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You searched for subject:( organic chemistry). Showing records 1 – 30 of 8137 total matches.

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1. Jayasekara, Himali Devika. Photochemical Elimination Reactions that Proceed via Triplet Excited State Electrocyclic Ring Closures.

Degree: 2014, Marquette University

 Cage compounds have become an important tool for the study of biological processes. The research focuses on new cage compounds that can unmask functional groups… (more)

Subjects/Keywords: Organic chemistry; Chemistry; Organic Chemistry

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APA (6th Edition):

Jayasekara, H. D. (2014). Photochemical Elimination Reactions that Proceed via Triplet Excited State Electrocyclic Ring Closures. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/theses_open/247

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):

Jayasekara, Himali Devika. “Photochemical Elimination Reactions that Proceed via Triplet Excited State Electrocyclic Ring Closures.” 2014. Thesis, Marquette University. Accessed June 25, 2019. https://epublications.marquette.edu/theses_open/247.

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

MLA Handbook (7th Edition):

Jayasekara, Himali Devika. “Photochemical Elimination Reactions that Proceed via Triplet Excited State Electrocyclic Ring Closures.” 2014. Web. 25 Jun 2019.

Vancouver:

Jayasekara HD. Photochemical Elimination Reactions that Proceed via Triplet Excited State Electrocyclic Ring Closures. [Internet] [Thesis]. Marquette University; 2014. [cited 2019 Jun 25]. Available from: https://epublications.marquette.edu/theses_open/247.

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

Council of Science Editors:

Jayasekara HD. Photochemical Elimination Reactions that Proceed via Triplet Excited State Electrocyclic Ring Closures. [Thesis]. Marquette University; 2014. Available from: https://epublications.marquette.edu/theses_open/247

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


Iowa State University

2. Drochner, Dana Lynn. Rational design and characterization of electron-deficient heterocycles for organic photovoltaic materials.

Degree: 2015, Iowa State University

 This research explores the synthesis and evaluation of new building blocks and polymers for organic photovoltaic materials. Through the development of new synthetic routes and… (more)

Subjects/Keywords: Organic Chemistry; Chemistry; Organic Chemistry

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APA (6th Edition):

Drochner, D. L. (2015). Rational design and characterization of electron-deficient heterocycles for organic photovoltaic materials. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/14793

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):

Drochner, Dana Lynn. “Rational design and characterization of electron-deficient heterocycles for organic photovoltaic materials.” 2015. Thesis, Iowa State University. Accessed June 25, 2019. https://lib.dr.iastate.edu/etd/14793.

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

MLA Handbook (7th Edition):

Drochner, Dana Lynn. “Rational design and characterization of electron-deficient heterocycles for organic photovoltaic materials.” 2015. Web. 25 Jun 2019.

Vancouver:

Drochner DL. Rational design and characterization of electron-deficient heterocycles for organic photovoltaic materials. [Internet] [Thesis]. Iowa State University; 2015. [cited 2019 Jun 25]. Available from: https://lib.dr.iastate.edu/etd/14793.

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

Council of Science Editors:

Drochner DL. Rational design and characterization of electron-deficient heterocycles for organic photovoltaic materials. [Thesis]. Iowa State University; 2015. Available from: https://lib.dr.iastate.edu/etd/14793

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


University of Oxford

3. Liddon, John Timothy Ruskin. The versatile chemistry of azidoalkyl enol ethers and their equivalents.

Degree: PhD, 2015, University of Oxford

 This thesis describes the synthesis and intramolecular cycloaddition products of azides tethered to olefins bearing a heteroatom in an attempt to access a proposed triazolium… (more)

Subjects/Keywords: 547; Chemistry; Organic Chemistry; Organic

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APA (6th Edition):

Liddon, J. T. R. (2015). The versatile chemistry of azidoalkyl enol ethers and their equivalents. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:a5554d44-d251-4ca5-8b2d-d07a7c95138a ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664830

Chicago Manual of Style (16th Edition):

Liddon, John Timothy Ruskin. “The versatile chemistry of azidoalkyl enol ethers and their equivalents.” 2015. Doctoral Dissertation, University of Oxford. Accessed June 25, 2019. http://ora.ox.ac.uk/objects/uuid:a5554d44-d251-4ca5-8b2d-d07a7c95138a ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664830.

MLA Handbook (7th Edition):

Liddon, John Timothy Ruskin. “The versatile chemistry of azidoalkyl enol ethers and their equivalents.” 2015. Web. 25 Jun 2019.

Vancouver:

Liddon JTR. The versatile chemistry of azidoalkyl enol ethers and their equivalents. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2019 Jun 25]. Available from: http://ora.ox.ac.uk/objects/uuid:a5554d44-d251-4ca5-8b2d-d07a7c95138a ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664830.

Council of Science Editors:

Liddon JTR. The versatile chemistry of azidoalkyl enol ethers and their equivalents. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:a5554d44-d251-4ca5-8b2d-d07a7c95138a ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664830


University of Helsinki

4. Raffaelli, Barbara. Synthesis of lignano-9,9'-lactones and rearrangement studies.

Degree: Department of Chemistry, Laboratory of Organic Chemistry, 2012, University of Helsinki

Lignans are found as naturally occurring compounds in plants, and also as metabolites in mammals. Due to their biological activity, lignans have attracted the interest… (more)

Subjects/Keywords: organic Chemistry; organic Chemistry

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APA (6th Edition):

Raffaelli, B. (2012). Synthesis of lignano-9,9'-lactones and rearrangement studies. (Doctoral Dissertation). University of Helsinki. Retrieved from http://hdl.handle.net/10138/37066

Chicago Manual of Style (16th Edition):

Raffaelli, Barbara. “Synthesis of lignano-9,9'-lactones and rearrangement studies.” 2012. Doctoral Dissertation, University of Helsinki. Accessed June 25, 2019. http://hdl.handle.net/10138/37066.

MLA Handbook (7th Edition):

Raffaelli, Barbara. “Synthesis of lignano-9,9'-lactones and rearrangement studies.” 2012. Web. 25 Jun 2019.

Vancouver:

Raffaelli B. Synthesis of lignano-9,9'-lactones and rearrangement studies. [Internet] [Doctoral dissertation]. University of Helsinki; 2012. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10138/37066.

Council of Science Editors:

Raffaelli B. Synthesis of lignano-9,9'-lactones and rearrangement studies. [Doctoral Dissertation]. University of Helsinki; 2012. Available from: http://hdl.handle.net/10138/37066

5. Lee, Jennifer Jiyoung. Platform approach to diversification: bio-based methyl coumalate to functionalized aromatics via a Diels-Alder strategy.

