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You searched for subject:(Organic compounds Synthesis ). Showing records 1 – 30 of 33665 total matches.

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University of Hawaii

1. Ebisu, Kikuye. The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde.

Degree: PhD, 2009, University of Hawaii

Typescript.

Bibliography: leaves [60]-64.

x, 64 l illus

The highly strained bicyclo[2.1.1]hexane system has been of considerable interest to chemists especially in connection with bond… (more)

Subjects/Keywords: Organic compounds  – Synthesis

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

APA (6th Edition):

Ebisu, K. (2009). The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde. (Doctoral Dissertation). University of Hawaii. Retrieved from http://hdl.handle.net/10125/11389

Chicago Manual of Style (16th Edition):

Ebisu, Kikuye. “The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde.” 2009. Doctoral Dissertation, University of Hawaii. Accessed October 17, 2019. http://hdl.handle.net/10125/11389.

MLA Handbook (7th Edition):

Ebisu, Kikuye. “The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde.” 2009. Web. 17 Oct 2019.

Vancouver:

Ebisu K. The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde. [Internet] [Doctoral dissertation]. University of Hawaii; 2009. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10125/11389.

Council of Science Editors:

Ebisu K. The synthesis of 5, 5-dimethylbicyclo [2.1.1] hexane-1-carboxaldehyde. [Doctoral Dissertation]. University of Hawaii; 2009. Available from: http://hdl.handle.net/10125/11389


University of Hong Kong

2. He, Jiayun. Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine.

Degree: PhD, 2017, University of Hong Kong

The intramolecular (4+3) cycloadditions of epoxy enolsilane substrates 1.89 generated polycyclic cycloadducts 1.90 having bicyclo[5.3.0]decane frameworks, a skeleton which is common among terpenoid natural products… (more)

Subjects/Keywords: Organic compounds - Synthesis

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APA (6th Edition):

He, J. (2017). Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/241419

Chicago Manual of Style (16th Edition):

He, Jiayun. “Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine.” 2017. Doctoral Dissertation, University of Hong Kong. Accessed October 17, 2019. http://hdl.handle.net/10722/241419.

MLA Handbook (7th Edition):

He, Jiayun. “Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine.” 2017. Web. 17 Oct 2019.

Vancouver:

He J. Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine. [Internet] [Doctoral dissertation]. University of Hong Kong; 2017. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10722/241419.

Council of Science Editors:

He J. Investigations on the intramolecular (4+3) cycloadditions of epoxy enolsilanes, and applications towards the asymmetric synthesis of himandrine. [Doctoral Dissertation]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/241419


Brock University

3. Gilmet, Jacqueline. Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine .

Degree: Department of Chemistry, 2010, Brock University

 The present thesis reviews the development of a formal enantiodivergent synthesis of the (+)- and (-)-isomers of balanol. This approach commences from a cis-dihydrodiol derived… (more)

Subjects/Keywords: Organic compounds  – Synthesis; Codeine  – Synthesis

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APA (6th Edition):

Gilmet, J. (2010). Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/3033

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):

Gilmet, Jacqueline. “Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine .” 2010. Thesis, Brock University. Accessed October 17, 2019. http://hdl.handle.net/10464/3033.

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

MLA Handbook (7th Edition):

Gilmet, Jacqueline. “Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine .” 2010. Web. 17 Oct 2019.

Vancouver:

Gilmet J. Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine . [Internet] [Thesis]. Brock University; 2010. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10464/3033.

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

Council of Science Editors:

Gilmet J. Enantiodivergent chemoenzymatic synthesis of Balanol and approaches to the synthesis of (+)-Codine . [Thesis]. Brock University; 2010. Available from: http://hdl.handle.net/10464/3033

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


Brock University

4. Metcalf, Thomas A. Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine .

Degree: Department of Chemistry, 2011, Brock University

 The present studies describe our recent work on expanding the use of the Burgess reagent and its reaction with oxiranes. Several new variants of the… (more)

Subjects/Keywords: Organic compounds  – Synthesis; Morphine  – Synthesis.

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APA (6th Edition):

Metcalf, T. A. (2011). Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/3417

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):

Metcalf, Thomas A. “Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine .” 2011. Thesis, Brock University. Accessed October 17, 2019. http://hdl.handle.net/10464/3417.

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

MLA Handbook (7th Edition):

Metcalf, Thomas A. “Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine .” 2011. Web. 17 Oct 2019.

Vancouver:

Metcalf TA. Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine . [Internet] [Thesis]. Brock University; 2011. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10464/3417.

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

Council of Science Editors:

Metcalf TA. Development of thermally stable versions of the Burgess Reagent : approaches to the chemoenzymatic total synthesis of morphine . [Thesis]. Brock University; 2011. Available from: http://hdl.handle.net/10464/3417

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


Nelson Mandela Metropolitan University

5. Mahanjana, Lungelwa. Reactions towards the synthesis of the uncommon P57 cymarose moiety.

Degree: Faculty of Science, 2013, Nelson Mandela Metropolitan University

 The work described in this study aims to investigate methods that will improve a lengthy synthetic pathway in the synthesis of the P57 cymarose moiety,… (more)

Subjects/Keywords: Chemistry, Organic; Organic compounds  – Synthesis

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APA (6th Edition):

Mahanjana, L. (2013). Reactions towards the synthesis of the uncommon P57 cymarose moiety. (Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/6711

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):

Mahanjana, Lungelwa. “Reactions towards the synthesis of the uncommon P57 cymarose moiety.” 2013. Thesis, Nelson Mandela Metropolitan University. Accessed October 17, 2019. http://hdl.handle.net/10948/6711.

