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You searched for subject:(Synthetic organic chemistry). Showing records 1 – 30 of 147 total matches.

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Texas State University – San Marcos

1. 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 November 17, 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. 17 Nov 2019.

Vancouver:

Taylor BC. Glucuronide Prodrug of a Naturally Derived Cytotoxic Product. [Internet] [Masters thesis]. Texas State University – San Marcos; 2019. [cited 2019 Nov 17]. 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 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 November 17, 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. 17 Nov 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 Nov 17]. 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 Oxford

3. 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 November 17, 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. 17 Nov 2019.

Vancouver:

Ilupeju JO. Synthesis and use of new chiral DABCO derivatives for asymmetric fluorination. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2019 Nov 17]. 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

4. 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 November 17, 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. 17 Nov 2019.

Vancouver:

Tatebe CJ. Synthesis of Sugar-Derived Esters and Carbamate Compounds. [Internet] [Masters thesis]. Youngstown State University; 2014. [cited 2019 Nov 17]. 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


University of Oxford

5. 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 (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 November 17, 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. 17 Nov 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 Nov 17]. 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


UCLA

6. 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 November 17, 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. 17 Nov 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 Nov 17]. 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 Arkansas

7. 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 November 17, 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. 17 Nov 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 Nov 17]. 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 Cambridge

8. 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 November 17, 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. 17 Nov 2019.

Vancouver:

Phillips A. Studies Towards the Total Synthesis of Patellazole B . [Internet] [Thesis]. University of Cambridge; 2017. [cited 2019 Nov 17]. 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

9. 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 November 17, 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. 17 Nov 2019.

Vancouver:

Phillips A. Studies towards the total synthesis of patellazole B. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2019 Nov 17]. 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 Sydney

10. 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 November 17, 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. 17 Nov 2019.

Vancouver:

Norman AR. Catalytic Photoredox Approaches to Reactive Intermediates . [Internet] [Thesis]. University of Sydney; 2018. [cited 2019 Nov 17]. 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 Oxford

11. 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 November 17, 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. 17 Nov 2019.

Vancouver:

Pearson JM. Hydrogen-bonding motifs for non-covalent synthesis. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Nov 17]. 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

12. 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 November 17, 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. 17 Nov 2019.

Vancouver:

Arif T. Studies towards the stereoselective synthesis of alkenes. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Nov 17]. 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


The Ohio State University

13. 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 (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 November 17, 2019. 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. 17 Nov 2019.

Vancouver:

Dewese KR. Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2019 Nov 17]. 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


University of Oregon

14. White, Brittany. The Synthesis of Functionalized Cycloparaphenylenes as Novel Biocompatible Fluorescent Probes and Organic Materials.

Degree: 2019, University of Oregon

 Conjugated macrocycles have emerged as novel structural motifs that modulate the electronic properties of organic molecules because of their strained and contorted structures. Cycloparaphenylenes, known… (more)

Subjects/Keywords: Biocompatible fluorophores; Nanohoops; Organic materials; Physical organic chemistry; Synthetic chemistry

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APA (6th Edition):

White, B. (2019). The Synthesis of Functionalized Cycloparaphenylenes as Novel Biocompatible Fluorescent Probes and Organic Materials. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/24521

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):

White, Brittany. “The Synthesis of Functionalized Cycloparaphenylenes as Novel Biocompatible Fluorescent Probes and Organic Materials.” 2019. Thesis, University of Oregon. Accessed November 17, 2019. http://hdl.handle.net/1794/24521.

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

MLA Handbook (7th Edition):

White, Brittany. “The Synthesis of Functionalized Cycloparaphenylenes as Novel Biocompatible Fluorescent Probes and Organic Materials.” 2019. Web. 17 Nov 2019.

Vancouver:

White B. The Synthesis of Functionalized Cycloparaphenylenes as Novel Biocompatible Fluorescent Probes and Organic Materials. [Internet] [Thesis]. University of Oregon; 2019. [cited 2019 Nov 17]. Available from: http://hdl.handle.net/1794/24521.

