investigation into Higher Dendralenes .” 2016. Web. 14 Oct 2019.

Vancouver:

Saglam MF. Investigation into Higher Dendralenes . [Internet] [Thesis]. Australian National University; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/1885/107105.

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

Council of Science Editors:

Saglam MF. Investigation into Higher Dendralenes . [Thesis]. Australian National University; 2016. Available from: http://hdl.handle.net/1885/107105

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


KTH

4. Lakó, Ágnes. Towards Nickel Boride Catalyzed C-C Coupling Reactions.

Degree: Chemical Science and Engineering (CHE), 2017, KTH

  This thesis focuses on the study of nickel boride as a catalyst in various coupling reactions. The nickel boride catalyst was investigated in three… (more)

Subjects/Keywords: heterogeneous catalysis; nickel catalysis; coupling reactions; cross-coupling; homocoupling; Engineering and Technology; Teknik och teknologier

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APA (6th Edition):

Lakó, . (2017). Towards Nickel Boride Catalyzed C-C Coupling Reactions. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-216398

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):

Lakó, Ágnes. “Towards Nickel Boride Catalyzed C-C Coupling Reactions.” 2017. Thesis, KTH. Accessed October 14, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-216398.

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

MLA Handbook (7th Edition):

Lakó, Ágnes. “Towards Nickel Boride Catalyzed C-C Coupling Reactions.” 2017. Web. 14 Oct 2019.

Vancouver:

Lakó . Towards Nickel Boride Catalyzed C-C Coupling Reactions. [Internet] [Thesis]. KTH; 2017. [cited 2019 Oct 14]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-216398.

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

Council of Science Editors:

Lakó . Towards Nickel Boride Catalyzed C-C Coupling Reactions. [Thesis]. KTH; 2017. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-216398

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


University of Ottawa

5. Ben Halima, Taoufik. Engaging Esters as Cross-Coupling Electrophiles .

Degree: 2019, University of Ottawa

Cross-coupling reactions, where a transition metal catalyst facilitates the formation of a new carbon-carbon or carbon-heteroatom bond between two coupling partners, has become one of… (more)

Subjects/Keywords: Esters; Electrophiles; cross-coupling reactions; Suzuki-Miyaura coupling; Amide bond formation; High-throughput screening

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APA (6th Edition):

Ben Halima, T. (2019). Engaging Esters as Cross-Coupling Electrophiles . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/39493

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):

Ben Halima, Taoufik. “Engaging Esters as Cross-Coupling Electrophiles .” 2019. Thesis, University of Ottawa. Accessed October 14, 2019. http://hdl.handle.net/10393/39493.

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

MLA Handbook (7th Edition):

Ben Halima, Taoufik. “Engaging Esters as Cross-Coupling Electrophiles .” 2019. Web. 14 Oct 2019.

Vancouver:

Ben Halima T. Engaging Esters as Cross-Coupling Electrophiles . [Internet] [Thesis]. University of Ottawa; 2019. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10393/39493.

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

Council of Science Editors:

Ben Halima T. Engaging Esters as Cross-Coupling Electrophiles . [Thesis]. University of Ottawa; 2019. Available from: http://hdl.handle.net/10393/39493

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


University of California – Irvine

6. Osborne, Charlotte A. Development of Transition Metal-Catalyzed Reactions for the Synthesis and Biological Evaluation of Enantioenriched Diarylalkanes and Homopropargylic Sultams.

Degree: Chemistry, 2015, University of California – Irvine

 Methodology for the synthesis of enantioenriched compounds is critical to the discovery of new pharmaceuticals. To access single enantiomers of biologically relevant molecules for evaluation,… (more)

Subjects/Keywords: Chemistry; anti-breast-cancer activity; cross-coupling reactions; nickel catalysis; propargylation reactions; silver catalysis

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APA (6th Edition):

Osborne, C. A. (2015). Development of Transition Metal-Catalyzed Reactions for the Synthesis and Biological Evaluation of Enantioenriched Diarylalkanes and Homopropargylic Sultams. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/3ch4c75g

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):

Osborne, Charlotte A. “Development of Transition Metal-Catalyzed Reactions for the Synthesis and Biological Evaluation of Enantioenriched Diarylalkanes and Homopropargylic Sultams.” 2015. Thesis, University of California – Irvine. Accessed October 14, 2019. http://www.escholarship.org/uc/item/3ch4c75g.