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

MLA Handbook (7th Edition):

Mahanjana, Lungelwa. “Reactions towards the synthesis of the uncommon P57 cymarose moiety.” 2013. Web. 17 Oct 2019.

Vancouver:

Mahanjana L. Reactions towards the synthesis of the uncommon P57 cymarose moiety. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2013. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10948/6711.

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

Council of Science Editors:

Mahanjana L. Reactions towards the synthesis of the uncommon P57 cymarose moiety. [Thesis]. Nelson Mandela Metropolitan University; 2013. Available from: http://hdl.handle.net/10948/6711

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


University of Oxford

6. Akhtar, Wasim. The α-alkylation of ketones using hydrogen borrowing catalysis.

Degree: PhD, 2018, University of Oxford

 <b>Introduction - Hydrogen Borrowing Alkylation Reactions Using Alcohols</b> The introduction reviews the origins of hydrogen borrowing catalysis and how it has been applied to utilise… (more)

Subjects/Keywords: Organic Chemistry; Organic compounds – Synthesis

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APA (6th Edition):

Akhtar, W. (2018). The α-alkylation of ketones using hydrogen borrowing catalysis. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:a8afbade-c195-4b20-ac37-b710a869304e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780421

Chicago Manual of Style (16th Edition):

Akhtar, Wasim. “The α-alkylation of ketones using hydrogen borrowing catalysis.” 2018. Doctoral Dissertation, University of Oxford. Accessed October 17, 2019. http://ora.ox.ac.uk/objects/uuid:a8afbade-c195-4b20-ac37-b710a869304e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780421.

MLA Handbook (7th Edition):

Akhtar, Wasim. “The α-alkylation of ketones using hydrogen borrowing catalysis.” 2018. Web. 17 Oct 2019.

Vancouver:

Akhtar W. The α-alkylation of ketones using hydrogen borrowing catalysis. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2019 Oct 17]. Available from: http://ora.ox.ac.uk/objects/uuid:a8afbade-c195-4b20-ac37-b710a869304e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780421.

Council of Science Editors:

Akhtar W. The α-alkylation of ketones using hydrogen borrowing catalysis. [Doctoral Dissertation]. University of Oxford; 2018. Available from: http://ora.ox.ac.uk/objects/uuid:a8afbade-c195-4b20-ac37-b710a869304e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780421


Rutgers University

7. Ramanathan, Ahalya. I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily.

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

TMC-95A is a natural product which has demonstrated inhibition activity against the proteasomal pathway. Though its biological activity is proven, the total synthesis of the… (more)

Subjects/Keywords: Chemistry, Organic; Organic compounds – Synthesis

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APA (6th Edition):

Ramanathan, A. (2011). I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673

Chicago Manual of Style (16th Edition):

Ramanathan, Ahalya. “I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily.” 2011. Doctoral Dissertation, Rutgers University. Accessed October 17, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673.

MLA Handbook (7th Edition):

Ramanathan, Ahalya. “I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily.” 2011. Web. 17 Oct 2019.

Vancouver:

Ramanathan A. I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2019 Oct 17]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673.

Council of Science Editors:

Ramanathan A. I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673


University of Johannesburg

8. Crous, Renier. Approaches to the synthesis of selected nitrogenous heterocycles.

Degree: PhD, 2012, University of Johannesburg

 The first part of the research described in this thesis involves the development of a new methodology for the synthesis of N-hydroxy pyrrolidines, starting from… (more)

Subjects/Keywords: Organic compounds - Synthesis.; Nitrogen compounds.; Heterocyclic compounds.

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APA (6th Edition):

Crous, R. (2012). Approaches to the synthesis of selected nitrogenous heterocycles. (Doctoral Dissertation). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/6287

Chicago Manual of Style (16th Edition):

Crous, Renier. “Approaches to the synthesis of selected nitrogenous heterocycles.” 2012. Doctoral Dissertation, University of Johannesburg. Accessed October 17, 2019. http://hdl.handle.net/10210/6287.

MLA Handbook (7th Edition):

Crous, Renier. “Approaches to the synthesis of selected nitrogenous heterocycles.” 2012. Web. 17 Oct 2019.

Vancouver:

Crous R. Approaches to the synthesis of selected nitrogenous heterocycles. [Internet] [Doctoral dissertation]. University of Johannesburg; 2012. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10210/6287.

