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You searched for subject:(synthetic chemistry). Showing records 1 – 30 of 303 total matches.

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1. Nikolaev, Andrei. Palladium (II) Mediated Transformation: Exploring Synthetic Methodology for the Synthesis of Cyclopentenones from Tertiary-Cyclobutanois.

Degree: MSc -MS, Chemistry, 2015, York University

 A new method for the synthesis of ring-fused cyclopentenone is described. The method utilizes the built-in strain of tertiary cyclobutanol to drive the palladium(II)-catalyzed rearrangement… (more)

Subjects/Keywords: Chemistry; Chemistry; Synthetic chemistry; Organometallics; Organopalladium chemistry; Cyclopentenone; Strain; Synthetic methodology.

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

APA (6th Edition):

Nikolaev, A. (2015). Palladium (II) Mediated Transformation: Exploring Synthetic Methodology for the Synthesis of Cyclopentenones from Tertiary-Cyclobutanois. (Masters Thesis). York University. Retrieved from http://hdl.handle.net/10315/30036

Chicago Manual of Style (16th Edition):

Nikolaev, Andrei. “Palladium (II) Mediated Transformation: Exploring Synthetic Methodology for the Synthesis of Cyclopentenones from Tertiary-Cyclobutanois.” 2015. Masters Thesis, York University. Accessed July 09, 2020. http://hdl.handle.net/10315/30036.

MLA Handbook (7th Edition):

Nikolaev, Andrei. “Palladium (II) Mediated Transformation: Exploring Synthetic Methodology for the Synthesis of Cyclopentenones from Tertiary-Cyclobutanois.” 2015. Web. 09 Jul 2020.

Vancouver:

Nikolaev A. Palladium (II) Mediated Transformation: Exploring Synthetic Methodology for the Synthesis of Cyclopentenones from Tertiary-Cyclobutanois. [Internet] [Masters thesis]. York University; 2015. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10315/30036.

Council of Science Editors:

Nikolaev A. Palladium (II) Mediated Transformation: Exploring Synthetic Methodology for the Synthesis of Cyclopentenones from Tertiary-Cyclobutanois. [Masters Thesis]. York University; 2015. Available from: http://hdl.handle.net/10315/30036


University of Ottawa

2. Jamshidi, Mohammad. Formaldehyde as a Catalyst: Investigations on the Role of Formaldehyde as a Potential Prebiotic Catalyst and Desymmetrization Agent .

Degree: 2017, University of Ottawa

 Life, as we know it, has emerged from the association of simple building blocks (e.g. HCN, NH3, aldehydes, etc). The reactions required to form the… (more)

Subjects/Keywords: Organic Chemistry; Prebiotic Chemistry; Synthetic Organic Chemistry

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APA (6th Edition):

Jamshidi, M. (2017). Formaldehyde as a Catalyst: Investigations on the Role of Formaldehyde as a Potential Prebiotic Catalyst and Desymmetrization Agent . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/36609

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):

Jamshidi, Mohammad. “Formaldehyde as a Catalyst: Investigations on the Role of Formaldehyde as a Potential Prebiotic Catalyst and Desymmetrization Agent .” 2017. Thesis, University of Ottawa. Accessed July 09, 2020. http://hdl.handle.net/10393/36609.

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

MLA Handbook (7th Edition):

Jamshidi, Mohammad. “Formaldehyde as a Catalyst: Investigations on the Role of Formaldehyde as a Potential Prebiotic Catalyst and Desymmetrization Agent .” 2017. Web. 09 Jul 2020.

Vancouver:

Jamshidi M. Formaldehyde as a Catalyst: Investigations on the Role of Formaldehyde as a Potential Prebiotic Catalyst and Desymmetrization Agent . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10393/36609.

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

Council of Science Editors:

Jamshidi M. Formaldehyde as a Catalyst: Investigations on the Role of Formaldehyde as a Potential Prebiotic Catalyst and Desymmetrization Agent . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/36609

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


Rochester Institute of Technology

3. Brodsky, Kathy-Jo. The Synthesis and characterization of a BIS(4-(3-(4-Phenoxy)Propionitrile))-N,N'-disalicylidene-1,2-phenylenediamino)zirconium(IV),Zr(Nitrile)2 and the attempted sythesis of Zr(Amine)2 and coordination polymers contaning Zr(dspOH)2.

Degree: School of Chemistry and Materials Science (COS), 1994, Rochester Institute of Technology

  The synthesis of a series of bis(quadridentate)zirconium(IV) complexes, that can be considered as derivatives of the model complex, bis(N,N'-disalicylidene-l,2-phenylenediaminozirconium (IV), Zr(dsp)2, was conducted in… (more)

Subjects/Keywords: Synthetic chemistry

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APA (6th Edition):

Brodsky, K. (1994). The Synthesis and characterization of a BIS(4-(3-(4-Phenoxy)Propionitrile))-N,N'-disalicylidene-1,2-phenylenediamino)zirconium(IV),Zr(Nitrile)2 and the attempted sythesis of Zr(Amine)2 and coordination polymers contaning Zr(dspOH)2. (Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/6045

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):

Brodsky, Kathy-Jo. “The Synthesis and characterization of a BIS(4-(3-(4-Phenoxy)Propionitrile))-N,N'-disalicylidene-1,2-phenylenediamino)zirconium(IV),Zr(Nitrile)2 and the attempted sythesis of Zr(Amine)2 and coordination polymers contaning Zr(dspOH)2.” 1994. Thesis, Rochester Institute of Technology. Accessed July 09, 2020. https://scholarworks.rit.edu/theses/6045.

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

MLA Handbook (7th Edition):

Brodsky, Kathy-Jo. “The Synthesis and characterization of a BIS(4-(3-(4-Phenoxy)Propionitrile))-N,N'-disalicylidene-1,2-phenylenediamino)zirconium(IV),Zr(Nitrile)2 and the attempted sythesis of Zr(Amine)2 and coordination polymers contaning Zr(dspOH)2.” 1994. Web. 09 Jul 2020.

