Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Stereoselective). Showing records 1 – 30 of 132 total matches.

[1] [2] [3] [4] [5]

Search Limiters

Last 2 Years | English Only

Degrees

Languages

Country

▼ Search Limiters


Cornell University

1. Widger, Peter. Stereoselective Epoxide Polymerization: Exploring Isoselective Bimetallic Catalysts, Ionic Cocatalysts, And The Use Of Alcohols As Chain Transfer Agents.

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

 For over 50 years, researchers have attempted to create catalysts for stereoselectively polymerizing epoxides. Until very recently, catalysts for the polymerization of racemic epoxides gave… (more)

Subjects/Keywords: Catalysis; Polyether; Stereoselective

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Widger, P. (2011). Stereoselective Epoxide Polymerization: Exploring Isoselective Bimetallic Catalysts, Ionic Cocatalysts, And The Use Of Alcohols As Chain Transfer Agents. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/30705

Chicago Manual of Style (16th Edition):

Widger, Peter. “Stereoselective Epoxide Polymerization: Exploring Isoselective Bimetallic Catalysts, Ionic Cocatalysts, And The Use Of Alcohols As Chain Transfer Agents.” 2011. Doctoral Dissertation, Cornell University. Accessed May 09, 2021. http://hdl.handle.net/1813/30705.

MLA Handbook (7th Edition):

Widger, Peter. “Stereoselective Epoxide Polymerization: Exploring Isoselective Bimetallic Catalysts, Ionic Cocatalysts, And The Use Of Alcohols As Chain Transfer Agents.” 2011. Web. 09 May 2021.

Vancouver:

Widger P. Stereoselective Epoxide Polymerization: Exploring Isoselective Bimetallic Catalysts, Ionic Cocatalysts, And The Use Of Alcohols As Chain Transfer Agents. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2021 May 09]. Available from: http://hdl.handle.net/1813/30705.

Council of Science Editors:

Widger P. Stereoselective Epoxide Polymerization: Exploring Isoselective Bimetallic Catalysts, Ionic Cocatalysts, And The Use Of Alcohols As Chain Transfer Agents. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/30705


University of Utah

2. Boyarskikh, Vyacheslav Vladimirovich. Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement.

Degree: PhD, Chemistry;, 2010, University of Utah

 Sulfonium ylides are formed using mild conditions and a diazo decomposition reaction catalyzed by a transition metal. These intermediates can undergo a variety of synthetically… (more)

Subjects/Keywords: Sigmatropic rearrangement; Stereoselective; Sulfonium ylide

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Boyarskikh, V. V. (2010). Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1242/rec/113

Chicago Manual of Style (16th Edition):

Boyarskikh, Vyacheslav Vladimirovich. “Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement.” 2010. Doctoral Dissertation, University of Utah. Accessed May 09, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1242/rec/113.

MLA Handbook (7th Edition):

Boyarskikh, Vyacheslav Vladimirovich. “Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement.” 2010. Web. 09 May 2021.

Vancouver:

Boyarskikh VV. Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2021 May 09]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1242/rec/113.

Council of Science Editors:

Boyarskikh VV. Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1242/rec/113

3. Balasubramanyam, P. Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -.

Degree: Chemistry, 2012, Jawaharlal Nehru Technological University, Hyderabad

The thesis entitled Stereoselective Total Synthesis of Biologically Active Lactones: Synargentolide A, Cryptofolione and newlineCryptocaryalactone along with the Development of Novel Synthetic Methodologies has been… (more)

Subjects/Keywords: biologically; lactones; methodologies; Stereoselective; synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Balasubramanyam, P. (2012). Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -. (Thesis). Jawaharlal Nehru Technological University, Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19106

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):

Balasubramanyam, P. “Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -.” 2012. Thesis, Jawaharlal Nehru Technological University, Hyderabad. Accessed May 09, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/19106.

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

MLA Handbook (7th Edition):

Balasubramanyam, P. “Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -.” 2012. Web. 09 May 2021.

Vancouver:

Balasubramanyam P. Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2012. [cited 2021 May 09]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19106.

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

Council of Science Editors:

Balasubramanyam P. Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -. [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19106

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


University of Adelaide

4. Licari, Giovanni. The stereoselective pharmacodynamics of the enantiomers of perhexiline.

Degree: 2013, University of Adelaide

 In the past decade there has been growing interest and evidence that altered myocardial energy metabolism plays a major role in the onset and/or progression… (more)

Subjects/Keywords: stereoselective; pharmacodynamics; enantiomers; perhexiline

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Licari, G. (2013). The stereoselective pharmacodynamics of the enantiomers of perhexiline. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/84991

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):

Licari, Giovanni. “The stereoselective pharmacodynamics of the enantiomers of perhexiline.” 2013. Thesis, University of Adelaide. Accessed May 09, 2021. http://hdl.handle.net/2440/84991.

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

MLA Handbook (7th Edition):

Licari, Giovanni. “The stereoselective pharmacodynamics of the enantiomers of perhexiline.” 2013. Web. 09 May 2021.

Vancouver:

Licari G. The stereoselective pharmacodynamics of the enantiomers of perhexiline. [Internet] [Thesis]. University of Adelaide; 2013. [cited 2021 May 09]. Available from: http://hdl.handle.net/2440/84991.

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

Council of Science Editors:

Licari G. The stereoselective pharmacodynamics of the enantiomers of perhexiline. [Thesis]. University of Adelaide; 2013. Available from: http://hdl.handle.net/2440/84991

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


University of Illinois – Urbana-Champaign

5. Roth, Aaron. Stereoselective synthesis of 1,2-disubstitued βeta-amino alcohols and amino thiols.

Degree: PhD, Chemistry, 2020, University of Illinois – Urbana-Champaign

 This thesis covers the development and implementation of two distinct methodologies, both of which provide access to enantiomerically enriched, vicinally functionalized products. Chapter 1 provides… (more)

Subjects/Keywords: Lewis base Catalysis; Stereoselective; Enantioselective

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Roth, A. (2020). Stereoselective synthesis of 1,2-disubstitued βeta-amino alcohols and amino thiols. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/108470

Chicago Manual of Style (16th Edition):

Roth, Aaron. “Stereoselective synthesis of 1,2-disubstitued βeta-amino alcohols and amino thiols.” 2020. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed May 09, 2021. http://hdl.handle.net/2142/108470.

