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You searched for subject:(Heterocycle). Showing records 1 – 30 of 115 total matches.

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University of Oregon

1. Young, Brian. Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations.

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

 Highly conjugated, extended heterocycles are recognized as important materials for use in electronic applications, and therefore the synthesis and characterization of new molecules of this… (more)

Subjects/Keywords: Coarctate; Heterocycle; Synthetic chemistry

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

APA (6th Edition):

Young, B. (2013). Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations. (Doctoral Dissertation). University of Oregon. Retrieved from http://hdl.handle.net/1794/13260

Chicago Manual of Style (16th Edition):

Young, Brian. “Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations.” 2013. Doctoral Dissertation, University of Oregon. Accessed April 18, 2021. http://hdl.handle.net/1794/13260.

MLA Handbook (7th Edition):

Young, Brian. “Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations.” 2013. Web. 18 Apr 2021.

Vancouver:

Young B. Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations. [Internet] [Doctoral dissertation]. University of Oregon; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1794/13260.

Council of Science Editors:

Young B. Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations. [Doctoral Dissertation]. University of Oregon; 2013. Available from: http://hdl.handle.net/1794/13260


Oklahoma State University

2. Bryant, Daniel James. Palladium-catalyzed cyclization of drug candidates.

Degree: Chemistry, 2020, Oklahoma State University

 Ovarian cancer is both difficult to detect and difficult to treat, therefore the discovery of new therapies is important. Retinoids (retinoic acid derivatives) are known… (more)

Subjects/Keywords: anticancer; catalysis; heterocycle; sheta2

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APA (6th Edition):

Bryant, D. J. (2020). Palladium-catalyzed cyclization of drug candidates. (Thesis). Oklahoma State University. Retrieved from http://hdl.handle.net/11244/325527

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):

Bryant, Daniel James. “Palladium-catalyzed cyclization of drug candidates.” 2020. Thesis, Oklahoma State University. Accessed April 18, 2021. http://hdl.handle.net/11244/325527.

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

MLA Handbook (7th Edition):

Bryant, Daniel James. “Palladium-catalyzed cyclization of drug candidates.” 2020. Web. 18 Apr 2021.

Vancouver:

Bryant DJ. Palladium-catalyzed cyclization of drug candidates. [Internet] [Thesis]. Oklahoma State University; 2020. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/11244/325527.

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

Council of Science Editors:

Bryant DJ. Palladium-catalyzed cyclization of drug candidates. [Thesis]. Oklahoma State University; 2020. Available from: http://hdl.handle.net/11244/325527

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

3. L. Basolo. SYNTHESIS AND REACTIVITY OF N-CONTAINING HETEROCYCLES THROUGH CATALYTIC SYSTEMS.

Degree: 2010, Università degli Studi di Milano

 N-containing heterocycles are the more represented in natural products and drugs. Our research has been focused on various aspects of heterocycles synthesis and reactivity. For… (more)

Subjects/Keywords: palladium; heterocycle; Settore CHIM/06 - Chimica Organica

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APA (6th Edition):

Basolo, L. (2010). SYNTHESIS AND REACTIVITY OF N-CONTAINING HETEROCYCLES THROUGH CATALYTIC SYSTEMS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/150083

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):

Basolo, L.. “SYNTHESIS AND REACTIVITY OF N-CONTAINING HETEROCYCLES THROUGH CATALYTIC SYSTEMS.” 2010. Thesis, Università degli Studi di Milano. Accessed April 18, 2021. http://hdl.handle.net/2434/150083.

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

MLA Handbook (7th Edition):

Basolo, L.. “SYNTHESIS AND REACTIVITY OF N-CONTAINING HETEROCYCLES THROUGH CATALYTIC SYSTEMS.” 2010. Web. 18 Apr 2021.

Vancouver:

Basolo L. SYNTHESIS AND REACTIVITY OF N-CONTAINING HETEROCYCLES THROUGH CATALYTIC SYSTEMS. [Internet] [Thesis]. Università degli Studi di Milano; 2010. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2434/150083.

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

Council of Science Editors:

Basolo L. SYNTHESIS AND REACTIVITY OF N-CONTAINING HETEROCYCLES THROUGH CATALYTIC SYSTEMS. [Thesis]. Università degli Studi di Milano; 2010. Available from: http://hdl.handle.net/2434/150083

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


Iowa State University

4. Fang, Yuesi. Synthesis of Bioactive Nitrogen-Containing Heterocycles via Aryne Methodologies.

Degree: 2012, Iowa State University

 The six chapters of this dissertation exemplify the application of aryne chemistry in medicinally-relevant, nitrogen-containing heterocycle synthesis. The arynes discussed in this dissertation are generated… (more)

Subjects/Keywords: aryne; benzyne; bioactive; heterocycle; organic synthesis; Chemistry

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APA (6th Edition):

Fang, Y. (2012). Synthesis of Bioactive Nitrogen-Containing Heterocycles via Aryne Methodologies. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/12674

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):

Fang, Yuesi. “Synthesis of Bioactive Nitrogen-Containing Heterocycles via Aryne Methodologies.” 2012. Thesis, Iowa State University. Accessed April 18, 2021. https://lib.dr.iastate.edu/etd/12674.

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

MLA Handbook (7th Edition):

Fang, Yuesi. “Synthesis of Bioactive Nitrogen-Containing Heterocycles via Aryne Methodologies.” 2012. Web. 18 Apr 2021.

Vancouver:

Fang Y. Synthesis of Bioactive Nitrogen-Containing Heterocycles via Aryne Methodologies. [Internet] [Thesis]. Iowa State University; 2012. [cited 2021 Apr 18]. Available from: https://lib.dr.iastate.edu/etd/12674.

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

Council of Science Editors:

Fang Y. Synthesis of Bioactive Nitrogen-Containing Heterocycles via Aryne Methodologies. [Thesis]. Iowa State University; 2012. Available from: https://lib.dr.iastate.edu/etd/12674

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

5. Zhao, Guangkuan. Reduction of thioketals by TMSCl/NaI association and synthesis of heterocycles from ortho-substituted arylalkynes : Réduction de thiocétals par l'association TMSCl/NaI et synthèse d'hétérocycles à partir d'alcynes ortho-substitués.