Vancouver:

Brodsky K. The Synthesis and characterization of a BIS(4-(3-(4-Phenoxy)Propionitrile))-N,N'-disalicylidene-1,2-phenylenediamino)zirconium(IV),Zr(Nitrile)2 and the attempted sythesis of Zr(Amine)2 and coordination polymers contaning Zr(dspOH)2. [Internet] [Thesis]. Rochester Institute of Technology; 1994. [cited 2020 Jul 09]. Available from: https://scholarworks.rit.edu/theses/6045.

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

Council of Science Editors:

Brodsky K. The Synthesis and characterization of a BIS(4-(3-(4-Phenoxy)Propionitrile))-N,N'-disalicylidene-1,2-phenylenediamino)zirconium(IV),Zr(Nitrile)2 and the attempted sythesis of Zr(Amine)2 and coordination polymers contaning Zr(dspOH)2. [Thesis]. Rochester Institute of Technology; 1994. Available from: https://scholarworks.rit.edu/theses/6045

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


Boston University

4. Ward, Jessamyn. Surface-enhanced Raman spectroscopy (SERS) for the qualitative analysis of synthetic piperazines.

Degree: MS, Biomedical Forensic Sciences, 2017, Boston University

 Designer drugs are some of the most commonly abused substances in the world. They are synthesized through slight chemical modifications of existing substances, evading the… (more)

Subjects/Keywords: Chemistry; SERS; Synthetic piperazines

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APA (6th Edition):

Ward, J. (2017). Surface-enhanced Raman spectroscopy (SERS) for the qualitative analysis of synthetic piperazines. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/26942

Chicago Manual of Style (16th Edition):

Ward, Jessamyn. “Surface-enhanced Raman spectroscopy (SERS) for the qualitative analysis of synthetic piperazines.” 2017. Masters Thesis, Boston University. Accessed July 09, 2020. http://hdl.handle.net/2144/26942.

MLA Handbook (7th Edition):

Ward, Jessamyn. “Surface-enhanced Raman spectroscopy (SERS) for the qualitative analysis of synthetic piperazines.” 2017. Web. 09 Jul 2020.

Vancouver:

Ward J. Surface-enhanced Raman spectroscopy (SERS) for the qualitative analysis of synthetic piperazines. [Internet] [Masters thesis]. Boston University; 2017. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2144/26942.

Council of Science Editors:

Ward J. Surface-enhanced Raman spectroscopy (SERS) for the qualitative analysis of synthetic piperazines. [Masters Thesis]. Boston University; 2017. Available from: http://hdl.handle.net/2144/26942


University of Texas Southwestern Medical Center

5. Bayeh, Liela Antoinette. Synthetic Studies in the Selective Functionalization of Unsaturated Compounds: From Initial Applications in Medicinal Chemistry to General Applications in Unactivated Systems.

Degree: 2016, University of Texas Southwestern Medical Center

 Medicinal chemistry and reaction development have influenced one another in the field of organic chemistry. The synthesis of therapeutic small molecules often requires the use… (more)

Subjects/Keywords: Alkenes; Catalysis; Chemistry Techniques, Synthetic

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APA (6th Edition):

Bayeh, L. A. (2016). Synthetic Studies in the Selective Functionalization of Unsaturated Compounds: From Initial Applications in Medicinal Chemistry to General Applications in Unactivated Systems. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6135

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):

Bayeh, Liela Antoinette. “Synthetic Studies in the Selective Functionalization of Unsaturated Compounds: From Initial Applications in Medicinal Chemistry to General Applications in Unactivated Systems.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/6135.

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

MLA Handbook (7th Edition):

Bayeh, Liela Antoinette. “Synthetic Studies in the Selective Functionalization of Unsaturated Compounds: From Initial Applications in Medicinal Chemistry to General Applications in Unactivated Systems.” 2016. Web. 09 Jul 2020.

Vancouver:

Bayeh LA. Synthetic Studies in the Selective Functionalization of Unsaturated Compounds: From Initial Applications in Medicinal Chemistry to General Applications in Unactivated Systems. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/6135.

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

Council of Science Editors:

Bayeh LA. Synthetic Studies in the Selective Functionalization of Unsaturated Compounds: From Initial Applications in Medicinal Chemistry to General Applications in Unactivated Systems. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/6135

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


University of Oregon

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

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

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

Subjects/Keywords: Coarctate; Heterocycle; Synthetic chemistry

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Young, Brian. “Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations.” 2013. Doctoral Dissertation, University of Oregon. Accessed July 09, 2020. http://hdl.handle.net/1794/13260.

MLA Handbook (7th Edition):

Young, Brian. “Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations.” 2013. Web. 09 Jul 2020.

Vancouver:

Young B. Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations. [Internet] [Doctoral dissertation]. University of Oregon; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/1794/13260.

Council of Science Editors:

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

7. Ingham, Richard Jeremy. Control tools for flow chemistry processing and their application to the synthesis of bromodomain inhibitors.

Degree: PhD, 2014, University of Cambridge

 Flow chemistry and continuous processing techniques are now frequently used in synthetic laboratories, taking advantage of the ability to contain reactive or hazardous intermediates and… (more)

Subjects/Keywords: Laboratory automation; Flow chemistry; Synthetic chemistry

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APA (6th Edition):

Ingham, R. J. (2014). Control tools for flow chemistry processing and their application to the synthesis of bromodomain inhibitors. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/246534https://www.repository.cam.ac.uk/bitstream/1810/246534/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/246534/6/Thesis.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/246534/7/Thesis.pdf.jpg

Chicago Manual of Style (16th Edition):

Ingham, Richard Jeremy. “Control tools for flow chemistry processing and their application to the synthesis of bromodomain inhibitors.” 2014. Doctoral Dissertation, University of Cambridge. Accessed July 09, 2020. https://www.repository.cam.ac.uk/handle/1810/246534https://www.repository.cam.ac.uk/bitstream/1810/246534/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/246534/6/Thesis.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/246534/7/Thesis.pdf.jpg.

MLA Handbook (7th Edition):

Ingham, Richard Jeremy. “Control tools for flow chemistry processing and their application to the synthesis of bromodomain inhibitors.” 2014. Web. 09 Jul 2020.

Vancouver:

Ingham RJ. Control tools for flow chemistry processing and their application to the synthesis of bromodomain inhibitors. [Internet] [Doctoral dissertation]. University of Cambridge; 2014. [cited 2020 Jul 09]. Available from: https://www.repository.cam.ac.uk/handle/1810/246534https://www.repository.cam.ac.uk/bitstream/1810/246534/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/246534/6/Thesis.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/246534/7/Thesis.pdf.jpg.