MLA Handbook (7th Edition):

Roth, Aaron. “Stereoselective synthesis of 1,2-disubstitued βeta-amino alcohols and amino thiols.” 2020. Web. 09 May 2021.

Vancouver:

Roth A. Stereoselective synthesis of 1,2-disubstitued βeta-amino alcohols and amino thiols. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2020. [cited 2021 May 09]. Available from: http://hdl.handle.net/2142/108470.

Council of Science Editors:

Roth A. Stereoselective synthesis of 1,2-disubstitued βeta-amino alcohols and amino thiols. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2020. Available from: http://hdl.handle.net/2142/108470


University of Illinois – Urbana-Champaign

6. Ickes, Andrew R. The development of a rhodium-catalyzed chemo- and stereoselective hydroamination for the synthesis of 1,2-diamines.

Degree: MS, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Amines are a prominent functionality found throughout organic molecules, including pharmaceuticals, agrochemicals, organic materials, and organic dyes.1 However, incorporation of amines into organic frameworks in… (more)

Subjects/Keywords: rhodium; hydroamination; intermolecular; stereoselective; chemoselective

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ickes, A. R. (2016). The development of a rhodium-catalyzed chemo- and stereoselective hydroamination for the synthesis of 1,2-diamines. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95603

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):

Ickes, Andrew R. “The development of a rhodium-catalyzed chemo- and stereoselective hydroamination for the synthesis of 1,2-diamines.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed May 09, 2021. http://hdl.handle.net/2142/95603.

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

MLA Handbook (7th Edition):

Ickes, Andrew R. “The development of a rhodium-catalyzed chemo- and stereoselective hydroamination for the synthesis of 1,2-diamines.” 2016. Web. 09 May 2021.

Vancouver:

Ickes AR. The development of a rhodium-catalyzed chemo- and stereoselective hydroamination for the synthesis of 1,2-diamines. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/2142/95603.

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

Council of Science Editors:

Ickes AR. The development of a rhodium-catalyzed chemo- and stereoselective hydroamination for the synthesis of 1,2-diamines. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95603

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


University of Canterbury

7. Singh, Govind Pratap. New approaches to stereocontrolled glycosylation.

Degree: PhD, Chemistry, 2015, University of Canterbury

 The conceptually simple process of linking carbohydrate units by glycosylation has proven to be one of the most difficult synthetic processes to control from a… (more)

Subjects/Keywords: carbohydrate; glycosylation; stereoselective; NGP; organocatalysis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Singh, G. P. (2015). New approaches to stereocontrolled glycosylation. (Doctoral Dissertation). University of Canterbury. Retrieved from http://dx.doi.org/10.26021/6577

Chicago Manual of Style (16th Edition):

Singh, Govind Pratap. “New approaches to stereocontrolled glycosylation.” 2015. Doctoral Dissertation, University of Canterbury. Accessed May 09, 2021. http://dx.doi.org/10.26021/6577.

MLA Handbook (7th Edition):

Singh, Govind Pratap. “New approaches to stereocontrolled glycosylation.” 2015. Web. 09 May 2021.

Vancouver:

Singh GP. New approaches to stereocontrolled glycosylation. [Internet] [Doctoral dissertation]. University of Canterbury; 2015. [cited 2021 May 09]. Available from: http://dx.doi.org/10.26021/6577.

Council of Science Editors:

Singh GP. New approaches to stereocontrolled glycosylation. [Doctoral Dissertation]. University of Canterbury; 2015. Available from: http://dx.doi.org/10.26021/6577


University of Alberta

8. Sun, Ho-Yan. Breaking New Ground with the Suzuki-Miyaura Reaction: Stereoselective Cross-Couplings of 1,1-Diboronyl Alkanes.

Degree: PhD, Department of Chemistry, 2015, University of Alberta

 Synthetic organic chemistry is an area that has seen incredible growth through the years. The level of molecular complexity that can be achieved through available… (more)

Subjects/Keywords: Suzuki-Miyaura; organoboronates; stereoselective couplings; palladium; catalysis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sun, H. (2015). Breaking New Ground with the Suzuki-Miyaura Reaction: Stereoselective Cross-Couplings of 1,1-Diboronyl Alkanes. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/pk02cd596

Chicago Manual of Style (16th Edition):

Sun, Ho-Yan. “Breaking New Ground with the Suzuki-Miyaura Reaction: Stereoselective Cross-Couplings of 1,1-Diboronyl Alkanes.” 2015. Doctoral Dissertation, University of Alberta. Accessed May 09, 2021. https://era.library.ualberta.ca/files/pk02cd596.

MLA Handbook (7th Edition):

Sun, Ho-Yan. “Breaking New Ground with the Suzuki-Miyaura Reaction: Stereoselective Cross-Couplings of 1,1-Diboronyl Alkanes.” 2015. Web. 09 May 2021.

Vancouver:

Sun H. Breaking New Ground with the Suzuki-Miyaura Reaction: Stereoselective Cross-Couplings of 1,1-Diboronyl Alkanes. [Internet] [Doctoral dissertation]. University of Alberta; 2015. [cited 2021 May 09]. Available from: https://era.library.ualberta.ca/files/pk02cd596.

Council of Science Editors:

Sun H. Breaking New Ground with the Suzuki-Miyaura Reaction: Stereoselective Cross-Couplings of 1,1-Diboronyl Alkanes. [Doctoral Dissertation]. University of Alberta; 2015. Available from: https://era.library.ualberta.ca/files/pk02cd596

9. Wu, Zhenhua. Development of Methods for Stereoselective Carbon-Carbon Bond Formation.

Degree: PhD, Chemistry, 2016, Oregon State University

 Three distinct methods to achieve the stereoselective synthesis of carbon-carbon bonds were investigated, encompassing: (i) the formation of axially chiral biaryl molecules by enantioselective Suzuki… (more)

Subjects/Keywords: Stereoselective; Stereochemistry

…Continued) Figure Page Scheme 17. Stereoselective synthesis of a conjugated diene 213 from… …61 Development of Methods for Stereoselective Carbon-Carbon Bond Formation 2 Preface… …Three different projects focused on different stereoselective C–C bond formation are… …in principle applicable to the stereoselective synthesis of essentially any type of… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wu, Z. (2016). Development of Methods for Stereoselective Carbon-Carbon Bond Formation. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/59817

Chicago Manual of Style (16th Edition):

Wu, Zhenhua. “Development of Methods for Stereoselective Carbon-Carbon Bond Formation.” 2016. Doctoral Dissertation, Oregon State University. Accessed May 09, 2021. http://hdl.handle.net/1957/59817.