Degree: 2014, Iowa State University

 The chemical industry relies on crude oil to manufacture the vast majority of chemicals. However, the increasing demand cannot be supported with the simultaneous decrease… (more)

Subjects/Keywords: Organic Chemistry; Organic Chemistry

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APA (6th Edition):

Lee, J. J. (2014). Platform approach to diversification: bio-based methyl coumalate to functionalized aromatics via a Diels-Alder strategy. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/14190

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):

Lee, Jennifer Jiyoung. “Platform approach to diversification: bio-based methyl coumalate to functionalized aromatics via a Diels-Alder strategy.” 2014. Thesis, Iowa State University. Accessed June 25, 2019. https://lib.dr.iastate.edu/etd/14190.

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

MLA Handbook (7th Edition):

Lee, Jennifer Jiyoung. “Platform approach to diversification: bio-based methyl coumalate to functionalized aromatics via a Diels-Alder strategy.” 2014. Web. 25 Jun 2019.

Vancouver:

Lee JJ. Platform approach to diversification: bio-based methyl coumalate to functionalized aromatics via a Diels-Alder strategy. [Internet] [Thesis]. Iowa State University; 2014. [cited 2019 Jun 25]. Available from: https://lib.dr.iastate.edu/etd/14190.

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

Council of Science Editors:

Lee JJ. Platform approach to diversification: bio-based methyl coumalate to functionalized aromatics via a Diels-Alder strategy. [Thesis]. Iowa State University; 2014. Available from: https://lib.dr.iastate.edu/etd/14190

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


McMaster University

6. Jeyakanthan, Ketharagowry. A STUDY OF THE EFFECTS INTRAMOLECULAR π-COMPLEXATION ON THE REACTIVITY OF TRANSIENT ARYL(3-BUTENYL)GERMYLENES.

Degree: MSc, 2014, McMaster University

Three novel 1-aryl-1-(3-butenyl)germacyclopent-3-enes (26a, 26b and 26c) were synthesized and their photochemistry in hexane solution was studied by steady state and laser flash photolysis… (more)

Subjects/Keywords: Organic Chemistry; Organic Chemistry

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APA (6th Edition):

Jeyakanthan, K. (2014). A STUDY OF THE EFFECTS INTRAMOLECULAR π-COMPLEXATION ON THE REACTIVITY OF TRANSIENT ARYL(3-BUTENYL)GERMYLENES. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/14137

Chicago Manual of Style (16th Edition):

Jeyakanthan, Ketharagowry. “A STUDY OF THE EFFECTS INTRAMOLECULAR π-COMPLEXATION ON THE REACTIVITY OF TRANSIENT ARYL(3-BUTENYL)GERMYLENES.” 2014. Masters Thesis, McMaster University. Accessed June 25, 2019. http://hdl.handle.net/11375/14137.

MLA Handbook (7th Edition):

Jeyakanthan, Ketharagowry. “A STUDY OF THE EFFECTS INTRAMOLECULAR π-COMPLEXATION ON THE REACTIVITY OF TRANSIENT ARYL(3-BUTENYL)GERMYLENES.” 2014. Web. 25 Jun 2019.

Vancouver:

Jeyakanthan K. A STUDY OF THE EFFECTS INTRAMOLECULAR π-COMPLEXATION ON THE REACTIVITY OF TRANSIENT ARYL(3-BUTENYL)GERMYLENES. [Internet] [Masters thesis]. McMaster University; 2014. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/11375/14137.

Council of Science Editors:

Jeyakanthan K. A STUDY OF THE EFFECTS INTRAMOLECULAR π-COMPLEXATION ON THE REACTIVITY OF TRANSIENT ARYL(3-BUTENYL)GERMYLENES. [Masters Thesis]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/14137


Iowa State University

7. Goswami, Pratik Pran. Development of light- and chemo-sensitive probes for biochemical methods.

Degree: 2015, Iowa State University

 Part I. Photocages, which are light cleavable protecting groups, are an important class of chemical tools that allow light to unmask bioactive substrates with precise… (more)

Subjects/Keywords: Organic Chemistry; Organic Chemistry

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APA (6th Edition):

Goswami, P. P. (2015). Development of light- and chemo-sensitive probes for biochemical methods. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/14369

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):

Goswami, Pratik Pran. “Development of light- and chemo-sensitive probes for biochemical methods.” 2015. Thesis, Iowa State University. Accessed June 25, 2019. https://lib.dr.iastate.edu/etd/14369.

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

MLA Handbook (7th Edition):

Goswami, Pratik Pran. “Development of light- and chemo-sensitive probes for biochemical methods.” 2015. Web. 25 Jun 2019.

Vancouver:

Goswami PP. Development of light- and chemo-sensitive probes for biochemical methods. [Internet] [Thesis]. Iowa State University; 2015. [cited 2019 Jun 25]. Available from: https://lib.dr.iastate.edu/etd/14369.

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

Council of Science Editors:

Goswami PP. Development of light- and chemo-sensitive probes for biochemical methods. [Thesis]. Iowa State University; 2015. Available from: https://lib.dr.iastate.edu/etd/14369

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


Iowa State University

8. Bhuwalka, Achala. Design and synthesis of novel heterocycles for organic semiconducting materials.

Degree: 2014, Iowa State University

Organic semiconductors have attracted much attention as alternatives to silicon based photovoltaic technology. Currently, the best power conversion efficiencies use small molecules and conjugated polymers… (more)

Subjects/Keywords: Organic Chemistry; Organic Chemistry

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APA (6th Edition):

Bhuwalka, A. (2014). Design and synthesis of novel heterocycles for organic semiconducting materials. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/14123

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):

Bhuwalka, Achala. “Design and synthesis of novel heterocycles for organic semiconducting materials.” 2014. Thesis, Iowa State University. Accessed June 25, 2019. https://lib.dr.iastate.edu/etd/14123.

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

MLA Handbook (7th Edition):

Bhuwalka, Achala. “Design and synthesis of novel heterocycles for organic semiconducting materials.” 2014. Web. 25 Jun 2019.

Vancouver:

Bhuwalka A. Design and synthesis of novel heterocycles for organic semiconducting materials. [Internet] [Thesis]. Iowa State University; 2014. [cited 2019 Jun 25]. Available from: https://lib.dr.iastate.edu/etd/14123.