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

Council of Science Editors:

White B. The Synthesis of Functionalized Cycloparaphenylenes as Novel Biocompatible Fluorescent Probes and Organic Materials. [Thesis]. University of Oregon; 2019. Available from: http://hdl.handle.net/1794/24521

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


University of Oxford

15. Hawkins, Alison. Studies towards the total synthesis of manzamine A.

Degree: PhD, 2013, University of Oxford

 This thesis describes studies towards the total synthesis of manzamine A (9), a marine alkaloid. Two routes are presented. The first route applied a novel… (more)

Subjects/Keywords: 547; Organic synthesis; Organic chemistry; Natural products; Chemistry & allied sciences; Synthetic organic chemistry

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APA (6th Edition):

Hawkins, A. (2013). Studies towards the total synthesis of manzamine A. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:0ca64b5d-bc7c-4624-b9c2-4b5f7b6967e3 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581268

Chicago Manual of Style (16th Edition):

Hawkins, Alison. “Studies towards the total synthesis of manzamine A.” 2013. Doctoral Dissertation, University of Oxford. Accessed November 17, 2019. http://ora.ox.ac.uk/objects/uuid:0ca64b5d-bc7c-4624-b9c2-4b5f7b6967e3 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581268.

MLA Handbook (7th Edition):

Hawkins, Alison. “Studies towards the total synthesis of manzamine A.” 2013. Web. 17 Nov 2019.

Vancouver:

Hawkins A. Studies towards the total synthesis of manzamine A. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Nov 17]. Available from: http://ora.ox.ac.uk/objects/uuid:0ca64b5d-bc7c-4624-b9c2-4b5f7b6967e3 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581268.

Council of Science Editors:

Hawkins A. Studies towards the total synthesis of manzamine A. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:0ca64b5d-bc7c-4624-b9c2-4b5f7b6967e3 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581268


University of Oxford

16. Kyle, Andrew F. Total synthesis of (–)-nakadomarin A and an approach to the diazatricyclic core of the madangamines.

Degree: PhD, 2012, University of Oxford

 This dissertation describes work towards two marine alkaloid natural products of the manzamine family. The total synthesis of (–)-nakadomarin A, via two conceptually different strategies… (more)

Subjects/Keywords: 547; Chemistry & allied sciences; Asymmetric catalysis; Natural products; Organic chemistry; Organic synthesis; Synthetic organic chemistry

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APA (6th Edition):

Kyle, A. F. (2012). Total synthesis of (–)-nakadomarin A and an approach to the diazatricyclic core of the madangamines. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:43e8044f-6860-47a2-9850-5f42990d4a68 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580987

Chicago Manual of Style (16th Edition):

Kyle, Andrew F. “Total synthesis of (–)-nakadomarin A and an approach to the diazatricyclic core of the madangamines.” 2012. Doctoral Dissertation, University of Oxford. Accessed November 17, 2019. http://ora.ox.ac.uk/objects/uuid:43e8044f-6860-47a2-9850-5f42990d4a68 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580987.

MLA Handbook (7th Edition):

Kyle, Andrew F. “Total synthesis of (–)-nakadomarin A and an approach to the diazatricyclic core of the madangamines.” 2012. Web. 17 Nov 2019.

Vancouver:

Kyle AF. Total synthesis of (–)-nakadomarin A and an approach to the diazatricyclic core of the madangamines. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2019 Nov 17]. Available from: http://ora.ox.ac.uk/objects/uuid:43e8044f-6860-47a2-9850-5f42990d4a68 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580987.

Council of Science Editors:

Kyle AF. Total synthesis of (–)-nakadomarin A and an approach to the diazatricyclic core of the madangamines. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:43e8044f-6860-47a2-9850-5f42990d4a68 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580987


University of California – Irvine

17. 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 November 17, 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. 17 Nov 2019.

Vancouver:

Sizemore NBL. Intramolecular Diels-Alder Reactions in Organic Synthesis. [Internet] [Thesis]. University of California – Irvine; 2014. [cited 2019 Nov 17]. 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 Cambridge

18. 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/1810/273347 ; 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 November 17, 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. 17 Nov 2019.