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

MLA Handbook (7th Edition):

Osborne, Charlotte A. “Development of Transition Metal-Catalyzed Reactions for the Synthesis and Biological Evaluation of Enantioenriched Diarylalkanes and Homopropargylic Sultams.” 2015. Web. 14 Oct 2019.

Vancouver:

Osborne CA. Development of Transition Metal-Catalyzed Reactions for the Synthesis and Biological Evaluation of Enantioenriched Diarylalkanes and Homopropargylic Sultams. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2019 Oct 14]. Available from: http://www.escholarship.org/uc/item/3ch4c75g.

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

Council of Science Editors:

Osborne CA. Development of Transition Metal-Catalyzed Reactions for the Synthesis and Biological Evaluation of Enantioenriched Diarylalkanes and Homopropargylic Sultams. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/3ch4c75g

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


University of Edinburgh

7. Clavadetscher, Jessica Veronica. Transition metal catalysis : a new paradigm in bioorthogonal drug activation.

Degree: PhD, 2017, University of Edinburgh

 Powerful tools have emerged in the past few years to allow the sensing, imaging and modulation of biological processes in living systems. Bioorthogonal organometallic reactions(more)

Subjects/Keywords: bioorthogonal reactions; nanoparticle catalysts; zebrafish; bioorthogonal organometallic reactions; palladium-mediated cross-coupling; decaging; copper nanoparticles

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APA (6th Edition):

Clavadetscher, J. V. (2017). Transition metal catalysis : a new paradigm in bioorthogonal drug activation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/29580

Chicago Manual of Style (16th Edition):

Clavadetscher, Jessica Veronica. “Transition metal catalysis : a new paradigm in bioorthogonal drug activation.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed October 14, 2019. http://hdl.handle.net/1842/29580.

MLA Handbook (7th Edition):

Clavadetscher, Jessica Veronica. “Transition metal catalysis : a new paradigm in bioorthogonal drug activation.” 2017. Web. 14 Oct 2019.

Vancouver:

Clavadetscher JV. Transition metal catalysis : a new paradigm in bioorthogonal drug activation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/1842/29580.

Council of Science Editors:

Clavadetscher JV. Transition metal catalysis : a new paradigm in bioorthogonal drug activation. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/29580


Australian National University

8. Joshua William, Boyle. A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis .

Degree: 2015, Australian National University

 [3]Dendralene is a small π-­rich hydrocarbon that is capable of taking part in a wide range of chemical reactions, not least of which is the… (more)

Subjects/Keywords: Diels-Alder; DTDA; Total Synthesis; Methodology; Domino reactions; Cross-coupling reactions; xestoquinone

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APA (6th Edition):

Joshua William, B. (2015). A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/101992

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):

Joshua William, Boyle. “A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis .” 2015. Thesis, Australian National University. Accessed October 14, 2019. http://hdl.handle.net/1885/101992.

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

MLA Handbook (7th Edition):

Joshua William, Boyle. “A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis .” 2015. Web. 14 Oct 2019.

Vancouver:

Joshua William B. A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis . [Internet] [Thesis]. Australian National University; 2015. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/1885/101992.

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

Council of Science Editors:

Joshua William B. A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis . [Thesis]. Australian National University; 2015. Available from: http://hdl.handle.net/1885/101992

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


University of Illinois – Urbana-Champaign

9. Bailey, Aaron D. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.

Degree: MS, 0335, 2011, University of Illinois – Urbana-Champaign

 Palladium-catalyzed cross-coupling of ??-substituted allylic silanolates with aryl bromides was investigated. It was discovered that ??-selectivity is heavily influenced by the substituents at silicon. It… (more)

Subjects/Keywords: Palladium-catalyzed cross-coupling reactions; allylic silanes; vinylsilanes

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APA (6th Edition):

Bailey, A. D. (2011). Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24450

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):

Bailey, Aaron D. “Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.” 2011. Thesis, University of Illinois – Urbana-Champaign. Accessed October 14, 2019. http://hdl.handle.net/2142/24450.

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

MLA Handbook (7th Edition):

Bailey, Aaron D. “Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.” 2011. Web. 14 Oct 2019.

Vancouver:

Bailey AD. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2142/24450.