Council of Science Editors:

Ingham RJ. Control tools for flow chemistry processing and their application to the synthesis of bromodomain inhibitors. [Doctoral Dissertation]. University of Cambridge; 2014. Available from: https://www.repository.cam.ac.uk/handle/1810/246534https://www.repository.cam.ac.uk/bitstream/1810/246534/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/246534/6/Thesis.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/246534/7/Thesis.pdf.jpg


University of Oxford

8. Ilupeju, John Oluwafemi. Synthesis and use of new chiral DABCO derivatives for asymmetric fluorination.

Degree: PhD, 2012, University of Oxford

 In this thesis, the synthesis, reactivity and enantioselectivity of novel chiral Selectfluor Analogues were investigated. Chapter 1: Discussed is a general introduction to Selectfluor as… (more)

Subjects/Keywords: 547; Chemistry & allied sciences; Synthetic organic chemistry

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APA (6th Edition):

Ilupeju, J. O. (2012). Synthesis and use of new chiral DABCO derivatives for asymmetric fluorination. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:1ee07d47-49ce-4072-a739-c20857d3b468 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588384

Chicago Manual of Style (16th Edition):

Ilupeju, John Oluwafemi. “Synthesis and use of new chiral DABCO derivatives for asymmetric fluorination.” 2012. Doctoral Dissertation, University of Oxford. Accessed July 09, 2020. http://ora.ox.ac.uk/objects/uuid:1ee07d47-49ce-4072-a739-c20857d3b468 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588384.

MLA Handbook (7th Edition):

Ilupeju, John Oluwafemi. “Synthesis and use of new chiral DABCO derivatives for asymmetric fluorination.” 2012. Web. 09 Jul 2020.

Vancouver:

Ilupeju JO. Synthesis and use of new chiral DABCO derivatives for asymmetric fluorination. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2020 Jul 09]. Available from: http://ora.ox.ac.uk/objects/uuid:1ee07d47-49ce-4072-a739-c20857d3b468 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588384.

Council of Science Editors:

Ilupeju JO. Synthesis and use of new chiral DABCO derivatives for asymmetric fluorination. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:1ee07d47-49ce-4072-a739-c20857d3b468 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588384


Youngstown State University

9. Tatebe, Caleb J. Synthesis of Sugar-Derived Esters and Carbamate Compounds.

Degree: MSin Chemistry, Department of Chemistry, 2014, Youngstown State University

 This thesis deals with the synthesis of sugar-derived esters and carbamate compounds. The attempted decomposition of diazo ester sugars is also a topic of this… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Synthetic chemistry; Carbamate; Ester; Organic chemistry

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APA (6th Edition):

Tatebe, C. J. (2014). Synthesis of Sugar-Derived Esters and Carbamate Compounds. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409833972

Chicago Manual of Style (16th Edition):

Tatebe, Caleb J. “Synthesis of Sugar-Derived Esters and Carbamate Compounds.” 2014. Masters Thesis, Youngstown State University. Accessed July 09, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409833972.

MLA Handbook (7th Edition):

Tatebe, Caleb J. “Synthesis of Sugar-Derived Esters and Carbamate Compounds.” 2014. Web. 09 Jul 2020.

Vancouver:

Tatebe CJ. Synthesis of Sugar-Derived Esters and Carbamate Compounds. [Internet] [Masters thesis]. Youngstown State University; 2014. [cited 2020 Jul 09]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409833972.

Council of Science Editors:

Tatebe CJ. Synthesis of Sugar-Derived Esters and Carbamate Compounds. [Masters Thesis]. Youngstown State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409833972

10. Bansal, Priti. Studies on degradation and mineralization of synthetic dyes present in industrial effluents by heterogeneous Photocatalysis; -.

Degree: Chemistry, 2007, INFLIBNET

Industrial effluents detoxification is one of the most challenging global problems. Dyes, phenols, pesticides, fertilizers, detergents, herbicides, surfactants and other synthetic organic compounds are disposed… (more)

Subjects/Keywords: Synthetic Dyes; Mineralization; Heterogeneous Photocatalysis; Chemistry

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APA (6th Edition):

Bansal, P. (2007). Studies on degradation and mineralization of synthetic dyes present in industrial effluents by heterogeneous Photocatalysis; -. (Thesis). INFLIBNET. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/5202

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):

Bansal, Priti. “Studies on degradation and mineralization of synthetic dyes present in industrial effluents by heterogeneous Photocatalysis; -.” 2007. Thesis, INFLIBNET. Accessed July 09, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/5202.

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

MLA Handbook (7th Edition):

Bansal, Priti. “Studies on degradation and mineralization of synthetic dyes present in industrial effluents by heterogeneous Photocatalysis; -.” 2007. Web. 09 Jul 2020.

Vancouver:

Bansal P. Studies on degradation and mineralization of synthetic dyes present in industrial effluents by heterogeneous Photocatalysis; -. [Internet] [Thesis]. INFLIBNET; 2007. [cited 2020 Jul 09]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/5202.

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

Council of Science Editors:

Bansal P. Studies on degradation and mineralization of synthetic dyes present in industrial effluents by heterogeneous Photocatalysis; -. [Thesis]. INFLIBNET; 2007. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/5202

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


University of Cambridge

11. Phillips, Andrew. Studies Towards the Total Synthesis of Patellazole B.

Degree: PhD, 2017, University of Cambridge

 The patellazoles are a family of marine polyketide natural products first isolated from Lissoclinum patella in 1988 by both the Moore and Ireland groups. They… (more)

Subjects/Keywords: Synthetic organic chemistry; total synthesis; natural products

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APA (6th Edition):

Phillips, A. (2017). Studies Towards the Total Synthesis of Patellazole B. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/269364

Chicago Manual of Style (16th Edition):

Phillips, Andrew. “Studies Towards the Total Synthesis of Patellazole B.” 2017. Doctoral Dissertation, University of Cambridge. Accessed July 09, 2020. https://www.repository.cam.ac.uk/handle/1810/269364.

MLA Handbook (7th Edition):

Phillips, Andrew. “Studies Towards the Total Synthesis of Patellazole B.” 2017. Web. 09 Jul 2020.