Vancouver:

Lau SH. Organic synthesis : taming chemistry using enabling technologies. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Nov 17]. 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

19. 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 November 17, 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. 17 Nov 2019.

Vancouver:

Lau SH. Organic Synthesis: Taming Chemistry using Enabling Technologies . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Nov 17]. 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


University of Michigan

20. 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 November 17, 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. 17 Nov 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 Nov 17]. 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

21. Connolly, Matthew James. Selective routes to substituted dihydropyridones.

Degree: 2011, University of Oxford

 Introduction: The introduction provides a survey of the natural product and pharmaceutical targets accessible from dihydropyridines and dihydropyridones as well as an overview of previous… (more)

Subjects/Keywords: 547.59; Organic chemistry : Organic synthesis : Synthetic organic chemistry : dihydropyridones : reduction : pyridines : asymmetric synthesis

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APA (6th Edition):

Connolly, M. J. (2011). Selective routes to substituted dihydropyridones. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:2e670c3f-e928-46c5-a1db-28bc1a6609e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.547454

Chicago Manual of Style (16th Edition):

Connolly, Matthew James. “Selective routes to substituted dihydropyridones.” 2011. Doctoral Dissertation, University of Oxford. Accessed November 17, 2019. http://ora.ox.ac.uk/objects/uuid:2e670c3f-e928-46c5-a1db-28bc1a6609e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.547454.

MLA Handbook (7th Edition):

Connolly, Matthew James. “Selective routes to substituted dihydropyridones.” 2011. Web. 17 Nov 2019.

Vancouver:

Connolly MJ. Selective routes to substituted dihydropyridones. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Nov 17]. Available from: http://ora.ox.ac.uk/objects/uuid:2e670c3f-e928-46c5-a1db-28bc1a6609e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.547454.

Council of Science Editors:

Connolly MJ. Selective routes to substituted dihydropyridones. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:2e670c3f-e928-46c5-a1db-28bc1a6609e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.547454


University of Oxford

22. Ling, Kenneth B. Stereoselective cyclopropanations of allylic amines and derivatives.

Degree: 2009, University of Oxford

 This thesis is concerned with the development and application of methods for the stereoselective cyclopropanation of allylic amines and derivatives. Firstly, a highly chemo- and… (more)

Subjects/Keywords: 547.5; Organic chemistry : Organic synthesis : Synthetic organic chemistry : cyclopropanation : allylic amines : Shi's carbenoid

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APA (6th Edition):

Ling, K. B. (2009). Stereoselective cyclopropanations of allylic amines and derivatives. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:15907329-15e7-4cbd-ba46-2735ff4129ea ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526079

Chicago Manual of Style (16th Edition):

Ling, Kenneth B. “Stereoselective cyclopropanations of allylic amines and derivatives.” 2009. Doctoral Dissertation, University of Oxford. Accessed November 17, 2019. http://ora.ox.ac.uk/objects/uuid:15907329-15e7-4cbd-ba46-2735ff4129ea ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526079.

MLA Handbook (7th Edition):

Ling, Kenneth B. “Stereoselective cyclopropanations of allylic amines and derivatives.” 2009. Web. 17 Nov 2019.

Vancouver:

Ling KB. Stereoselective cyclopropanations of allylic amines and derivatives. [Internet] [Doctoral dissertation]. University of Oxford; 2009. [cited 2019 Nov 17]. Available from: http://ora.ox.ac.uk/objects/uuid:15907329-15e7-4cbd-ba46-2735ff4129ea ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526079.

Council of Science Editors:

Ling KB. Stereoselective cyclopropanations of allylic amines and derivatives. [Doctoral Dissertation]. University of Oxford; 2009. Available from: http://ora.ox.ac.uk/objects/uuid:15907329-15e7-4cbd-ba46-2735ff4129ea ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526079


University of Oxford

23. Saliba, Regis C. Design and synthesis of nanoparticles functionalised with Lewis oligosaccharides for selective targeting of DC-SIGN.