MLA Handbook (7th Edition):

Wu, Zhenhua. “Development of Methods for Stereoselective Carbon-Carbon Bond Formation.” 2016. Web. 09 May 2021.

Vancouver:

Wu Z. Development of Methods for Stereoselective Carbon-Carbon Bond Formation. [Internet] [Doctoral dissertation]. Oregon State University; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/1957/59817.

Council of Science Editors:

Wu Z. Development of Methods for Stereoselective Carbon-Carbon Bond Formation. [Doctoral Dissertation]. Oregon State University; 2016. Available from: http://hdl.handle.net/1957/59817


Cornell University

10. Childers, Matthew. Bimetallic Epoxide Polymerization Catalysts.

Degree: PhD, Chemistry and Chemical Biology, 2015, Cornell University

 Atactic poly(propylene oxide) is a commonly produced polyether that is used as the soft segment in polyurethanes as it is amorphous with a T g… (more)

Subjects/Keywords: epoxide polymerization bimetallic; isotactic stereoselective stereoregular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Childers, M. (2015). Bimetallic Epoxide Polymerization Catalysts. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/41133

Chicago Manual of Style (16th Edition):

Childers, Matthew. “Bimetallic Epoxide Polymerization Catalysts.” 2015. Doctoral Dissertation, Cornell University. Accessed May 09, 2021. http://hdl.handle.net/1813/41133.

MLA Handbook (7th Edition):

Childers, Matthew. “Bimetallic Epoxide Polymerization Catalysts.” 2015. Web. 09 May 2021.

Vancouver:

Childers M. Bimetallic Epoxide Polymerization Catalysts. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/1813/41133.

Council of Science Editors:

Childers M. Bimetallic Epoxide Polymerization Catalysts. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41133

11. Thakur, Pallavi. Stereoselective Total Synthesis of Biologically Active Natural Products Achaetolide Panaxjapyne C, Goniothalesdiol A and ( 5 R, 6 S)- Acetoxyhexadecanolide; -.

Degree: Chemistry, 2013, Jawaharlal Nehru Technological University, Hyderabad

The Thesis entitled STEREOSELECTIVE TOTAL SYNTHESIS OF BIOLOGICALY ACTIVE NATURAL PRODUCTS ACHAETOLIDE, PANAXJAPYNE C, GONIOTHALESDIOL A AND (5R,6S)- newlineACETOXYHEXADECANOLIDE has been divided into four chapters.… (more)

Subjects/Keywords: Acetoxyhexadecanolide; Active; Biologically; Goniothalesdio; Stereoselective; Synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Thakur, P. (2013). Stereoselective Total Synthesis of Biologically Active Natural Products Achaetolide Panaxjapyne C, Goniothalesdiol A and ( 5 R, 6 S)- Acetoxyhexadecanolide; -. (Thesis). Jawaharlal Nehru Technological University, Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19277

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):

Thakur, Pallavi. “Stereoselective Total Synthesis of Biologically Active Natural Products Achaetolide Panaxjapyne C, Goniothalesdiol A and ( 5 R, 6 S)- Acetoxyhexadecanolide; -.” 2013. Thesis, Jawaharlal Nehru Technological University, Hyderabad. Accessed May 09, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/19277.

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

MLA Handbook (7th Edition):

Thakur, Pallavi. “Stereoselective Total Synthesis of Biologically Active Natural Products Achaetolide Panaxjapyne C, Goniothalesdiol A and ( 5 R, 6 S)- Acetoxyhexadecanolide; -.” 2013. Web. 09 May 2021.

Vancouver:

Thakur P. Stereoselective Total Synthesis of Biologically Active Natural Products Achaetolide Panaxjapyne C, Goniothalesdiol A and ( 5 R, 6 S)- Acetoxyhexadecanolide; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. [cited 2021 May 09]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19277.

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

Council of Science Editors:

Thakur P. Stereoselective Total Synthesis of Biologically Active Natural Products Achaetolide Panaxjapyne C, Goniothalesdiol A and ( 5 R, 6 S)- Acetoxyhexadecanolide; -. [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19277

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


University of Saskatchewan

12. Truong, Tram Tu 1992-. Stereoselective Synthesis of (E)-Enol Borinates via Borylation of Lithum Enolates.

Degree: 2018, University of Saskatchewan

 Aldol reactions of enol borinates constitute one the most powerful and reliable methods for asymmetric synthesis. Crucial to this success is the stereoselective preparation of… (more)

Subjects/Keywords: Stereoselective; (E)-Enol Borinates; Borylation; Lithum Enolates

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Truong, T. T. 1. (2018). Stereoselective Synthesis of (E)-Enol Borinates via Borylation of Lithum Enolates. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/11828

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):

Truong, Tram Tu 1992-. “Stereoselective Synthesis of (E)-Enol Borinates via Borylation of Lithum Enolates.” 2018. Thesis, University of Saskatchewan. Accessed May 09, 2021. http://hdl.handle.net/10388/11828.

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

MLA Handbook (7th Edition):

Truong, Tram Tu 1992-. “Stereoselective Synthesis of (E)-Enol Borinates via Borylation of Lithum Enolates.” 2018. Web. 09 May 2021.

Vancouver:

Truong TT1. Stereoselective Synthesis of (E)-Enol Borinates via Borylation of Lithum Enolates. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2021 May 09]. Available from: http://hdl.handle.net/10388/11828.

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

Council of Science Editors:

Truong TT1. Stereoselective Synthesis of (E)-Enol Borinates via Borylation of Lithum Enolates. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/11828

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


University of Sydney

13. Corcilius, Leo. Stereoselective Synthesis of Plant and Animal-Derived O-linked Glycopeptides .

Degree: 2016, University of Sydney

 This thesis describes efforts towards the stereoselective synthesis of homogeneous plant and animal-derived O-linked glycopeptides for the purposes of interrogating structure-function relationships. The first section… (more)

Subjects/Keywords: stereoselective; glycosylation; CLE; CEP; MUC1; IAD

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Corcilius, L. (2016). Stereoselective Synthesis of Plant and Animal-Derived O-linked Glycopeptides . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/16017

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):

Corcilius, Leo. “Stereoselective Synthesis of Plant and Animal-Derived O-linked Glycopeptides .” 2016. Thesis, University of Sydney. Accessed May 09, 2021. http://hdl.handle.net/2123/16017.

