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You searched for subject:(Diversity oriented synthesis). Showing records 1 – 30 of 35 total matches.

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Universitat de Valencia

1. Herrera Muñoz, Lidia. DOS vs TOS. Estrategias complementarias en la cobertura del espacio químico .

Degree: 2017, Universitat de Valencia

 Las moléculas pequeñas siempre han sido de interés en química debido a su capacidad para ejercer poderosos efectos sobre las funciones de las macromoléculas presentes… (more)

Subjects/Keywords: diversity oriented synthesis; target oriented synthesis

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APA (6th Edition):

Herrera Muñoz, L. (2017). DOS vs TOS. Estrategias complementarias en la cobertura del espacio químico . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/58661

Chicago Manual of Style (16th Edition):

Herrera Muñoz, Lidia. “DOS vs TOS. Estrategias complementarias en la cobertura del espacio químico .” 2017. Doctoral Dissertation, Universitat de Valencia. Accessed November 27, 2020. http://hdl.handle.net/10550/58661.

MLA Handbook (7th Edition):

Herrera Muñoz, Lidia. “DOS vs TOS. Estrategias complementarias en la cobertura del espacio químico .” 2017. Web. 27 Nov 2020.

Vancouver:

Herrera Muñoz L. DOS vs TOS. Estrategias complementarias en la cobertura del espacio químico . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10550/58661.

Council of Science Editors:

Herrera Muñoz L. DOS vs TOS. Estrategias complementarias en la cobertura del espacio químico . [Doctoral Dissertation]. Universitat de Valencia; 2017. Available from: http://hdl.handle.net/10550/58661


University of Southern California

2. Munoz, Socrates Benjamin. Sustainable metal catalysis for organic and organofluorine small molecule library generation: a diversity oriented synthesis approach.

Degree: PhD, Chemistry, 2015, University of Southern California

 Chemical processes occupy a vital for pretty much every aspect of human life. As a consequence, in order to fulfill the requirements for a sustainable… (more)

Subjects/Keywords: fluorine chemistry; diversity oriented synthesis; catalysis

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APA (6th Edition):

Munoz, S. B. (2015). Sustainable metal catalysis for organic and organofluorine small molecule library generation: a diversity oriented synthesis approach. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/612416/rec/6253

Chicago Manual of Style (16th Edition):

Munoz, Socrates Benjamin. “Sustainable metal catalysis for organic and organofluorine small molecule library generation: a diversity oriented synthesis approach.” 2015. Doctoral Dissertation, University of Southern California. Accessed November 27, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/612416/rec/6253.

MLA Handbook (7th Edition):

Munoz, Socrates Benjamin. “Sustainable metal catalysis for organic and organofluorine small molecule library generation: a diversity oriented synthesis approach.” 2015. Web. 27 Nov 2020.

Vancouver:

Munoz SB. Sustainable metal catalysis for organic and organofluorine small molecule library generation: a diversity oriented synthesis approach. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2020 Nov 27]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/612416/rec/6253.

Council of Science Editors:

Munoz SB. Sustainable metal catalysis for organic and organofluorine small molecule library generation: a diversity oriented synthesis approach. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/612416/rec/6253


University of Cambridge

3. North, Andrew James Peter. Fragment synthesis : pharmacophore and diversity oriented approaches.

Degree: PhD, 2019, University of Cambridge

 This thesis explores two approaches to fragment-based drug discovery. First, protein target CK2 was chosen due to its importance in the cancer phenotype. A literature… (more)

Subjects/Keywords: Organic chemistry; synthesis; fragment based drug discovery; diversity oriented synthesis; CK2

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APA (6th Edition):

North, A. J. P. (2019). Fragment synthesis : pharmacophore and diversity oriented approaches. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.37301 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767876

Chicago Manual of Style (16th Edition):

North, Andrew James Peter. “Fragment synthesis : pharmacophore and diversity oriented approaches.” 2019. Doctoral Dissertation, University of Cambridge. Accessed November 27, 2020. https://doi.org/10.17863/CAM.37301 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767876.

MLA Handbook (7th Edition):

North, Andrew James Peter. “Fragment synthesis : pharmacophore and diversity oriented approaches.” 2019. Web. 27 Nov 2020.

Vancouver:

North AJP. Fragment synthesis : pharmacophore and diversity oriented approaches. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Nov 27]. Available from: https://doi.org/10.17863/CAM.37301 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767876.

Council of Science Editors:

North AJP. Fragment synthesis : pharmacophore and diversity oriented approaches. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.37301 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767876


Boston College

4. Marineau, Jason Joseph. New Applications of Cyclobutadiene Cycloadditions: Diversity and Target Oriented Synthesis.

Degree: PhD, Chemistry, 2010, Boston College

 Cyclobutadiene cycloadditions provide rapid access to rigid polycyclic systems with high strain energy and unusual molecular geometries. Further functionalization of these systems allows entry into… (more)

Subjects/Keywords: cyclobutadiene; diversity oriented synthesis; guaiane; solid phase organic synthesis; torilin; total synthesis

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APA (6th Edition):

Marineau, J. J. (2010). New Applications of Cyclobutadiene Cycloadditions: Diversity and Target Oriented Synthesis. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101751

Chicago Manual of Style (16th Edition):

Marineau, Jason Joseph. “New Applications of Cyclobutadiene Cycloadditions: Diversity and Target Oriented Synthesis.” 2010. Doctoral Dissertation, Boston College. Accessed November 27, 2020. http://dlib.bc.edu/islandora/object/bc-ir:101751.

MLA Handbook (7th Edition):

Marineau, Jason Joseph. “New Applications of Cyclobutadiene Cycloadditions: Diversity and Target Oriented Synthesis.” 2010. Web. 27 Nov 2020.

Vancouver:

Marineau JJ. New Applications of Cyclobutadiene Cycloadditions: Diversity and Target Oriented Synthesis. [Internet] [Doctoral dissertation]. Boston College; 2010. [cited 2020 Nov 27]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101751.

Council of Science Editors:

Marineau JJ. New Applications of Cyclobutadiene Cycloadditions: Diversity and Target Oriented Synthesis. [Doctoral Dissertation]. Boston College; 2010. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101751


University of Kansas

5. Hur, Moon Young. Synthesis of Novel Sultam Scaffolds: Method and Library Development.

Degree: PhD, Chemistry, 2015, University of Kansas

 The development of methods to produce diverse set of small molecules to be utilized as chemical probes in chemical biology is a continuing emerging area… (more)

Subjects/Keywords: Organic chemistry; diversity oriented synthesis; sultam; tetramic acid

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APA (6th Edition):

Hur, M. Y. (2015). Synthesis of Novel Sultam Scaffolds: Method and Library Development. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/25373

Chicago Manual of Style (16th Edition):

Hur, Moon Young. “Synthesis of Novel Sultam Scaffolds: Method and Library Development.” 2015. Doctoral Dissertation, University of Kansas. Accessed November 27, 2020. http://hdl.handle.net/1808/25373.