Council of Science Editors:

Crous R. Approaches to the synthesis of selected nitrogenous heterocycles. [Doctoral Dissertation]. University of Johannesburg; 2012. Available from: http://hdl.handle.net/10210/6287


University of KwaZulu-Natal

9. Naicker, Tricia. Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis .

Degree: Chemistry, 2008, University of KwaZulu-Natal

 There is enormous interest in the design and development of efficient chiral ligands for asymmetric catalysis, as a result, this field has become one of… (more)

Subjects/Keywords: Organic compounds – Synthesis.; Catalysis.; Chemistry.

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APA (6th Edition):

Naicker, T. (2008). Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis . (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/427

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):

Naicker, Tricia. “Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis .” 2008. Thesis, University of KwaZulu-Natal. Accessed October 17, 2019. http://hdl.handle.net/10413/427.

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

MLA Handbook (7th Edition):

Naicker, Tricia. “Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis .” 2008. Web. 17 Oct 2019.

Vancouver:

Naicker T. Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis . [Internet] [Thesis]. University of KwaZulu-Natal; 2008. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10413/427.

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

Council of Science Editors:

Naicker T. Synthesis of novel pentacyclo-undecane chiral ligands for application in asymmetric catalysis . [Thesis]. University of KwaZulu-Natal; 2008. Available from: http://hdl.handle.net/10413/427

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


University of Hawaii

10. Siṃha, Īśvara. Synthetic approaches toward napthazarin derivatives.

Degree: PhD, 2009, University of Hawaii

Typescript.

Bibliography: leaves [114]-116.

ix, 116 l illus., tables

The sea urchin pigments, spinochromes A, C, D, and E (I, II, III, and IV) are… (more)

Subjects/Keywords: Naphthazarin; Organic compounds  – Synthesis

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APA (6th Edition):

Siṃha, I. (2009). Synthetic approaches toward napthazarin derivatives. (Doctoral Dissertation). University of Hawaii. Retrieved from http://hdl.handle.net/10125/11394

Chicago Manual of Style (16th Edition):

Siṃha, Īśvara. “Synthetic approaches toward napthazarin derivatives.” 2009. Doctoral Dissertation, University of Hawaii. Accessed October 17, 2019. http://hdl.handle.net/10125/11394.

MLA Handbook (7th Edition):

Siṃha, Īśvara. “Synthetic approaches toward napthazarin derivatives.” 2009. Web. 17 Oct 2019.

Vancouver:

Siṃha I. Synthetic approaches toward napthazarin derivatives. [Internet] [Doctoral dissertation]. University of Hawaii; 2009. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10125/11394.

Council of Science Editors:

Siṃha I. Synthetic approaches toward napthazarin derivatives. [Doctoral Dissertation]. University of Hawaii; 2009. Available from: http://hdl.handle.net/10125/11394


Hong Kong University of Science and Technology

11. Li, Zhilong. Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products.

Degree: 2017, Hong Kong University of Science and Technology

 This thesis consists of four chapters, describing the development of new synthetic methodology and total syntheses of natural products: chapter one is focused on the… (more)

Subjects/Keywords: Natural products; Synthesis; Organic compounds

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APA (6th Edition):

Li, Z. (2017). Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1781125 ; http://repository.ust.hk/ir/bitstream/1783.1-88075/1/th_redirect.html

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):

Li, Zhilong. “Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products.” 2017. Thesis, Hong Kong University of Science and Technology. Accessed October 17, 2019. https://doi.org/10.14711/thesis-b1781125 ; http://repository.ust.hk/ir/bitstream/1783.1-88075/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Li, Zhilong. “Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products.” 2017. Web. 17 Oct 2019.

Vancouver:

Li Z. Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2017. [cited 2019 Oct 17]. Available from: https://doi.org/10.14711/thesis-b1781125 ; http://repository.ust.hk/ir/bitstream/1783.1-88075/1/th_redirect.html.

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

Council of Science Editors:

Li Z. Achmatowicz rearrangement in total syntheses of diarylheptanoid natural products. [Thesis]. Hong Kong University of Science and Technology; 2017. Available from: https://doi.org/10.14711/thesis-b1781125 ; http://repository.ust.hk/ir/bitstream/1783.1-88075/1/th_redirect.html

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


Hong Kong University of Science and Technology

12. Zhou, Jiangbin. Synthesis of the C8-C12 fragment of amphidinolactone B.

Degree: 2015, Hong Kong University of Science and Technology

 In connection with the total synthesis of a marine macrolide, amphidinolactone B, this thesis deals with the synthesis of the C8–C12 fragment of this molecule.… (more)

Subjects/Keywords: Chemistry, Organic; Synthesis; Macrocyclic compounds

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APA (6th Edition):

Zhou, J. (2015). Synthesis of the C8-C12 fragment of amphidinolactone B. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1514996 ; http://repository.ust.hk/ir/bitstream/1783.1-80263/1/th_redirect.html

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):

Zhou, Jiangbin. “Synthesis of the C8-C12 fragment of amphidinolactone B.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed October 17, 2019. https://doi.org/10.14711/thesis-b1514996 ; http://repository.ust.hk/ir/bitstream/1783.1-80263/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Zhou, Jiangbin. “Synthesis of the C8-C12 fragment of amphidinolactone B.” 2015. Web. 17 Oct 2019.