Degree: PhD, 2014, University of Oxford

 Dendritic cells (DC) are one of the major antigen presenting cells (APC) of the body. They, by capture of antigen and cross-presentation of these antigens,… (more)

Subjects/Keywords: 547; Organic chemistry; Chemical biology; Organic synthesis; Natural products; Synthetic organic chemistry

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APA (6th Edition):

Saliba, R. C. (2014). Design and synthesis of nanoparticles functionalised with Lewis oligosaccharides for selective targeting of DC-SIGN. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:21906fcb-b29f-415b-a1b7-bca375f06a2b ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635259

Chicago Manual of Style (16th Edition):

Saliba, Regis C. “Design and synthesis of nanoparticles functionalised with Lewis oligosaccharides for selective targeting of DC-SIGN.” 2014. Doctoral Dissertation, University of Oxford. Accessed November 17, 2019. http://ora.ox.ac.uk/objects/uuid:21906fcb-b29f-415b-a1b7-bca375f06a2b ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635259.

MLA Handbook (7th Edition):

Saliba, Regis C. “Design and synthesis of nanoparticles functionalised with Lewis oligosaccharides for selective targeting of DC-SIGN.” 2014. Web. 17 Nov 2019.

Vancouver:

Saliba RC. Design and synthesis of nanoparticles functionalised with Lewis oligosaccharides for selective targeting of DC-SIGN. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2019 Nov 17]. Available from: http://ora.ox.ac.uk/objects/uuid:21906fcb-b29f-415b-a1b7-bca375f06a2b ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635259.

Council of Science Editors:

Saliba RC. Design and synthesis of nanoparticles functionalised with Lewis oligosaccharides for selective targeting of DC-SIGN. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:21906fcb-b29f-415b-a1b7-bca375f06a2b ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635259


University of Oxford

24. Wu, Boshen. Synthesis of taurospongin A and other biologically active natural products.

Degree: PhD, 2017, University of Oxford

 This thesis firstly describes a synthesis of the natural product taurospongin A, a potent DNA polymerase beta inhibitor. Sharpless asymmetric dihydroxylation on olefin <b>E-1.60</b> followed… (more)

Subjects/Keywords: 572.86; Organic chemistry; Organic synthesis; Synthetic organic chemistry; Total Synthesis; natural products; structural elucidation

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APA (6th Edition):

Wu, B. (2017). Synthesis of taurospongin A and other biologically active natural products. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:37a34bc4-efb4-4a6b-9d44-a3ad1c8ae0be ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.565957

Chicago Manual of Style (16th Edition):

Wu, Boshen. “Synthesis of taurospongin A and other biologically active natural products.” 2017. Doctoral Dissertation, University of Oxford. Accessed November 17, 2019. http://ora.ox.ac.uk/objects/uuid:37a34bc4-efb4-4a6b-9d44-a3ad1c8ae0be ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.565957.

MLA Handbook (7th Edition):

Wu, Boshen. “Synthesis of taurospongin A and other biologically active natural products.” 2017. Web. 17 Nov 2019.

Vancouver:

Wu B. Synthesis of taurospongin A and other biologically active natural products. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2019 Nov 17]. Available from: http://ora.ox.ac.uk/objects/uuid:37a34bc4-efb4-4a6b-9d44-a3ad1c8ae0be ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.565957.

Council of Science Editors:

Wu B. Synthesis of taurospongin A and other biologically active natural products. [Doctoral Dissertation]. University of Oxford; 2017. Available from: http://ora.ox.ac.uk/objects/uuid:37a34bc4-efb4-4a6b-9d44-a3ad1c8ae0be ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.565957


University of Oxford

25. Cresswell, Alex. New methods for nucleophilic fluorination.

Degree: PhD, 2011, University of Oxford

 This thesis describes investigations into the utility of boron fluorides and tetrafluoroborates as sources of nucleophilic fluorine. Chapter 1 discusses the history and importance of… (more)

Subjects/Keywords: 661.0731; Organic synthesis; Organic chemistry; Synthetic organic chemistry; fluorination; boron trifluoride; epoxides

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APA (6th Edition):

Cresswell, A. (2011). New methods for nucleophilic fluorination. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:612ea592-2f52-407b-b761-36b02b746e9d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.556275

Chicago Manual of Style (16th Edition):

Cresswell, Alex. “New methods for nucleophilic fluorination.” 2011. Doctoral Dissertation, University of Oxford. Accessed November 17, 2019. http://ora.ox.ac.uk/objects/uuid:612ea592-2f52-407b-b761-36b02b746e9d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.556275.