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

MLA Handbook (7th Edition):

Corcilius, Leo. “Stereoselective Synthesis of Plant and Animal-Derived O-linked Glycopeptides .” 2016. Web. 09 May 2021.

Vancouver:

Corcilius L. Stereoselective Synthesis of Plant and Animal-Derived O-linked Glycopeptides . [Internet] [Thesis]. University of Sydney; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/2123/16017.

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

Council of Science Editors:

Corcilius L. Stereoselective Synthesis of Plant and Animal-Derived O-linked Glycopeptides . [Thesis]. University of Sydney; 2016. Available from: http://hdl.handle.net/2123/16017

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


University of California – Irvine

14. Hill, Richard. Lithium 4,4’-Di-Tert-Butylbiphenylide: Characterization, Use in Spirocyclic Synthesis and Applications in Flow Reactors.

Degree: Chemistry, 2016, University of California – Irvine

 The first part of the dissertation describes the characterization of lithium 4,4’-di-tert-butylbiphenylide (LiDBB). The rates of formation and degradation of LiDBB were investigated and decomposition… (more)

Subjects/Keywords: Chemistry; flow reactor; LiDBB; lithium; radical; spirocycle; stereoselective

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hill, R. (2016). Lithium 4,4’-Di-Tert-Butylbiphenylide: Characterization, Use in Spirocyclic Synthesis and Applications in Flow Reactors. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/4zp5z2qm

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):

Hill, Richard. “Lithium 4,4’-Di-Tert-Butylbiphenylide: Characterization, Use in Spirocyclic Synthesis and Applications in Flow Reactors.” 2016. Thesis, University of California – Irvine. Accessed May 09, 2021. http://www.escholarship.org/uc/item/4zp5z2qm.

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

MLA Handbook (7th Edition):

Hill, Richard. “Lithium 4,4’-Di-Tert-Butylbiphenylide: Characterization, Use in Spirocyclic Synthesis and Applications in Flow Reactors.” 2016. Web. 09 May 2021.

Vancouver:

Hill R. Lithium 4,4’-Di-Tert-Butylbiphenylide: Characterization, Use in Spirocyclic Synthesis and Applications in Flow Reactors. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2021 May 09]. Available from: http://www.escholarship.org/uc/item/4zp5z2qm.

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

Council of Science Editors:

Hill R. Lithium 4,4’-Di-Tert-Butylbiphenylide: Characterization, Use in Spirocyclic Synthesis and Applications in Flow Reactors. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/4zp5z2qm

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

15. Kumar, Vinoth V. Preparation and utility of and#945; chlorosulfides in organic synthesis, stereoselective synthesis of the C1 C8 and C9 C19subunits of peloruside A; -.

Degree: Chemistry, 2012, Acharya Nagarjuna University

None

Bibliography given

Advisors/Committee Members: Raghavan, S.

Subjects/Keywords: chlorosulfides; organic synthesis; stereoselective synthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kumar, V. V. (2012). Preparation and utility of and#945; chlorosulfides in organic synthesis, stereoselective synthesis of the C1 C8 and C9 C19subunits of peloruside A; -. (Thesis). Acharya Nagarjuna University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/49354

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):

Kumar, Vinoth V. “Preparation and utility of and#945; chlorosulfides in organic synthesis, stereoselective synthesis of the C1 C8 and C9 C19subunits of peloruside A; -.” 2012. Thesis, Acharya Nagarjuna University. Accessed May 09, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/49354.

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

MLA Handbook (7th Edition):

Kumar, Vinoth V. “Preparation and utility of and#945; chlorosulfides in organic synthesis, stereoselective synthesis of the C1 C8 and C9 C19subunits of peloruside A; -.” 2012. Web. 09 May 2021.

Vancouver:

Kumar VV. Preparation and utility of and#945; chlorosulfides in organic synthesis, stereoselective synthesis of the C1 C8 and C9 C19subunits of peloruside A; -. [Internet] [Thesis]. Acharya Nagarjuna University; 2012. [cited 2021 May 09]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/49354.

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

Council of Science Editors:

Kumar VV. Preparation and utility of and#945; chlorosulfides in organic synthesis, stereoselective synthesis of the C1 C8 and C9 C19subunits of peloruside A; -. [Thesis]. Acharya Nagarjuna University; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/49354

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


University of Hyderabad

16. Surisetti, Suresh. Stereoselective cc bond forming reactions using titanium reagents: synthesis of chiral B amino esters, B lectams 3 aryl amineds, 1 2 diamines and coumarin derivatives; _.

Degree: chemistry, 2005, University of Hyderabad

None

Appendix p.224-262

Advisors/Committee Members: Periasamy, M.

Subjects/Keywords: Stereoselective; forming reactions; titanium

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Surisetti, S. (2005). Stereoselective cc bond forming reactions using titanium reagents: synthesis of chiral B amino esters, B lectams 3 aryl amineds, 1 2 diamines and coumarin derivatives; _. (Thesis). University of Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/25855

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):

Surisetti, Suresh. “Stereoselective cc bond forming reactions using titanium reagents: synthesis of chiral B amino esters, B lectams 3 aryl amineds, 1 2 diamines and coumarin derivatives; _.” 2005. Thesis, University of Hyderabad. Accessed May 09, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/25855.

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

MLA Handbook (7th Edition):

Surisetti, Suresh. “Stereoselective cc bond forming reactions using titanium reagents: synthesis of chiral B amino esters, B lectams 3 aryl amineds, 1 2 diamines and coumarin derivatives; _.” 2005. Web. 09 May 2021.

Vancouver:

Surisetti S. Stereoselective cc bond forming reactions using titanium reagents: synthesis of chiral B amino esters, B lectams 3 aryl amineds, 1 2 diamines and coumarin derivatives; _. [Internet] [Thesis]. University of Hyderabad; 2005. [cited 2021 May 09]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25855.