Degree: Docteur es, Chimie thérapeutique, 2019, Université Paris-Saclay (ComUE)

La thèse est divisée en deux parties distinctes.La première consiste, après une étude exhaustive concernant les réactions de désulfurisation de thiocétals répertoriées dans la littérature,… (more)

Subjects/Keywords: Hétérocycle; Synthèse; Catalyse; Heterocycle; Synthesis; Catalysis

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APA (6th Edition):

Zhao, G. (2019). Reduction of thioketals by TMSCl/NaI association and synthesis of heterocycles from ortho-substituted arylalkynes : Réduction de thiocétals par l'association TMSCl/NaI et synthèse d'hétérocycles à partir d'alcynes ortho-substitués. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS392

Chicago Manual of Style (16th Edition):

Zhao, Guangkuan. “Reduction of thioketals by TMSCl/NaI association and synthesis of heterocycles from ortho-substituted arylalkynes : Réduction de thiocétals par l'association TMSCl/NaI et synthèse d'hétérocycles à partir d'alcynes ortho-substitués.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 18, 2021. http://www.theses.fr/2019SACLS392.

MLA Handbook (7th Edition):

Zhao, Guangkuan. “Reduction of thioketals by TMSCl/NaI association and synthesis of heterocycles from ortho-substituted arylalkynes : Réduction de thiocétals par l'association TMSCl/NaI et synthèse d'hétérocycles à partir d'alcynes ortho-substitués.” 2019. Web. 18 Apr 2021.

Vancouver:

Zhao G. Reduction of thioketals by TMSCl/NaI association and synthesis of heterocycles from ortho-substituted arylalkynes : Réduction de thiocétals par l'association TMSCl/NaI et synthèse d'hétérocycles à partir d'alcynes ortho-substitués. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2021 Apr 18]. Available from: http://www.theses.fr/2019SACLS392.

Council of Science Editors:

Zhao G. Reduction of thioketals by TMSCl/NaI association and synthesis of heterocycles from ortho-substituted arylalkynes : Réduction de thiocétals par l'association TMSCl/NaI et synthèse d'hétérocycles à partir d'alcynes ortho-substitués. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS392


University of Oregon

6. Campbell, Patrick. Hydrogen Storage Applications of 1,2-Azaborines.

Degree: 2012, University of Oregon

 The development of safe and efficient hydrogen storage materials will aid in the transition away from fossil fuels toward a renewable, hydrogen-based energy infrastructure. Boron-nitrogen… (more)

Subjects/Keywords: Aryl-phosphine; Boron; Heterocycle; Hydrogen; Nitrogen; Storage

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APA (6th Edition):

Campbell, P. (2012). Hydrogen Storage Applications of 1,2-Azaborines. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/12555

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):

Campbell, Patrick. “Hydrogen Storage Applications of 1,2-Azaborines.” 2012. Thesis, University of Oregon. Accessed April 18, 2021. http://hdl.handle.net/1794/12555.

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

MLA Handbook (7th Edition):

Campbell, Patrick. “Hydrogen Storage Applications of 1,2-Azaborines.” 2012. Web. 18 Apr 2021.

Vancouver:

Campbell P. Hydrogen Storage Applications of 1,2-Azaborines. [Internet] [Thesis]. University of Oregon; 2012. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1794/12555.

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

Council of Science Editors:

Campbell P. Hydrogen Storage Applications of 1,2-Azaborines. [Thesis]. University of Oregon; 2012. Available from: http://hdl.handle.net/1794/12555

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


University of Toronto

7. Bancerz, Matthew. Verdazyl Radicals as Substrates for Organic Synthesis.

Degree: 2012, University of Toronto

Verdazyl radicals, discovered in 1963, are a family of exceptionally stable radicals defined by their 6-membered ring containing four nitrogen atoms. Verdazyl radicals are highly… (more)

Subjects/Keywords: verdazyl; radical; cycloaddition; heterocycle; rearrangement; 0490

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APA (6th Edition):

Bancerz, M. (2012). Verdazyl Radicals as Substrates for Organic Synthesis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/43376

Chicago Manual of Style (16th Edition):

Bancerz, Matthew. “Verdazyl Radicals as Substrates for Organic Synthesis.” 2012. Doctoral Dissertation, University of Toronto. Accessed April 18, 2021. http://hdl.handle.net/1807/43376.

MLA Handbook (7th Edition):

Bancerz, Matthew. “Verdazyl Radicals as Substrates for Organic Synthesis.” 2012. Web. 18 Apr 2021.

Vancouver:

Bancerz M. Verdazyl Radicals as Substrates for Organic Synthesis. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1807/43376.

Council of Science Editors:

Bancerz M. Verdazyl Radicals as Substrates for Organic Synthesis. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/43376


University of Minnesota

8. Seki, Hajime. Cyclic enaminones: methodology development, total synthesis, and library construction.

Degree: PhD, Chemistry, 2011, University of Minnesota

 The cyclic enaminone lies at the core of this entire doctoral work. It possesses exceptionally versatile reactivities, and can thus be utilized in the synthesis… (more)

Subjects/Keywords: Alkaloid; Enaminone; Heterocycle; Indolizidine; Methodology; Quinolizidine; Chemistry

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APA (6th Edition):

Seki, H. (2011). Cyclic enaminones: methodology development, total synthesis, and library construction. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/127080

Chicago Manual of Style (16th Edition):

Seki, Hajime. “Cyclic enaminones: methodology development, total synthesis, and library construction.” 2011. Doctoral Dissertation, University of Minnesota. Accessed April 18, 2021. http://purl.umn.edu/127080.

MLA Handbook (7th Edition):

Seki, Hajime. “Cyclic enaminones: methodology development, total synthesis, and library construction.” 2011. Web. 18 Apr 2021.

Vancouver:

Seki H. Cyclic enaminones: methodology development, total synthesis, and library construction. [Internet] [Doctoral dissertation]. University of Minnesota; 2011. [cited 2021 Apr 18]. Available from: http://purl.umn.edu/127080.

Council of Science Editors:

Seki H. Cyclic enaminones: methodology development, total synthesis, and library construction. [Doctoral Dissertation]. University of Minnesota; 2011. Available from: http://purl.umn.edu/127080


Clemson University

9. Belina, Steven Paul. The Synthesis and Characterization of Novel Pentafluorosulfanyl-Containing Heterocycles and Pentafluorosulfanyldifluoromethane.