Vancouver:

Zhou J. Synthesis of the C8-C12 fragment of amphidinolactone B. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2019 Oct 17]. Available from: https://doi.org/10.14711/thesis-b1514996 ; http://repository.ust.hk/ir/bitstream/1783.1-80263/1/th_redirect.html.

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

Council of Science Editors:

Zhou J. Synthesis of the C8-C12 fragment of amphidinolactone B. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: https://doi.org/10.14711/thesis-b1514996 ; http://repository.ust.hk/ir/bitstream/1783.1-80263/1/th_redirect.html

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


University of Hong Kong

13. 陳肇人; Chan, Diana. Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A.

Degree: PhD, 2016, University of Hong Kong

The first transannular (4+3) cycloadditions based on the activation of epoxy enolsilanes have been realized. Six macrocyclic epoxy ketones were converted to enolsilanes, then treated… (more)

Subjects/Keywords: Organic cyclic compounds - Synthesis

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APA (6th Edition):

陳肇人; Chan, D. (2016). Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/238343

Chicago Manual of Style (16th Edition):

陳肇人; Chan, Diana. “Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A.” 2016. Doctoral Dissertation, University of Hong Kong. Accessed October 17, 2019. http://hdl.handle.net/10722/238343.

MLA Handbook (7th Edition):

陳肇人; Chan, Diana. “Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A.” 2016. Web. 17 Oct 2019.

Vancouver:

陳肇人; Chan D. Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A. [Internet] [Doctoral dissertation]. University of Hong Kong; 2016. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10722/238343.

Council of Science Editors:

陳肇人; Chan D. Studies of transannular (4+3) cycloadditions and application to the synthesis of (+)-cortistatin A. [Doctoral Dissertation]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/238343


Hong Kong University of Science and Technology

14. Feng, Gaofeng. Total synthesis of 24-demethylbafilomycins using diester-tethered ring-closing metathesis.

Degree: 2010, Hong Kong University of Science and Technology

 Total synthesis of complex natural products, such as 24-demethylbafilomycins, not only serves as the purposes for confirming the structures and accessing to synthetic derivatives for… (more)

Subjects/Keywords: Organic compounds  – Synthesis; Metathesis (Chemistry)

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

APA (6th Edition):

Feng, G. (2010). Total synthesis of 24-demethylbafilomycins using diester-tethered ring-closing metathesis. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1097883 ; http://repository.ust.hk/ir/bitstream/1783.1-6464/1/th_redirect.html

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):

Feng, Gaofeng. “Total synthesis of 24-demethylbafilomycins using diester-tethered ring-closing metathesis.” 2010. Thesis, Hong Kong University of Science and Technology. Accessed October 17, 2019. https://doi.org/10.14711/thesis-b1097883 ; http://repository.ust.hk/ir/bitstream/1783.1-6464/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Feng, Gaofeng. “Total synthesis of 24-demethylbafilomycins using diester-tethered ring-closing metathesis.” 2010. Web. 17 Oct 2019.

Vancouver:

Feng G. Total synthesis of 24-demethylbafilomycins using diester-tethered ring-closing metathesis. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2010. [cited 2019 Oct 17]. Available from: https://doi.org/10.14711/thesis-b1097883 ; http://repository.ust.hk/ir/bitstream/1783.1-6464/1/th_redirect.html.

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

Council of Science Editors:

Feng G. Total synthesis of 24-demethylbafilomycins using diester-tethered ring-closing metathesis. [Thesis]. Hong Kong University of Science and Technology; 2010. Available from: https://doi.org/10.14711/thesis-b1097883 ; http://repository.ust.hk/ir/bitstream/1783.1-6464/1/th_redirect.html

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


Nelson Mandela Metropolitan University

15. Sagandira, Cloudius Ray. Exploring acyl azides chemistry in continuous flow systems.

Degree: Faculty of Science, 2017, Nelson Mandela Metropolitan University

Organic azides are important in the synthesis of many target molecules of great use in fine chemical and pharmaceutical production. The use of this class… (more)

Subjects/Keywords: Organic compounds  – Synthesis; Flow chemistry

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

APA (6th Edition):

Sagandira, C. R. (2017). Exploring acyl azides chemistry in continuous flow systems. (Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/12065

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):

Sagandira, Cloudius Ray. “Exploring acyl azides chemistry in continuous flow systems.” 2017. Thesis, Nelson Mandela Metropolitan University. Accessed October 17, 2019. http://hdl.handle.net/10948/12065.

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

MLA Handbook (7th Edition):

Sagandira, Cloudius Ray. “Exploring acyl azides chemistry in continuous flow systems.” 2017. Web. 17 Oct 2019.

Vancouver:

Sagandira CR. Exploring acyl azides chemistry in continuous flow systems. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2017. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10948/12065.