Vancouver:

Phillips A. Studies Towards the Total Synthesis of Patellazole B. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2020 Jul 09]. Available from: https://www.repository.cam.ac.uk/handle/1810/269364.

Council of Science Editors:

Phillips A. Studies Towards the Total Synthesis of Patellazole B. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/269364


University of Illinois – Chicago

12. Muhammad, Maryam Bint. Synthetic Biology Tools for Polyketide Engineering.

Degree: 2017, University of Illinois – Chicago

 This thesis discusses the advancement of synthetic biology tools for polyketide engineering, specifically in the construction of a genetic device for the biosynthesis of a… (more)

Subjects/Keywords: Synthetic biology; polyketides; fluorine chemistry; Streptomyces

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APA (6th Edition):

Muhammad, M. B. (2017). Synthetic Biology Tools for Polyketide Engineering. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22166

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):

Muhammad, Maryam Bint. “Synthetic Biology Tools for Polyketide Engineering.” 2017. Thesis, University of Illinois – Chicago. Accessed July 09, 2020. http://hdl.handle.net/10027/22166.

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

MLA Handbook (7th Edition):

Muhammad, Maryam Bint. “Synthetic Biology Tools for Polyketide Engineering.” 2017. Web. 09 Jul 2020.

Vancouver:

Muhammad MB. Synthetic Biology Tools for Polyketide Engineering. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10027/22166.

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

Council of Science Editors:

Muhammad MB. Synthetic Biology Tools for Polyketide Engineering. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22166

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


University of Sydney

13. Norman, Alexander Roderick. Catalytic Photoredox Approaches to Reactive Intermediates .

Degree: 2018, University of Sydney

 Photoredox catalysis is a rapidly evolving field enabling chemists to design novel methods for chemical synthesis, under mild and benign conditions. The application of radical… (more)

Subjects/Keywords: Photoredox; Catalysis; Synthetic; Organic; Radical; Chemistry

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APA (6th Edition):

Norman, A. R. (2018). Catalytic Photoredox Approaches to Reactive Intermediates . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/19897

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):

Norman, Alexander Roderick. “Catalytic Photoredox Approaches to Reactive Intermediates .” 2018. Thesis, University of Sydney. Accessed July 09, 2020. http://hdl.handle.net/2123/19897.

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

MLA Handbook (7th Edition):

Norman, Alexander Roderick. “Catalytic Photoredox Approaches to Reactive Intermediates .” 2018. Web. 09 Jul 2020.

Vancouver:

Norman AR. Catalytic Photoredox Approaches to Reactive Intermediates . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2123/19897.

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

Council of Science Editors:

Norman AR. Catalytic Photoredox Approaches to Reactive Intermediates . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/19897

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


University of Minnesota

14. Willoughby, Patrick. Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction.

Degree: Chemistry, 2013, University of Minnesota

 Part I: The salinosporamides are a subset of polyketide-derived marine natural products that have as their key structural feature a fused γ-lactam/β-lactone moiety. These molecules… (more)

Subjects/Keywords: Natural products; Synthetic methodology; Total synthesis; Chemistry

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APA (6th Edition):

Willoughby, P. (2013). Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction. (Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/167685

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):

Willoughby, Patrick. “Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction.” 2013. Thesis, University of Minnesota. Accessed July 09, 2020. http://hdl.handle.net/11299/167685.

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

MLA Handbook (7th Edition):

Willoughby, Patrick. “Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction.” 2013. Web. 09 Jul 2020.

Vancouver:

Willoughby P. Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction. [Internet] [Thesis]. University of Minnesota; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/11299/167685.

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

Council of Science Editors:

Willoughby P. Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction. [Thesis]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/167685

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


University of Melbourne

15. Wiltshire, James Thomas. Design and synthesis of star macromolecular architectures with degradable functionality.

Degree: 2007, University of Melbourne

 Polymers with star shaped architectures represent an interesting class of macromolecule. Core cross-linked star (CCS) polymers in particular have shown potential for use in various… (more)

Subjects/Keywords: polymers; synthetic chemistry

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APA (6th Edition):

Wiltshire, J. T. (2007). Design and synthesis of star macromolecular architectures with degradable functionality. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/39365

Chicago Manual of Style (16th Edition):

Wiltshire, James Thomas. “Design and synthesis of star macromolecular architectures with degradable functionality.” 2007. Doctoral Dissertation, University of Melbourne. Accessed July 09, 2020. http://hdl.handle.net/11343/39365.

MLA Handbook (7th Edition):

Wiltshire, James Thomas. “Design and synthesis of star macromolecular architectures with degradable functionality.” 2007. Web. 09 Jul 2020.

Vancouver:

Wiltshire JT. Design and synthesis of star macromolecular architectures with degradable functionality. [Internet] [Doctoral dissertation]. University of Melbourne; 2007. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/11343/39365.

Council of Science Editors:

Wiltshire JT. Design and synthesis of star macromolecular architectures with degradable functionality. [Doctoral Dissertation]. University of Melbourne; 2007. Available from: http://hdl.handle.net/11343/39365


University of Texas Southwestern Medical Center

16. Butler, John R. Enantioselective Total Synthesis of the Kibdelones.

Degree: PhD, Biological Chemistry, 2012, University of Texas Southwestern Medical Center

 The kibdelones are a family of aromatic polyketides reported in 2006 by Capon and co-workers. These compounds possess potent antibiotic and cytotoxic activities and operate… (more)

Subjects/Keywords: Xanthones; Antineoplastic Agents; Chemistry Techniques, Synthetic

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APA (6th Edition):

Butler, J. R. (2012). Enantioselective Total Synthesis of the Kibdelones. (Doctoral Dissertation). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1016

Chicago Manual of Style (16th Edition):

Butler, John R. “Enantioselective Total Synthesis of the Kibdelones.” 2012. Doctoral Dissertation, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/1016.

MLA Handbook (7th Edition):

Butler, John R. “Enantioselective Total Synthesis of the Kibdelones.” 2012. Web. 09 Jul 2020.

Vancouver:

Butler JR. Enantioselective Total Synthesis of the Kibdelones. [Internet] [Doctoral dissertation]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/1016.