MLA Handbook (7th Edition):

Hur, Moon Young. “Synthesis of Novel Sultam Scaffolds: Method and Library Development.” 2015. Web. 27 Nov 2020.

Vancouver:

Hur MY. Synthesis of Novel Sultam Scaffolds: Method and Library Development. [Internet] [Doctoral dissertation]. University of Kansas; 2015. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1808/25373.

Council of Science Editors:

Hur MY. Synthesis of Novel Sultam Scaffolds: Method and Library Development. [Doctoral Dissertation]. University of Kansas; 2015. Available from: http://hdl.handle.net/1808/25373


University of Pennsylvania

6. Han, Heeoon. Applications of Type II Anion Relay Chemistry (ARC) Part 1: Diversity-Oriented Synthesis of Polysubstituted Piperidine Analogues via Type II Arc, Part 2: A Highly Convergent Synthesis of (-)-Secu'amamine A Exploiting Type II Arc, Part 3: Facile Access To Diverse Carbobicyclic Systems via Type II Arc.

Degree: 2013, University of Pennsylvania

 In this dissertation, three successful applications of Type II Anion Relay Chemistry (ARC), a versatile multi-component union tactic, are described. Part 1: An effective, general… (more)

Subjects/Keywords: Anion Relay Chemistry; Cascade Reaction; Diversity Oriented Synthesis; Organic Chemistry

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APA (6th Edition):

Han, H. (2013). Applications of Type II Anion Relay Chemistry (ARC) Part 1: Diversity-Oriented Synthesis of Polysubstituted Piperidine Analogues via Type II Arc, Part 2: A Highly Convergent Synthesis of (-)-Secu'amamine A Exploiting Type II Arc, Part 3: Facile Access To Diverse Carbobicyclic Systems via Type II Arc. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/760

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):

Han, Heeoon. “Applications of Type II Anion Relay Chemistry (ARC) Part 1: Diversity-Oriented Synthesis of Polysubstituted Piperidine Analogues via Type II Arc, Part 2: A Highly Convergent Synthesis of (-)-Secu'amamine A Exploiting Type II Arc, Part 3: Facile Access To Diverse Carbobicyclic Systems via Type II Arc.” 2013. Thesis, University of Pennsylvania. Accessed November 27, 2020. https://repository.upenn.edu/edissertations/760.

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

MLA Handbook (7th Edition):

Han, Heeoon. “Applications of Type II Anion Relay Chemistry (ARC) Part 1: Diversity-Oriented Synthesis of Polysubstituted Piperidine Analogues via Type II Arc, Part 2: A Highly Convergent Synthesis of (-)-Secu'amamine A Exploiting Type II Arc, Part 3: Facile Access To Diverse Carbobicyclic Systems via Type II Arc.” 2013. Web. 27 Nov 2020.

Vancouver:

Han H. Applications of Type II Anion Relay Chemistry (ARC) Part 1: Diversity-Oriented Synthesis of Polysubstituted Piperidine Analogues via Type II Arc, Part 2: A Highly Convergent Synthesis of (-)-Secu'amamine A Exploiting Type II Arc, Part 3: Facile Access To Diverse Carbobicyclic Systems via Type II Arc. [Internet] [Thesis]. University of Pennsylvania; 2013. [cited 2020 Nov 27]. Available from: https://repository.upenn.edu/edissertations/760.

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

Council of Science Editors:

Han H. Applications of Type II Anion Relay Chemistry (ARC) Part 1: Diversity-Oriented Synthesis of Polysubstituted Piperidine Analogues via Type II Arc, Part 2: A Highly Convergent Synthesis of (-)-Secu'amamine A Exploiting Type II Arc, Part 3: Facile Access To Diverse Carbobicyclic Systems via Type II Arc. [Thesis]. University of Pennsylvania; 2013. Available from: https://repository.upenn.edu/edissertations/760

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


Vrije Universiteit Amsterdam

7. Scheffelaar, R. Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential .

Degree: 2010, Vrije Universiteit Amsterdam

Subjects/Keywords: Multicomponent Reactions • Diversity-Oriented Synthesis • Complexity • Synthesis • Scaffold Diversity

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APA (6th Edition):

Scheffelaar, R. (2010). Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/16149

Chicago Manual of Style (16th Edition):

Scheffelaar, R. “Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential .” 2010. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed November 27, 2020. http://hdl.handle.net/1871/16149.

MLA Handbook (7th Edition):

Scheffelaar, R. “Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential .” 2010. Web. 27 Nov 2020.

Vancouver:

Scheffelaar R. Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2010. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1871/16149.

Council of Science Editors:

Scheffelaar R. Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2010. Available from: http://hdl.handle.net/1871/16149


University of Cambridge

8. Kidd, Sarah Louise. Synthesis of Structurally Diverse N-Substituted Quaternary Carbon Containing Small Molecules and Their Application as Novel Starting Points for Drug Discovery.

Degree: PhD, 2019, University of Cambridge

 New bioactive small molecules are urgently required to seed both medicinal chemistry and chemical biology research. Within the two last decades, however, organic synthesis has… (more)

Subjects/Keywords: Fragment-based drug discovery; medicinal chemistry; organic synthesis; organic methodology; Diversity-oriented synthesis; drug discovery; molecular diversity

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APA (6th Edition):

Kidd, S. L. (2019). Synthesis of Structurally Diverse N-Substituted Quaternary Carbon Containing Small Molecules and Their Application as Novel Starting Points for Drug Discovery. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/291122

Chicago Manual of Style (16th Edition):

Kidd, Sarah Louise. “Synthesis of Structurally Diverse N-Substituted Quaternary Carbon Containing Small Molecules and Their Application as Novel Starting Points for Drug Discovery.” 2019. Doctoral Dissertation, University of Cambridge. Accessed November 27, 2020. https://www.repository.cam.ac.uk/handle/1810/291122.

MLA Handbook (7th Edition):

Kidd, Sarah Louise. “Synthesis of Structurally Diverse N-Substituted Quaternary Carbon Containing Small Molecules and Their Application as Novel Starting Points for Drug Discovery.” 2019. Web. 27 Nov 2020.

Vancouver:

Kidd SL. Synthesis of Structurally Diverse N-Substituted Quaternary Carbon Containing Small Molecules and Their Application as Novel Starting Points for Drug Discovery. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Nov 27]. Available from: https://www.repository.cam.ac.uk/handle/1810/291122.