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

Council of Science Editors:

Bailey AD. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. [Thesis]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24450

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


University of Rochester

10. 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 14, 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. 14 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 14]. 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

11. Toste, F.D. Visible light-mediated gold-catalysed carbon(sp2)-carbon(sp) cross-coupling.

Degree: 2018, Royal Society of Chemistry

Subjects/Keywords: Catalysis; Chemical reactions; Cross coupling reactions; Oxidative additions; Química

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APA (6th Edition):

Toste, F. D. (2018). Visible light-mediated gold-catalysed carbon(sp2)-carbon(sp) cross-coupling. (Thesis). Royal Society of Chemistry. Retrieved from http://hdl.handle.net/10486/676080

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):

Toste, F D. “Visible light-mediated gold-catalysed carbon(sp2)-carbon(sp) cross-coupling.” 2018. Thesis, Royal Society of Chemistry. Accessed October 14, 2019. http://hdl.handle.net/10486/676080.

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

MLA Handbook (7th Edition):

Toste, F D. “Visible light-mediated gold-catalysed carbon(sp2)-carbon(sp) cross-coupling.” 2018. Web. 14 Oct 2019.

Vancouver:

Toste FD. Visible light-mediated gold-catalysed carbon(sp2)-carbon(sp) cross-coupling. [Internet] [Thesis]. Royal Society of Chemistry; 2018. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10486/676080.

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

Council of Science Editors:

Toste FD. Visible light-mediated gold-catalysed carbon(sp2)-carbon(sp) cross-coupling. [Thesis]. Royal Society of Chemistry; 2018. Available from: http://hdl.handle.net/10486/676080

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


University of Illinois – Urbana-Champaign

12. Yousaf, Zain. Development of organosilicon cross-coupling reaction.

Degree: MS, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Use of palladium catalyzed cross-couplings have found widespread use in the pharmaceutical industry and there is a significant ongoing effort to either improve or devise… (more)

Subjects/Keywords: silanolate; cross-coupling

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APA (6th Edition):

Yousaf, Z. (2015). Development of organosilicon cross-coupling reaction. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89275

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):

Yousaf, Zain. “Development of organosilicon cross-coupling reaction.” 2015. Thesis, University of Illinois – Urbana-Champaign. Accessed October 14, 2019. http://hdl.handle.net/2142/89275.

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

MLA Handbook (7th Edition):

Yousaf, Zain. “Development of organosilicon cross-coupling reaction.” 2015. Web. 14 Oct 2019.

Vancouver:

Yousaf Z. Development of organosilicon cross-coupling reaction. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2142/89275.

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

Council of Science Editors:

Yousaf Z. Development of organosilicon cross-coupling reaction. [Thesis]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89275

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


University of Ottawa

13. Masson-Makdissi, Jeanne. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .

Degree: 2018, University of Ottawa

 First popularized in the 1970s, transition metal-catalyzed cross-couplings now constitute staple reactions for the formation of carbon-carbon and carbon-heteroatom bonds. Recent endeavours in the field… (more)

Subjects/Keywords: cross-coupling; esters

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APA (6th Edition):

Masson-Makdissi, J. (2018). Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/38398

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):

Masson-Makdissi, Jeanne. “Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .” 2018. Thesis, University of Ottawa. Accessed October 14, 2019. http://hdl.handle.net/10393/38398.

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

MLA Handbook (7th Edition):

Masson-Makdissi, Jeanne. “Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .” 2018. Web. 14 Oct 2019.

Vancouver:

Masson-Makdissi J. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10393/38398.

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

Council of Science Editors:

Masson-Makdissi J. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/38398

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


Queens University

14. Holland, Amy Marie. INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS .

Degree: Chemistry, 2010, Queens University

 Until recently, secondary organoboronic esters were not viable substrates in the Suzuki-Miyaura cross-coupling reaction; however under recently reported conditions from the Crudden group1, which includes… (more)

Subjects/Keywords: Organometallics; Cross-Coupling

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

APA (6th Edition):

Holland, A. M. (2010). INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6071

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):

Holland, Amy Marie. “INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS .” 2010. Thesis, Queens University. Accessed October 14, 2019. http://hdl.handle.net/1974/6071.

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

MLA Handbook (7th Edition):

Holland, Amy Marie. “INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS .” 2010. Web. 14 Oct 2019.

Vancouver:

Holland AM. INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS . [Internet] [Thesis]. Queens University; 2010. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/1974/6071.