Degree: PhD, Chemistry, 2019, Clemson University

  Beginning in the early 1960s, scientists began to experiment with the pentafluorosulfanyl moiety. The unique properties of the functional group has attracted interest among… (more)

Subjects/Keywords: heterocycle; pentafluorosulfanyl; raman spectroscopy; x-ray crystallography

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APA (6th Edition):

Belina, S. P. (2019). The Synthesis and Characterization of Novel Pentafluorosulfanyl-Containing Heterocycles and Pentafluorosulfanyldifluoromethane. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/2373

Chicago Manual of Style (16th Edition):

Belina, Steven Paul. “The Synthesis and Characterization of Novel Pentafluorosulfanyl-Containing Heterocycles and Pentafluorosulfanyldifluoromethane.” 2019. Doctoral Dissertation, Clemson University. Accessed April 18, 2021. https://tigerprints.clemson.edu/all_dissertations/2373.

MLA Handbook (7th Edition):

Belina, Steven Paul. “The Synthesis and Characterization of Novel Pentafluorosulfanyl-Containing Heterocycles and Pentafluorosulfanyldifluoromethane.” 2019. Web. 18 Apr 2021.

Vancouver:

Belina SP. The Synthesis and Characterization of Novel Pentafluorosulfanyl-Containing Heterocycles and Pentafluorosulfanyldifluoromethane. [Internet] [Doctoral dissertation]. Clemson University; 2019. [cited 2021 Apr 18]. Available from: https://tigerprints.clemson.edu/all_dissertations/2373.

Council of Science Editors:

Belina SP. The Synthesis and Characterization of Novel Pentafluorosulfanyl-Containing Heterocycles and Pentafluorosulfanyldifluoromethane. [Doctoral Dissertation]. Clemson University; 2019. Available from: https://tigerprints.clemson.edu/all_dissertations/2373


University of New South Wales

10. Islam, Md. Exploring bio-active natural products as potential therapeutics leads.

Degree: Chemistry, 2015, University of New South Wales

 This thesis describes screening, mechanistic studies, design and synthesis of natural product analogs. Chapter 2 describes screening of a natural products library for their antibacterial… (more)

Subjects/Keywords: Macrocycle; Natural products; Heterocycle; Mechanistic study

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APA (6th Edition):

Islam, M. (2015). Exploring bio-active natural products as potential therapeutics leads. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/54756 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35865/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Islam, Md. “Exploring bio-active natural products as potential therapeutics leads.” 2015. Doctoral Dissertation, University of New South Wales. Accessed April 18, 2021. http://handle.unsw.edu.au/1959.4/54756 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35865/SOURCE02?view=true.

MLA Handbook (7th Edition):

Islam, Md. “Exploring bio-active natural products as potential therapeutics leads.” 2015. Web. 18 Apr 2021.

Vancouver:

Islam M. Exploring bio-active natural products as potential therapeutics leads. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2021 Apr 18]. Available from: http://handle.unsw.edu.au/1959.4/54756 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35865/SOURCE02?view=true.

Council of Science Editors:

Islam M. Exploring bio-active natural products as potential therapeutics leads. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/54756 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35865/SOURCE02?view=true


University of New South Wales

11. Sengul, Ibrahim Fazil. Synthesis of new heterocycle-linked BIS-indole systems.

Degree: Chemistry, 2011, University of New South Wales

 The primary aim of this project was to synthesize relatively large molecular structures derived from novel 2- and 3-indolyl compounds and to investigate their properties… (more)

Subjects/Keywords: BIS-indole system; heterocycle-linked; synthesis

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APA (6th Edition):

Sengul, I. F. (2011). Synthesis of new heterocycle-linked BIS-indole systems. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10251/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Sengul, Ibrahim Fazil. “Synthesis of new heterocycle-linked BIS-indole systems.” 2011. Doctoral Dissertation, University of New South Wales. Accessed April 18, 2021. http://handle.unsw.edu.au/1959.4/51584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10251/SOURCE02?view=true.

MLA Handbook (7th Edition):

Sengul, Ibrahim Fazil. “Synthesis of new heterocycle-linked BIS-indole systems.” 2011. Web. 18 Apr 2021.

Vancouver:

Sengul IF. Synthesis of new heterocycle-linked BIS-indole systems. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2021 Apr 18]. Available from: http://handle.unsw.edu.au/1959.4/51584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10251/SOURCE02?view=true.

Council of Science Editors:

Sengul IF. Synthesis of new heterocycle-linked BIS-indole systems. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10251/SOURCE02?view=true


RMIT University

12. Leonard, M. A novel hydantoin synthesis and exploration of related reactions.

Degree: 2015, RMIT University

 Chapter one gives a short history of the discovery of hydantoins, followed by their chemical properties and reactivity and concluding with the many ways to… (more)

Subjects/Keywords: Fields of Research; Hydantoin; Nucleophilic substitution; Heterocycle; Isocyanate; 2-Nitropropane

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APA (6th Edition):

Leonard, M. (2015). A novel hydantoin synthesis and exploration of related reactions. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:161425

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):

Leonard, M. “A novel hydantoin synthesis and exploration of related reactions.” 2015. Thesis, RMIT University. Accessed April 18, 2021. http://researchbank.rmit.edu.au/view/rmit:161425.

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

MLA Handbook (7th Edition):

Leonard, M. “A novel hydantoin synthesis and exploration of related reactions.” 2015. Web. 18 Apr 2021.

Vancouver:

Leonard M. A novel hydantoin synthesis and exploration of related reactions. [Internet] [Thesis]. RMIT University; 2015. [cited 2021 Apr 18]. Available from: http://researchbank.rmit.edu.au/view/rmit:161425.