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

Council of Science Editors:

Bhuwalka A. Design and synthesis of novel heterocycles for organic semiconducting materials. [Thesis]. Iowa State University; 2014. Available from: https://lib.dr.iastate.edu/etd/14123

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


Wright State University

9. Boyer, Amanda Merrill. Potential Tau Directed Imaging Agents.

Degree: MS, Chemistry, 2015, Wright State University

 Given the ambident reactivity of oxindoles in terms of N- versus C-alkylation, realization of the three points of diversity available to (presumably benzenoid substituted) benzylidene… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; chemistry; organic chemistry

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APA (6th Edition):

Boyer, A. M. (2015). Potential Tau Directed Imaging Agents. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1453210267

Chicago Manual of Style (16th Edition):

Boyer, Amanda Merrill. “Potential Tau Directed Imaging Agents.” 2015. Masters Thesis, Wright State University. Accessed June 25, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1453210267.

MLA Handbook (7th Edition):

Boyer, Amanda Merrill. “Potential Tau Directed Imaging Agents.” 2015. Web. 25 Jun 2019.

Vancouver:

Boyer AM. Potential Tau Directed Imaging Agents. [Internet] [Masters thesis]. Wright State University; 2015. [cited 2019 Jun 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1453210267.

Council of Science Editors:

Boyer AM. Potential Tau Directed Imaging Agents. [Masters Thesis]. Wright State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1453210267

10. Omran, Anahid. Synthesis of N-Functionalized Chiral 3-Hydroxyphenylpyrrolidines and Their Evaluation as Selective D3 Receptor Ligands.

Degree: 2017, Southern Illinois University at Edwardsville

  Dysfunction of dopaminergic receptor signaling in the brain is a hallmark of a number of neurodegenerative pathologies. Of the five dopamine receptors, the D3(more)

Subjects/Keywords: Chemistry; Organic chemistry

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APA (6th Edition):

Omran, A. (2017). Synthesis of N-Functionalized Chiral 3-Hydroxyphenylpyrrolidines and Their Evaluation as Selective D3 Receptor Ligands. (Thesis). Southern Illinois University at Edwardsville. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=10616167

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):

Omran, Anahid. “Synthesis of N-Functionalized Chiral 3-Hydroxyphenylpyrrolidines and Their Evaluation as Selective D3 Receptor Ligands.” 2017. Thesis, Southern Illinois University at Edwardsville. Accessed June 25, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=10616167.

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

MLA Handbook (7th Edition):

Omran, Anahid. “Synthesis of N-Functionalized Chiral 3-Hydroxyphenylpyrrolidines and Their Evaluation as Selective D3 Receptor Ligands.” 2017. Web. 25 Jun 2019.

Vancouver:

Omran A. Synthesis of N-Functionalized Chiral 3-Hydroxyphenylpyrrolidines and Their Evaluation as Selective D3 Receptor Ligands. [Internet] [Thesis]. Southern Illinois University at Edwardsville; 2017. [cited 2019 Jun 25]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10616167.

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

Council of Science Editors:

Omran A. Synthesis of N-Functionalized Chiral 3-Hydroxyphenylpyrrolidines and Their Evaluation as Selective D3 Receptor Ligands. [Thesis]. Southern Illinois University at Edwardsville; 2017. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10616167

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


Temple University

11. GADDIRAJU, NARENDRA VARMA. Asymmetric Synthesis of C-1 Substituted Cocaine Analogues Using Sulfinimine (N-Sulfinyl Imine) Chemistry And Vinylaluminum Addition to Sulfinimines (N-Sulfinyl Imines) For The Asymmetric Synthesis Of Alpha-Substituted-Beta-Amino Esters.

Degree: PhD, 2013, Temple University

Chemistry

Organic nitrogen containing chiral compounds are widely found in nature, and a number of them exhibit important biological and medicinal properties. The main objective… (more)

Subjects/Keywords: Chemistry; Organic chemistry

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APA (6th Edition):

GADDIRAJU, N. V. (2013). Asymmetric Synthesis of C-1 Substituted Cocaine Analogues Using Sulfinimine (N-Sulfinyl Imine) Chemistry And Vinylaluminum Addition to Sulfinimines (N-Sulfinyl Imines) For The Asymmetric Synthesis Of Alpha-Substituted-Beta-Amino Esters. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,225834

Chicago Manual of Style (16th Edition):

GADDIRAJU, NARENDRA VARMA. “Asymmetric Synthesis of C-1 Substituted Cocaine Analogues Using Sulfinimine (N-Sulfinyl Imine) Chemistry And Vinylaluminum Addition to Sulfinimines (N-Sulfinyl Imines) For The Asymmetric Synthesis Of Alpha-Substituted-Beta-Amino Esters.” 2013. Doctoral Dissertation, Temple University. Accessed June 25, 2019. http://digital.library.temple.edu/u?/p245801coll10,225834.

MLA Handbook (7th Edition):

GADDIRAJU, NARENDRA VARMA. “Asymmetric Synthesis of C-1 Substituted Cocaine Analogues Using Sulfinimine (N-Sulfinyl Imine) Chemistry And Vinylaluminum Addition to Sulfinimines (N-Sulfinyl Imines) For The Asymmetric Synthesis Of Alpha-Substituted-Beta-Amino Esters.” 2013. Web. 25 Jun 2019.

Vancouver:

GADDIRAJU NV. Asymmetric Synthesis of C-1 Substituted Cocaine Analogues Using Sulfinimine (N-Sulfinyl Imine) Chemistry And Vinylaluminum Addition to Sulfinimines (N-Sulfinyl Imines) For The Asymmetric Synthesis Of Alpha-Substituted-Beta-Amino Esters. [Internet] [Doctoral dissertation]. Temple University; 2013. [cited 2019 Jun 25]. Available from: http://digital.library.temple.edu/u?/p245801coll10,225834.

Council of Science Editors:

GADDIRAJU NV. Asymmetric Synthesis of C-1 Substituted Cocaine Analogues Using Sulfinimine (N-Sulfinyl Imine) Chemistry And Vinylaluminum Addition to Sulfinimines (N-Sulfinyl Imines) For The Asymmetric Synthesis Of Alpha-Substituted-Beta-Amino Esters. [Doctoral Dissertation]. Temple University; 2013. Available from: http://digital.library.temple.edu/u?/p245801coll10,225834

12. Guerrera, Cessandra. Stereoselective Synthesis of alpha,alpha-Disubstituted Amino Acids Utilizing Porcine Liver Esterase and the Petasis Borono-Mannich Reaction.