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

Council of Science Editors:

Holland AM. INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS . [Thesis]. Queens University; 2010. Available from: http://hdl.handle.net/1974/6071

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


Queensland University of Technology

15. Xiao, Qi. Visible light photocatalytic synthesis of fine organic chemicals with new photocatalysts.

Degree: 2015, Queensland University of Technology

 This project was a step forward in developing new recyclable photocatalysts for chemical reactions. These new photocatalysts can facilitate reactions by using visible light under… (more)

Subjects/Keywords: Photocatalysis; Visible light; Localized surface plasmon resonance; Plasmonic photocatalysts; Plasmonic metal nanoparticles; Gold nanoparticles; Alloy nanoparticles; Cross-coupling reactions; Organic synthesis

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

APA (6th Edition):

Xiao, Q. (2015). Visible light photocatalytic synthesis of fine organic chemicals with new photocatalysts. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/84078/

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):

Xiao, Qi. “Visible light photocatalytic synthesis of fine organic chemicals with new photocatalysts.” 2015. Thesis, Queensland University of Technology. Accessed October 14, 2019. https://eprints.qut.edu.au/84078/.

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

MLA Handbook (7th Edition):

Xiao, Qi. “Visible light photocatalytic synthesis of fine organic chemicals with new photocatalysts.” 2015. Web. 14 Oct 2019.

Vancouver:

Xiao Q. Visible light photocatalytic synthesis of fine organic chemicals with new photocatalysts. [Internet] [Thesis]. Queensland University of Technology; 2015. [cited 2019 Oct 14]. Available from: https://eprints.qut.edu.au/84078/.

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

Council of Science Editors:

Xiao Q. Visible light photocatalytic synthesis of fine organic chemicals with new photocatalysts. [Thesis]. Queensland University of Technology; 2015. Available from: https://eprints.qut.edu.au/84078/

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


Kyoto University / 京都大学

16. Kitano, Masaaki. Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学.

Degree: 博士(理学), 2016, Kyoto University / 京都大学

新制・課程博士

甲第19516号

理博第4176号

Subjects/Keywords: porphyrinoids; subporphyrins; cross-coupling reactions; substitution; borylation

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APA (6th Edition):

Kitano, M. (2016). Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516

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):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学.” 2016. Thesis, Kyoto University / 京都大学. Accessed October 14, 2019. http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516.

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

MLA Handbook (7th Edition):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学.” 2016. Web. 14 Oct 2019.

Vancouver:

Kitano M. Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学. [Internet] [Thesis]. Kyoto University / 京都大学; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516.

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

Council of Science Editors:

Kitano M. Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学. [Thesis]. Kyoto University / 京都大学; 2016. Available from: http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516

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


Kyoto University / 京都大学

17. Yamamoto, Yutaro. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.

Degree: 博士(理学), 2017, Kyoto University / 京都大学

新制・課程博士

甲第20205号

理博第4290号

Subjects/Keywords: palladium; aryl chloride; borylation; hydrodechlorination; cross-coupling reactions

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APA (6th Edition):

Yamamoto, Y. (2017). Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205

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):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.” 2017. Thesis, Kyoto University / 京都大学. Accessed October 14, 2019. http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205.

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

MLA Handbook (7th Edition):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.” 2017. Web. 14 Oct 2019.

Vancouver:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2017. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205.

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

Council of Science Editors:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. [Thesis]. Kyoto University / 京都大学; 2017. Available from: http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205

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

18. Stamatopoulos, Ioannis. Σύνθεση, χαρακτηρισμός και μελέτη της καταλυτικής δραστικότητας συμπλόκων του τύπου Μ(P,P)X2, M(P,E)X2 και M(E,E)X2, M = Ni, Pd, Pt, E = O, S, Se, X = Cl, Br.

Degree: 2014, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

In this PhD thesis was studied the synthesis of bidental ligands of phosphorus-nitrogenphosphorustype (P-N-P) was studied along with the preparation of the correspondingcomplexes of nickel,… (more)

Subjects/Keywords: Αμινοδιφωσφινικοί υποκαταστάτες; Ακινητοποίηση συμπλόκων ενώσεων; Καταλυτικές αντιδράσεις διασταυρούμενης σύζευξης; Ομογενής κατάλυση; Aminobiphosphine ligands; Complex immobilization; Catalytic cross-coupling reactions; Homogenous catalysis

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APA (6th Edition):

Stamatopoulos, I. (2014). Σύνθεση, χαρακτηρισμός και μελέτη της καταλυτικής δραστικότητας συμπλόκων του τύπου Μ(P,P)X2, M(P,E)X2 και M(E,E)X2, M = Ni, Pd, Pt, E = O, S, Se, X = Cl, Br. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/40395

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):

Stamatopoulos, Ioannis. “Σύνθεση, χαρακτηρισμός και μελέτη της καταλυτικής δραστικότητας συμπλόκων του τύπου Μ(P,P)X2, M(P,E)X2 και M(E,E)X2, M = Ni, Pd, Pt, E = O, S, Se, X = Cl, Br.” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 14, 2019. http://hdl.handle.net/10442/hedi/40395.