Council of Science Editors:

Kidd SL. Synthesis of Structurally Diverse N-Substituted Quaternary Carbon Containing Small Molecules and Their Application as Novel Starting Points for Drug Discovery. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/291122


University of Cambridge

9. Kidd, Sarah Louise. Synthesis of structurally diverse N-substituted quaternary carbon containing small molecules and their application as novel starting points for drug discovery.

Degree: PhD, 2019, University of Cambridge

 New bioactive small molecules are urgently required to seed both medicinal chemistry and chemical biology research. Within the two last decades, however, organic synthesis has… (more)

Subjects/Keywords: Fragment-based drug discovery; medicinal chemistry; organic synthesis; organic methodology; Diversity-oriented synthesis; drug discovery; molecular diversity

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APA (6th Edition):

Kidd, S. L. (2019). Synthesis of structurally diverse N-substituted quaternary carbon containing small molecules and their application as novel starting points for drug discovery. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.38303 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774677

Chicago Manual of Style (16th Edition):

Kidd, Sarah Louise. “Synthesis of structurally diverse N-substituted quaternary carbon containing small molecules and their application as novel starting points for drug discovery.” 2019. Doctoral Dissertation, University of Cambridge. Accessed November 27, 2020. https://doi.org/10.17863/CAM.38303 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774677.

MLA Handbook (7th Edition):

Kidd, Sarah Louise. “Synthesis of structurally diverse N-substituted quaternary carbon containing small molecules and their application as novel starting points for drug discovery.” 2019. Web. 27 Nov 2020.

Vancouver:

Kidd SL. Synthesis of structurally diverse N-substituted quaternary carbon containing small molecules and their application as novel starting points for drug discovery. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Nov 27]. Available from: https://doi.org/10.17863/CAM.38303 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774677.

Council of Science Editors:

Kidd SL. Synthesis of structurally diverse N-substituted quaternary carbon containing small molecules and their application as novel starting points for drug discovery. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.38303 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774677

10. Umstead, Weston James. Photoassisted Generation of Complex N, O, S Polyheterocycles.

Degree: PhD, Chemistry and Biochemistry, 2016, U of Denver

  This research set out to continue the exploration and diversification of excited state o-azaxylylene cycloadditions, utilizing both pre-photochemical and post-photochemical modifications. Pre-photochemical modifications came… (more)

Subjects/Keywords: Beta-lactams; Diversity oriented synthesis; Hydantoins; O-azaxylylenes; Photochemistry; Polyheterocycles; Organic Chemistry

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APA (6th Edition):

Umstead, W. J. (2016). Photoassisted Generation of Complex N, O, S Polyheterocycles. (Doctoral Dissertation). U of Denver. Retrieved from https://digitalcommons.du.edu/etd/1117

Chicago Manual of Style (16th Edition):

Umstead, Weston James. “Photoassisted Generation of Complex N, O, S Polyheterocycles.” 2016. Doctoral Dissertation, U of Denver. Accessed November 27, 2020. https://digitalcommons.du.edu/etd/1117.

MLA Handbook (7th Edition):

Umstead, Weston James. “Photoassisted Generation of Complex N, O, S Polyheterocycles.” 2016. Web. 27 Nov 2020.

Vancouver:

Umstead WJ. Photoassisted Generation of Complex N, O, S Polyheterocycles. [Internet] [Doctoral dissertation]. U of Denver; 2016. [cited 2020 Nov 27]. Available from: https://digitalcommons.du.edu/etd/1117.

Council of Science Editors:

Umstead WJ. Photoassisted Generation of Complex N, O, S Polyheterocycles. [Doctoral Dissertation]. U of Denver; 2016. Available from: https://digitalcommons.du.edu/etd/1117

11. Semina, Elena. Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives.

Degree: 2016, Ghent University

 The discovery of non-proteinogenic amino acids among natural products has significantly increased interest in this class of compounds as they may possess interesting biological activity… (more)

Subjects/Keywords: Chemistry; Azetidines; Aziridines; Piperidines; Non-proteinogenic amino acids; Diversity oriented synthesis; Epoxides

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APA (6th Edition):

Semina, E. (2016). Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives. (Thesis). Ghent University. Retrieved from http://hdl.handle.net/1854/LU-7041917

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):

Semina, Elena. “Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives.” 2016. Thesis, Ghent University. Accessed November 27, 2020. http://hdl.handle.net/1854/LU-7041917.

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

MLA Handbook (7th Edition):

Semina, Elena. “Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives.” 2016. Web. 27 Nov 2020.

Vancouver:

Semina E. Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives. [Internet] [Thesis]. Ghent University; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1854/LU-7041917.

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

Council of Science Editors:

Semina E. Synthesis of new cyclic and acyclic biologically relevant amino acid derivatives. [Thesis]. Ghent University; 2016. Available from: http://hdl.handle.net/1854/LU-7041917

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


University of Texas – Austin

12. -7231-5317. Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines.

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

 The ways in which torsional strain in the bound form of a ligand affects the energetics of protein binding are poorly understood. In order to… (more)

Subjects/Keywords: Protein; Protein-ligand interaction; Diversity oriented synthesis; Iminium ion; Allylsilane; 2-arylpiperidine

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APA (6th Edition):

-7231-5317. (2016). Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/45584

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-7231-5317. “Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines.” 2016. Masters Thesis, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/45584.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-7231-5317. “Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines.” 2016. Web. 27 Nov 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-7231-5317. Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines. [Internet] [Masters thesis]. University of Texas – Austin; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/45584.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-7231-5317. Design and synthesis of conformationally constrained ligands for Grb2 SH2 binding and thermodynamic evaluation and the development of a diversity oriented synthesis of 2-arylpiperidines. [Masters Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/45584

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

13. Lepitre, Thomas. Modulation des Processus Domino au départ des Accepteurs de Michael en série Chromone : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Modulation of domino processes from the chromone based Michael acceptors platform : access to structural diversity through metal-catalyzed aza-cyclization, arylation and aryloxylation.

Degree: Docteur es, Chimie organique, 2017, Normandie

Le concept de la DOS (Diversity-Oriented Synthesis) est une nouvelle approche qui vise à générer des collections de petites molécules avec des hauts degrés de… (more)

Subjects/Keywords: DOS (Diversity-Oriented Synthesis); Processus domino; 3-formylchromone; Accepteurs de Michael-1,6; Diversité structurale; Synthèse organique; Méthodologie de synthèse; Hétérocycles; DOS (Diversity-Oriented Synthesis); Domino process; 3-formylchromone; Acceptors of Michael-1,6; Structural diversity; Organic synthesis; Synthetic methodology; Heterocycles

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APA (6th Edition):

Lepitre, T. (2017). Modulation des Processus Domino au départ des Accepteurs de Michael en série Chromone : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Modulation of domino processes from the chromone based Michael acceptors platform : access to structural diversity through metal-catalyzed aza-cyclization, arylation and aryloxylation. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2017NORMLH31

Chicago Manual of Style (16th Edition):

Lepitre, Thomas. “Modulation des Processus Domino au départ des Accepteurs de Michael en série Chromone : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Modulation of domino processes from the chromone based Michael acceptors platform : access to structural diversity through metal-catalyzed aza-cyclization, arylation and aryloxylation.” 2017. Doctoral Dissertation, Normandie. Accessed November 27, 2020. http://www.theses.fr/2017NORMLH31.