Degree: 2017, Southern Connecticut State University

  Arginase is a manganese-containing enzyme that catalyzes the hydrolysis of L-arginine to yield L-ornithine and urea. It has been suggested that inhibition of arginase… (more)

Subjects/Keywords: Chemistry; Organic chemistry

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APA (6th Edition):

Guerrera, C. (2017). Stereoselective Synthesis of alpha,alpha-Disubstituted Amino Acids Utilizing Porcine Liver Esterase and the Petasis Borono-Mannich Reaction. (Thesis). Southern Connecticut State University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=10283110

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):

Guerrera, Cessandra. “Stereoselective Synthesis of alpha,alpha-Disubstituted Amino Acids Utilizing Porcine Liver Esterase and the Petasis Borono-Mannich Reaction.” 2017. Thesis, Southern Connecticut State University. Accessed June 25, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=10283110.

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

MLA Handbook (7th Edition):

Guerrera, Cessandra. “Stereoselective Synthesis of alpha,alpha-Disubstituted Amino Acids Utilizing Porcine Liver Esterase and the Petasis Borono-Mannich Reaction.” 2017. Web. 25 Jun 2019.

Vancouver:

Guerrera C. Stereoselective Synthesis of alpha,alpha-Disubstituted Amino Acids Utilizing Porcine Liver Esterase and the Petasis Borono-Mannich Reaction. [Internet] [Thesis]. Southern Connecticut State University; 2017. [cited 2019 Jun 25]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10283110.

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

Council of Science Editors:

Guerrera C. Stereoselective Synthesis of alpha,alpha-Disubstituted Amino Acids Utilizing Porcine Liver Esterase and the Petasis Borono-Mannich Reaction. [Thesis]. Southern Connecticut State University; 2017. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10283110

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


University of Vermont

13. Machamer, Natalie Kay. I. A New Route To Azomethine Ylides: Shifting The Reliance On Amino Ester Precursors II. Applications In Total Synthesis.

Degree: PhD, Chemistry, 2015, University of Vermont

  Nitrogen-containing heterocycles have great utility in the biomedical and medicinal fields and one such heterocycle is the 5-membered pyrrolidine ring. The synthesis of pyrrolidine… (more)

Subjects/Keywords: Chemistry; Organic Chemistry

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APA (6th Edition):

Machamer, N. K. (2015). I. A New Route To Azomethine Ylides: Shifting The Reliance On Amino Ester Precursors II. Applications In Total Synthesis. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/407

Chicago Manual of Style (16th Edition):

Machamer, Natalie Kay. “I. A New Route To Azomethine Ylides: Shifting The Reliance On Amino Ester Precursors II. Applications In Total Synthesis.” 2015. Doctoral Dissertation, University of Vermont. Accessed June 25, 2019. https://scholarworks.uvm.edu/graddis/407.

MLA Handbook (7th Edition):

Machamer, Natalie Kay. “I. A New Route To Azomethine Ylides: Shifting The Reliance On Amino Ester Precursors II. Applications In Total Synthesis.” 2015. Web. 25 Jun 2019.

Vancouver:

Machamer NK. I. A New Route To Azomethine Ylides: Shifting The Reliance On Amino Ester Precursors II. Applications In Total Synthesis. [Internet] [Doctoral dissertation]. University of Vermont; 2015. [cited 2019 Jun 25]. Available from: https://scholarworks.uvm.edu/graddis/407.

Council of Science Editors:

Machamer NK. I. A New Route To Azomethine Ylides: Shifting The Reliance On Amino Ester Precursors II. Applications In Total Synthesis. [Doctoral Dissertation]. University of Vermont; 2015. Available from: https://scholarworks.uvm.edu/graddis/407

14. Borikar, Sanjay P. Novel organic transformations using ultrasound Ionic liquid and their application towards the synthesis of biological active molecules/intermediates.

Degree: 2011, University of Pune

 “Novel Organic Transformations Using Ultrasound, Ionic Liquid and Their Application Towards the Synthesis of Biological Active Molecules/Intermediates” Thesis is divided into three chapters: CHAPTER-1: Synthesis… (more)

Subjects/Keywords: Chemistry; Organic Chemistry

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APA (6th Edition):

Borikar, S. P. (2011). Novel organic transformations using ultrasound Ionic liquid and their application towards the synthesis of biological active molecules/intermediates. (Thesis). University of Pune. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/2375

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):

Borikar, Sanjay P. “Novel organic transformations using ultrasound Ionic liquid and their application towards the synthesis of biological active molecules/intermediates.” 2011. Thesis, University of Pune. Accessed June 25, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/2375.

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

MLA Handbook (7th Edition):

Borikar, Sanjay P. “Novel organic transformations using ultrasound Ionic liquid and their application towards the synthesis of biological active molecules/intermediates.” 2011. Web. 25 Jun 2019.

Vancouver:

Borikar SP. Novel organic transformations using ultrasound Ionic liquid and their application towards the synthesis of biological active molecules/intermediates. [Internet] [Thesis]. University of Pune; 2011. [cited 2019 Jun 25]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2375.

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

Council of Science Editors:

Borikar SP. Novel organic transformations using ultrasound Ionic liquid and their application towards the synthesis of biological active molecules/intermediates. [Thesis]. University of Pune; 2011. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2375

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

15. Ayala, Malerie. Synthesis of a second generation naphthopyran metal-binding photoswitch.

Degree: 2015, California State University, Los Angeles

  The aim of this project was to increase the calcium binding affinity of our previously developed photochromic 3H-naphtho[2,1-b]pyran <b>1,</b> a light-controlled reversible binding switch… (more)

Subjects/Keywords: Chemistry; Organic chemistry

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APA (6th Edition):

Ayala, M. (2015). Synthesis of a second generation naphthopyran metal-binding photoswitch. (Thesis). California State University, Los Angeles. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=1597156

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):

Ayala, Malerie. “Synthesis of a second generation naphthopyran metal-binding photoswitch.” 2015. Thesis, California State University, Los Angeles. Accessed June 25, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=1597156.

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

MLA Handbook (7th Edition):

Ayala, Malerie. “Synthesis of a second generation naphthopyran metal-binding photoswitch.” 2015. Web. 25 Jun 2019.

Vancouver:

Ayala M. Synthesis of a second generation naphthopyran metal-binding photoswitch. [Internet] [Thesis]. California State University, Los Angeles; 2015. [cited 2019 Jun 25]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1597156.