Council of Science Editors:

Butler JR. Enantioselective Total Synthesis of the Kibdelones. [Doctoral Dissertation]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1016


University of Arkansas

17. Spahn, Elizabeth Suzanne. The Large-Scale Synthesis and Asymmetric Hydrosilylations of CuIPhEt, a C2-Symmetric N-Heterocyclic Carbene.

Degree: PhD, 2016, University of Arkansas

  CuIPhEt is a C2-symmetric N-heterocyclic carbene catalyst used in the asymmetric hydrosilylation of a variety of prochiral ketones with good yields and selectivities. The… (more)

Subjects/Keywords: Pure Sciences; Assymetic synthetic; Organic Chemistry

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APA (6th Edition):

Spahn, E. S. (2016). The Large-Scale Synthesis and Asymmetric Hydrosilylations of CuIPhEt, a C2-Symmetric N-Heterocyclic Carbene. (Doctoral Dissertation). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/1693

Chicago Manual of Style (16th Edition):

Spahn, Elizabeth Suzanne. “The Large-Scale Synthesis and Asymmetric Hydrosilylations of CuIPhEt, a C2-Symmetric N-Heterocyclic Carbene.” 2016. Doctoral Dissertation, University of Arkansas. Accessed July 09, 2020. https://scholarworks.uark.edu/etd/1693.

MLA Handbook (7th Edition):

Spahn, Elizabeth Suzanne. “The Large-Scale Synthesis and Asymmetric Hydrosilylations of CuIPhEt, a C2-Symmetric N-Heterocyclic Carbene.” 2016. Web. 09 Jul 2020.

Vancouver:

Spahn ES. The Large-Scale Synthesis and Asymmetric Hydrosilylations of CuIPhEt, a C2-Symmetric N-Heterocyclic Carbene. [Internet] [Doctoral dissertation]. University of Arkansas; 2016. [cited 2020 Jul 09]. Available from: https://scholarworks.uark.edu/etd/1693.

Council of Science Editors:

Spahn ES. The Large-Scale Synthesis and Asymmetric Hydrosilylations of CuIPhEt, a C2-Symmetric N-Heterocyclic Carbene. [Doctoral Dissertation]. University of Arkansas; 2016. Available from: https://scholarworks.uark.edu/etd/1693

18. Swain, Jonathan. Phenylacetylene oligomers as synthetic information molecules.

Degree: PhD, 2018, University of Cambridge

 Nucleic acids store genetic information in the sequence of nucleobases. Through duplex formation and template directed synthesis, the information stored in nucleic acids determines their… (more)

Subjects/Keywords: Phenylacetylene; oligomers; chemistry; synthetic; information; molecules

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APA (6th Edition):

Swain, J. (2018). Phenylacetylene oligomers as synthetic information molecules. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/279084 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753444

Chicago Manual of Style (16th Edition):

Swain, Jonathan. “Phenylacetylene oligomers as synthetic information molecules.” 2018. Doctoral Dissertation, University of Cambridge. Accessed July 09, 2020. https://www.repository.cam.ac.uk/handle/1810/279084 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753444.

MLA Handbook (7th Edition):

Swain, Jonathan. “Phenylacetylene oligomers as synthetic information molecules.” 2018. Web. 09 Jul 2020.

Vancouver:

Swain J. Phenylacetylene oligomers as synthetic information molecules. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2020 Jul 09]. Available from: https://www.repository.cam.ac.uk/handle/1810/279084 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753444.

Council of Science Editors:

Swain J. Phenylacetylene oligomers as synthetic information molecules. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/279084 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753444


Eastern Illinois University

19. Priyadarshana, Lokugama Widanelage Vidula. Developing a Basket-Shaped Host Molecule Based on P-Tert-Butylcalix[4]arene Featuring Urea Groups for Encapsulating Volatile Guest Molecules.

Degree: MS, Chemistry and Biochemistry, 2019, Eastern Illinois University

  Molecular baskets are a group of synthetic host molecules which are designed to govern the inclusion of small guest molecules. The basic structural features… (more)

Subjects/Keywords: Molecular baskets; synthetic host molecules; Physical Chemistry

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APA (6th Edition):

Priyadarshana, L. W. V. (2019). Developing a Basket-Shaped Host Molecule Based on P-Tert-Butylcalix[4]arene Featuring Urea Groups for Encapsulating Volatile Guest Molecules. (Masters Thesis). Eastern Illinois University. Retrieved from https://thekeep.eiu.edu/theses/4467

Chicago Manual of Style (16th Edition):

Priyadarshana, Lokugama Widanelage Vidula. “Developing a Basket-Shaped Host Molecule Based on P-Tert-Butylcalix[4]arene Featuring Urea Groups for Encapsulating Volatile Guest Molecules.” 2019. Masters Thesis, Eastern Illinois University. Accessed July 09, 2020. https://thekeep.eiu.edu/theses/4467.

MLA Handbook (7th Edition):

Priyadarshana, Lokugama Widanelage Vidula. “Developing a Basket-Shaped Host Molecule Based on P-Tert-Butylcalix[4]arene Featuring Urea Groups for Encapsulating Volatile Guest Molecules.” 2019. Web. 09 Jul 2020.

Vancouver:

Priyadarshana LWV. Developing a Basket-Shaped Host Molecule Based on P-Tert-Butylcalix[4]arene Featuring Urea Groups for Encapsulating Volatile Guest Molecules. [Internet] [Masters thesis]. Eastern Illinois University; 2019. [cited 2020 Jul 09]. Available from: https://thekeep.eiu.edu/theses/4467.

Council of Science Editors:

Priyadarshana LWV. Developing a Basket-Shaped Host Molecule Based on P-Tert-Butylcalix[4]arene Featuring Urea Groups for Encapsulating Volatile Guest Molecules. [Masters Thesis]. Eastern Illinois University; 2019. Available from: https://thekeep.eiu.edu/theses/4467


Texas State University – San Marcos

20. Taylor, Brandie C. Glucuronide Prodrug of a Naturally Derived Cytotoxic Product.

Degree: MS, Biochemistry, 2019, Texas State University – San Marcos

 African Potato (Hypoxis hemerocallidea) is utilized as a medicinal plant in South Africa to treat disorders such as cancer, prostate hyperplasia, and cardiac disease. The… (more)

Subjects/Keywords: Synthetic Chemistry; Organic Chemistry; Glucuronide; Cancer – Treatment – Research; Chemistry, Organic; Hpoxidaceae

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APA (6th Edition):

Taylor, B. C. (2019). Glucuronide Prodrug of a Naturally Derived Cytotoxic Product. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/7991

Chicago Manual of Style (16th Edition):

Taylor, Brandie C. “Glucuronide Prodrug of a Naturally Derived Cytotoxic Product.” 2019. Masters Thesis, Texas State University – San Marcos. Accessed July 09, 2020. https://digital.library.txstate.edu/handle/10877/7991.