MLA Handbook (7th Edition):

Lepitre, Thomas. “Modulation des Processus Domino au départ des Accepteurs de Michael en série Chromone : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Modulation of domino processes from the chromone based Michael acceptors platform : access to structural diversity through metal-catalyzed aza-cyclization, arylation and aryloxylation.” 2017. Web. 27 Nov 2020.

Vancouver:

Lepitre T. Modulation des Processus Domino au départ des Accepteurs de Michael en série Chromone : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Modulation of domino processes from the chromone based Michael acceptors platform : access to structural diversity through metal-catalyzed aza-cyclization, arylation and aryloxylation. [Internet] [Doctoral dissertation]. Normandie; 2017. [cited 2020 Nov 27]. Available from: http://www.theses.fr/2017NORMLH31.

Council of Science Editors:

Lepitre T. Modulation des Processus Domino au départ des Accepteurs de Michael en série Chromone : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Modulation of domino processes from the chromone based Michael acceptors platform : access to structural diversity through metal-catalyzed aza-cyclization, arylation and aryloxylation. [Doctoral Dissertation]. Normandie; 2017. Available from: http://www.theses.fr/2017NORMLH31


Cornell University

14. Moilanen, Sirkka. SYNTHESIS OF A STRUCTURALLY AND STEREOCHEMICALLY DIVERSE SPIROKETAL LIBRARY USING NOVEL STEREOSELECTIVE SPIROCYCLIZATIONS OF C1-SUBSTITUTED GLYCAL EPOXIDES.

Degree: 2007, Cornell University

 A chemical genetic approach that uses small organic molecules to modulate protein function has the potential to overcome the limitations of classical genetic techniques for… (more)

Subjects/Keywords: spiroketal; small molecule library; glycal; glycoside; diversity-oriented synthesis

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

APA (6th Edition):

Moilanen, S. (2007). SYNTHESIS OF A STRUCTURALLY AND STEREOCHEMICALLY DIVERSE SPIROKETAL LIBRARY USING NOVEL STEREOSELECTIVE SPIROCYCLIZATIONS OF C1-SUBSTITUTED GLYCAL EPOXIDES. (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/7635

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):

Moilanen, Sirkka. “SYNTHESIS OF A STRUCTURALLY AND STEREOCHEMICALLY DIVERSE SPIROKETAL LIBRARY USING NOVEL STEREOSELECTIVE SPIROCYCLIZATIONS OF C1-SUBSTITUTED GLYCAL EPOXIDES.” 2007. Thesis, Cornell University. Accessed November 27, 2020. http://hdl.handle.net/1813/7635.

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

MLA Handbook (7th Edition):

Moilanen, Sirkka. “SYNTHESIS OF A STRUCTURALLY AND STEREOCHEMICALLY DIVERSE SPIROKETAL LIBRARY USING NOVEL STEREOSELECTIVE SPIROCYCLIZATIONS OF C1-SUBSTITUTED GLYCAL EPOXIDES.” 2007. Web. 27 Nov 2020.

Vancouver:

Moilanen S. SYNTHESIS OF A STRUCTURALLY AND STEREOCHEMICALLY DIVERSE SPIROKETAL LIBRARY USING NOVEL STEREOSELECTIVE SPIROCYCLIZATIONS OF C1-SUBSTITUTED GLYCAL EPOXIDES. [Internet] [Thesis]. Cornell University; 2007. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1813/7635.

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

Council of Science Editors:

Moilanen S. SYNTHESIS OF A STRUCTURALLY AND STEREOCHEMICALLY DIVERSE SPIROKETAL LIBRARY USING NOVEL STEREOSELECTIVE SPIROCYCLIZATIONS OF C1-SUBSTITUTED GLYCAL EPOXIDES. [Thesis]. Cornell University; 2007. Available from: http://hdl.handle.net/1813/7635

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


Jawaharlal Nehru University

15. Shailesh Kumar. Studies on diversity oriented synthesis of bioactive compounds;.

Degree: Medicinal chemistry, 2009, Jawaharlal Nehru University

None

Reference included in chapters, List of publications

Advisors/Committee Members: Sahu, D P.

Subjects/Keywords: Medicinal chemistry; Bioactive compounds; Diversity oriented synthesis

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APA (6th Edition):

Kumar, S. (2009). Studies on diversity oriented synthesis of bioactive compounds;. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/13541

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):

Kumar, Shailesh. “Studies on diversity oriented synthesis of bioactive compounds;.” 2009. Thesis, Jawaharlal Nehru University. Accessed November 27, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/13541.

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

MLA Handbook (7th Edition):

Kumar, Shailesh. “Studies on diversity oriented synthesis of bioactive compounds;.” 2009. Web. 27 Nov 2020.

Vancouver:

Kumar S. Studies on diversity oriented synthesis of bioactive compounds;. [Internet] [Thesis]. Jawaharlal Nehru University; 2009. [cited 2020 Nov 27]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/13541.

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

Council of Science Editors:

Kumar S. Studies on diversity oriented synthesis of bioactive compounds;. [Thesis]. Jawaharlal Nehru University; 2009. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/13541

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


Jawaharlal Nehru University

16. Das, Sajal Kumar. Diversity oriented organic synthesis of biologically important molecules; -.

Degree: Pharmacy, 2008, Jawaharlal Nehru University

None

References given chapter wise

Advisors/Committee Members: Panda, Gautam.

Subjects/Keywords: Drugs research; Diversity oriented organic synthesis; molecules

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APA (6th Edition):

Das, S. K. (2008). Diversity oriented organic synthesis of biologically important molecules; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/14744

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):

Das, Sajal Kumar. “Diversity oriented organic synthesis of biologically important molecules; -.” 2008. Thesis, Jawaharlal Nehru University. Accessed November 27, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/14744.

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

MLA Handbook (7th Edition):

Das, Sajal Kumar. “Diversity oriented organic synthesis of biologically important molecules; -.” 2008. Web. 27 Nov 2020.

Vancouver:

Das SK. Diversity oriented organic synthesis of biologically important molecules; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2008. [cited 2020 Nov 27]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/14744.