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

Council of Science Editors:

Ayala M. Synthesis of a second generation naphthopyran metal-binding photoswitch. [Thesis]. California State University, Los Angeles; 2015. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1597156

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


Purdue University

16. Kuriakose, Jerrin. Development of novel strategies to combat multidrug resistance mediated by efflux transporters and intracellular bacteria.

Degree: PhD, Chemistry, 2014, Purdue University

  Multidrug resistance (MDR) is the condition where cancer cells or microorganisms cease to respond to multiple drugs. MDR conferred by efflux transporters, that deprive… (more)

Subjects/Keywords: Chemistry; Organic Chemistry

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APA (6th Edition):

Kuriakose, J. (2014). Development of novel strategies to combat multidrug resistance mediated by efflux transporters and intracellular bacteria. (Doctoral Dissertation). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_dissertations/312

Chicago Manual of Style (16th Edition):

Kuriakose, Jerrin. “Development of novel strategies to combat multidrug resistance mediated by efflux transporters and intracellular bacteria.” 2014. Doctoral Dissertation, Purdue University. Accessed June 25, 2019. http://docs.lib.purdue.edu/open_access_dissertations/312.

MLA Handbook (7th Edition):

Kuriakose, Jerrin. “Development of novel strategies to combat multidrug resistance mediated by efflux transporters and intracellular bacteria.” 2014. Web. 25 Jun 2019.

Vancouver:

Kuriakose J. Development of novel strategies to combat multidrug resistance mediated by efflux transporters and intracellular bacteria. [Internet] [Doctoral dissertation]. Purdue University; 2014. [cited 2019 Jun 25]. Available from: http://docs.lib.purdue.edu/open_access_dissertations/312.

Council of Science Editors:

Kuriakose J. Development of novel strategies to combat multidrug resistance mediated by efflux transporters and intracellular bacteria. [Doctoral Dissertation]. Purdue University; 2014. Available from: http://docs.lib.purdue.edu/open_access_dissertations/312


Wayne State University

17. Mandhapati, Appi Reddy. Synthesis of apramycin and paromomycin derivatives as potential next generation aminoglycoside antibiotics and chemistry of isothiocyanato sialyl donors.

Degree: 2016, Wayne State University

  AGAs are clinically important antibacterials for human therapy and have long been used as highly potent antibiotics for treating several bacterial infections. The fidelity… (more)

Subjects/Keywords: Chemistry; Organic chemistry

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APA (6th Edition):

Mandhapati, A. R. (2016). Synthesis of apramycin and paromomycin derivatives as potential next generation aminoglycoside antibiotics and chemistry of isothiocyanato sialyl donors. (Thesis). Wayne State University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=10153408

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):

Mandhapati, Appi Reddy. “Synthesis of apramycin and paromomycin derivatives as potential next generation aminoglycoside antibiotics and chemistry of isothiocyanato sialyl donors.” 2016. Thesis, Wayne State University. Accessed June 25, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=10153408.

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

MLA Handbook (7th Edition):

Mandhapati, Appi Reddy. “Synthesis of apramycin and paromomycin derivatives as potential next generation aminoglycoside antibiotics and chemistry of isothiocyanato sialyl donors.” 2016. Web. 25 Jun 2019.

Vancouver:

Mandhapati AR. Synthesis of apramycin and paromomycin derivatives as potential next generation aminoglycoside antibiotics and chemistry of isothiocyanato sialyl donors. [Internet] [Thesis]. Wayne State University; 2016. [cited 2019 Jun 25]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10153408.

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

Council of Science Editors:

Mandhapati AR. Synthesis of apramycin and paromomycin derivatives as potential next generation aminoglycoside antibiotics and chemistry of isothiocyanato sialyl donors. [Thesis]. Wayne State University; 2016. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10153408

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


Florida State University

18. Gold, Brian, 1987-. Stereoelectronic Control of Cycloadditions and Fragmentations.

Degree: PhD, Chemistry and Biochemistry, 2014, Florida State University

 The stereoelectronic control of reactivity provides a special, yet necessary challenge. Pericyclic reactions play an important role in the development of theoretical organic chemistry, and… (more)

Subjects/Keywords: Chemistry; Chemistry, Organic

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APA (6th Edition):

Gold, Brian, 1. (2014). Stereoelectronic Control of Cycloadditions and Fragmentations. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_migr_etd-9178 ;

Chicago Manual of Style (16th Edition):

Gold, Brian, 1987-. “Stereoelectronic Control of Cycloadditions and Fragmentations.” 2014. Doctoral Dissertation, Florida State University. Accessed June 25, 2019. http://purl.flvc.org/fsu/fd/FSU_migr_etd-9178 ;.

MLA Handbook (7th Edition):

Gold, Brian, 1987-. “Stereoelectronic Control of Cycloadditions and Fragmentations.” 2014. Web. 25 Jun 2019.

Vancouver:

Gold, Brian 1. Stereoelectronic Control of Cycloadditions and Fragmentations. [Internet] [Doctoral dissertation]. Florida State University; 2014. [cited 2019 Jun 25]. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-9178 ;.

Council of Science Editors:

Gold, Brian 1. Stereoelectronic Control of Cycloadditions and Fragmentations. [Doctoral Dissertation]. Florida State University; 2014. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-9178 ;


Florida State University

19. Brassard, Christopher J. Rapid and Selective Syntheses of Trisubstituted -1,2,3-Triazoles Through Copper Mediated Azide Alkyne Cycloaddition.

Degree: PhD, Chemistry and Biochemistry, 2016, Florida State University

 This dissertation describes the development of alternative products from the copper-catalyzed azide-alkyne cycloaddition (CuAAC). The first chapter provides an introduction to the CuAAC through the… (more)

Subjects/Keywords: Chemistry, Organic; Chemistry

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APA (6th Edition):

Brassard, C. J. (2016). Rapid and Selective Syntheses of Trisubstituted -1,2,3-Triazoles Through Copper Mediated Azide Alkyne Cycloaddition. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_2016SU_Brassard_fsu_0071E_13324-C ;

Chicago Manual of Style (16th Edition):

Brassard, Christopher J. “Rapid and Selective Syntheses of Trisubstituted -1,2,3-Triazoles Through Copper Mediated Azide Alkyne Cycloaddition.” 2016. Doctoral Dissertation, Florida State University. Accessed June 25, 2019. http://purl.flvc.org/fsu/fd/FSU_2016SU_Brassard_fsu_0071E_13324-C ;.