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

MLA Handbook (7th Edition):

Stamatopoulos, Ioannis. “Σύνθεση, χαρακτηρισμός και μελέτη της καταλυτικής δραστικότητας συμπλόκων του τύπου Μ(P,P)X2, M(P,E)X2 και M(E,E)X2, M = Ni, Pd, Pt, E = O, S, Se, X = Cl, Br.” 2014. Web. 14 Oct 2019.

Vancouver:

Stamatopoulos I. Σύνθεση, χαρακτηρισμός και μελέτη της καταλυτικής δραστικότητας συμπλόκων του τύπου Μ(P,P)X2, M(P,E)X2 και M(E,E)X2, M = Ni, Pd, Pt, E = O, S, Se, X = Cl, Br. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10442/hedi/40395.

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

Council of Science Editors:

Stamatopoulos I. Σύνθεση, χαρακτηρισμός και μελέτη της καταλυτικής δραστικότητας συμπλόκων του τύπου Μ(P,P)X2, M(P,E)X2 και M(E,E)X2, M = Ni, Pd, Pt, E = O, S, Se, X = Cl, Br. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/40395

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


Kyoto University

19. Kitano, Masaaki. Chemistry of meso-Free Subporphyrins .

Degree: 2016, Kyoto University

Subjects/Keywords: porphyrinoids; subporphyrins; cross-coupling reactions; substitution; borylation

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

APA (6th Edition):

Kitano, M. (2016). Chemistry of meso-Free Subporphyrins . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/215329

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):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins .” 2016. Thesis, Kyoto University. Accessed October 14, 2019. http://hdl.handle.net/2433/215329.

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

MLA Handbook (7th Edition):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins .” 2016. Web. 14 Oct 2019.

Vancouver:

Kitano M. Chemistry of meso-Free Subporphyrins . [Internet] [Thesis]. Kyoto University; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2433/215329.

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

Council of Science Editors:

Kitano M. Chemistry of meso-Free Subporphyrins . [Thesis]. Kyoto University; 2016. Available from: http://hdl.handle.net/2433/215329

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


Kyoto University

20. Yamamoto, Yutaro. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .

Degree: 2017, Kyoto University

Subjects/Keywords: palladium; aryl chloride; borylation; hydrodechlorination; cross-coupling reactions

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

APA (6th Edition):

Yamamoto, Y. (2017). Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/225430

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):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .” 2017. Thesis, Kyoto University. Accessed October 14, 2019. http://hdl.handle.net/2433/225430.

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

MLA Handbook (7th Edition):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .” 2017. Web. 14 Oct 2019.

Vancouver:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . [Internet] [Thesis]. Kyoto University; 2017. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2433/225430.

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

Council of Science Editors:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . [Thesis]. Kyoto University; 2017. Available from: http://hdl.handle.net/2433/225430

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


Universitat Rovira i Virgili

21. Lillo García, Vanesa. Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach.

Degree: Departament de Química Física i Inorgànica, 2009, Universitat Rovira i Virgili

 Organoboron compounds are some of the most useful reagents in organic synthesis. The carbon-boron bond, once formed, can be cleaved in a variety of ways,… (more)

Subjects/Keywords: Hydroboration; Diboration; B-addition; Tandem reactions; C-C cross coupling; Carbene; Homogeneous Catalysis; 54; 542; 546

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APA (6th Edition):

Lillo García, V. (2009). Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/9101

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):

Lillo García, Vanesa. “Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach.” 2009. Thesis, Universitat Rovira i Virgili. Accessed October 14, 2019. http://hdl.handle.net/10803/9101.

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

MLA Handbook (7th Edition):

Lillo García, Vanesa. “Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach.” 2009. Web. 14 Oct 2019.

Vancouver:

Lillo García V. Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach. [Internet] [Thesis]. Universitat Rovira i Virgili; 2009. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10803/9101.

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

Council of Science Editors:

Lillo García V. Transition metal catalysed functionalisation of c=c through boron chemistry: a tandem approach. [Thesis]. Universitat Rovira i Virgili; 2009. Available from: http://hdl.handle.net/10803/9101

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

22. Guilarte Moreno, Verónica. 2,3-Dihalofenoles: sustratos de partida versátiles para la síntesis de heterociclos funcionalizados regioselectivamente.