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

Council of Science Editors:

Sagandira CR. Exploring acyl azides chemistry in continuous flow systems. [Thesis]. Nelson Mandela Metropolitan University; 2017. Available from: http://hdl.handle.net/10948/12065

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


Hong Kong University of Science and Technology

16. Wu, Yandong. Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain.

Degree: 2014, Hong Kong University of Science and Technology

 Marine microorganisms are widely viewed as an emerging source of novel natural products. A variety of butenolides [or furan-2(5H)-ones], featured with an α,β-unsaturated lactone core,… (more)

Subjects/Keywords: Organic compounds; Synthesis; Lactones; Stereochemistry

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

APA (6th Edition):

Wu, Y. (2014). Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/th_redirect.html

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):

Wu, Yandong. “Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed October 17, 2019. https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Wu, Yandong. “Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain.” 2014. Web. 17 Oct 2019.

Vancouver:

Wu Y. Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2019 Oct 17]. Available from: https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/th_redirect.html.

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

Council of Science Editors:

Wu Y. Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/th_redirect.html

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


Hong Kong University of Science and Technology

17. Ye, Ning. Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies.

Degree: 2014, Hong Kong University of Science and Technology

 Total synthesis of natural products is the Holy Grail of chemical science. Not only does it serve for structural elucidation, but also as an enabling… (more)

Subjects/Keywords: Organic compounds; Synthesis; Stereoisomers; Lactones

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APA (6th Edition):

Ye, N. (2014). Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/th_redirect.html

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):

Ye, Ning. “Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed October 17, 2019. https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Ye, Ning. “Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies.” 2014. Web. 17 Oct 2019.

Vancouver:

Ye N. Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2019 Oct 17]. Available from: https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/th_redirect.html.

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

Council of Science Editors:

Ye N. Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/th_redirect.html

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


Victoria University of Wellington

18. Hewitt, Russell James. Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B.

Degree: 2010, Victoria University of Wellington

 Cyclopropanes and carbohydrates are materials of great interest to chemists. Ring opening reactions of cyclopropanated carbohydrates have excellent potential for synthesis, due to the many… (more)

Subjects/Keywords: Organic compounds; Synthesis; Carbohydrates; Cyclopropane

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

APA (6th Edition):

Hewitt, R. J. (2010). Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/1249

Chicago Manual of Style (16th Edition):

Hewitt, Russell James. “Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B.” 2010. Doctoral Dissertation, Victoria University of Wellington. Accessed October 17, 2019. http://hdl.handle.net/10063/1249.

MLA Handbook (7th Edition):

Hewitt, Russell James. “Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B.” 2010. Web. 17 Oct 2019.

Vancouver:

Hewitt RJ. Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2010. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10063/1249.

Council of Science Editors:

Hewitt RJ. Investigations of Ring-Opening Reactions of Cyclopropanated Carbohydrates: Towards the Synthesis of the Natural Product ( – )-TAN-2483B. [Doctoral Dissertation]. Victoria University of Wellington; 2010. Available from: http://hdl.handle.net/10063/1249


University of Missouri – Columbia

19. Calkins, Nathan L., 1982-. 2,1-Benzothiazines: preparation and reactivity.

Degree: 2010, University of Missouri – Columbia

 The synthesis of chiral ligands to tune the reactivity and stereoselectivity of many catalytic asymmetric reactions has been given considerable attention in synthetic organic chemistry… (more)

Subjects/Keywords: Benzothiazine; Organic compounds  – Synthesis; Sulfoximines

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APA (6th Edition):

Calkins, Nathan L., 1. (2010). 2,1-Benzothiazines: preparation and reactivity. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/8309

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):

Calkins, Nathan L., 1982-. “2,1-Benzothiazines: preparation and reactivity.” 2010. Thesis, University of Missouri – Columbia. Accessed October 17, 2019. http://hdl.handle.net/10355/8309.

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

MLA Handbook (7th Edition):

Calkins, Nathan L., 1982-. “2,1-Benzothiazines: preparation and reactivity.” 2010. Web. 17 Oct 2019.

Vancouver:

Calkins, Nathan L. 1. 2,1-Benzothiazines: preparation and reactivity. [Internet] [Thesis]. University of Missouri – Columbia; 2010. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10355/8309.

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

Council of Science Editors:

Calkins, Nathan L. 1. 2,1-Benzothiazines: preparation and reactivity. [Thesis]. University of Missouri – Columbia; 2010. Available from: http://hdl.handle.net/10355/8309

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


University of Johannesburg

20. Braithwaite, Dana Helen. New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides.

Degree: 2014, University of Johannesburg

M.Sc. (Chemistry)

The aim of this study waa to develop new methodology for the synthesis of chiral pyrrolidine derivatives Crom monosaccharides. An overview of the… (more)

Subjects/Keywords: Monosaccharides; Organic compounds - Synthesis

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APA (6th Edition):

Braithwaite, D. H. (2014). New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/10144

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):

Braithwaite, Dana Helen. “New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides.” 2014. Thesis, University of Johannesburg. Accessed October 17, 2019. http://hdl.handle.net/10210/10144.

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

MLA Handbook (7th Edition):

Braithwaite, Dana Helen. “New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides.” 2014. Web. 17 Oct 2019.

Vancouver:

Braithwaite DH. New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10210/10144.