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

Council of Science Editors:

Leonard M. A novel hydantoin synthesis and exploration of related reactions. [Thesis]. RMIT University; 2015. Available from: http://researchbank.rmit.edu.au/view/rmit:161425

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


University of California – Irvine

13. McCutcheon, David Clark. Expansion of the bioluminescence toolkit for in vivo imaging.

Degree: Chemistry, 2015, University of California – Irvine

 Bioluminescence imaging is among the most popular methods for visualizing biologicalprocesses in vitro, in live cells, and even in whole organisms. At the core of… (more)

Subjects/Keywords: Chemistry; Bioluminescence; Heterocycle; Imaging; Luciferin; Organic chemistry; Synthesis

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APA (6th Edition):

McCutcheon, D. C. (2015). Expansion of the bioluminescence toolkit for in vivo imaging. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/16c295pd

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):

McCutcheon, David Clark. “Expansion of the bioluminescence toolkit for in vivo imaging.” 2015. Thesis, University of California – Irvine. Accessed April 18, 2021. http://www.escholarship.org/uc/item/16c295pd.

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

MLA Handbook (7th Edition):

McCutcheon, David Clark. “Expansion of the bioluminescence toolkit for in vivo imaging.” 2015. Web. 18 Apr 2021.

Vancouver:

McCutcheon DC. Expansion of the bioluminescence toolkit for in vivo imaging. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2021 Apr 18]. Available from: http://www.escholarship.org/uc/item/16c295pd.

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

Council of Science Editors:

McCutcheon DC. Expansion of the bioluminescence toolkit for in vivo imaging. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/16c295pd

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


UCLA

14. Miller, Kevin L. Unique Properties and Reactivity of Electrophilic Metal Centers Supported by Ferrocene Diamide Ligands.

Degree: Chemistry, 2014, UCLA

 The work reported herein represents various studies of group 3 metal complexes supported by ferrocene diamide ligands. Chapter 1 is a brief introduction and survey… (more)

Subjects/Keywords: Inorganic chemistry; electronic communication; ferrocene; hydrodenitrogenation; lanthanide; N-heterocycle

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APA (6th Edition):

Miller, K. L. (2014). Unique Properties and Reactivity of Electrophilic Metal Centers Supported by Ferrocene Diamide Ligands. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1k33f451

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):

Miller, Kevin L. “Unique Properties and Reactivity of Electrophilic Metal Centers Supported by Ferrocene Diamide Ligands.” 2014. Thesis, UCLA. Accessed April 18, 2021. http://www.escholarship.org/uc/item/1k33f451.

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

MLA Handbook (7th Edition):

Miller, Kevin L. “Unique Properties and Reactivity of Electrophilic Metal Centers Supported by Ferrocene Diamide Ligands.” 2014. Web. 18 Apr 2021.

Vancouver:

Miller KL. Unique Properties and Reactivity of Electrophilic Metal Centers Supported by Ferrocene Diamide Ligands. [Internet] [Thesis]. UCLA; 2014. [cited 2021 Apr 18]. Available from: http://www.escholarship.org/uc/item/1k33f451.

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

Council of Science Editors:

Miller KL. Unique Properties and Reactivity of Electrophilic Metal Centers Supported by Ferrocene Diamide Ligands. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/1k33f451

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


University of Rochester

15. Li, Ling (1980 - ). Transition metal mediated synthesis of heterocycles via carbon-hydrogen bond activation.

Degree: PhD, 2011, University of Rochester

 Dicobalt octacarbonyl was found to be an efficient catalyst for the selective conversion of diallylanilines to quinolines in good yields under mild conditions in the… (more)

Subjects/Keywords: Transition metal; Carbon-hydrogen bond activation; Heterocycle; Quinoline; Isoquinoline; Catalyst

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APA (6th Edition):

Li, L. (. -. ). (2011). Transition metal mediated synthesis of heterocycles via carbon-hydrogen bond activation. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/14546

Chicago Manual of Style (16th Edition):

Li, Ling (1980 - ). “Transition metal mediated synthesis of heterocycles via carbon-hydrogen bond activation.” 2011. Doctoral Dissertation, University of Rochester. Accessed April 18, 2021. http://hdl.handle.net/1802/14546.

MLA Handbook (7th Edition):

Li, Ling (1980 - ). “Transition metal mediated synthesis of heterocycles via carbon-hydrogen bond activation.” 2011. Web. 18 Apr 2021.

Vancouver:

Li L(-). Transition metal mediated synthesis of heterocycles via carbon-hydrogen bond activation. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1802/14546.

Council of Science Editors:

Li L(-). Transition metal mediated synthesis of heterocycles via carbon-hydrogen bond activation. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/14546


University of Tasmania

16. James, AN. Steric and electronic investigations into Samarium (II) dinitrogen, heteroalkyne and heterocycle reductions .

Degree: 2011, University of Tasmania

 This thesis describes the synthesis, characterisation and reactivity of a range of samarium(II) and samarium(III) complexes of a modified porphyrinogen, trans-N,Nʹ-dimethyl-meso-octaethylporphyrinogen, `Et8N4Me2H2`. Various related reactivity… (more)

Subjects/Keywords: samarium; organometallic; reduction; dinitrogen; heterocycle; heteroalkyne; steric; electronic

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APA (6th Edition):

James, A. (2011). Steric and electronic investigations into Samarium (II) dinitrogen, heteroalkyne and heterocycle reductions . (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/12478/1/James_Adam_021413_PhD_thesis.pdf ; https://eprints.utas.edu.au/12478/2/Appendix_C.zip ; https://eprints.utas.edu.au/12478/3/Appendix_D.zip

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):

James, AN. “Steric and electronic investigations into Samarium (II) dinitrogen, heteroalkyne and heterocycle reductions .” 2011. Thesis, University of Tasmania. Accessed April 18, 2021. https://eprints.utas.edu.au/12478/1/James_Adam_021413_PhD_thesis.pdf ; https://eprints.utas.edu.au/12478/2/Appendix_C.zip ; https://eprints.utas.edu.au/12478/3/Appendix_D.zip.

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

MLA Handbook (7th Edition):

James, AN. “Steric and electronic investigations into Samarium (II) dinitrogen, heteroalkyne and heterocycle reductions .” 2011. Web. 18 Apr 2021.

Vancouver:

James A. Steric and electronic investigations into Samarium (II) dinitrogen, heteroalkyne and heterocycle reductions . [Internet] [Thesis]. University of Tasmania; 2011. [cited 2021 Apr 18]. Available from: https://eprints.utas.edu.au/12478/1/James_Adam_021413_PhD_thesis.pdf ; https://eprints.utas.edu.au/12478/2/Appendix_C.zip ; https://eprints.utas.edu.au/12478/3/Appendix_D.zip.