MLA Handbook (7th Edition):

Taylor, Brandie C. “Glucuronide Prodrug of a Naturally Derived Cytotoxic Product.” 2019. Web. 09 Jul 2020.

Vancouver:

Taylor BC. Glucuronide Prodrug of a Naturally Derived Cytotoxic Product. [Internet] [Masters thesis]. Texas State University – San Marcos; 2019. [cited 2020 Jul 09]. Available from: https://digital.library.txstate.edu/handle/10877/7991.

Council of Science Editors:

Taylor BC. Glucuronide Prodrug of a Naturally Derived Cytotoxic Product. [Masters Thesis]. Texas State University – San Marcos; 2019. Available from: https://digital.library.txstate.edu/handle/10877/7991


University of Cambridge

21. Lau, Shing Hing. Organic Synthesis: Taming Chemistry using Enabling Technologies.

Degree: PhD, 2018, University of Cambridge

 This thesis describes the application of flow chemistry to discovery and development of medicinal compound synthesis and new chemical methodologies respectively. It is divided into… (more)

Subjects/Keywords: Synthetic Organic Chemistry; Flow Chemistry; API Syntheses; Chemistry

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APA (6th Edition):

Lau, S. H. (2018). Organic Synthesis: Taming Chemistry using Enabling Technologies. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/273347https://www.repository.cam.ac.uk/bitstream/1810/273347/2/3bda936b-67a7-41c8-9361-cdda5597f874_confirmations.txt

Chicago Manual of Style (16th Edition):

Lau, Shing Hing. “Organic Synthesis: Taming Chemistry using Enabling Technologies.” 2018. Doctoral Dissertation, University of Cambridge. Accessed July 09, 2020. https://www.repository.cam.ac.uk/handle/1810/273347https://www.repository.cam.ac.uk/bitstream/1810/273347/2/3bda936b-67a7-41c8-9361-cdda5597f874_confirmations.txt.

MLA Handbook (7th Edition):

Lau, Shing Hing. “Organic Synthesis: Taming Chemistry using Enabling Technologies.” 2018. Web. 09 Jul 2020.

Vancouver:

Lau SH. Organic Synthesis: Taming Chemistry using Enabling Technologies. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2020 Jul 09]. Available from: https://www.repository.cam.ac.uk/handle/1810/273347https://www.repository.cam.ac.uk/bitstream/1810/273347/2/3bda936b-67a7-41c8-9361-cdda5597f874_confirmations.txt.

Council of Science Editors:

Lau SH. Organic Synthesis: Taming Chemistry using Enabling Technologies. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/273347https://www.repository.cam.ac.uk/bitstream/1810/273347/2/3bda936b-67a7-41c8-9361-cdda5597f874_confirmations.txt


UCLA

22. Simmons, Bryan Joseph. Nickel-Catalyzed Reactions of Amides and New Methods for the Synthesis of Nitrogen-Containing Heterocycles.

Degree: Chemistry, 2019, UCLA

 This dissertation is divided into two main themes concerning transition metal-mediatedmethodologies and the synthesis of nitrogen-containing heterocycles. The first part of thisdissertation focuses on the… (more)

Subjects/Keywords: Organic chemistry; Amides; Heterocycles; Nitrogen; Organic Chemistry; Synthetic Chemistry; Transition Metals

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APA (6th Edition):

Simmons, B. J. (2019). Nickel-Catalyzed Reactions of Amides and New Methods for the Synthesis of Nitrogen-Containing Heterocycles. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/2f21p451

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):

Simmons, Bryan Joseph. “Nickel-Catalyzed Reactions of Amides and New Methods for the Synthesis of Nitrogen-Containing Heterocycles.” 2019. Thesis, UCLA. Accessed July 09, 2020. http://www.escholarship.org/uc/item/2f21p451.

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

MLA Handbook (7th Edition):

Simmons, Bryan Joseph. “Nickel-Catalyzed Reactions of Amides and New Methods for the Synthesis of Nitrogen-Containing Heterocycles.” 2019. Web. 09 Jul 2020.

Vancouver:

Simmons BJ. Nickel-Catalyzed Reactions of Amides and New Methods for the Synthesis of Nitrogen-Containing Heterocycles. [Internet] [Thesis]. UCLA; 2019. [cited 2020 Jul 09]. Available from: http://www.escholarship.org/uc/item/2f21p451.

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

Council of Science Editors:

Simmons BJ. Nickel-Catalyzed Reactions of Amides and New Methods for the Synthesis of Nitrogen-Containing Heterocycles. [Thesis]. UCLA; 2019. Available from: http://www.escholarship.org/uc/item/2f21p451

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


University of Michigan

23. Hinds, Elsa. Development of Strategies for the Synthesis of Heterocycles and Carbocycles; and Investigation of Chemistry Course Placement on Undergraduate Students.

Degree: PhD, Chemistry, 2018, University of Michigan

 Heterocycles and carbocycles are important motifs in synthetic chemistry as they are present in many natural products and pharmaceuticals and possess biological activities. Among other… (more)

Subjects/Keywords: synthetic organic chemistry; chemistry education research; Chemistry; Science

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APA (6th Edition):

Hinds, E. (2018). Development of Strategies for the Synthesis of Heterocycles and Carbocycles; and Investigation of Chemistry Course Placement on Undergraduate Students. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/150019

Chicago Manual of Style (16th Edition):

Hinds, Elsa. “Development of Strategies for the Synthesis of Heterocycles and Carbocycles; and Investigation of Chemistry Course Placement on Undergraduate Students.” 2018. Doctoral Dissertation, University of Michigan. Accessed July 09, 2020. http://hdl.handle.net/2027.42/150019.