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

Council of Science Editors:

Surisetti S. Stereoselective cc bond forming reactions using titanium reagents: synthesis of chiral B amino esters, B lectams 3 aryl amineds, 1 2 diamines and coumarin derivatives; _. [Thesis]. University of Hyderabad; 2005. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25855

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


McMaster University

17. McLeod, David. STEREOSELECTIVE OLEFINATIONS EMPLOYING TRIALKYLPHOSPHORANYLIDES: NEW METHODS AND SYNTHETIC APPLICATIONS.

Degree: PhD, 2016, McMaster University

The Wittig reaction has constantly evolved during the last half-century and is one of the most strategic, reliable, widely-applicable carbon-carbon olefin bond forming processes available… (more)

Subjects/Keywords: Olefination; Alkene; Wittig; Phosphorane; Organic Chemistry; Natural Products; Ylid; Stereoselective

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

McLeod, D. (2016). STEREOSELECTIVE OLEFINATIONS EMPLOYING TRIALKYLPHOSPHORANYLIDES: NEW METHODS AND SYNTHETIC APPLICATIONS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/20458

Chicago Manual of Style (16th Edition):

McLeod, David. “STEREOSELECTIVE OLEFINATIONS EMPLOYING TRIALKYLPHOSPHORANYLIDES: NEW METHODS AND SYNTHETIC APPLICATIONS.” 2016. Doctoral Dissertation, McMaster University. Accessed May 09, 2021. http://hdl.handle.net/11375/20458.

MLA Handbook (7th Edition):

McLeod, David. “STEREOSELECTIVE OLEFINATIONS EMPLOYING TRIALKYLPHOSPHORANYLIDES: NEW METHODS AND SYNTHETIC APPLICATIONS.” 2016. Web. 09 May 2021.

Vancouver:

McLeod D. STEREOSELECTIVE OLEFINATIONS EMPLOYING TRIALKYLPHOSPHORANYLIDES: NEW METHODS AND SYNTHETIC APPLICATIONS. [Internet] [Doctoral dissertation]. McMaster University; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/11375/20458.

Council of Science Editors:

McLeod D. STEREOSELECTIVE OLEFINATIONS EMPLOYING TRIALKYLPHOSPHORANYLIDES: NEW METHODS AND SYNTHETIC APPLICATIONS. [Doctoral Dissertation]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20458


University of Toronto

18. D'Angelo, Kyan Anthony. Glycosyl Methanesulfonates in Regio- and Stereoselective Glycosylations Catalyzed by Borinic Acids.

Degree: 2015, University of Toronto

Stoichiometric and catalytic activation of unprotected glycosyl acceptors toward reaction with glycosyl donors represent a growing breadth of methodologies recently developed with the goal of… (more)

Subjects/Keywords: Borinic Acid; Carbohydrate; Glycosylation; Regioselective; Stereoselective; Sulfonate; 0490

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

D'Angelo, K. A. (2015). Glycosyl Methanesulfonates in Regio- and Stereoselective Glycosylations Catalyzed by Borinic Acids. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/74690

Chicago Manual of Style (16th Edition):

D'Angelo, Kyan Anthony. “Glycosyl Methanesulfonates in Regio- and Stereoselective Glycosylations Catalyzed by Borinic Acids.” 2015. Masters Thesis, University of Toronto. Accessed May 09, 2021. http://hdl.handle.net/1807/74690.

MLA Handbook (7th Edition):

D'Angelo, Kyan Anthony. “Glycosyl Methanesulfonates in Regio- and Stereoselective Glycosylations Catalyzed by Borinic Acids.” 2015. Web. 09 May 2021.

Vancouver:

D'Angelo KA. Glycosyl Methanesulfonates in Regio- and Stereoselective Glycosylations Catalyzed by Borinic Acids. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/1807/74690.

Council of Science Editors:

D'Angelo KA. Glycosyl Methanesulfonates in Regio- and Stereoselective Glycosylations Catalyzed by Borinic Acids. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/74690


University of Wollongong

19. Abdel-Megeed, Ashraf Mostafa Kamal. Design and synthesis of chiral ligands for the stereoselective synthesis of atropisomeric natural products.

Degree: PhD, 2014, University of Wollongong

  An investigation into the design and synthesis of chiral helical ligands for application in stereoselective synthesis of atropisomeric natural products by Suzuki coupling reaction… (more)

Subjects/Keywords: atropisomerism; stereoselective synthesis; 2; 2'-bipyrrolidine; 2'2-blindoline; DFT calculation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Abdel-Megeed, A. M. K. (2014). Design and synthesis of chiral ligands for the stereoselective synthesis of atropisomeric natural products. (Doctoral Dissertation). University of Wollongong. Retrieved from 0305 ORGANIC CHEMISTRY, 0304 MEDICINAL AND BIOMOLECULAR CHEMISTRY ; https://ro.uow.edu.au/theses/4209

Chicago Manual of Style (16th Edition):

Abdel-Megeed, Ashraf Mostafa Kamal. “Design and synthesis of chiral ligands for the stereoselective synthesis of atropisomeric natural products.” 2014. Doctoral Dissertation, University of Wollongong. Accessed May 09, 2021. 0305 ORGANIC CHEMISTRY, 0304 MEDICINAL AND BIOMOLECULAR CHEMISTRY ; https://ro.uow.edu.au/theses/4209.

MLA Handbook (7th Edition):

Abdel-Megeed, Ashraf Mostafa Kamal. “Design and synthesis of chiral ligands for the stereoselective synthesis of atropisomeric natural products.” 2014. Web. 09 May 2021.

Vancouver:

Abdel-Megeed AMK. Design and synthesis of chiral ligands for the stereoselective synthesis of atropisomeric natural products. [Internet] [Doctoral dissertation]. University of Wollongong; 2014. [cited 2021 May 09]. Available from: 0305 ORGANIC CHEMISTRY, 0304 MEDICINAL AND BIOMOLECULAR CHEMISTRY ; https://ro.uow.edu.au/theses/4209.