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

Council of Science Editors:

Das SK. Diversity oriented organic synthesis of biologically important molecules; -. [Thesis]. Jawaharlal Nehru University; 2008. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/14744

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


Harvard University

17. Chou, Danny Hung-Chieh. Small-Molecule Suppressors of Cytokine-Induced Beta-Cell Apoptosis.

Degree: PhD, Chemistry and Chemical Biology, 2011, Harvard University

Type-1 diabetes is caused by the autoimmune destruction of insulin-producing beta cells in the pancreas. Beta-cell apoptosis involves a complex set of signaling cascades initiated… (more)

Subjects/Keywords: beta cells; cytokines; diversity-oriented synthesis; high-throughput screening; histone deacetylase inhibitors; small-molecule probes; chemistry; organic chemistry; cellular biology

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APA (6th Edition):

Chou, D. H. (2011). Small-Molecule Suppressors of Cytokine-Induced Beta-Cell Apoptosis. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:10121978

Chicago Manual of Style (16th Edition):

Chou, Danny Hung-Chieh. “Small-Molecule Suppressors of Cytokine-Induced Beta-Cell Apoptosis.” 2011. Doctoral Dissertation, Harvard University. Accessed November 27, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:10121978.

MLA Handbook (7th Edition):

Chou, Danny Hung-Chieh. “Small-Molecule Suppressors of Cytokine-Induced Beta-Cell Apoptosis.” 2011. Web. 27 Nov 2020.

Vancouver:

Chou DH. Small-Molecule Suppressors of Cytokine-Induced Beta-Cell Apoptosis. [Internet] [Doctoral dissertation]. Harvard University; 2011. [cited 2020 Nov 27]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10121978.

Council of Science Editors:

Chou DH. Small-Molecule Suppressors of Cytokine-Induced Beta-Cell Apoptosis. [Doctoral Dissertation]. Harvard University; 2011. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10121978


University of Notre Dame

18. Timothy Adam Wencewicz. Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>.

Degree: Chemistry and Biochemistry, 2011, University of Notre Dame

  Anitibiotic resistance is developing at an alarming rate and is one of the world’s most pressing health problems. New methods for developing microbe-selective antibacterial… (more)

Subjects/Keywords: sideromycin; hydroxylamine; antibiotic delivery; salmycin; albomycin; drug delivery; structure-activity relationship; siderophore; active transport; diversity-oriented synthesis; microcin; nitroso; hydroxamic acid

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APA (6th Edition):

Wencewicz, T. A. (2011). Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/5m60qr48p6n

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):

Wencewicz, Timothy Adam. “Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>.” 2011. Thesis, University of Notre Dame. Accessed November 27, 2020. https://curate.nd.edu/show/5m60qr48p6n.

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

MLA Handbook (7th Edition):

Wencewicz, Timothy Adam. “Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>.” 2011. Web. 27 Nov 2020.

Vancouver:

Wencewicz TA. Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>. [Internet] [Thesis]. University of Notre Dame; 2011. [cited 2020 Nov 27]. Available from: https://curate.nd.edu/show/5m60qr48p6n.

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

Council of Science Editors:

Wencewicz TA. Development of Microbe-Selective Antibacterial Agents: From Small Molecules to Siderophores</h1>. [Thesis]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/5m60qr48p6n

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

19. Valiulin, Roman Askatovich. Novel Photochemical Methodologies for Diversity Oriented Synthesis and Screening of Combinatorial Libraries.

Degree: PhD, Chemistry and Biochemistry, 2010, U of Denver

  The main goal of this project was to develop an efficient methodology allowing rapid access to structurally diverse scaffolds decorated with various functional groups.… (more)

Subjects/Keywords: Combinatorial; Diversity; Library; Oriented; Photochemistry; Synthesis; Organic Chemistry

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

APA (6th Edition):

Valiulin, R. A. (2010). Novel Photochemical Methodologies for Diversity Oriented Synthesis and Screening of Combinatorial Libraries. (Doctoral Dissertation). U of Denver. Retrieved from https://digitalcommons.du.edu/etd/943

Chicago Manual of Style (16th Edition):

Valiulin, Roman Askatovich. “Novel Photochemical Methodologies for Diversity Oriented Synthesis and Screening of Combinatorial Libraries.” 2010. Doctoral Dissertation, U of Denver. Accessed November 27, 2020. https://digitalcommons.du.edu/etd/943.

MLA Handbook (7th Edition):

Valiulin, Roman Askatovich. “Novel Photochemical Methodologies for Diversity Oriented Synthesis and Screening of Combinatorial Libraries.” 2010. Web. 27 Nov 2020.

Vancouver:

Valiulin RA. Novel Photochemical Methodologies for Diversity Oriented Synthesis and Screening of Combinatorial Libraries. [Internet] [Doctoral dissertation]. U of Denver; 2010. [cited 2020 Nov 27]. Available from: https://digitalcommons.du.edu/etd/943.

Council of Science Editors:

Valiulin RA. Novel Photochemical Methodologies for Diversity Oriented Synthesis and Screening of Combinatorial Libraries. [Doctoral Dissertation]. U of Denver; 2010. Available from: https://digitalcommons.du.edu/etd/943


Duke University

20. Morgan, Brittany Suzanne. Towards Guiding Principles for Targeting RNA: Rational Approaches to Design and Synthesize RNA-Biased Small Molecule Libraries .

Degree: 2018, Duke University

  RNA is increasingly recognized as a therapeutic target in many diseases, including viral and bacterial infections, neurodegenerative disease, and cancer. Despite this, no FDA-approved… (more)

Subjects/Keywords: Organic chemistry; Biochemistry; 2-Oxazolidinone; Chemical Biology; Diversity-Oriented Synthesis; Guiding Principles; RNA Bulge Motifs; RNA Recognition

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APA (6th Edition):

Morgan, B. S. (2018). Towards Guiding Principles for Targeting RNA: Rational Approaches to Design and Synthesize RNA-Biased Small Molecule Libraries . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/17473

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):

Morgan, Brittany Suzanne. “Towards Guiding Principles for Targeting RNA: Rational Approaches to Design and Synthesize RNA-Biased Small Molecule Libraries .” 2018. Thesis, Duke University. Accessed November 27, 2020. http://hdl.handle.net/10161/17473.

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

MLA Handbook (7th Edition):

Morgan, Brittany Suzanne. “Towards Guiding Principles for Targeting RNA: Rational Approaches to Design and Synthesize RNA-Biased Small Molecule Libraries .” 2018. Web. 27 Nov 2020.

Vancouver:

Morgan BS. Towards Guiding Principles for Targeting RNA: Rational Approaches to Design and Synthesize RNA-Biased Small Molecule Libraries . [Internet] [Thesis]. Duke University; 2018. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10161/17473.