MLA Handbook (7th Edition):

Cresswell, Alex. “New methods for nucleophilic fluorination.” 2011. Web. 17 Nov 2019.

Vancouver:

Cresswell A. New methods for nucleophilic fluorination. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Nov 17]. Available from: http://ora.ox.ac.uk/objects/uuid:612ea592-2f52-407b-b761-36b02b746e9d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.556275.

Council of Science Editors:

Cresswell A. New methods for nucleophilic fluorination. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:612ea592-2f52-407b-b761-36b02b746e9d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.556275


University of Oxford

26. Lenden, Philip. Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation.

Degree: PhD, 2011, University of Oxford

 This work describes the extension of rhodium-catalysed intermolecular hydroacylation to encompass some tandem catalytic processes, wherein a further catalytic process is enacted on the product… (more)

Subjects/Keywords: 547.215; Chemistry & allied sciences; Catalysis; Heterocyclic chemistry; Organic chemistry; Organic synthesis; Organometallic Chemistry; Synthetic organic chemistry; chemistry; catalysis; heterocycles; rhodium; hydroacylation

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APA (6th Edition):

Lenden, P. (2011). Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:e63f5fd7-f92f-47dd-b06f-face73729804 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555255

Chicago Manual of Style (16th Edition):

Lenden, Philip. “Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation.” 2011. Doctoral Dissertation, University of Oxford. Accessed November 17, 2019. http://ora.ox.ac.uk/objects/uuid:e63f5fd7-f92f-47dd-b06f-face73729804 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555255.

MLA Handbook (7th Edition):

Lenden, Philip. “Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation.” 2011. Web. 17 Nov 2019.

Vancouver:

Lenden P. Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Nov 17]. Available from: http://ora.ox.ac.uk/objects/uuid:e63f5fd7-f92f-47dd-b06f-face73729804 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555255.

Council of Science Editors:

Lenden P. Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:e63f5fd7-f92f-47dd-b06f-face73729804 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555255


University of Oxford

27. Knipe, Peter Clarke. Chiral counter-ion controlled asymmetric electrocyclic reactions.

Degree: PhD, 2012, University of Oxford

 The aim of this project was to develop new catalytic methods to control asymmetry in electrocyclic reactions, and to apply these methods to generate complex… (more)

Subjects/Keywords: 547; Chemistry & allied sciences; Asymmetric catalysis; Catalysis; Heterocyclic chemistry; Organic chemistry; Organic synthesis; Synthetic organic chemistry; Electrocyclization; asymmetric; organic

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

APA (6th Edition):

Knipe, P. C. (2012). Chiral counter-ion controlled asymmetric electrocyclic reactions. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:c981f724-c783-4913-b224-92fcebf94d37 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580964

Chicago Manual of Style (16th Edition):

Knipe, Peter Clarke. “Chiral counter-ion controlled asymmetric electrocyclic reactions.” 2012. Doctoral Dissertation, University of Oxford. Accessed November 17, 2019. http://ora.ox.ac.uk/objects/uuid:c981f724-c783-4913-b224-92fcebf94d37 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580964.

MLA Handbook (7th Edition):

Knipe, Peter Clarke. “Chiral counter-ion controlled asymmetric electrocyclic reactions.” 2012. Web. 17 Nov 2019.

Vancouver:

Knipe PC. Chiral counter-ion controlled asymmetric electrocyclic reactions. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2019 Nov 17]. Available from: http://ora.ox.ac.uk/objects/uuid:c981f724-c783-4913-b224-92fcebf94d37 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580964.