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

Council of Science Editors:

James A. Steric and electronic investigations into Samarium (II) dinitrogen, heteroalkyne and heterocycle reductions . [Thesis]. University of Tasmania; 2011. Available from: https://eprints.utas.edu.au/12478/1/James_Adam_021413_PhD_thesis.pdf ; https://eprints.utas.edu.au/12478/2/Appendix_C.zip ; https://eprints.utas.edu.au/12478/3/Appendix_D.zip

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

17. Sharma, Mani. Synthesis of substituted aromatic heterocycle based dpp iv inhibitors fluoropyrrolidine and related structural types; -.

Degree: Pharmacy, 2013, University of Delhi

None

Reference p.105-115

Advisors/Committee Members: Gupta, Monica.

Subjects/Keywords: aromatic heterocycle; fluoropyrrolidine; substituted aromatic

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APA (6th Edition):

Sharma, M. (2013). Synthesis of substituted aromatic heterocycle based dpp iv inhibitors fluoropyrrolidine and related structural types; -. (Thesis). University of Delhi. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/31575

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):

Sharma, Mani. “Synthesis of substituted aromatic heterocycle based dpp iv inhibitors fluoropyrrolidine and related structural types; -.” 2013. Thesis, University of Delhi. Accessed April 18, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/31575.

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

MLA Handbook (7th Edition):

Sharma, Mani. “Synthesis of substituted aromatic heterocycle based dpp iv inhibitors fluoropyrrolidine and related structural types; -.” 2013. Web. 18 Apr 2021.

Vancouver:

Sharma M. Synthesis of substituted aromatic heterocycle based dpp iv inhibitors fluoropyrrolidine and related structural types; -. [Internet] [Thesis]. University of Delhi; 2013. [cited 2021 Apr 18]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/31575.

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

Council of Science Editors:

Sharma M. Synthesis of substituted aromatic heterocycle based dpp iv inhibitors fluoropyrrolidine and related structural types; -. [Thesis]. University of Delhi; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/31575

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


Texas A&M University

18. Giles, Ian. Experimental and Theoretical Investigations of Anion-pi Interactions Metallacyclic Architectures of First-Row Transition Metals and N-Heteroaromatic Ligands.

Degree: PhD, Chemistry, 2012, Texas A&M University

 Research into anion-pi interactions has shifted from attempts to establish the legitimacy of the interaction to the incorporation of anion-pi interactions into supramolecular architectures. The… (more)

Subjects/Keywords: supramolecular chemistry; inorganic chemistry; anion-pi interactions; metallacycle; N-heterocycle

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APA (6th Edition):

Giles, I. (2012). Experimental and Theoretical Investigations of Anion-pi Interactions Metallacyclic Architectures of First-Row Transition Metals and N-Heteroaromatic Ligands. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11026

Chicago Manual of Style (16th Edition):

Giles, Ian. “Experimental and Theoretical Investigations of Anion-pi Interactions Metallacyclic Architectures of First-Row Transition Metals and N-Heteroaromatic Ligands.” 2012. Doctoral Dissertation, Texas A&M University. Accessed April 18, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11026.

MLA Handbook (7th Edition):

Giles, Ian. “Experimental and Theoretical Investigations of Anion-pi Interactions Metallacyclic Architectures of First-Row Transition Metals and N-Heteroaromatic Ligands.” 2012. Web. 18 Apr 2021.

Vancouver:

Giles I. Experimental and Theoretical Investigations of Anion-pi Interactions Metallacyclic Architectures of First-Row Transition Metals and N-Heteroaromatic Ligands. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11026.

Council of Science Editors:

Giles I. Experimental and Theoretical Investigations of Anion-pi Interactions Metallacyclic Architectures of First-Row Transition Metals and N-Heteroaromatic Ligands. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11026


University of Toronto

19. Kaldas, Sherif James. Development of Chemoselective Transformations for Organic Synthesis: From Amphoteric Boronates to Benzynes.

Degree: PhD, 2020, University of Toronto

 A significant challenge in organic chemistry is the development of methodologies capable of synthesizing new molecular motifs or previously inaccessible scaffolds. Previous research in the… (more)

Subjects/Keywords: benzyne; boron; catalysis; cross-coupling; heterocycle synthesis; MIDA; 0490

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APA (6th Edition):

Kaldas, S. J. (2020). Development of Chemoselective Transformations for Organic Synthesis: From Amphoteric Boronates to Benzynes. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/101198

Chicago Manual of Style (16th Edition):

Kaldas, Sherif James. “Development of Chemoselective Transformations for Organic Synthesis: From Amphoteric Boronates to Benzynes.” 2020. Doctoral Dissertation, University of Toronto. Accessed April 18, 2021. http://hdl.handle.net/1807/101198.

MLA Handbook (7th Edition):

Kaldas, Sherif James. “Development of Chemoselective Transformations for Organic Synthesis: From Amphoteric Boronates to Benzynes.” 2020. Web. 18 Apr 2021.

Vancouver:

Kaldas SJ. Development of Chemoselective Transformations for Organic Synthesis: From Amphoteric Boronates to Benzynes. [Internet] [Doctoral dissertation]. University of Toronto; 2020. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1807/101198.

Council of Science Editors:

Kaldas SJ. Development of Chemoselective Transformations for Organic Synthesis: From Amphoteric Boronates to Benzynes. [Doctoral Dissertation]. University of Toronto; 2020. Available from: http://hdl.handle.net/1807/101198


University of Illinois – Chicago

20. Kong, Chen. Transition Metal-Catalyzed Tandem Electrocyclization Migration Reaction Using Styryl Azides.

Degree: 2016, University of Illinois – Chicago

 This thesis describes transition metal-catalyzed tandem electrocyclization reaction employing styryl azides as the nitrogen source to form highly functionalized N-heterocycles. Chapter one briefly highlights methods… (more)

Subjects/Keywords: transition metal; electrocyclization; migration; azides; N-heterocycle; Nazarov; rearrangement

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APA (6th Edition):

Kong, C. (2016). Transition Metal-Catalyzed Tandem Electrocyclization Migration Reaction Using Styryl Azides. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/20167

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):

Kong, Chen. “Transition Metal-Catalyzed Tandem Electrocyclization Migration Reaction Using Styryl Azides.” 2016. Thesis, University of Illinois – Chicago. Accessed April 18, 2021. http://hdl.handle.net/10027/20167.