Council of Science Editors:

Abdel-Megeed AMK. Design and synthesis of chiral ligands for the stereoselective synthesis of atropisomeric natural products. [Doctoral Dissertation]. University of Wollongong; 2014. Available from: 0305 ORGANIC CHEMISTRY, 0304 MEDICINAL AND BIOMOLECULAR CHEMISTRY ; https://ro.uow.edu.au/theses/4209


Wayne State University

20. Dhakal, Bibek. Stereoselective Synthesis Of Legionaminic Acid And Pseudaminic Acid Glycosides.

Degree: PhD, Chemistry, 2018, Wayne State University

  Legionaminic acid (Leg) and pseudaminic acid (Pse) are deoxy acetamido analogues of the most common sialic acid, N-acetylneuraminic acid (NeuAc) that are found in… (more)

Subjects/Keywords: Legionaminic acid; Pseudaminic acid; Stereoselective glycosylation; Chemistry; Organic Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dhakal, B. (2018). Stereoselective Synthesis Of Legionaminic Acid And Pseudaminic Acid Glycosides. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/2155

Chicago Manual of Style (16th Edition):

Dhakal, Bibek. “Stereoselective Synthesis Of Legionaminic Acid And Pseudaminic Acid Glycosides.” 2018. Doctoral Dissertation, Wayne State University. Accessed May 09, 2021. https://digitalcommons.wayne.edu/oa_dissertations/2155.

MLA Handbook (7th Edition):

Dhakal, Bibek. “Stereoselective Synthesis Of Legionaminic Acid And Pseudaminic Acid Glycosides.” 2018. Web. 09 May 2021.

Vancouver:

Dhakal B. Stereoselective Synthesis Of Legionaminic Acid And Pseudaminic Acid Glycosides. [Internet] [Doctoral dissertation]. Wayne State University; 2018. [cited 2021 May 09]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/2155.

Council of Science Editors:

Dhakal B. Stereoselective Synthesis Of Legionaminic Acid And Pseudaminic Acid Glycosides. [Doctoral Dissertation]. Wayne State University; 2018. Available from: https://digitalcommons.wayne.edu/oa_dissertations/2155

21. Han, Bing Yuan. Studies towards the total synthesis of hemicalide.

Degree: PhD, 2019, University of Cambridge

 The discovery of a novel marine natural product hemicalide (1), with promising anticancer activity, has sparked interest in elucidating its full three-dimensional structure. Studies into… (more)

Subjects/Keywords: total synthesis; natural products; stereoselective; dp4; nmr; structural elucidation; polyketide; stereochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Han, B. Y. (2019). Studies towards the total synthesis of hemicalide. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.39381 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774743

Chicago Manual of Style (16th Edition):

Han, Bing Yuan. “Studies towards the total synthesis of hemicalide.” 2019. Doctoral Dissertation, University of Cambridge. Accessed May 09, 2021. https://doi.org/10.17863/CAM.39381 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774743.

MLA Handbook (7th Edition):

Han, Bing Yuan. “Studies towards the total synthesis of hemicalide.” 2019. Web. 09 May 2021.

Vancouver:

Han BY. Studies towards the total synthesis of hemicalide. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 May 09]. Available from: https://doi.org/10.17863/CAM.39381 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774743.

Council of Science Editors:

Han BY. Studies towards the total synthesis of hemicalide. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.39381 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774743


Bucknell University

22. Nelson, Brandon Nathaniel. Development of a Stereoselective Approach for the Synthesis of Allo Bile Acids.

Degree: 2016, Bucknell University

 Bile acids are natural products that are located within a variety of organisms through metabolism of cholesterol. The less common allo bile acids contain a… (more)

Subjects/Keywords: organic synthesis; bile acid; eudesmane; hydrogen atom transfer; stereoselective

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nelson, B. N. (2016). Development of a Stereoselective Approach for the Synthesis of Allo Bile Acids. (Thesis). Bucknell University. Retrieved from https://digitalcommons.bucknell.edu/masters_theses/167

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):

Nelson, Brandon Nathaniel. “Development of a Stereoselective Approach for the Synthesis of Allo Bile Acids.” 2016. Thesis, Bucknell University. Accessed May 09, 2021. https://digitalcommons.bucknell.edu/masters_theses/167.

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

MLA Handbook (7th Edition):

Nelson, Brandon Nathaniel. “Development of a Stereoselective Approach for the Synthesis of Allo Bile Acids.” 2016. Web. 09 May 2021.

Vancouver:

Nelson BN. Development of a Stereoselective Approach for the Synthesis of Allo Bile Acids. [Internet] [Thesis]. Bucknell University; 2016. [cited 2021 May 09]. Available from: https://digitalcommons.bucknell.edu/masters_theses/167.

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

Council of Science Editors:

Nelson BN. Development of a Stereoselective Approach for the Synthesis of Allo Bile Acids. [Thesis]. Bucknell University; 2016. Available from: https://digitalcommons.bucknell.edu/masters_theses/167

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


University of Colorado

23. Dockery, Lance Taylor. New Methods in Carbohydrate Chemistry: Dehydrative Glycosylation with Cyclic Phosphonium Anhydrides and α-Selective Glycosylation of Glycosyl Phosphinites.

Degree: MS, Chemistry & Biochemistry, 2016, University of Colorado

 Achieving a high level of efficiency in carbohydrate synthesis is dependent upon reactions that can provide high yields and stereoselectivity at the anomeric position. The… (more)

Subjects/Keywords: carbohydrate chemistry; dehydrative glycosylation; organic synthesis; phosphonium; stereoselective synthesis; Organic Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dockery, L. T. (2016). New Methods in Carbohydrate Chemistry: Dehydrative Glycosylation with Cyclic Phosphonium Anhydrides and α-Selective Glycosylation of Glycosyl Phosphinites. (Masters Thesis). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/201

Chicago Manual of Style (16th Edition):

Dockery, Lance Taylor. “New Methods in Carbohydrate Chemistry: Dehydrative Glycosylation with Cyclic Phosphonium Anhydrides and α-Selective Glycosylation of Glycosyl Phosphinites.” 2016. Masters Thesis, University of Colorado. Accessed May 09, 2021. https://scholar.colorado.edu/chem_gradetds/201.

MLA Handbook (7th Edition):

Dockery, Lance Taylor. “New Methods in Carbohydrate Chemistry: Dehydrative Glycosylation with Cyclic Phosphonium Anhydrides and α-Selective Glycosylation of Glycosyl Phosphinites.” 2016. Web. 09 May 2021.

Vancouver:

Dockery LT. New Methods in Carbohydrate Chemistry: Dehydrative Glycosylation with Cyclic Phosphonium Anhydrides and α-Selective Glycosylation of Glycosyl Phosphinites. [Internet] [Masters thesis]. University of Colorado; 2016. [cited 2021 May 09]. Available from: https://scholar.colorado.edu/chem_gradetds/201.