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

Council of Science Editors:

Morgan BS. Towards Guiding Principles for Targeting RNA: Rational Approaches to Design and Synthesize RNA-Biased Small Molecule Libraries . [Thesis]. Duke University; 2018. Available from: http://hdl.handle.net/10161/17473

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


University of Kansas

21. Charaschanya, Manwika. Advances in Heterocyclic Synthesis through Ring Expansions and Flow Chemistry.

Degree: PhD, Medicinal Chemistry, 2018, University of Kansas

 This dissertation comprises three chapters, which focus on the development of new synthetic methodologies and the construction of a screening collection. An Application of the… (more)

Subjects/Keywords: Chemistry; Pharmaceutical sciences; Diversity-oriented synthesis; Drug discovery; Flow chemistry; Medicinal chemistry; Organic chemistry; Synthetic methodology

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APA (6th Edition):

Charaschanya, M. (2018). Advances in Heterocyclic Synthesis through Ring Expansions and Flow Chemistry. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/27577

Chicago Manual of Style (16th Edition):

Charaschanya, Manwika. “Advances in Heterocyclic Synthesis through Ring Expansions and Flow Chemistry.” 2018. Doctoral Dissertation, University of Kansas. Accessed November 27, 2020. http://hdl.handle.net/1808/27577.

MLA Handbook (7th Edition):

Charaschanya, Manwika. “Advances in Heterocyclic Synthesis through Ring Expansions and Flow Chemistry.” 2018. Web. 27 Nov 2020.

Vancouver:

Charaschanya M. Advances in Heterocyclic Synthesis through Ring Expansions and Flow Chemistry. [Internet] [Doctoral dissertation]. University of Kansas; 2018. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1808/27577.

Council of Science Editors:

Charaschanya M. Advances in Heterocyclic Synthesis through Ring Expansions and Flow Chemistry. [Doctoral Dissertation]. University of Kansas; 2018. Available from: http://hdl.handle.net/1808/27577


University of Texas – Austin

22. Sunderhaus, James Dennis. The development of a four component reaction and its application to the synthesis of diverse heterocyclic scaffolds and the total synthesis of alkaloid natural products : the total synthesis of roelactamine and efforts towards the syntheses of rosicine and pseudotabersonine.

Degree: PhD, Chemistry, 2009, University of Texas – Austin

 A four component reaction involving the coupling of functionalized aldehydes, amines, acid chlorides, and [pi]- and organometallic nucleophiles has been developed to prepare multifunctional substrates… (more)

Subjects/Keywords: Diversity oriented synthesis; Multicomponent reaction; Isopavine alkaloids; Aspidosperma alkaloids

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APA (6th Edition):

Sunderhaus, J. D. (2009). The development of a four component reaction and its application to the synthesis of diverse heterocyclic scaffolds and the total synthesis of alkaloid natural products : the total synthesis of roelactamine and efforts towards the syntheses of rosicine and pseudotabersonine. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2009-05-170

Chicago Manual of Style (16th Edition):

Sunderhaus, James Dennis. “The development of a four component reaction and its application to the synthesis of diverse heterocyclic scaffolds and the total synthesis of alkaloid natural products : the total synthesis of roelactamine and efforts towards the syntheses of rosicine and pseudotabersonine.” 2009. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/ETD-UT-2009-05-170.

MLA Handbook (7th Edition):

Sunderhaus, James Dennis. “The development of a four component reaction and its application to the synthesis of diverse heterocyclic scaffolds and the total synthesis of alkaloid natural products : the total synthesis of roelactamine and efforts towards the syntheses of rosicine and pseudotabersonine.” 2009. Web. 27 Nov 2020.

Vancouver:

Sunderhaus JD. The development of a four component reaction and its application to the synthesis of diverse heterocyclic scaffolds and the total synthesis of alkaloid natural products : the total synthesis of roelactamine and efforts towards the syntheses of rosicine and pseudotabersonine. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2009. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/ETD-UT-2009-05-170.

Council of Science Editors:

Sunderhaus JD. The development of a four component reaction and its application to the synthesis of diverse heterocyclic scaffolds and the total synthesis of alkaloid natural products : the total synthesis of roelactamine and efforts towards the syntheses of rosicine and pseudotabersonine. [Doctoral Dissertation]. University of Texas – Austin; 2009. Available from: http://hdl.handle.net/2152/ETD-UT-2009-05-170

23. Gatbonton-Schwager, Tonibelle N. Biological and Chemical Analysis of Small Molecule Activators of Anti-inflammatory and Antioxidant Nrf2-Keap1 Signaling.

Degree: PhD, Pharmacology, 2014, Case Western Reserve University School of Graduate Studies

 The immune system provides a cellular defense mechanism against harmful agents in the form of inflammatory and antioxidant responses mediated by the Nrf2-Keap1 signaling pathway.… (more)

Subjects/Keywords: Biology; Chemistry; Pharmacology; Immunology; triterpenoids; lipid peroxidation; inflammation; antioxidant; Nrf2; bryonolic acid; 4-hydroxynonenal; macrophage; diversity oriented synthesis

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APA (6th Edition):

Gatbonton-Schwager, T. N. (2014). Biological and Chemical Analysis of Small Molecule Activators of Anti-inflammatory and Antioxidant Nrf2-Keap1 Signaling. (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1390560628

Chicago Manual of Style (16th Edition):

Gatbonton-Schwager, Tonibelle N. “Biological and Chemical Analysis of Small Molecule Activators of Anti-inflammatory and Antioxidant Nrf2-Keap1 Signaling.” 2014. Doctoral Dissertation, Case Western Reserve University School of Graduate Studies. Accessed November 27, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1390560628.

MLA Handbook (7th Edition):

Gatbonton-Schwager, Tonibelle N. “Biological and Chemical Analysis of Small Molecule Activators of Anti-inflammatory and Antioxidant Nrf2-Keap1 Signaling.” 2014. Web. 27 Nov 2020.

Vancouver:

Gatbonton-Schwager TN. Biological and Chemical Analysis of Small Molecule Activators of Anti-inflammatory and Antioxidant Nrf2-Keap1 Signaling. [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2014. [cited 2020 Nov 27]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1390560628.

Council of Science Editors:

Gatbonton-Schwager TN. Biological and Chemical Analysis of Small Molecule Activators of Anti-inflammatory and Antioxidant Nrf2-Keap1 Signaling. [Doctoral Dissertation]. Case Western Reserve University School of Graduate Studies; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1390560628

24. Alcover, Charlotte. Réseaux moléculaires et Chimie des Substances Naturelles : de l’isolement de composés inédits à de toutes nouvelles applications en synthèse biomimétique : Molecular Networking and Natural Products Chemistry : from novel compounds isolation to brand new applications in biomimetic synthesis.