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

Council of Science Editors:

Braithwaite DH. New methodology for the synthesis of chiral pyrrolidine derivatives from monosaccharides. [Thesis]. University of Johannesburg; 2014. Available from: http://hdl.handle.net/10210/10144

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


University of Johannesburg

21. Williams, Dennis Bradley Glen. Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems.

Degree: 2014, University of Johannesburg

M.Sc. (Chemistry)

Palladium-mediated carbon-earbon (and carbon-heteroatom) bond formation! is to an increasing extent playing a vital role in synthetic organic chemistry. The chemistry is usually… (more)

Subjects/Keywords: Palladium; Organic compounds - Synthesis

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APA (6th Edition):

Williams, D. B. G. (2014). Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/9145

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):

Williams, Dennis Bradley Glen. “Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems.” 2014. Thesis, University of Johannesburg. Accessed October 17, 2019. http://hdl.handle.net/10210/9145.

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

MLA Handbook (7th Edition):

Williams, Dennis Bradley Glen. “Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems.” 2014. Web. 17 Oct 2019.

Vancouver:

Williams DBG. Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10210/9145.

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

Council of Science Editors:

Williams DBG. Consecutive palladium-mediated reactions in the synthesis of some bicyclic systems. [Thesis]. University of Johannesburg; 2014. Available from: http://hdl.handle.net/10210/9145

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


University of Johannesburg

22. Thompson, Catherine. Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties.

Degree: 2014, University of Johannesburg

M.Sc. (Chemistry)

Barium titanate (BaTi03) is an important material in the electronics industry as a result of its excellent dielectric properties. It has been the… (more)

Subjects/Keywords: Barium metatitanate; Organic compounds - Synthesis

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APA (6th Edition):

Thompson, C. (2014). Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/10857

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):

Thompson, Catherine. “Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties.” 2014. Thesis, University of Johannesburg. Accessed October 17, 2019. http://hdl.handle.net/10210/10857.

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

MLA Handbook (7th Edition):

Thompson, Catherine. “Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties.” 2014. Web. 17 Oct 2019.

Vancouver:

Thompson C. Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10210/10857.

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

Council of Science Editors:

Thompson C. Barium titanate : the relationship between the conditions of synthesis and its structural and electrical properties. [Thesis]. University of Johannesburg; 2014. Available from: http://hdl.handle.net/10210/10857

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


Hong Kong University of Science and Technology

23. Wang, Yong CHEM. Regio- and stereoselective functionalization of thioalkynes and ynamides.

Degree: 2017, Hong Kong University of Science and Technology

 Functionalization of alkynes is a very important field in organic chemistry, because it provides straightforward synthesis of multi-substituted alkenes, which are widely present in biological… (more)

Subjects/Keywords: Alkynes; Catalysts; Organic compounds; Synthesis

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APA (6th Edition):

Wang, Y. C. (2017). Regio- and stereoselective functionalization of thioalkynes and ynamides. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1781152 ; http://repository.ust.hk/ir/bitstream/1783.1-97159/1/th_redirect.html

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):

Wang, Yong CHEM. “Regio- and stereoselective functionalization of thioalkynes and ynamides.” 2017. Thesis, Hong Kong University of Science and Technology. Accessed October 17, 2019. https://doi.org/10.14711/thesis-b1781152 ; http://repository.ust.hk/ir/bitstream/1783.1-97159/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Wang, Yong CHEM. “Regio- and stereoselective functionalization of thioalkynes and ynamides.” 2017. Web. 17 Oct 2019.

Vancouver:

Wang YC. Regio- and stereoselective functionalization of thioalkynes and ynamides. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2017. [cited 2019 Oct 17]. Available from: https://doi.org/10.14711/thesis-b1781152 ; http://repository.ust.hk/ir/bitstream/1783.1-97159/1/th_redirect.html.

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

Council of Science Editors:

Wang YC. Regio- and stereoselective functionalization of thioalkynes and ynamides. [Thesis]. Hong Kong University of Science and Technology; 2017. Available from: https://doi.org/10.14711/thesis-b1781152 ; http://repository.ust.hk/ir/bitstream/1783.1-97159/1/th_redirect.html

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


Drexel University

24. Tsetsakos, Panagiota. Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway.

Degree: 2014, Drexel University

Previously, ethyl 1-nitro-1,2,3,5,6,7,8,8a-octahydro-1- naphthalenecarboxylate was synthesized via tandem Mitsunobu cyclization - [3,3]-sigmatropic rearrangement of ethyl 5-(cyclohex-1-en-1-yl)-5-hydroxy-2- nitropentenoate. It was obtained in 48% yield as a… (more)

Subjects/Keywords: Chemistry; Organic compounds – Synthesis; Diastereoisomers

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APA (6th Edition):

Tsetsakos, P. (2014). Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/4501

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):

Tsetsakos, Panagiota. “Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway.” 2014. Thesis, Drexel University. Accessed October 17, 2019. http://hdl.handle.net/1860/4501.

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

MLA Handbook (7th Edition):

Tsetsakos, Panagiota. “Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway.” 2014. Web. 17 Oct 2019.

Vancouver:

Tsetsakos P. Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway. [Internet] [Thesis]. Drexel University; 2014. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1860/4501.