MLA Handbook (7th Edition):

Hinds, Elsa. “Development of Strategies for the Synthesis of Heterocycles and Carbocycles; and Investigation of Chemistry Course Placement on Undergraduate Students.” 2018. Web. 09 Jul 2020.

Vancouver:

Hinds E. Development of Strategies for the Synthesis of Heterocycles and Carbocycles; and Investigation of Chemistry Course Placement on Undergraduate Students. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2027.42/150019.

Council of Science Editors:

Hinds E. Development of Strategies for the Synthesis of Heterocycles and Carbocycles; and Investigation of Chemistry Course Placement on Undergraduate Students. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/150019


University of California – Irvine

24. Sizemore, Nicholas Blandford Luke. Intramolecular Diels-Alder Reactions in Organic Synthesis.

Degree: Chemistry, 2014, University of California – Irvine

 Intramolecular Diels-Alder (IMDA) reactions are an important class of reactions in synthetic organic chemistry for the rapid construction of polycyclic frameworks. Three classes of IMDA… (more)

Subjects/Keywords: Chemistry; Organic chemistry; computational chemistry; Intramolecular Diels-Alder reaction; maoecrystal Z; palhinine; synthetic organic chemistry

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APA (6th Edition):

Sizemore, N. B. L. (2014). Intramolecular Diels-Alder Reactions in Organic Synthesis. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/9r20m5s6

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):

Sizemore, Nicholas Blandford Luke. “Intramolecular Diels-Alder Reactions in Organic Synthesis.” 2014. Thesis, University of California – Irvine. Accessed July 09, 2020. http://www.escholarship.org/uc/item/9r20m5s6.

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

MLA Handbook (7th Edition):

Sizemore, Nicholas Blandford Luke. “Intramolecular Diels-Alder Reactions in Organic Synthesis.” 2014. Web. 09 Jul 2020.

Vancouver:

Sizemore NBL. Intramolecular Diels-Alder Reactions in Organic Synthesis. [Internet] [Thesis]. University of California – Irvine; 2014. [cited 2020 Jul 09]. Available from: http://www.escholarship.org/uc/item/9r20m5s6.

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

Council of Science Editors:

Sizemore NBL. Intramolecular Diels-Alder Reactions in Organic Synthesis. [Thesis]. University of California – Irvine; 2014. Available from: http://www.escholarship.org/uc/item/9r20m5s6

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


University of Oxford

25. Arif, Tanzeel. Studies towards the stereoselective synthesis of alkenes.

Degree: PhD, 2011, University of Oxford

 The work presented in this thesis mainly describes the development of new reactions of β-lithiooxyphosphonium ylides to access stereodefined substituted alkenes in a highly convergent… (more)

Subjects/Keywords: 547.4; Chemistry & allied sciences; Organic chemistry; Organic synthesis; Organometallic Chemistry; Synthetic organic chemistry

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APA (6th Edition):

Arif, T. (2011). Studies towards the stereoselective synthesis of alkenes. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:7c1fffe2-1bf5-4c8c-bfb7-d46dd4a68342 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543045

Chicago Manual of Style (16th Edition):

Arif, Tanzeel. “Studies towards the stereoselective synthesis of alkenes.” 2011. Doctoral Dissertation, University of Oxford. Accessed July 09, 2020. http://ora.ox.ac.uk/objects/uuid:7c1fffe2-1bf5-4c8c-bfb7-d46dd4a68342 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543045.

MLA Handbook (7th Edition):

Arif, Tanzeel. “Studies towards the stereoselective synthesis of alkenes.” 2011. Web. 09 Jul 2020.

Vancouver:

Arif T. Studies towards the stereoselective synthesis of alkenes. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2020 Jul 09]. Available from: http://ora.ox.ac.uk/objects/uuid:7c1fffe2-1bf5-4c8c-bfb7-d46dd4a68342 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543045.

Council of Science Editors:

Arif T. Studies towards the stereoselective synthesis of alkenes. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:7c1fffe2-1bf5-4c8c-bfb7-d46dd4a68342 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543045


University of Oxford

26. Pearson, Jem M. Hydrogen-bonding motifs for non-covalent synthesis.

Degree: PhD, 2013, University of Oxford

 This work describes the design and synthesis of a set of four organic molecules that are intended to hydrogen-bond to each other in a pairwise… (more)

Subjects/Keywords: 541; Organic chemistry; Organic synthesis; Supramolecular chemistry; Synthetic organic chemistry; chemistry; synthesis; hydrogen-bond; supramolecular

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APA (6th Edition):

Pearson, J. M. (2013). Hydrogen-bonding motifs for non-covalent synthesis. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:f0630898-35b4-4c74-bc31-dfd252c2ee26 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627783

Chicago Manual of Style (16th Edition):

Pearson, Jem M. “Hydrogen-bonding motifs for non-covalent synthesis.” 2013. Doctoral Dissertation, University of Oxford. Accessed July 09, 2020. http://ora.ox.ac.uk/objects/uuid:f0630898-35b4-4c74-bc31-dfd252c2ee26 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627783.

MLA Handbook (7th Edition):

Pearson, Jem M. “Hydrogen-bonding motifs for non-covalent synthesis.” 2013. Web. 09 Jul 2020.

Vancouver:

Pearson JM. Hydrogen-bonding motifs for non-covalent synthesis. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jul 09]. Available from: http://ora.ox.ac.uk/objects/uuid:f0630898-35b4-4c74-bc31-dfd252c2ee26 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627783.

Council of Science Editors:

Pearson JM. Hydrogen-bonding motifs for non-covalent synthesis. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:f0630898-35b4-4c74-bc31-dfd252c2ee26 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627783


Temple University

27. Chatare, Vijay K. METHODOLOGY AND NATURAL PRODUCT SYNTEHSIS: (A) NOVEL GLYCOSYL DONORS; (B) N-SULFINYL METALLODIENAMINES AND THEIR APPLICATION TO THE TOTAL SYNTHESIS OF (–)-ALBOCYCLINE.