Council of Science Editors:

Dockery LT. New Methods in Carbohydrate Chemistry: Dehydrative Glycosylation with Cyclic Phosphonium Anhydrides and α-Selective Glycosylation of Glycosyl Phosphinites. [Masters Thesis]. University of Colorado; 2016. Available from: https://scholar.colorado.edu/chem_gradetds/201


University of Adelaide

24. Davies, Benjamin James Lloyd. The stereoselective pharmacokinetics of the enantiomers of perhexiline in poor and extensive metabolisers of the cytochrome P450 2D6.

Degree: 2008, University of Adelaide

 Perhexiline maleate was first introduced for the prophylaxis of exertional angina in the 1970s but reports of adverse reactions, including potentially fatal hepatotoxicity, increasingly restricted… (more)

Subjects/Keywords: pharmacokinetics; Perhexiline; stereoselective; CYP2D6

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Davies, B. J. L. (2008). The stereoselective pharmacokinetics of the enantiomers of perhexiline in poor and extensive metabolisers of the cytochrome P450 2D6. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/52002

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):

Davies, Benjamin James Lloyd. “The stereoselective pharmacokinetics of the enantiomers of perhexiline in poor and extensive metabolisers of the cytochrome P450 2D6.” 2008. Thesis, University of Adelaide. Accessed May 09, 2021. http://hdl.handle.net/2440/52002.

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

MLA Handbook (7th Edition):

Davies, Benjamin James Lloyd. “The stereoselective pharmacokinetics of the enantiomers of perhexiline in poor and extensive metabolisers of the cytochrome P450 2D6.” 2008. Web. 09 May 2021.

Vancouver:

Davies BJL. The stereoselective pharmacokinetics of the enantiomers of perhexiline in poor and extensive metabolisers of the cytochrome P450 2D6. [Internet] [Thesis]. University of Adelaide; 2008. [cited 2021 May 09]. Available from: http://hdl.handle.net/2440/52002.

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

Council of Science Editors:

Davies BJL. The stereoselective pharmacokinetics of the enantiomers of perhexiline in poor and extensive metabolisers of the cytochrome P450 2D6. [Thesis]. University of Adelaide; 2008. Available from: http://hdl.handle.net/2440/52002

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


IUPUI

25. Masters, Andrea Renee. Stereoselective disposition of bupropion and its three major metabolites : 4-hydroxybupropion, erythro-dihydrobupropion, and threo-dihydrobupropion.

Degree: 2016, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

A version of this thesis was published as: Masters AR, McCoy M, Jones DR, and Desta Z. Stereoselective method to… (more)

Subjects/Keywords: Bupropion; Stereoselective; HPLC-MS/MS; 4-Hydroxybupropion; Threo-dihydrobupropion; Erythro-dihydrobupropion

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Masters, A. R. (2016). Stereoselective disposition of bupropion and its three major metabolites : 4-hydroxybupropion, erythro-dihydrobupropion, and threo-dihydrobupropion. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/10935

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):

Masters, Andrea Renee. “Stereoselective disposition of bupropion and its three major metabolites : 4-hydroxybupropion, erythro-dihydrobupropion, and threo-dihydrobupropion.” 2016. Thesis, IUPUI. Accessed May 09, 2021. http://hdl.handle.net/1805/10935.

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

MLA Handbook (7th Edition):

Masters, Andrea Renee. “Stereoselective disposition of bupropion and its three major metabolites : 4-hydroxybupropion, erythro-dihydrobupropion, and threo-dihydrobupropion.” 2016. Web. 09 May 2021.

Vancouver:

Masters AR. Stereoselective disposition of bupropion and its three major metabolites : 4-hydroxybupropion, erythro-dihydrobupropion, and threo-dihydrobupropion. [Internet] [Thesis]. IUPUI; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/1805/10935.

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

Council of Science Editors:

Masters AR. Stereoselective disposition of bupropion and its three major metabolites : 4-hydroxybupropion, erythro-dihydrobupropion, and threo-dihydrobupropion. [Thesis]. IUPUI; 2016. Available from: http://hdl.handle.net/1805/10935

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

26. White, Lorenzo. Stereochemical Control in Complex Molecule Synthesis .

Degree: 2015, Australian National University

 The body of this thesis is comprised of eight scientific articles and is preceded by an overview that contextualises all of this submitted/published work. The… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Synthesis; Natural Products; Stereochemistry; Stereoselective; Radical Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

White, L. (2015). Stereochemical Control in Complex Molecule Synthesis . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/101922

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, Lorenzo. “Stereochemical Control in Complex Molecule Synthesis .” 2015. Thesis, Australian National University. Accessed May 09, 2021. http://hdl.handle.net/1885/101922.

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

MLA Handbook (7th Edition):

White, Lorenzo. “Stereochemical Control in Complex Molecule Synthesis .” 2015. Web. 09 May 2021.

Vancouver:

White L. Stereochemical Control in Complex Molecule Synthesis . [Internet] [Thesis]. Australian National University; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/1885/101922.

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

Council of Science Editors:

White L. Stereochemical Control in Complex Molecule Synthesis . [Thesis]. Australian National University; 2015. Available from: http://hdl.handle.net/1885/101922

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


Brock University

27. Cadwallader, Dusty. Epimeric L-Proline Derived Imidazolone Chiral Auxiliaries for the Stereoselective Alkylative Birch Reduction of Aromatic Esters and Benzonitriles .