Degree: Departamento de Química, 2012, Universidad de Burgos

 Esta Tesis Doctoral se ha centrado en la preparación de diferentes heterociclos funcionalizados que presentan gran interés en Química Orgánica, al formar parte del esqueleto… (more)

Subjects/Keywords: heterociclos funcionalizados; orto-metalación; reacciones de acoplamiento; heterociclación; functionalized heterocycles; ortho-metalation; cross-coupling reactions; heterocyclization; Química orgánica; Chemistry, Organic; 230610

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APA (6th Edition):

Guilarte Moreno, V. (2012). 2,3-Dihalofenoles: sustratos de partida versátiles para la síntesis de heterociclos funcionalizados regioselectivamente. (Thesis). Universidad de Burgos. Retrieved from http://hdl.handle.net/10259/179

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):

Guilarte Moreno, Verónica. “2,3-Dihalofenoles: sustratos de partida versátiles para la síntesis de heterociclos funcionalizados regioselectivamente.” 2012. Thesis, Universidad de Burgos. Accessed October 14, 2019. http://hdl.handle.net/10259/179.

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

MLA Handbook (7th Edition):

Guilarte Moreno, Verónica. “2,3-Dihalofenoles: sustratos de partida versátiles para la síntesis de heterociclos funcionalizados regioselectivamente.” 2012. Web. 14 Oct 2019.

Vancouver:

Guilarte Moreno V. 2,3-Dihalofenoles: sustratos de partida versátiles para la síntesis de heterociclos funcionalizados regioselectivamente. [Internet] [Thesis]. Universidad de Burgos; 2012. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10259/179.

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

Council of Science Editors:

Guilarte Moreno V. 2,3-Dihalofenoles: sustratos de partida versátiles para la síntesis de heterociclos funcionalizados regioselectivamente. [Thesis]. Universidad de Burgos; 2012. Available from: http://hdl.handle.net/10259/179

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


University of Pennsylvania

23. Nguyen, Minh Huu. Part 1 Design, Synthesis, and Validation of Polymer-Supported Siloxane Transfer Agents for Transition-Metal-Mediated Cross-Coupling Reactions of Organolithiums Part 2 Total Synthesis of (-)-Mandelalide a Exploiting Anion Relay Chemistry.

Degree: 2016, University of Pennsylvania

 Part 1: Recent development of Anion Relay Chemistry (ARC) has revealed a “new ARC dimension”, namely the discovery of siloxane transfer agents for efficient palladium-catalyzed… (more)

Subjects/Keywords: anion relay chemistry; cross-coupling reactions; glycosylated polyketide macrolide; organolithium reagents; polymer-supported reagents; total synthesis; Organic Chemistry; Polymer Chemistry

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

APA (6th Edition):

Nguyen, M. H. (2016). Part 1 Design, Synthesis, and Validation of Polymer-Supported Siloxane Transfer Agents for Transition-Metal-Mediated Cross-Coupling Reactions of Organolithiums Part 2 Total Synthesis of (-)-Mandelalide a Exploiting Anion Relay Chemistry. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1914

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):

Nguyen, Minh Huu. “Part 1 Design, Synthesis, and Validation of Polymer-Supported Siloxane Transfer Agents for Transition-Metal-Mediated Cross-Coupling Reactions of Organolithiums Part 2 Total Synthesis of (-)-Mandelalide a Exploiting Anion Relay Chemistry.” 2016. Thesis, University of Pennsylvania. Accessed October 14, 2019. https://repository.upenn.edu/edissertations/1914.

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

MLA Handbook (7th Edition):

Nguyen, Minh Huu. “Part 1 Design, Synthesis, and Validation of Polymer-Supported Siloxane Transfer Agents for Transition-Metal-Mediated Cross-Coupling Reactions of Organolithiums Part 2 Total Synthesis of (-)-Mandelalide a Exploiting Anion Relay Chemistry.” 2016. Web. 14 Oct 2019.

Vancouver:

Nguyen MH. Part 1 Design, Synthesis, and Validation of Polymer-Supported Siloxane Transfer Agents for Transition-Metal-Mediated Cross-Coupling Reactions of Organolithiums Part 2 Total Synthesis of (-)-Mandelalide a Exploiting Anion Relay Chemistry. [Internet] [Thesis]. University of Pennsylvania; 2016. [cited 2019 Oct 14]. Available from: https://repository.upenn.edu/edissertations/1914.