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

Council of Science Editors:

Tsetsakos P. Synthesis of Ethyl 1-Nitro-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenecarboxylate Via a Diels- Alder Pathway. [Thesis]. Drexel University; 2014. Available from: http://hdl.handle.net/1860/4501

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


Texas Christian University

25. Bian, Zhiguo. Synthetic approaches to the skeleton of crinine-type alkaloids from isoquinoline and the total synthesis of (?)-crinine.

Degree: PhD, 2010, Texas Christian University

 The crinine-type alkaloids, which have the 5,10b-ethanophenanthridine skeleton as the core structure, represent an important sub-class of the family of Amaryllidaceae alkaloids. Considering the obvious… (more)

Subjects/Keywords: Alkaloids.; Isoquinoline.; Organic compounds Synthesis.

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APA (6th Edition):

Bian, Z. (2010). Synthetic approaches to the skeleton of crinine-type alkaloids from isoquinoline and the total synthesis of (?)-crinine. (Doctoral Dissertation). Texas Christian University. Retrieved from https://repository.tcu.edu:443/handle/116099117/4209

Chicago Manual of Style (16th Edition):

Bian, Zhiguo. “Synthetic approaches to the skeleton of crinine-type alkaloids from isoquinoline and the total synthesis of (?)-crinine.” 2010. Doctoral Dissertation, Texas Christian University. Accessed October 17, 2019. https://repository.tcu.edu:443/handle/116099117/4209.

MLA Handbook (7th Edition):

Bian, Zhiguo. “Synthetic approaches to the skeleton of crinine-type alkaloids from isoquinoline and the total synthesis of (?)-crinine.” 2010. Web. 17 Oct 2019.

Vancouver:

Bian Z. Synthetic approaches to the skeleton of crinine-type alkaloids from isoquinoline and the total synthesis of (?)-crinine. [Internet] [Doctoral dissertation]. Texas Christian University; 2010. [cited 2019 Oct 17]. Available from: https://repository.tcu.edu:443/handle/116099117/4209.

Council of Science Editors:

Bian Z. Synthetic approaches to the skeleton of crinine-type alkaloids from isoquinoline and the total synthesis of (?)-crinine. [Doctoral Dissertation]. Texas Christian University; 2010. Available from: https://repository.tcu.edu:443/handle/116099117/4209


Texas Christian University

26. Ding, Lixin. Total synthesis of the crinane-type Amaryllidaceae alkaloids (+)-maritidine and (+)-oxomaritidine.

Degree: PhD, 2010, Texas Christian University

 The crinane-type alkaloids are characterized by the presence of the 5,10b-ethanophenanthridine skeleton and represent an important subgroup within the large family of Amaryllidaceae alkaloids, many… (more)

Subjects/Keywords: Alkaloids.; Amaryllidaceae.; Organic compounds Synthesis.

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APA (6th Edition):

Ding, L. (2010). Total synthesis of the crinane-type Amaryllidaceae alkaloids (+)-maritidine and (+)-oxomaritidine. (Doctoral Dissertation). Texas Christian University. Retrieved from https://repository.tcu.edu:443/handle/116099117/4222

Chicago Manual of Style (16th Edition):

Ding, Lixin. “Total synthesis of the crinane-type Amaryllidaceae alkaloids (+)-maritidine and (+)-oxomaritidine.” 2010. Doctoral Dissertation, Texas Christian University. Accessed October 17, 2019. https://repository.tcu.edu:443/handle/116099117/4222.

MLA Handbook (7th Edition):

Ding, Lixin. “Total synthesis of the crinane-type Amaryllidaceae alkaloids (+)-maritidine and (+)-oxomaritidine.” 2010. Web. 17 Oct 2019.

Vancouver:

Ding L. Total synthesis of the crinane-type Amaryllidaceae alkaloids (+)-maritidine and (+)-oxomaritidine. [Internet] [Doctoral dissertation]. Texas Christian University; 2010. [cited 2019 Oct 17]. Available from: https://repository.tcu.edu:443/handle/116099117/4222.

Council of Science Editors:

Ding L. Total synthesis of the crinane-type Amaryllidaceae alkaloids (+)-maritidine and (+)-oxomaritidine. [Doctoral Dissertation]. Texas Christian University; 2010. Available from: https://repository.tcu.edu:443/handle/116099117/4222


Hong Kong University of Science and Technology

27. Bendel, Lars Erik CHEM. Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid.

Degree: 2018, Hong Kong University of Science and Technology

 The SmI2-mediated reductive coupling reaction between non-conjugated aldehydes and two 2-(dialkylamido)aryl 2,3-disubstituted α,β-unsaturated esters has been investigated. In contrast to the corresponding 2- or 3-monosubstituted… (more)

Subjects/Keywords: Organic compounds; Synthesis; Inorganic compounds; Aldehydes; Samarium

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APA (6th Edition):

Bendel, L. E. C. (2018). Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-991012662567503412 ; http://repository.ust.hk/ir/bitstream/1783.1-97892/1/th_redirect.html

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):

Bendel, Lars Erik CHEM. “Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid.” 2018. Thesis, Hong Kong University of Science and Technology. Accessed October 17, 2019. https://doi.org/10.14711/thesis-991012662567503412 ; http://repository.ust.hk/ir/bitstream/1783.1-97892/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Bendel, Lars Erik CHEM. “Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid.” 2018. Web. 17 Oct 2019.