MLA Handbook (7th Edition):

Brassard, Christopher J. “Rapid and Selective Syntheses of Trisubstituted -1,2,3-Triazoles Through Copper Mediated Azide Alkyne Cycloaddition.” 2016. Web. 25 Jun 2019.

Vancouver:

Brassard CJ. Rapid and Selective Syntheses of Trisubstituted -1,2,3-Triazoles Through Copper Mediated Azide Alkyne Cycloaddition. [Internet] [Doctoral dissertation]. Florida State University; 2016. [cited 2019 Jun 25]. Available from: http://purl.flvc.org/fsu/fd/FSU_2016SU_Brassard_fsu_0071E_13324-C ;.

Council of Science Editors:

Brassard CJ. Rapid and Selective Syntheses of Trisubstituted -1,2,3-Triazoles Through Copper Mediated Azide Alkyne Cycloaddition. [Doctoral Dissertation]. Florida State University; 2016. Available from: http://purl.flvc.org/fsu/fd/FSU_2016SU_Brassard_fsu_0071E_13324-C ;


Florida State University

20. Zhang, Xiaoguang. The Study on the Copper(II)-Mediated Azide-Alkyne Cycloaddition Reactions.

Degree: PhD, Chemistry and Biochemistry, 2017, Florida State University

 The copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction is an efficient technique for linking two molecules in different applications. Generally, Cu(II) salts were used to generate active… (more)

Subjects/Keywords: Chemistry; Chemistry, Organic

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APA (6th Edition):

Zhang, X. (2017). The Study on the Copper(II)-Mediated Azide-Alkyne Cycloaddition Reactions. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_SUMMER2017_Zhang_fsu_0071E_14063 ;

Chicago Manual of Style (16th Edition):

Zhang, Xiaoguang. “The Study on the Copper(II)-Mediated Azide-Alkyne Cycloaddition Reactions.” 2017. Doctoral Dissertation, Florida State University. Accessed June 25, 2019. http://purl.flvc.org/fsu/fd/FSU_SUMMER2017_Zhang_fsu_0071E_14063 ;.

MLA Handbook (7th Edition):

Zhang, Xiaoguang. “The Study on the Copper(II)-Mediated Azide-Alkyne Cycloaddition Reactions.” 2017. Web. 25 Jun 2019.

Vancouver:

Zhang X. The Study on the Copper(II)-Mediated Azide-Alkyne Cycloaddition Reactions. [Internet] [Doctoral dissertation]. Florida State University; 2017. [cited 2019 Jun 25]. Available from: http://purl.flvc.org/fsu/fd/FSU_SUMMER2017_Zhang_fsu_0071E_14063 ;.

Council of Science Editors:

Zhang X. The Study on the Copper(II)-Mediated Azide-Alkyne Cycloaddition Reactions. [Doctoral Dissertation]. Florida State University; 2017. Available from: http://purl.flvc.org/fsu/fd/FSU_SUMMER2017_Zhang_fsu_0071E_14063 ;


University of Toledo

21. Khatri, Hem Raj. Synthesis of Complex ortho-Allyliodoarenes via Reductive Iodonio-Claisen Rearrangement and Total Synthesis of Antitumor Antibiotic Derhodinosylurdamycin A.

Degree: PhD, Chemistry, 2015, University of Toledo

 The chemistry related to hypervalent iodine compounds has been extensively studied in the past few decades due to the environmentally benign character of hypervalent iodine… (more)

Subjects/Keywords: Organic Chemistry; Chemistry

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APA (6th Edition):

Khatri, H. R. (2015). Synthesis of Complex ortho-Allyliodoarenes via Reductive Iodonio-Claisen Rearrangement and Total Synthesis of Antitumor Antibiotic Derhodinosylurdamycin A. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1431342601

Chicago Manual of Style (16th Edition):

Khatri, Hem Raj. “Synthesis of Complex ortho-Allyliodoarenes via Reductive Iodonio-Claisen Rearrangement and Total Synthesis of Antitumor Antibiotic Derhodinosylurdamycin A.” 2015. Doctoral Dissertation, University of Toledo. Accessed June 25, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1431342601.

MLA Handbook (7th Edition):

Khatri, Hem Raj. “Synthesis of Complex ortho-Allyliodoarenes via Reductive Iodonio-Claisen Rearrangement and Total Synthesis of Antitumor Antibiotic Derhodinosylurdamycin A.” 2015. Web. 25 Jun 2019.

Vancouver:

Khatri HR. Synthesis of Complex ortho-Allyliodoarenes via Reductive Iodonio-Claisen Rearrangement and Total Synthesis of Antitumor Antibiotic Derhodinosylurdamycin A. [Internet] [Doctoral dissertation]. University of Toledo; 2015. [cited 2019 Jun 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1431342601.

Council of Science Editors:

Khatri HR. Synthesis of Complex ortho-Allyliodoarenes via Reductive Iodonio-Claisen Rearrangement and Total Synthesis of Antitumor Antibiotic Derhodinosylurdamycin A. [Doctoral Dissertation]. University of Toledo; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1431342601


University of Toledo

22. Starr, Matthew J. Synthesis of a C5'-Pseudouridinyl Radical Precursor.

Degree: MS, Medicinal Chemistry, 2015, University of Toledo

 Reactive oxygen species can cause damage to proteins, lipids, and nucleic acids through the generation of free radicals. Oxidative damage in DNA has been studied… (more)

Subjects/Keywords: Chemistry; Organic Chemistry

…precursors are made using synthetic organic chemistry to install special photolabile groups, such… …combined organic layers were dried using magnesium sulfate, and concentrated under reduced… …EtOAc (30 ml x 3), and the combined organic layers dried over magnesium sulfate. The crude was… 

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APA (6th Edition):

Starr, M. J. (2015). Synthesis of a C5'-Pseudouridinyl Radical Precursor. (Masters Thesis). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1449675404

Chicago Manual of Style (16th Edition):

Starr, Matthew J. “Synthesis of a C5'-Pseudouridinyl Radical Precursor.” 2015. Masters Thesis, University of Toledo. Accessed June 25, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1449675404.

MLA Handbook (7th Edition):

Starr, Matthew J. “Synthesis of a C5'-Pseudouridinyl Radical Precursor.” 2015. Web. 25 Jun 2019.

Vancouver:

Starr MJ. Synthesis of a C5'-Pseudouridinyl Radical Precursor. [Internet] [Masters thesis]. University of Toledo; 2015. [cited 2019 Jun 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1449675404.