Degree: Docteur es, Chimie des substances naturelles, 2019, Université Paris-Saclay (ComUE)

La découverte de nouvelles entités naturelles est un processus particulièrement long et coûteux ; il faut donc réussir le plus tôt possible à détecter les… (more)

Subjects/Keywords: Substances naturelles; Synthèse organique; Biosynthèse; Biomimétisme; Criblage biologique; Synthèse orientée vers la diversité; Natural substances; Organic synthesis; Biosynthesis; Biomimetics; Biological screening; Diversity oriented synthesis

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APA (6th Edition):

Alcover, C. (2019). Réseaux moléculaires et Chimie des Substances Naturelles : de l’isolement de composés inédits à de toutes nouvelles applications en synthèse biomimétique : Molecular Networking and Natural Products Chemistry : from novel compounds isolation to brand new applications in biomimetic synthesis. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS569

Chicago Manual of Style (16th Edition):

Alcover, Charlotte. “Réseaux moléculaires et Chimie des Substances Naturelles : de l’isolement de composés inédits à de toutes nouvelles applications en synthèse biomimétique : Molecular Networking and Natural Products Chemistry : from novel compounds isolation to brand new applications in biomimetic synthesis.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed November 27, 2020. http://www.theses.fr/2019SACLS569.

MLA Handbook (7th Edition):

Alcover, Charlotte. “Réseaux moléculaires et Chimie des Substances Naturelles : de l’isolement de composés inédits à de toutes nouvelles applications en synthèse biomimétique : Molecular Networking and Natural Products Chemistry : from novel compounds isolation to brand new applications in biomimetic synthesis.” 2019. Web. 27 Nov 2020.

Vancouver:

Alcover C. Réseaux moléculaires et Chimie des Substances Naturelles : de l’isolement de composés inédits à de toutes nouvelles applications en synthèse biomimétique : Molecular Networking and Natural Products Chemistry : from novel compounds isolation to brand new applications in biomimetic synthesis. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Nov 27]. Available from: http://www.theses.fr/2019SACLS569.

Council of Science Editors:

Alcover C. Réseaux moléculaires et Chimie des Substances Naturelles : de l’isolement de composés inédits à de toutes nouvelles applications en synthèse biomimétique : Molecular Networking and Natural Products Chemistry : from novel compounds isolation to brand new applications in biomimetic synthesis. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS569


University of Ottawa

25. Legault, Marc. From Probes to Cell Surface Labelling: Towards the Development of New Chemical Biology Compounds and Methods .

Degree: 2011, University of Ottawa

 Chemical biology encompasses the study and manipulation of biological system using chemistry, often by virtue of small molecules or unnatural amino acids. Much insight has… (more)

Subjects/Keywords: CuAAC; click chemistry; N-heterocyclic carbene; intramolecular cyclization; diversity oriented synthesis; unnatural amino acid; metabolic labelling; rearrangement; small molecule library; chemical biology; bioorthogonal

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APA (6th Edition):

Legault, M. (2011). From Probes to Cell Surface Labelling: Towards the Development of New Chemical Biology Compounds and Methods . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/20084

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):

Legault, Marc. “From Probes to Cell Surface Labelling: Towards the Development of New Chemical Biology Compounds and Methods .” 2011. Thesis, University of Ottawa. Accessed November 27, 2020. http://hdl.handle.net/10393/20084.

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

MLA Handbook (7th Edition):

Legault, Marc. “From Probes to Cell Surface Labelling: Towards the Development of New Chemical Biology Compounds and Methods .” 2011. Web. 27 Nov 2020.

Vancouver:

Legault M. From Probes to Cell Surface Labelling: Towards the Development of New Chemical Biology Compounds and Methods . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10393/20084.

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

Council of Science Editors:

Legault M. From Probes to Cell Surface Labelling: Towards the Development of New Chemical Biology Compounds and Methods . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/20084

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


University of Bradford

26. Neves dos Santos, Ana Rita. Exploration of [2+2+2] cyclotrimerisation reactions of alkynes : a new methodology for the synthesis of small molecules to probe biological systems.

Degree: PhD, 2013, University of Bradford

 The generation of new chemical entities (NCEs) for use in chemical biology and drug discovery is of wide interest to both academia and the pharmaceutical… (more)

Subjects/Keywords: 616.99; [2+2+2] cyclotrimerisation; Alkynes; Biological probe; Diversity-oriented synthesis (DOS); Tetrahydroisoquinoline; Transition-metal chemistry; Organometallic chemistry; Microwave chemistry; Tetrahydronaphthyridine; Dihydropyrrolopyridine

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APA (6th Edition):

Neves dos Santos, A. R. (2013). Exploration of [2+2+2] cyclotrimerisation reactions of alkynes : a new methodology for the synthesis of small molecules to probe biological systems. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/6311

Chicago Manual of Style (16th Edition):

Neves dos Santos, Ana Rita. “Exploration of [2+2+2] cyclotrimerisation reactions of alkynes : a new methodology for the synthesis of small molecules to probe biological systems.” 2013. Doctoral Dissertation, University of Bradford. Accessed November 27, 2020. http://hdl.handle.net/10454/6311.

MLA Handbook (7th Edition):

Neves dos Santos, Ana Rita. “Exploration of [2+2+2] cyclotrimerisation reactions of alkynes : a new methodology for the synthesis of small molecules to probe biological systems.” 2013. Web. 27 Nov 2020.

Vancouver:

Neves dos Santos AR. Exploration of [2+2+2] cyclotrimerisation reactions of alkynes : a new methodology for the synthesis of small molecules to probe biological systems. [Internet] [Doctoral dissertation]. University of Bradford; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10454/6311.

Council of Science Editors:

Neves dos Santos AR. Exploration of [2+2+2] cyclotrimerisation reactions of alkynes : a new methodology for the synthesis of small molecules to probe biological systems. [Doctoral Dissertation]. University of Bradford; 2013. Available from: http://hdl.handle.net/10454/6311

27. Ignatenko, Vasily A. MOLECULAR LIBRARY SYNTHESIS USING NATURAL PRODUCTS: EXPANDING THE FRAMEWORK OF STEROIDS AND PENTACYCLIC TRITERPENOIDS.

Degree: PhD, Chemistry, 2013, Case Western Reserve University School of Graduate Studies

 Triterpenoids are a broad and structurally diverse class of natural products primarily derived from the plant kingdom. The triterpenoid family consists of nearly thirty thousand… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Pharmaceuticals; diversity oriented synthesis; DOS; terpene; triterpenoid; steroid; natural product; molecular library; carocyclic framework; pentacycllic; tetracyclic; aldol; Norrish; Yang; divergent; photocyclization; transannular; lanosterol; bryonolic acid; polyketone

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APA (6th Edition):

Ignatenko, V. A. (2013). MOLECULAR LIBRARY SYNTHESIS USING NATURAL PRODUCTS: EXPANDING THE FRAMEWORK OF STEROIDS AND PENTACYCLIC TRITERPENOIDS. (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1384382654

Chicago Manual of Style (16th Edition):

Ignatenko, Vasily A. “MOLECULAR LIBRARY SYNTHESIS USING NATURAL PRODUCTS: EXPANDING THE FRAMEWORK OF STEROIDS AND PENTACYCLIC TRITERPENOIDS.” 2013. Doctoral Dissertation, Case Western Reserve University School of Graduate Studies. Accessed November 27, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1384382654.