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

MLA Handbook (7th Edition):

Kong, Chen. “Transition Metal-Catalyzed Tandem Electrocyclization Migration Reaction Using Styryl Azides.” 2016. Web. 18 Apr 2021.

Vancouver:

Kong C. Transition Metal-Catalyzed Tandem Electrocyclization Migration Reaction Using Styryl Azides. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10027/20167.

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

Council of Science Editors:

Kong C. Transition Metal-Catalyzed Tandem Electrocyclization Migration Reaction Using Styryl Azides. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/20167

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

21. 深澤, 甲. Ugi 反応によるヘテロ環を含むアズレンアミド誘導体の合成 : FACILE SYNTHESIS OF AZULENE AMIDE DERIVATIVES WITH HETEROCYCLIC RESIDUES USING UGI REACTION.

Degree: 2008, Hosei University / 法政大学

 Many synthetic research reports on heterocyclic compounds by Ugi reaction have appeared in recentyears. Starting from 3-isocyanoguaiazulene (3-isocyano-7-isopropyl-1,4-dimethylazulene), there wereperformed our synthetic studies by Ugi… (more)

Subjects/Keywords: 3-isocyanoguaiazulene; Ugi reaction; heterocycle

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APA (6th Edition):

深澤, . (2008). Ugi 反応によるヘテロ環を含むアズレンアミド誘導体の合成 : FACILE SYNTHESIS OF AZULENE AMIDE DERIVATIVES WITH HETEROCYCLIC RESIDUES USING UGI REACTION. (Thesis). Hosei University / 法政大学. Retrieved from http://hdl.handle.net/10114/6195

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):

深澤, 甲. “Ugi 反応によるヘテロ環を含むアズレンアミド誘導体の合成 : FACILE SYNTHESIS OF AZULENE AMIDE DERIVATIVES WITH HETEROCYCLIC RESIDUES USING UGI REACTION.” 2008. Thesis, Hosei University / 法政大学. Accessed April 18, 2021. http://hdl.handle.net/10114/6195.

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

MLA Handbook (7th Edition):

深澤, 甲. “Ugi 反応によるヘテロ環を含むアズレンアミド誘導体の合成 : FACILE SYNTHESIS OF AZULENE AMIDE DERIVATIVES WITH HETEROCYCLIC RESIDUES USING UGI REACTION.” 2008. Web. 18 Apr 2021.

Vancouver:

深澤 . Ugi 反応によるヘテロ環を含むアズレンアミド誘導体の合成 : FACILE SYNTHESIS OF AZULENE AMIDE DERIVATIVES WITH HETEROCYCLIC RESIDUES USING UGI REACTION. [Internet] [Thesis]. Hosei University / 法政大学; 2008. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10114/6195.

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

Council of Science Editors:

深澤 . Ugi 反応によるヘテロ環を含むアズレンアミド誘導体の合成 : FACILE SYNTHESIS OF AZULENE AMIDE DERIVATIVES WITH HETEROCYCLIC RESIDUES USING UGI REACTION. [Thesis]. Hosei University / 法政大学; 2008. Available from: http://hdl.handle.net/10114/6195

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


Boston College

22. Baggett, Andrew William. New Strategies Enabling Diverse Functionalization of Aromatic 1,2-Azaborine Motifs.

Degree: PhD, Chemistry, 2016, Boston College

 Described herein are four projects focused on the elaboration of aromatic 1,2-azaborine core structures through late-stage functionalization strategies. In the first chapter, the gram scale,… (more)

Subjects/Keywords: Aromaticity; Azaborine; Boron; C-H Functionalization; Heterocycle; Nitrogen

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APA (6th Edition):

Baggett, A. W. (2016). New Strategies Enabling Diverse Functionalization of Aromatic 1,2-Azaborine Motifs. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:105027

Chicago Manual of Style (16th Edition):

Baggett, Andrew William. “New Strategies Enabling Diverse Functionalization of Aromatic 1,2-Azaborine Motifs.” 2016. Doctoral Dissertation, Boston College. Accessed April 18, 2021. http://dlib.bc.edu/islandora/object/bc-ir:105027.

MLA Handbook (7th Edition):

Baggett, Andrew William. “New Strategies Enabling Diverse Functionalization of Aromatic 1,2-Azaborine Motifs.” 2016. Web. 18 Apr 2021.

Vancouver:

Baggett AW. New Strategies Enabling Diverse Functionalization of Aromatic 1,2-Azaborine Motifs. [Internet] [Doctoral dissertation]. Boston College; 2016. [cited 2021 Apr 18]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:105027.

Council of Science Editors:

Baggett AW. New Strategies Enabling Diverse Functionalization of Aromatic 1,2-Azaborine Motifs. [Doctoral Dissertation]. Boston College; 2016. Available from: http://dlib.bc.edu/islandora/object/bc-ir:105027


Boston College

23. McConnell, Cameron Reed. Leveraging 1,2-Azaborine's Distinct Electronic Structure to Access New Building Blocks.

Degree: PhD, Chemistry, 2019, Boston College

 Described herein are three projects that derive from in-depth studies of the distinct electronic structure of monocyclic 1,2-dihydro-1,2-azaborine (heretofore referred to as simply 1,2-azaborine). In… (more)

Subjects/Keywords: 1,2-azaborine; BN-heterocycle; functionalization; ligand; polymer; regioselective

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APA (6th Edition):

McConnell, C. R. (2019). Leveraging 1,2-Azaborine's Distinct Electronic Structure to Access New Building Blocks. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:108607

Chicago Manual of Style (16th Edition):

McConnell, Cameron Reed. “Leveraging 1,2-Azaborine's Distinct Electronic Structure to Access New Building Blocks.” 2019. Doctoral Dissertation, Boston College. Accessed April 18, 2021. http://dlib.bc.edu/islandora/object/bc-ir:108607.

MLA Handbook (7th Edition):

McConnell, Cameron Reed. “Leveraging 1,2-Azaborine's Distinct Electronic Structure to Access New Building Blocks.” 2019. Web. 18 Apr 2021.