Council of Science Editors:

Knipe PC. Chiral counter-ion controlled asymmetric electrocyclic reactions. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:c981f724-c783-4913-b224-92fcebf94d37 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580964


East Carolina University

28. Duffy, Brian. Solvent and Solubility Effects on Quinone Ratios.

Degree: 2012, East Carolina University

 Monoquinones and diquinones are a biologically and chemically important class of compounds that can be found in numerous natural products such as: thymoquinone, oosporein, coenzyme… (more)

Subjects/Keywords: Chemistry; Chemistry, Organic; Diquinone; Quinone; Synthesis; Organic chemistry; Quinone – Synthesis – Research; Synthetic products

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APA (6th Edition):

Duffy, B. (2012). Solvent and Solubility Effects on Quinone Ratios. (Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4003

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):

Duffy, Brian. “Solvent and Solubility Effects on Quinone Ratios.” 2012. Thesis, East Carolina University. Accessed November 17, 2019. http://hdl.handle.net/10342/4003.

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

MLA Handbook (7th Edition):

Duffy, Brian. “Solvent and Solubility Effects on Quinone Ratios.” 2012. Web. 17 Nov 2019.

Vancouver:

Duffy B. Solvent and Solubility Effects on Quinone Ratios. [Internet] [Thesis]. East Carolina University; 2012. [cited 2019 Nov 17]. Available from: http://hdl.handle.net/10342/4003.

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

Council of Science Editors:

Duffy B. Solvent and Solubility Effects on Quinone Ratios. [Thesis]. East Carolina University; 2012. Available from: http://hdl.handle.net/10342/4003

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


University of Manchester

29. Hussain, Shahed. The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines.

Degree: 2017, University of Manchester

 Chiral amines represent a pervasive structural motif found in various natural products, pharmaceuticals, agrochemicals and fine chemicals. Their preparation in single-enantiomer form continues to attract… (more)

Subjects/Keywords: Biocatalysis; Biotechnology; Bioorganic Chemistry; Chemical Biology; Synthetic Organic Chemistry; Enzymes

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

APA (6th Edition):

Hussain, S. (2017). The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:309577

Chicago Manual of Style (16th Edition):

Hussain, Shahed. “The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines.” 2017. Doctoral Dissertation, University of Manchester. Accessed November 17, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:309577.

MLA Handbook (7th Edition):

Hussain, Shahed. “The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines.” 2017. Web. 17 Nov 2019.

Vancouver:

Hussain S. The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2019 Nov 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:309577.

Council of Science Editors:

Hussain S. The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:309577


University of Manchester

30. Hussain, Shahed. The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines.

Degree: PhD, 2017, University of Manchester

 Chiral amines represent a pervasive structural motif found in various natural products, pharmaceuticals, agrochemicals and fine chemicals. Their preparation in single-enantiomer form continues to attract… (more)

Subjects/Keywords: 540; Enzymes; Synthetic Organic Chemistry; Chemical Biology; Biocatalysis; Biotechnology; Bioorganic Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hussain, S. (2017). The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-development-of-novel-biocatalytic-routes-for-the-synthesis-of-enantiomericallypure-chiral-amines(eba89b88-6801-40cc-a3c3-9c5f1c518d0f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748025

Chicago Manual of Style (16th Edition):

Hussain, Shahed. “The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines.” 2017. Doctoral Dissertation, University of Manchester. Accessed November 17, 2019. https://www.research.manchester.ac.uk/portal/en/theses/the-development-of-novel-biocatalytic-routes-for-the-synthesis-of-enantiomericallypure-chiral-amines(eba89b88-6801-40cc-a3c3-9c5f1c518d0f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748025.

MLA Handbook (7th Edition):

Hussain, Shahed. “The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines.” 2017. Web. 17 Nov 2019.

Vancouver:

Hussain S. The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2019 Nov 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-development-of-novel-biocatalytic-routes-for-the-synthesis-of-enantiomericallypure-chiral-amines(eba89b88-6801-40cc-a3c3-9c5f1c518d0f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748025.

Council of Science Editors:

Hussain S. The development of novel biocatalytic routes for the synthesis of enantiomerically-pure chiral amines. [Doctoral Dissertation]. University of Manchester; 2017. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-development-of-novel-biocatalytic-routes-for-the-synthesis-of-enantiomericallypure-chiral-amines(eba89b88-6801-40cc-a3c3-9c5f1c518d0f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748025

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