Degree: PhD, 2017, Temple University

Chemistry

My research involved in two different areas, development of novel glycosylation methodology and scope in oligosaccharide synthesis. A new scaffold for antibiotic development targeting… (more)

Subjects/Keywords: Organic chemistry;

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APA (6th Edition):

Chatare, V. K. (2017). METHODOLOGY AND NATURAL PRODUCT SYNTEHSIS: (A) NOVEL GLYCOSYL DONORS; (B) N-SULFINYL METALLODIENAMINES AND THEIR APPLICATION TO THE TOTAL SYNTHESIS OF (–)-ALBOCYCLINE. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,456762

Chicago Manual of Style (16th Edition):

Chatare, Vijay K. “METHODOLOGY AND NATURAL PRODUCT SYNTEHSIS: (A) NOVEL GLYCOSYL DONORS; (B) N-SULFINYL METALLODIENAMINES AND THEIR APPLICATION TO THE TOTAL SYNTHESIS OF (–)-ALBOCYCLINE.” 2017. Doctoral Dissertation, Temple University. Accessed July 09, 2020. http://digital.library.temple.edu/u?/p245801coll10,456762.

MLA Handbook (7th Edition):

Chatare, Vijay K. “METHODOLOGY AND NATURAL PRODUCT SYNTEHSIS: (A) NOVEL GLYCOSYL DONORS; (B) N-SULFINYL METALLODIENAMINES AND THEIR APPLICATION TO THE TOTAL SYNTHESIS OF (–)-ALBOCYCLINE.” 2017. Web. 09 Jul 2020.

Vancouver:

Chatare VK. METHODOLOGY AND NATURAL PRODUCT SYNTEHSIS: (A) NOVEL GLYCOSYL DONORS; (B) N-SULFINYL METALLODIENAMINES AND THEIR APPLICATION TO THE TOTAL SYNTHESIS OF (–)-ALBOCYCLINE. [Internet] [Doctoral dissertation]. Temple University; 2017. [cited 2020 Jul 09]. Available from: http://digital.library.temple.edu/u?/p245801coll10,456762.

Council of Science Editors:

Chatare VK. METHODOLOGY AND NATURAL PRODUCT SYNTEHSIS: (A) NOVEL GLYCOSYL DONORS; (B) N-SULFINYL METALLODIENAMINES AND THEIR APPLICATION TO THE TOTAL SYNTHESIS OF (–)-ALBOCYCLINE. [Doctoral Dissertation]. Temple University; 2017. Available from: http://digital.library.temple.edu/u?/p245801coll10,456762


The Ohio State University

28. Dewese, Kendra R. Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes.

Degree: PhD, Chemistry, 2016, The Ohio State University

 The catalysis of organic reactions by metal complexes is an effective way to improve atom economy and environmental friendliness for many synthetic transformations. Particularly, the… (more)

Subjects/Keywords: Organic Chemistry; Cobalt-Catalyzed Hydrofunctionalization; 1,3-Dienes; organic chemistry; synthetic transformations

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

APA (6th Edition):

Dewese, K. R. (2016). Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1471783775

Chicago Manual of Style (16th Edition):

Dewese, Kendra R. “Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes.” 2016. Doctoral Dissertation, The Ohio State University. Accessed July 09, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1471783775.

MLA Handbook (7th Edition):

Dewese, Kendra R. “Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes.” 2016. Web. 09 Jul 2020.

Vancouver:

Dewese KR. Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2020 Jul 09]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1471783775.

Council of Science Editors:

Dewese KR. Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1471783775

29. Dhonde M G. Synthetic and Structural Chemistry of N Glucosylated Nitrogen and Sulphur Containing 5 and 6 Membered Heterocyclic Compounds;.

Degree: Science, 2014, Sant Gadge Baba Amravati University

None newline

Advisors/Committee Members: Deshmukh S P.

Subjects/Keywords: Chemistry Synthetic and Structural Chemistry

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

APA (6th Edition):

G, D. M. (2014). Synthetic and Structural Chemistry of N Glucosylated Nitrogen and Sulphur Containing 5 and 6 Membered Heterocyclic Compounds;. (Thesis). Sant Gadge Baba Amravati University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19788

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):

G, Dhonde M. “Synthetic and Structural Chemistry of N Glucosylated Nitrogen and Sulphur Containing 5 and 6 Membered Heterocyclic Compounds;.” 2014. Thesis, Sant Gadge Baba Amravati University. Accessed July 09, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/19788.

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

MLA Handbook (7th Edition):

G, Dhonde M. “Synthetic and Structural Chemistry of N Glucosylated Nitrogen and Sulphur Containing 5 and 6 Membered Heterocyclic Compounds;.” 2014. Web. 09 Jul 2020.

Vancouver:

G DM. Synthetic and Structural Chemistry of N Glucosylated Nitrogen and Sulphur Containing 5 and 6 Membered Heterocyclic Compounds;. [Internet] [Thesis]. Sant Gadge Baba Amravati University; 2014. [cited 2020 Jul 09]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19788.

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

Council of Science Editors:

G DM. Synthetic and Structural Chemistry of N Glucosylated Nitrogen and Sulphur Containing 5 and 6 Membered Heterocyclic Compounds;. [Thesis]. Sant Gadge Baba Amravati University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19788

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


University of Oxford

30. Baker, David Bawden. Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C.

Degree: PhD, 2014, University of Oxford

 The Heck reaction has become a fundamental reaction for synthetic organic chemists over the last half century and is utilised heavily in the fine chemical… (more)

Subjects/Keywords: 547; Organic chemistry; Organic synthesis; Synthetic organic chemistry; Heck reaction; Pyridines

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

APA (6th Edition):

Baker, D. B. (2014). Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:09765f4e-83b9-4bb6-9130-7da3520752e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627840

Chicago Manual of Style (16th Edition):

Baker, David Bawden. “Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C.” 2014. Doctoral Dissertation, University of Oxford. Accessed July 09, 2020. http://ora.ox.ac.uk/objects/uuid:09765f4e-83b9-4bb6-9130-7da3520752e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627840.

MLA Handbook (7th Edition):

Baker, David Bawden. “Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C.” 2014. Web. 09 Jul 2020.

Vancouver:

Baker DB. Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jul 09]. Available from: http://ora.ox.ac.uk/objects/uuid:09765f4e-83b9-4bb6-9130-7da3520752e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627840.

Council of Science Editors:

Baker DB. Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:09765f4e-83b9-4bb6-9130-7da3520752e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627840

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