Vancouver:

McConnell CR. Leveraging 1,2-Azaborine's Distinct Electronic Structure to Access New Building Blocks. [Internet] [Doctoral dissertation]. Boston College; 2019. [cited 2021 Apr 18]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:108607.

Council of Science Editors:

McConnell CR. Leveraging 1,2-Azaborine's Distinct Electronic Structure to Access New Building Blocks. [Doctoral Dissertation]. Boston College; 2019. Available from: http://dlib.bc.edu/islandora/object/bc-ir:108607

24. Wang, Yanzhao. Homogeneous Gold Catalysis: Ligand Design and Reactions of Alkynes.

Degree: 2014, University of California – eScholarship, University of California

 In the past dozen years, great progress has been made in developing highly efficient homogenous gold catalysis. As soft Lewis acids, cationic gold(I) complexes are… (more)

Subjects/Keywords: Organic chemistry; alkyne; catalysis; gold; heterocycle; homogeneous; ligand

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APA (6th Edition):

Wang, Y. (2014). Homogeneous Gold Catalysis: Ligand Design and Reactions of Alkynes. (Thesis). University of California – eScholarship, University of California. Retrieved from http://www.escholarship.org/uc/item/8jk9p7wz

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

Chicago Manual of Style (16th Edition):

Wang, Yanzhao. “Homogeneous Gold Catalysis: Ligand Design and Reactions of Alkynes.” 2014. Thesis, University of California – eScholarship, University of California. Accessed April 18, 2021. http://www.escholarship.org/uc/item/8jk9p7wz.

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

MLA Handbook (7th Edition):

Wang, Yanzhao. “Homogeneous Gold Catalysis: Ligand Design and Reactions of Alkynes.” 2014. Web. 18 Apr 2021.

Vancouver:

Wang Y. Homogeneous Gold Catalysis: Ligand Design and Reactions of Alkynes. [Internet] [Thesis]. University of California – eScholarship, University of California; 2014. [cited 2021 Apr 18]. Available from: http://www.escholarship.org/uc/item/8jk9p7wz.

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

Council of Science Editors:

Wang Y. Homogeneous Gold Catalysis: Ligand Design and Reactions of Alkynes. [Thesis]. University of California – eScholarship, University of California; 2014. Available from: http://www.escholarship.org/uc/item/8jk9p7wz

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


University of Bradford

25. Alasmary, Fatmah Ali Saeed. Synthesis and evaluation of selected benzimidazole derivatives as potential antimicrobial agents : an investigation into the synthesis of substituted benzimidazoles and their evaluation in vitro for antimicrobial activity.

Degree: PhD, 2013, University of Bradford

 Microbe resistence is a serious issue, especially as they have become resistant to most well known drugs. Therefore this is considered as a global problem… (more)

Subjects/Keywords: 615.1; Benzimidazole; Heterocycle; Antibacterial activity; Antifungal activity; Antimicrobial activity; Silver complexes

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

APA (6th Edition):

Alasmary, F. A. S. (2013). Synthesis and evaluation of selected benzimidazole derivatives as potential antimicrobial agents : an investigation into the synthesis of substituted benzimidazoles and their evaluation in vitro for antimicrobial activity. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/6325

Chicago Manual of Style (16th Edition):

Alasmary, Fatmah Ali Saeed. “Synthesis and evaluation of selected benzimidazole derivatives as potential antimicrobial agents : an investigation into the synthesis of substituted benzimidazoles and their evaluation in vitro for antimicrobial activity.” 2013. Doctoral Dissertation, University of Bradford. Accessed April 18, 2021. http://hdl.handle.net/10454/6325.

MLA Handbook (7th Edition):

Alasmary, Fatmah Ali Saeed. “Synthesis and evaluation of selected benzimidazole derivatives as potential antimicrobial agents : an investigation into the synthesis of substituted benzimidazoles and their evaluation in vitro for antimicrobial activity.” 2013. Web. 18 Apr 2021.

Vancouver:

Alasmary FAS. Synthesis and evaluation of selected benzimidazole derivatives as potential antimicrobial agents : an investigation into the synthesis of substituted benzimidazoles and their evaluation in vitro for antimicrobial activity. [Internet] [Doctoral dissertation]. University of Bradford; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10454/6325.

Council of Science Editors:

Alasmary FAS. Synthesis and evaluation of selected benzimidazole derivatives as potential antimicrobial agents : an investigation into the synthesis of substituted benzimidazoles and their evaluation in vitro for antimicrobial activity. [Doctoral Dissertation]. University of Bradford; 2013. Available from: http://hdl.handle.net/10454/6325


University of Oregon

26. Abbey, Eric Ryan, 1980-. Boron in Disguise: Towards BN Biomimics: Towards BN Biomimics.

Degree: 2011, University of Oregon

 Chemists have long recognized the potential of the BN bond to mimic CC double bonds in aromatic systems. Phenyl and indole are two of the… (more)

Subjects/Keywords: Biochemistry; Inorganic chemistry; Pure sciences; Aromaticity; Biomimics; Boron; Heterocycle; Isosterism

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APA (6th Edition):

Abbey, Eric Ryan, 1. (2011). Boron in Disguise: Towards BN Biomimics: Towards BN Biomimics. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/11979

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):

Abbey, Eric Ryan, 1980-. “Boron in Disguise: Towards BN Biomimics: Towards BN Biomimics.” 2011. Thesis, University of Oregon. Accessed April 18, 2021. http://hdl.handle.net/1794/11979.

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

MLA Handbook (7th Edition):

Abbey, Eric Ryan, 1980-. “Boron in Disguise: Towards BN Biomimics: Towards BN Biomimics.” 2011. Web. 18 Apr 2021.

Vancouver:

Abbey, Eric Ryan 1. Boron in Disguise: Towards BN Biomimics: Towards BN Biomimics. [Internet] [Thesis]. University of Oregon; 2011. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1794/11979.