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

Council of Science Editors:

Nguyen MH. Part 1 Design, Synthesis, and Validation of Polymer-Supported Siloxane Transfer Agents for Transition-Metal-Mediated Cross-Coupling Reactions of Organolithiums Part 2 Total Synthesis of (-)-Mandelalide a Exploiting Anion Relay Chemistry. [Thesis]. University of Pennsylvania; 2016. Available from: https://repository.upenn.edu/edissertations/1914

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


Université Paris-Sud – Paris XI

24. Vabre, Roxane. Fonctionnalisation directe de liaisons C-H et couplages croisés pour la formation de liaisons C-C et C-N : synthèse de purines 6,8,9-trisubstituées : C-H bond direct functionalization and cross-coupling reactions for C-C and C-N bonds formation : synthesis of 6,8,9-trisubstituted purines.

Degree: Docteur es, Chimie organique, 2013, Université Paris-Sud – Paris XI

La grande variété de propriétés biologiques associées au noyau purine en fait une structure privilégiée pour la conception et la synthèse de nouvelles molécules à… (more)

Subjects/Keywords: Méthodologie; Purine; Fonctionnalisation directe de Liaison C-H; Couplages croisés; Methodology; Purine; Direct C-H bond functionalization; Cross-coupling reactions

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APA (6th Edition):

Vabre, R. (2013). Fonctionnalisation directe de liaisons C-H et couplages croisés pour la formation de liaisons C-C et C-N : synthèse de purines 6,8,9-trisubstituées : C-H bond direct functionalization and cross-coupling reactions for C-C and C-N bonds formation : synthesis of 6,8,9-trisubstituted purines. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA112228

Chicago Manual of Style (16th Edition):

Vabre, Roxane. “Fonctionnalisation directe de liaisons C-H et couplages croisés pour la formation de liaisons C-C et C-N : synthèse de purines 6,8,9-trisubstituées : C-H bond direct functionalization and cross-coupling reactions for C-C and C-N bonds formation : synthesis of 6,8,9-trisubstituted purines.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 14, 2019. http://www.theses.fr/2013PA112228.

MLA Handbook (7th Edition):

Vabre, Roxane. “Fonctionnalisation directe de liaisons C-H et couplages croisés pour la formation de liaisons C-C et C-N : synthèse de purines 6,8,9-trisubstituées : C-H bond direct functionalization and cross-coupling reactions for C-C and C-N bonds formation : synthesis of 6,8,9-trisubstituted purines.” 2013. Web. 14 Oct 2019.

Vancouver:

Vabre R. Fonctionnalisation directe de liaisons C-H et couplages croisés pour la formation de liaisons C-C et C-N : synthèse de purines 6,8,9-trisubstituées : C-H bond direct functionalization and cross-coupling reactions for C-C and C-N bonds formation : synthesis of 6,8,9-trisubstituted purines. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2019 Oct 14]. Available from: http://www.theses.fr/2013PA112228.

Council of Science Editors:

Vabre R. Fonctionnalisation directe de liaisons C-H et couplages croisés pour la formation de liaisons C-C et C-N : synthèse de purines 6,8,9-trisubstituées : C-H bond direct functionalization and cross-coupling reactions for C-C and C-N bonds formation : synthesis of 6,8,9-trisubstituted purines. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA112228


University of Cincinnati

25. Nambukara Wellala, Nadeesha P. Synthesis and Catalytic Activities of Nickel Complexes Bearing Flexible Tridentate Ligands.

Degree: PhD, Arts and Sciences: Chemistry, 2017, University of Cincinnati

 This dissertation research focuses on the development of tridentate ligand supported nickel complexes for both catalytic and stoichiometric bond activation reactions. One of the main… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Inorganic Chemistry; Nickel Complexes; Pincer Complexes; CO2 Reduction; C S Cross Coupling Reactions; Hydride Complexes; Protonation

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APA (6th Edition):

Nambukara Wellala, N. P. (2017). Synthesis and Catalytic Activities of Nickel Complexes Bearing Flexible Tridentate Ligands. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1491561548324255

Chicago Manual of Style (16th Edition):

Nambukara Wellala, Nadeesha P. “Synthesis and Catalytic Activities of Nickel Complexes Bearing Flexible Tridentate Ligands.” 2017. Doctoral Dissertation, University of Cincinnati. Accessed October 14, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1491561548324255.

MLA Handbook (7th Edition):

Nambukara Wellala, Nadeesha P. “Synthesis and Catalytic Activities of Nickel Complexes Bearing Flexible Tridentate Ligands.” 2017. Web. 14 Oct 2019.