Vancouver:

Bendel LEC. Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2018. [cited 2019 Oct 17]. Available from: https://doi.org/10.14711/thesis-991012662567503412 ; http://repository.ust.hk/ir/bitstream/1783.1-97892/1/th_redirect.html.

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

Council of Science Editors:

Bendel LEC. Samarium(II) iodide-mediated reductive coupling reaction of 2,3-disubstituted acrylates with non-conjugated aldehydes and synthesis of phaseolinic acid. [Thesis]. Hong Kong University of Science and Technology; 2018. Available from: https://doi.org/10.14711/thesis-991012662567503412 ; http://repository.ust.hk/ir/bitstream/1783.1-97892/1/th_redirect.html

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


University of Hong Kong

28. Ou, Jun. Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters.

Degree: PhD, 2011, University of Hong Kong

 Two syntheses of non-cross-linked polystyrene-supported TADDOL-based phosphoric acid organocatalyst have been developed. The optimal polymer-supported catalyst 2.29d exhibited comparable catalytic activity to its small molecule… (more)

Subjects/Keywords: Asymmetric synthesis.; Catalysis.; Organic compounds - Synthesis.

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APA (6th Edition):

Ou, J. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters. (Doctoral Dissertation). University of Hong Kong. Retrieved from Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528

Chicago Manual of Style (16th Edition):

Ou, Jun. “Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed October 17, 2019. Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528.

MLA Handbook (7th Edition):

Ou, Jun. “Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters.” 2011. Web. 17 Oct 2019.

Vancouver:

Ou J. Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2019 Oct 17]. Available from: Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528.

Council of Science Editors:

Ou J. Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: Ou, J. [欧军]. (2011). Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturated thioesters. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784970 ; http://dx.doi.org/10.5353/th_b4784970 ; http://hdl.handle.net/10722/174528


University of Hawaii – Manoa

29. Zou, Xianglong. Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs.

Degree: PhD, 2009, University of Hawaii – Manoa

Microfiche.

xi, 127 leaves, bound ill. 29 cm

Part I: The stereoselective total synthesis of each of the two diastereomeric C6-hydroxyhexahydrocannabinols is described. The extension… (more)

Subjects/Keywords: Cannabinoids  – Synthesis; Sarcophyton; Organic compounds  – Synthesis

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APA (6th Edition):

Zou, X. (2009). Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs. (Doctoral Dissertation). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/9527

Chicago Manual of Style (16th Edition):

Zou, Xianglong. “Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs.” 2009. Doctoral Dissertation, University of Hawaii – Manoa. Accessed October 17, 2019. http://hdl.handle.net/10125/9527.

MLA Handbook (7th Edition):

Zou, Xianglong. “Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs.” 2009. Web. 17 Oct 2019.

Vancouver:

Zou X. Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs. [Internet] [Doctoral dissertation]. University of Hawaii – Manoa; 2009. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10125/9527.

Council of Science Editors:

Zou X. Part I, The stereoselective synthesis of cannabinoids ; Part II, The total synthesis of sarcophytol A and its analogs. [Doctoral Dissertation]. University of Hawaii – Manoa; 2009. Available from: http://hdl.handle.net/10125/9527


Hong Kong University of Science and Technology

30. Au Yeung, Siu Fung. Synthesis and characterization of organo-borate solids.

Degree: 2011, Hong Kong University of Science and Technology

 Boric acid ‘flux’ synthesis was developed by our group and assisted the preparation of new borate materials solids. In this thesis apply the methodology to… (more)

Subjects/Keywords: Borates  – Synthesis; Organic compounds  – Synthesis; Salicylates

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

APA (6th Edition):

Au Yeung, S. F. (2011). Synthesis and characterization of organo-borate solids. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1155021 ; http://repository.ust.hk/ir/bitstream/1783.1-7306/1/th_redirect.html

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):

Au Yeung, Siu Fung. “Synthesis and characterization of organo-borate solids.” 2011. Thesis, Hong Kong University of Science and Technology. Accessed October 17, 2019. https://doi.org/10.14711/thesis-b1155021 ; http://repository.ust.hk/ir/bitstream/1783.1-7306/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Au Yeung, Siu Fung. “Synthesis and characterization of organo-borate solids.” 2011. Web. 17 Oct 2019.

Vancouver:

Au Yeung SF. Synthesis and characterization of organo-borate solids. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2019 Oct 17]. Available from: https://doi.org/10.14711/thesis-b1155021 ; http://repository.ust.hk/ir/bitstream/1783.1-7306/1/th_redirect.html.

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

Council of Science Editors:

Au Yeung SF. Synthesis and characterization of organo-borate solids. [Thesis]. Hong Kong University of Science and Technology; 2011. Available from: https://doi.org/10.14711/thesis-b1155021 ; http://repository.ust.hk/ir/bitstream/1783.1-7306/1/th_redirect.html

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

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