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

Council of Science Editors:

Abbey, Eric Ryan 1. Boron in Disguise: Towards BN Biomimics: Towards BN Biomimics. [Thesis]. University of Oregon; 2011. Available from: http://hdl.handle.net/1794/11979

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


University of Minnesota

27. Yu, Yiyun. Innate C-H functionalization of cyclic enaminones.

Degree: PhD, Chemistry, 2013, University of Minnesota

 Cyclic enaminones are versatile precursors for the synthesis of alkaloids and nitrogen-containing bioactive compounds. The development of efficient functionalization methods is vital to their synthetic… (more)

Subjects/Keywords: Catalysis; C-H Activation; Enaminone; Heterocycle; Palladium; Synthetic Methodology

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APA (6th Edition):

Yu, Y. (2013). Innate C-H functionalization of cyclic enaminones. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/162813

Chicago Manual of Style (16th Edition):

Yu, Yiyun. “Innate C-H functionalization of cyclic enaminones.” 2013. Doctoral Dissertation, University of Minnesota. Accessed April 18, 2021. http://hdl.handle.net/11299/162813.

MLA Handbook (7th Edition):

Yu, Yiyun. “Innate C-H functionalization of cyclic enaminones.” 2013. Web. 18 Apr 2021.

Vancouver:

Yu Y. Innate C-H functionalization of cyclic enaminones. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/11299/162813.

Council of Science Editors:

Yu Y. Innate C-H functionalization of cyclic enaminones. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/162813


Loughborough University

28. Li, Yuqi. Synthesis of fluorinated drug scaffolds using SNAr substitution reactions.

Degree: PhD, 2017, Loughborough University

 Fluorinated arenes are considered valuable in organic chemistry. They display different types of reactivity and physicochemical properties compared to their hydrogen analogues. In this project,… (more)

Subjects/Keywords: 547; Organofluorine; Drug scaffold; Heterocycle; Anti-trypanosomal agent; Medicinal chemistry

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APA (6th Edition):

Li, Y. (2017). Synthesis of fluorinated drug scaffolds using SNAr substitution reactions. (Doctoral Dissertation). Loughborough University. Retrieved from http://hdl.handle.net/2134/27541

Chicago Manual of Style (16th Edition):

Li, Yuqi. “Synthesis of fluorinated drug scaffolds using SNAr substitution reactions.” 2017. Doctoral Dissertation, Loughborough University. Accessed April 18, 2021. http://hdl.handle.net/2134/27541.

MLA Handbook (7th Edition):

Li, Yuqi. “Synthesis of fluorinated drug scaffolds using SNAr substitution reactions.” 2017. Web. 18 Apr 2021.

Vancouver:

Li Y. Synthesis of fluorinated drug scaffolds using SNAr substitution reactions. [Internet] [Doctoral dissertation]. Loughborough University; 2017. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2134/27541.

Council of Science Editors:

Li Y. Synthesis of fluorinated drug scaffolds using SNAr substitution reactions. [Doctoral Dissertation]. Loughborough University; 2017. Available from: http://hdl.handle.net/2134/27541


University of Akron

29. Tamgho, Ingrid-Suzy. Synthesis of Ligands and Macrocycles Based on 1,3-Diiminoisoindoline and Study of New Highly Fluorescent and Symmetric Pyrrole-BF2 Chromophores.

Degree: PhD, Chemistry, 2014, University of Akron

 Discovered in 1907 by Braun and Tcherniac, a phthalocyanine is a macrocycle composed of four isoindolines. The metal chemistry of this macrocycle is rich, as… (more)

Subjects/Keywords: Chemistry; phthalocyanine, DII, schiff bases, bodipy, bophy, fluorophores, isoindolines, N-heterocycle

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APA (6th Edition):

Tamgho, I. (2014). Synthesis of Ligands and Macrocycles Based on 1,3-Diiminoisoindoline and Study of New Highly Fluorescent and Symmetric Pyrrole-BF2 Chromophores. (Doctoral Dissertation). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron1412163224

Chicago Manual of Style (16th Edition):

Tamgho, Ingrid-Suzy. “Synthesis of Ligands and Macrocycles Based on 1,3-Diiminoisoindoline and Study of New Highly Fluorescent and Symmetric Pyrrole-BF2 Chromophores.” 2014. Doctoral Dissertation, University of Akron. Accessed April 18, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=akron1412163224.

MLA Handbook (7th Edition):

Tamgho, Ingrid-Suzy. “Synthesis of Ligands and Macrocycles Based on 1,3-Diiminoisoindoline and Study of New Highly Fluorescent and Symmetric Pyrrole-BF2 Chromophores.” 2014. Web. 18 Apr 2021.

Vancouver:

Tamgho I. Synthesis of Ligands and Macrocycles Based on 1,3-Diiminoisoindoline and Study of New Highly Fluorescent and Symmetric Pyrrole-BF2 Chromophores. [Internet] [Doctoral dissertation]. University of Akron; 2014. [cited 2021 Apr 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1412163224.

Council of Science Editors:

Tamgho I. Synthesis of Ligands and Macrocycles Based on 1,3-Diiminoisoindoline and Study of New Highly Fluorescent and Symmetric Pyrrole-BF2 Chromophores. [Doctoral Dissertation]. University of Akron; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1412163224


The Ohio State University

30. Counceller, Carla Marie. Development of Novel Methodologies for the Synthesis and Functionalization of Nitrogen Heterocycles.

Degree: PhD, Chemistry, 2010, The Ohio State University

  The following dissertation deals with two research projects. The first project describes an efficient metal-free synthesis of 1H-indazoles. Indazoles exhibit a diverse range of… (more)

Subjects/Keywords: Chemistry; indazole; oxazole; heterocycle

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

APA (6th Edition):

Counceller, C. M. (2010). Development of Novel Methodologies for the Synthesis and Functionalization of Nitrogen Heterocycles. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1275047798

Chicago Manual of Style (16th Edition):

Counceller, Carla Marie. “Development of Novel Methodologies for the Synthesis and Functionalization of Nitrogen Heterocycles.” 2010. Doctoral Dissertation, The Ohio State University. Accessed April 18, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1275047798.

MLA Handbook (7th Edition):

Counceller, Carla Marie. “Development of Novel Methodologies for the Synthesis and Functionalization of Nitrogen Heterocycles.” 2010. Web. 18 Apr 2021.

Vancouver:

Counceller CM. Development of Novel Methodologies for the Synthesis and Functionalization of Nitrogen Heterocycles. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2021 Apr 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1275047798.

Council of Science Editors:

Counceller CM. Development of Novel Methodologies for the Synthesis and Functionalization of Nitrogen Heterocycles. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1275047798

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