Council of Science Editors:

Starr MJ. Synthesis of a C5'-Pseudouridinyl Radical Precursor. [Masters Thesis]. University of Toledo; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1449675404


University of Toledo

23. Baryal, Kedar N. Stereoselective Synthesis of Digitoxin and S-Linked Glycosides.

Degree: PhD, Chemistry, 2016, University of Toledo

 Deoxy-sugars are an important class of carbohydrates in which one or more hydroxyl group/s are replaced by hydrogen atom/s. 2-Deoxy sugars exist in a wide… (more)

Subjects/Keywords: Chemistry; Organic Chemistry

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APA (6th Edition):

Baryal, K. N. (2016). Stereoselective Synthesis of Digitoxin and S-Linked Glycosides. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1438174529

Chicago Manual of Style (16th Edition):

Baryal, Kedar N. “Stereoselective Synthesis of Digitoxin and S-Linked Glycosides.” 2016. Doctoral Dissertation, University of Toledo. Accessed June 25, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1438174529.

MLA Handbook (7th Edition):

Baryal, Kedar N. “Stereoselective Synthesis of Digitoxin and S-Linked Glycosides.” 2016. Web. 25 Jun 2019.

Vancouver:

Baryal KN. Stereoselective Synthesis of Digitoxin and S-Linked Glycosides. [Internet] [Doctoral dissertation]. University of Toledo; 2016. [cited 2019 Jun 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1438174529.

Council of Science Editors:

Baryal KN. Stereoselective Synthesis of Digitoxin and S-Linked Glycosides. [Doctoral Dissertation]. University of Toledo; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1438174529


University of California – Irvine

24. Daub, Mary Elisabeth. A Unified Synthetic Approach Toward the Kalihinanes.

Degree: Chemistry, 2016, University of California – Irvine

 This dissertation describes our efforts toward developing a unified synthesis of the kalininane family of antimalarial marine isocyanoterpenes. Chapter 1 focuses on the isolation, structure… (more)

Subjects/Keywords: Chemistry; Organic chemistry

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APA (6th Edition):

Daub, M. E. (2016). A Unified Synthetic Approach Toward the Kalihinanes. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/5133j2rr

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):

Daub, Mary Elisabeth. “A Unified Synthetic Approach Toward the Kalihinanes.” 2016. Thesis, University of California – Irvine. Accessed June 25, 2019. http://www.escholarship.org/uc/item/5133j2rr.

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

MLA Handbook (7th Edition):

Daub, Mary Elisabeth. “A Unified Synthetic Approach Toward the Kalihinanes.” 2016. Web. 25 Jun 2019.

Vancouver:

Daub ME. A Unified Synthetic Approach Toward the Kalihinanes. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2019 Jun 25]. Available from: http://www.escholarship.org/uc/item/5133j2rr.

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

Council of Science Editors:

Daub ME. A Unified Synthetic Approach Toward the Kalihinanes. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/5133j2rr

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


University of California – San Diego

25. Hamill, Kristina. Overcoming Biological Barriers: Synthesis and Evaluation of Molecular Transporters.

Degree: Chemistry, 2016, University of California – San Diego

 High molecular weight and highly-charged biomolecules are emerging as drugs with high selectivity and efficacy; however, new strategies are needed to improve their efficiency and… (more)

Subjects/Keywords: Organic chemistry; Chemistry

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APA (6th Edition):

Hamill, K. (2016). Overcoming Biological Barriers: Synthesis and Evaluation of Molecular Transporters. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/9p90k8s4

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):

Hamill, Kristina. “Overcoming Biological Barriers: Synthesis and Evaluation of Molecular Transporters.” 2016. Thesis, University of California – San Diego. Accessed June 25, 2019. http://www.escholarship.org/uc/item/9p90k8s4.

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

MLA Handbook (7th Edition):

Hamill, Kristina. “Overcoming Biological Barriers: Synthesis and Evaluation of Molecular Transporters.” 2016. Web. 25 Jun 2019.

Vancouver:

Hamill K. Overcoming Biological Barriers: Synthesis and Evaluation of Molecular Transporters. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2019 Jun 25]. Available from: http://www.escholarship.org/uc/item/9p90k8s4.

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

Council of Science Editors:

Hamill K. Overcoming Biological Barriers: Synthesis and Evaluation of Molecular Transporters. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/9p90k8s4

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


University of California – Riverside

26. Bastin, Baback. Synthesis of Isotopically Labeled Co-Enzyme to Probe the Active Site of Tryptophan synthase/ New Synthetic Approach to Tetrahydrocannabinol Analogs.

Degree: Chemistry, 2015, University of California – Riverside

 Identifying enzyme mechanisms at proton level resolution is the ultimate goal of enzymology. Traditional enzyme mechanistic studies infer protonation states from x-ray crystal structure and… (more)

Subjects/Keywords: Chemistry; Organic chemistry

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APA (6th Edition):

Bastin, B. (2015). Synthesis of Isotopically Labeled Co-Enzyme to Probe the Active Site of Tryptophan synthase/ New Synthetic Approach to Tetrahydrocannabinol Analogs. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/68x2v2nr

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):

Bastin, Baback. “Synthesis of Isotopically Labeled Co-Enzyme to Probe the Active Site of Tryptophan synthase/ New Synthetic Approach to Tetrahydrocannabinol Analogs.” 2015. Thesis, University of California – Riverside. Accessed June 25, 2019. http://www.escholarship.org/uc/item/68x2v2nr.

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

MLA Handbook (7th Edition):

Bastin, Baback. “Synthesis of Isotopically Labeled Co-Enzyme to Probe the Active Site of Tryptophan synthase/ New Synthetic Approach to Tetrahydrocannabinol Analogs.” 2015. Web. 25 Jun 2019.

Vancouver:

Bastin B. Synthesis of Isotopically Labeled Co-Enzyme to Probe the Active Site of Tryptophan synthase/ New Synthetic Approach to Tetrahydrocannabinol Analogs. [Internet] [Thesis]. University of California – Riverside; 2015. [cited 2019 Jun 25]. Available from: http://www.escholarship.org/uc/item/68x2v2nr.

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

Council of Science Editors:

Bastin B. Synthesis of Isotopically Labeled Co-Enzyme to Probe the Active Site of Tryptophan synthase/ New Synthetic Approach to Tetrahydrocannabinol Analogs. [Thesis]. University of California – Riverside; 2015. Available from: http://www.escholarship.org/uc/item/68x2v2nr

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


UCLA

27. He, Cyndi Qixin. Origins of Reactivity and Selectivity of a Series of Proximity-Induced Transannular Diels-Alder Reactions.