Degree: Department of Chemistry, Brock University

 Described in this thesis are several advancements of imidazolidinone chiral auxiliaries. Initially, attempts were made to develop a N-heterocyclic carbene ligand derived from the N-benzyl… (more)

Subjects/Keywords: Stereoselective; Reductive alkylation; Birch reduction

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cadwallader, D. (n.d.). Epimeric L-Proline Derived Imidazolone Chiral Auxiliaries for the Stereoselective Alkylative Birch Reduction of Aromatic Esters and Benzonitriles . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/14813

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Cadwallader, Dusty. “Epimeric L-Proline Derived Imidazolone Chiral Auxiliaries for the Stereoselective Alkylative Birch Reduction of Aromatic Esters and Benzonitriles .” Thesis, Brock University. Accessed May 09, 2021. http://hdl.handle.net/10464/14813.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Cadwallader, Dusty. “Epimeric L-Proline Derived Imidazolone Chiral Auxiliaries for the Stereoselective Alkylative Birch Reduction of Aromatic Esters and Benzonitriles .” Web. 09 May 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Cadwallader D. Epimeric L-Proline Derived Imidazolone Chiral Auxiliaries for the Stereoselective Alkylative Birch Reduction of Aromatic Esters and Benzonitriles . [Internet] [Thesis]. Brock University; [cited 2021 May 09]. Available from: http://hdl.handle.net/10464/14813.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Cadwallader D. Epimeric L-Proline Derived Imidazolone Chiral Auxiliaries for the Stereoselective Alkylative Birch Reduction of Aromatic Esters and Benzonitriles . [Thesis]. Brock University; Available from: http://hdl.handle.net/10464/14813

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Notre Dame

28. William Danny Paquette. Toward the Total Synthesis of 20-Deoxyapoptolidin</h1>.

Degree: Chemistry and Biochemistry, 2006, University of Notre Dame

  Apoptolidin is a polyketide natural product isolated from the bacteria, Nocardiopsis sp. It is a selective apoptotic inducer of cells transformed with the adenovirus… (more)

Subjects/Keywords: apoptolidin; aldol; stereoselective; thionyl chloride

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Paquette, W. D. (2006). Toward the Total Synthesis of 20-Deoxyapoptolidin</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/gb19f47773d

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):

Paquette, William Danny. “Toward the Total Synthesis of 20-Deoxyapoptolidin</h1>.” 2006. Thesis, University of Notre Dame. Accessed May 09, 2021. https://curate.nd.edu/show/gb19f47773d.

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

MLA Handbook (7th Edition):

Paquette, William Danny. “Toward the Total Synthesis of 20-Deoxyapoptolidin</h1>.” 2006. Web. 09 May 2021.

Vancouver:

Paquette WD. Toward the Total Synthesis of 20-Deoxyapoptolidin</h1>. [Internet] [Thesis]. University of Notre Dame; 2006. [cited 2021 May 09]. Available from: https://curate.nd.edu/show/gb19f47773d.

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

Council of Science Editors:

Paquette WD. Toward the Total Synthesis of 20-Deoxyapoptolidin</h1>. [Thesis]. University of Notre Dame; 2006. Available from: https://curate.nd.edu/show/gb19f47773d

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


Duquesne University

29. Zhang, Zhiyu. Unsaturated Nitriles: Stereoselective Annulations and Alkylations.

Degree: PhD, Chemistry and Biochemistry, 2004, Duquesne University

 N-metallated nitriles are fundamental intermediate that have been used to generate new C-C bonds for over a century. C-metallated nitriles are new but equally important… (more)

Subjects/Keywords: Alkylations; Annulations; Nitriles; Stereoselective

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zhang, Z. (2004). Unsaturated Nitriles: Stereoselective Annulations and Alkylations. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1408

Chicago Manual of Style (16th Edition):

Zhang, Zhiyu. “Unsaturated Nitriles: Stereoselective Annulations and Alkylations.” 2004. Doctoral Dissertation, Duquesne University. Accessed May 09, 2021. https://dsc.duq.edu/etd/1408.

MLA Handbook (7th Edition):

Zhang, Zhiyu. “Unsaturated Nitriles: Stereoselective Annulations and Alkylations.” 2004. Web. 09 May 2021.

Vancouver:

Zhang Z. Unsaturated Nitriles: Stereoselective Annulations and Alkylations. [Internet] [Doctoral dissertation]. Duquesne University; 2004. [cited 2021 May 09]. Available from: https://dsc.duq.edu/etd/1408.

Council of Science Editors:

Zhang Z. Unsaturated Nitriles: Stereoselective Annulations and Alkylations. [Doctoral Dissertation]. Duquesne University; 2004. Available from: https://dsc.duq.edu/etd/1408


University of Maryland

30. Blakley, Cathryn Gail. Design and Synthesis of New Group (IV) Cyclopentadienyl Amidinate and Guanidinate Initiators for Controlling the Microstructure of Poly(α-olefins) During Living Coordinative Chain Transfer Polymerizations.

Degree: Chemistry, 2014, University of Maryland

 C1-symmetric, cationic group 4 metal (Zr and Hf) mono-methyl complexes, {(η5-C5Me5)M[N(tBu)C(Me)N(Et)](Me)}[B(C6F5)4], are highly active initiators for the living and stereo-selective (isotactic) coordinative polymerization of propene… (more)

Subjects/Keywords: Chemistry; Polymer chemistry; Living polymerization; Olefins; Stereoselective; Ziegler - Natta

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Blakley, C. G. (2014). Design and Synthesis of New Group (IV) Cyclopentadienyl Amidinate and Guanidinate Initiators for Controlling the Microstructure of Poly(α-olefins) During Living Coordinative Chain Transfer Polymerizations. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/16077

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):

Blakley, Cathryn Gail. “Design and Synthesis of New Group (IV) Cyclopentadienyl Amidinate and Guanidinate Initiators for Controlling the Microstructure of Poly(α-olefins) During Living Coordinative Chain Transfer Polymerizations.” 2014. Thesis, University of Maryland. Accessed May 09, 2021. http://hdl.handle.net/1903/16077.

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

MLA Handbook (7th Edition):

Blakley, Cathryn Gail. “Design and Synthesis of New Group (IV) Cyclopentadienyl Amidinate and Guanidinate Initiators for Controlling the Microstructure of Poly(α-olefins) During Living Coordinative Chain Transfer Polymerizations.” 2014. Web. 09 May 2021.

Vancouver:

Blakley CG. Design and Synthesis of New Group (IV) Cyclopentadienyl Amidinate and Guanidinate Initiators for Controlling the Microstructure of Poly(α-olefins) During Living Coordinative Chain Transfer Polymerizations. [Internet] [Thesis]. University of Maryland; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/1903/16077.

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

Council of Science Editors:

Blakley CG. Design and Synthesis of New Group (IV) Cyclopentadienyl Amidinate and Guanidinate Initiators for Controlling the Microstructure of Poly(α-olefins) During Living Coordinative Chain Transfer Polymerizations. [Thesis]. University of Maryland; 2014. Available from: http://hdl.handle.net/1903/16077

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

[1] [2] [3] [4] [5]

.