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You searched for subject:(Synthetic chemistry). Showing records 1 – 30 of 293 total matches.

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University of Edinburgh

1. O'Neill, William. New and novel cyclisation reactions of imidoylketenes.

Degree: PhD, 2009, University of Edinburgh

 The effect of scale on the conversion to products in flash vacuum pyrolysis experiments was studied using four model reactions. Overall, conversion was dependent on… (more)

Subjects/Keywords: 547.6; Chemistry; Synthetic chemistry

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APA (6th Edition):

O'Neill, W. (2009). New and novel cyclisation reactions of imidoylketenes. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/3124

Chicago Manual of Style (16th Edition):

O'Neill, William. “New and novel cyclisation reactions of imidoylketenes.” 2009. Doctoral Dissertation, University of Edinburgh. Accessed December 15, 2019. http://hdl.handle.net/1842/3124.

MLA Handbook (7th Edition):

O'Neill, William. “New and novel cyclisation reactions of imidoylketenes.” 2009. Web. 15 Dec 2019.

Vancouver:

O'Neill W. New and novel cyclisation reactions of imidoylketenes. [Internet] [Doctoral dissertation]. University of Edinburgh; 2009. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/1842/3124.

Council of Science Editors:

O'Neill W. New and novel cyclisation reactions of imidoylketenes. [Doctoral Dissertation]. University of Edinburgh; 2009. Available from: http://hdl.handle.net/1842/3124


Texas State University – San Marcos

2. 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

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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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Taylor BC. Glucuronide Prodrug of a Naturally Derived Cytotoxic Product. [Internet] [Masters thesis]. Texas State University – San Marcos; 2019. [cited 2019 Dec 15]. 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

3. 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 (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 December 15, 2019. 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. 15 Dec 2019.

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 2019 Dec 15]. 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

4. 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 December 15, 2019. 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. 15 Dec 2019.

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 2019 Dec 15]. 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


University of Oregon

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

Degree: 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. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/13260

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):

Young, Brian. “Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations.” 2013. Thesis, University of Oregon. Accessed December 15, 2019. http://hdl.handle.net/1794/13260.

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

MLA Handbook (7th Edition):

Young, Brian. “Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations.” 2013. Web. 15 Dec 2019.

Vancouver:

Young B. Synthesis of Aromatic Heterocycles via Pericyclic and Coarctate Cyclizations. [Internet] [Thesis]. University of Oregon; 2013. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/1794/13260.

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

Council of Science Editors:

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

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


Rochester Institute of Technology

6. 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 December 15, 2019. 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. 15 Dec 2019.

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 2019 Dec 15]. 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

7. 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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Ward J. Surface-enhanced Raman spectroscopy (SERS) for the qualitative analysis of synthetic piperazines. [Internet] [Masters thesis]. Boston University; 2017. [cited 2019 Dec 15]. 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

8. 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 December 15, 2019. 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. 15 Dec 2019.

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 2019 Dec 15]. 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 Oxford

9. 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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Ilupeju JO. Synthesis and use of new chiral DABCO derivatives for asymmetric fluorination. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2019 Dec 15]. 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

10. 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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Tatebe CJ. Synthesis of Sugar-Derived Esters and Carbamate Compounds. [Internet] [Masters thesis]. Youngstown State University; 2014. [cited 2019 Dec 15]. 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

11. 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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Bansal P. Studies on degradation and mineralization of synthetic dyes present in industrial effluents by heterogeneous Photocatalysis; -. [Internet] [Thesis]. INFLIBNET; 2007. [cited 2019 Dec 15]. 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 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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Muhammad MB. Synthetic Biology Tools for Polyketide Engineering. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Dec 15]. 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 Arkansas

13. 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 December 15, 2019. 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. 15 Dec 2019.

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 2019 Dec 15]. 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


University of Melbourne

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

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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Wiltshire JT. Design and synthesis of star macromolecular architectures with degradable functionality. [Internet] [Doctoral dissertation]. University of Melbourne; 2007. [cited 2019 Dec 15]. 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 Cambridge

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

Degree: 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 . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/269364

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):

Phillips, Andrew. “Studies Towards the Total Synthesis of Patellazole B .” 2017. Thesis, University of Cambridge. Accessed December 15, 2019. https://www.repository.cam.ac.uk/handle/1810/269364.

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

MLA Handbook (7th Edition):

Phillips, Andrew. “Studies Towards the Total Synthesis of Patellazole B .” 2017. Web. 15 Dec 2019.