Degree: Chemistry, 2013, UCLA

 Transannular Diels-Alder (TADA) reactions are a powerful tool for the construction of polycyclic structures with four stereogenic centers. A series of remarkably facile and stereoselective… (more)

Subjects/Keywords: Chemistry; Organic chemistry

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APA (6th Edition):

He, C. Q. (2013). Origins of Reactivity and Selectivity of a Series of Proximity-Induced Transannular Diels-Alder Reactions. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/4g93x5sn

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):

He, Cyndi Qixin. “Origins of Reactivity and Selectivity of a Series of Proximity-Induced Transannular Diels-Alder Reactions.” 2013. Thesis, UCLA. Accessed June 25, 2019. http://www.escholarship.org/uc/item/4g93x5sn.

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

MLA Handbook (7th Edition):

He, Cyndi Qixin. “Origins of Reactivity and Selectivity of a Series of Proximity-Induced Transannular Diels-Alder Reactions.” 2013. Web. 25 Jun 2019.

Vancouver:

He CQ. Origins of Reactivity and Selectivity of a Series of Proximity-Induced Transannular Diels-Alder Reactions. [Internet] [Thesis]. UCLA; 2013. [cited 2019 Jun 25]. Available from: http://www.escholarship.org/uc/item/4g93x5sn.

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

Council of Science Editors:

He CQ. Origins of Reactivity and Selectivity of a Series of Proximity-Induced Transannular Diels-Alder Reactions. [Thesis]. UCLA; 2013. Available from: http://www.escholarship.org/uc/item/4g93x5sn

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


Arizona State University

28. Trickey-Platt, Brindi. Combretastatin A-2 Synthetic Modifications.

Degree: MS, Chemistry, 2011, Arizona State University

 Combretastatin A-4 (CA-4) represents one of the most promising antineoplastic and cancer vascular targeting stilbenes that have been isolated from the South African bush willow,… (more)

Subjects/Keywords: Organic Chemistry; Chemistry

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

APA (6th Edition):

Trickey-Platt, B. (2011). Combretastatin A-2 Synthetic Modifications. (Masters Thesis). Arizona State University. Retrieved from http://repository.asu.edu/items/9441

Chicago Manual of Style (16th Edition):

Trickey-Platt, Brindi. “Combretastatin A-2 Synthetic Modifications.” 2011. Masters Thesis, Arizona State University. Accessed June 25, 2019. http://repository.asu.edu/items/9441.

MLA Handbook (7th Edition):

Trickey-Platt, Brindi. “Combretastatin A-2 Synthetic Modifications.” 2011. Web. 25 Jun 2019.

Vancouver:

Trickey-Platt B. Combretastatin A-2 Synthetic Modifications. [Internet] [Masters thesis]. Arizona State University; 2011. [cited 2019 Jun 25]. Available from: http://repository.asu.edu/items/9441.

Council of Science Editors:

Trickey-Platt B. Combretastatin A-2 Synthetic Modifications. [Masters Thesis]. Arizona State University; 2011. Available from: http://repository.asu.edu/items/9441


Washington University in St. Louis

29. Lu, Guojian. Part I Development of Nucleophilic Acylation Catalysts Part II Chiral Brønsted Acid Catalyzed Enantioselective Alcoholysis.

Degree: PhD, Chemistry, 2011, Washington University in St. Louis

  Chiral bicyclic amidines and isothioureas developed in our group have been showed as a new type of nucleophilic acyl transfer catalysts. Based on the… (more)

Subjects/Keywords: Chemistry; Organic chemistry

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

APA (6th Edition):

Lu, G. (2011). Part I Development of Nucleophilic Acylation Catalysts Part II Chiral Brønsted Acid Catalyzed Enantioselective Alcoholysis. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/612

Chicago Manual of Style (16th Edition):

Lu, Guojian. “Part I Development of Nucleophilic Acylation Catalysts Part II Chiral Brønsted Acid Catalyzed Enantioselective Alcoholysis.” 2011. Doctoral Dissertation, Washington University in St. Louis. Accessed June 25, 2019. https://openscholarship.wustl.edu/etd/612.

MLA Handbook (7th Edition):

Lu, Guojian. “Part I Development of Nucleophilic Acylation Catalysts Part II Chiral Brønsted Acid Catalyzed Enantioselective Alcoholysis.” 2011. Web. 25 Jun 2019.

Vancouver:

Lu G. Part I Development of Nucleophilic Acylation Catalysts Part II Chiral Brønsted Acid Catalyzed Enantioselective Alcoholysis. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2011. [cited 2019 Jun 25]. Available from: https://openscholarship.wustl.edu/etd/612.

Council of Science Editors:

Lu G. Part I Development of Nucleophilic Acylation Catalysts Part II Chiral Brønsted Acid Catalyzed Enantioselective Alcoholysis. [Doctoral Dissertation]. Washington University in St. Louis; 2011. Available from: https://openscholarship.wustl.edu/etd/612


Duke University

30. Brooner, Rachel. Mechanistic Studies of pi-Activation Catalysis by Cationic Gold(I) and Brønsted-acid .

Degree: 2013, Duke University

  Soluble gold(I) complexes are highly efficient catalysts for the functionalization of C-C multiple bonds through the addition of carbon- or heteroatom-nucleophiles across π-bonds or… (more)

Subjects/Keywords: Chemistry; Organic chemistry

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

APA (6th Edition):

Brooner, R. (2013). Mechanistic Studies of pi-Activation Catalysis by Cationic Gold(I) and Brønsted-acid . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/8070

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):

Brooner, Rachel. “Mechanistic Studies of pi-Activation Catalysis by Cationic Gold(I) and Brønsted-acid .” 2013. Thesis, Duke University. Accessed June 25, 2019. http://hdl.handle.net/10161/8070.

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

MLA Handbook (7th Edition):

Brooner, Rachel. “Mechanistic Studies of pi-Activation Catalysis by Cationic Gold(I) and Brønsted-acid .” 2013. Web. 25 Jun 2019.

Vancouver:

Brooner R. Mechanistic Studies of pi-Activation Catalysis by Cationic Gold(I) and Brønsted-acid . [Internet] [Thesis]. Duke University; 2013. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10161/8070.

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

Council of Science Editors:

Brooner R. Mechanistic Studies of pi-Activation Catalysis by Cationic Gold(I) and Brønsted-acid . [Thesis]. Duke University; 2013. Available from: http://hdl.handle.net/10161/8070

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

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