Vancouver:

Nambukara Wellala NP. Synthesis and Catalytic Activities of Nickel Complexes Bearing Flexible Tridentate Ligands. [Internet] [Doctoral dissertation]. University of Cincinnati; 2017. [cited 2019 Oct 14]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1491561548324255.

Council of Science Editors:

Nambukara Wellala NP. Synthesis and Catalytic Activities of Nickel Complexes Bearing Flexible Tridentate Ligands. [Doctoral Dissertation]. University of Cincinnati; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1491561548324255


Rutgers University

26. 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 October 14, 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. 14 Oct 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 Oct 14]. 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 California – Irvine

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

Degree: Chemistry, 2017, University of California – Irvine

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Erickson, Lucas William. “Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions.” 2017. Thesis, University of California – Irvine. Accessed October 14, 2019. http://www.escholarship.org/uc/item/3rr443q9.

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

MLA Handbook (7th Edition):

Erickson, Lucas William. “Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions.” 2017. Web. 14 Oct 2019.

Vancouver:

Erickson LW. Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2019 Oct 14]. Available from: http://www.escholarship.org/uc/item/3rr443q9.

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

Council of Science Editors:

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

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


Dalhousie University

28. Lundgren, Rylan. Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions.

Degree: PhD, Department of Chemistry, 2010, Dalhousie University

 Homogeneous organometallic species serve as useful catalysts for a vast number of chemical transformations. Ancillary ligands which bind to the metal center are employed to… (more)

Subjects/Keywords: Catalysis; organometallic; cross-coupling; hydrogenation

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APA (6th Edition):

Lundgren, R. (2010). Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/13115

Chicago Manual of Style (16th Edition):

Lundgren, Rylan. “Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions.” 2010. Doctoral Dissertation, Dalhousie University. Accessed October 14, 2019. http://hdl.handle.net/10222/13115.

MLA Handbook (7th Edition):

Lundgren, Rylan. “Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions.” 2010. Web. 14 Oct 2019.

Vancouver:

Lundgren R. Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions. [Internet] [Doctoral dissertation]. Dalhousie University; 2010. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10222/13115.

Council of Science Editors:

Lundgren R. Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions. [Doctoral Dissertation]. Dalhousie University; 2010. Available from: http://hdl.handle.net/10222/13115


University of Rochester

29. Prinsell, Michael R. (1986 - ). Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles.

Degree: PhD, 2014, University of Rochester

 The nickel-catalyzed reductive coupling of two organic electrophiles to form new carbon-carbon bonds is a fast emerging field of chemistry, with applications to the synthesis… (more)

Subjects/Keywords: Nickel; Electrophile; Cross-coupling

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APA (6th Edition):

Prinsell, M. R. (. -. ). (2014). Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/28613

Chicago Manual of Style (16th Edition):

Prinsell, Michael R (1986 - ). “Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles.” 2014. Doctoral Dissertation, University of Rochester. Accessed October 14, 2019. http://hdl.handle.net/1802/28613.

MLA Handbook (7th Edition):

Prinsell, Michael R (1986 - ). “Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles.” 2014. Web. 14 Oct 2019.

Vancouver:

Prinsell MR(-). Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles. [Internet] [Doctoral dissertation]. University of Rochester; 2014. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/1802/28613.

Council of Science Editors:

Prinsell MR(-). Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles. [Doctoral Dissertation]. University of Rochester; 2014. Available from: http://hdl.handle.net/1802/28613


Boston College

30. Heusser, Carolyn Andrea. Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement.

Degree: MS, Chemistry, 2013, Boston College

 Chapter 1: There are a limited number of examples of metal-catalyzed Brook rearrangements in the literature, none of which involve ruthenium, rhodium, or iridium which… (more)

Subjects/Keywords: Acylsilane; Brook rearrangement; Cross Coupling

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APA (6th Edition):

Heusser, C. A. (2013). Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101169

Chicago Manual of Style (16th Edition):

Heusser, Carolyn Andrea. “Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement.” 2013. Masters Thesis, Boston College. Accessed October 14, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101169.

MLA Handbook (7th Edition):

Heusser, Carolyn Andrea. “Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement.” 2013. Web. 14 Oct 2019.

Vancouver:

Heusser CA. Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement. [Internet] [Masters thesis]. Boston College; 2013. [cited 2019 Oct 14]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101169.

Council of Science Editors:

Heusser CA. Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement. [Masters Thesis]. Boston College; 2013. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101169

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