MLA Handbook (7th Edition):

Ignatenko, Vasily A. “MOLECULAR LIBRARY SYNTHESIS USING NATURAL PRODUCTS: EXPANDING THE FRAMEWORK OF STEROIDS AND PENTACYCLIC TRITERPENOIDS.” 2013. Web. 27 Nov 2020.

Vancouver:

Ignatenko VA. MOLECULAR LIBRARY SYNTHESIS USING NATURAL PRODUCTS: EXPANDING THE FRAMEWORK OF STEROIDS AND PENTACYCLIC TRITERPENOIDS. [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2013. [cited 2020 Nov 27]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1384382654.

Council of Science Editors:

Ignatenko VA. MOLECULAR LIBRARY SYNTHESIS USING NATURAL PRODUCTS: EXPANDING THE FRAMEWORK OF STEROIDS AND PENTACYCLIC TRITERPENOIDS. [Doctoral Dissertation]. Case Western Reserve University School of Graduate Studies; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1384382654

28. Gigant, Nicolas. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.

Degree: Docteur es, Chimie organique, 2012, Université d'Orléans

La nécessité grandissante de disposer d’une large librairie de diverses petites molécules pour le screening biologique constitue une puissante force motrice pour les chimistes organiciens… (more)

Subjects/Keywords: Enamide; Diversité moléculaire; Synthèse orientée vers la diversité; Phosphates vinyliques; Additions d’aza-Michaël; Nitrènes; Réactions de couplage pallado-catalysées; Réactions en cascades; Enamides; Molecular diversity; Diversity-oriented synthesis; Vinylphosphates; Aza-Michael additions; Nitrenes; Palladium-catalyzed cross-coupling reactions; Cascade reactions

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APA (6th Edition):

Gigant, N. (2012). Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2012ORLE2039

Chicago Manual of Style (16th Edition):

Gigant, Nicolas. “Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.” 2012. Doctoral Dissertation, Université d'Orléans. Accessed November 27, 2020. http://www.theses.fr/2012ORLE2039.

MLA Handbook (7th Edition):

Gigant, Nicolas. “Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.” 2012. Web. 27 Nov 2020.

Vancouver:

Gigant N. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. [Internet] [Doctoral dissertation]. Université d'Orléans; 2012. [cited 2020 Nov 27]. Available from: http://www.theses.fr/2012ORLE2039.

Council of Science Editors:

Gigant N. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. [Doctoral Dissertation]. Université d'Orléans; 2012. Available from: http://www.theses.fr/2012ORLE2039

29. North, Andrew James Peter. Fragment synthesis: pharmacophore and diversity oriented approaches.

Degree: PhD, 2019, University of Cambridge

 This thesis explores two approaches to fragment-based drug discovery. First, protein target CK2 was chosen due to its importance in the cancer phenotype. A literature… (more)

Subjects/Keywords: Organic chemistry; synthesis; fragment based drug discovery; diversity oriented synthesis; CK2

…54 Figure 3.1 The difference between target-oriented synthesis and diversity-oriented… …dd double doublet d doublet DOS diversity-oriented synthesis dr diastereomeric ratio… …30 2.3.2. Synthesis of fragment 29… …35 2.4.3. Synthesis of 39… …37 2.5.1. Synthesis of precursors… 

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APA (6th Edition):

North, A. J. P. (2019). Fragment synthesis: pharmacophore and diversity oriented approaches. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290076

Chicago Manual of Style (16th Edition):

North, Andrew James Peter. “Fragment synthesis: pharmacophore and diversity oriented approaches.” 2019. Doctoral Dissertation, University of Cambridge. Accessed November 27, 2020. https://www.repository.cam.ac.uk/handle/1810/290076.

MLA Handbook (7th Edition):

North, Andrew James Peter. “Fragment synthesis: pharmacophore and diversity oriented approaches.” 2019. Web. 27 Nov 2020.

Vancouver:

North AJP. Fragment synthesis: pharmacophore and diversity oriented approaches. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Nov 27]. Available from: https://www.repository.cam.ac.uk/handle/1810/290076.

Council of Science Editors:

North AJP. Fragment synthesis: pharmacophore and diversity oriented approaches. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290076

30. Wang, Yikai. Studies on Application of Silyl Groups in Ring-Closing Metathesis Reactions and Fragment-Based Probe Discovery.

Degree: PhD, Chemistry, 2012, Harvard University

In efforts to search for tool compounds that are capable of probing normal and disease-associated biological processes, both quality and identity of the screening collection… (more)

Subjects/Keywords: diversity-oriented synthesis; fragment-based drug discovery; macrocycle; ring-closing metathesis; stereoselective; vinylsiloxane; chemistry

…sulfoxide DOS diversity-oriented synthesis DPPF 1,1'-bis(diphenylphosphino)… …novel strategy in diversity-oriented synthesis (DOS)2 called build/couple/pair (… …acknowledge Alex Ramek for his participation in the synthesis of the initial library, and Dr. Taner… …Patrick Sheehan, Conor O'Herin, Dr. Alvin W. Hung all participated in the synthesis of… …stages: 1) a discovery phase, often requiring the synthesis and screening of candidate… 

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

APA (6th Edition):

Wang, Y. (2012). Studies on Application of Silyl Groups in Ring-Closing Metathesis Reactions and Fragment-Based Probe Discovery. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:10085991

Chicago Manual of Style (16th Edition):

Wang, Yikai. “Studies on Application of Silyl Groups in Ring-Closing Metathesis Reactions and Fragment-Based Probe Discovery.” 2012. Doctoral Dissertation, Harvard University. Accessed November 27, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:10085991.

MLA Handbook (7th Edition):

Wang, Yikai. “Studies on Application of Silyl Groups in Ring-Closing Metathesis Reactions and Fragment-Based Probe Discovery.” 2012. Web. 27 Nov 2020.

Vancouver:

Wang Y. Studies on Application of Silyl Groups in Ring-Closing Metathesis Reactions and Fragment-Based Probe Discovery. [Internet] [Doctoral dissertation]. Harvard University; 2012. [cited 2020 Nov 27]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10085991.

Council of Science Editors:

Wang Y. Studies on Application of Silyl Groups in Ring-Closing Metathesis Reactions and Fragment-Based Probe Discovery. [Doctoral Dissertation]. Harvard University; 2012. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10085991

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