Vancouver:

Phillips A. Studies Towards the Total Synthesis of Patellazole B . [Internet] [Thesis]. University of Cambridge; 2017. [cited 2019 Dec 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/269364.

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

Council of Science Editors:

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

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


University of Cambridge

16. 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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Swain J. Phenylacetylene oligomers as synthetic information molecules. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Dec 15]. 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


University of Cambridge

17. 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 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744298

Chicago Manual of Style (16th Edition):

Phillips, Andrew. “Studies towards the total synthesis of patellazole B.” 2017. Doctoral Dissertation, University of Cambridge. Accessed December 15, 2019. https://www.repository.cam.ac.uk/handle/1810/269364 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744298.

MLA Handbook (7th Edition):

Phillips, Andrew. “Studies towards the total synthesis of patellazole B.” 2017. Web. 15 Dec 2019.

Vancouver:

Phillips A. Studies towards the total synthesis of patellazole B. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2019 Dec 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/269364 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744298.

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 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744298


University of Minnesota

18. 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 December 15, 2019. 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. 15 Dec 2019.

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 2019 Dec 15]. 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 Texas Southwestern Medical Center

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

Degree: 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. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1016

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):

Butler, John R. “Enantioselective Total Synthesis of the Kibdelones.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed December 15, 2019. http://hdl.handle.net/2152.5/1016.

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

MLA Handbook (7th Edition):

Butler, John R. “Enantioselective Total Synthesis of the Kibdelones.” 2012. Web. 15 Dec 2019.

Vancouver:

Butler JR. Enantioselective Total Synthesis of the Kibdelones. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2152.5/1016.

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

Council of Science Editors:

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

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


Eastern Illinois University

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

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 December 15, 2019. 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. 15 Dec 2019.

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 2019 Dec 15]. 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


University of Sydney

21. 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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Norman AR. Catalytic Photoredox Approaches to Reactive Intermediates . [Internet] [Thesis]. University of Sydney; 2018. [cited 2019 Dec 15]. 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 Cambridge

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

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/1810/273347 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744550

Chicago Manual of Style (16th Edition):

Lau, Shing Hing. “Organic synthesis : taming chemistry using enabling technologies.” 2018. Doctoral Dissertation, University of Cambridge. Accessed December 15, 2019. https://www.repository.cam.ac.uk/handle/1810/273347 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744550.

MLA Handbook (7th Edition):

Lau, Shing Hing. “Organic synthesis : taming chemistry using enabling technologies.” 2018. Web. 15 Dec 2019.

Vancouver:

Lau SH. Organic synthesis : taming chemistry using enabling technologies. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Dec 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/273347 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744550.

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/1810/273347 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744550


University of Cambridge

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

Degree: 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 . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/273347

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):

Lau, Shing Hing. “Organic Synthesis: Taming Chemistry using Enabling Technologies .” 2018. Thesis, University of Cambridge. Accessed December 15, 2019. https://www.repository.cam.ac.uk/handle/1810/273347.

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

MLA Handbook (7th Edition):

Lau, Shing Hing. “Organic Synthesis: Taming Chemistry using Enabling Technologies .” 2018. Web. 15 Dec 2019.

Vancouver:

Lau SH. Organic Synthesis: Taming Chemistry using Enabling Technologies . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Dec 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/273347.

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

Council of Science Editors:

Lau SH. Organic Synthesis: Taming Chemistry using Enabling Technologies . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/273347

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


UCLA

24. 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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Simmons BJ. Nickel-Catalyzed Reactions of Amides and New Methods for the Synthesis of Nitrogen-Containing Heterocycles. [Internet] [Thesis]. UCLA; 2019. [cited 2019 Dec 15]. 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

25. 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 December 15, 2019. 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. 15 Dec 2019.

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 2019 Dec 15]. 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 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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Pearson JM. Hydrogen-bonding motifs for non-covalent synthesis. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Dec 15]. 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


University of Oxford

27. 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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Arif T. Studies towards the stereoselective synthesis of alkenes. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Dec 15]. 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 California – Irvine

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

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 December 15, 2019. 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. 15 Dec 2019.

Vancouver:

Sizemore NBL. Intramolecular Diels-Alder Reactions in Organic Synthesis. [Internet] [Thesis]. University of California – Irvine; 2014. [cited 2019 Dec 15]. 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

29. 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 December 15, 2019. 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. 15 Dec 2019.

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 2019 Dec 15]. 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


Temple University

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

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 December 15, 2019. 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. 15 Dec 2019.

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 2019 Dec 15]. 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

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