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You searched for subject:(asymmetric synthesis). Showing records 1 – 30 of 404 total matches.

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Osaka University

1. Kanbayashi, Naoya; 神林, 直哉. Studies on Novel Asymmetric Allylic Substitution and Asymmetric Polymerization Catalyzed by Planar-Chiral Cyclopentadienyl-Ruthenium Complex : 面不斉シクロペンタジエニルルテニウム錯体を用いた新規不斉アリル位置換反応と不斉重合反応に関する研究; メン フセイ シクロペンタジエニルルテニウム サクタイ ヲ モチイタ シンキ フセイ アリル イチカン ハンノウ ト フセイ ジュウゴウ ハンノウ 二 カンスル ケンキュウ.

Degree: 博士(理学), 2013, Osaka University

This is the author's version of a work that was accepted for publication in Angewandte Chemie International Edition. Changes resulting from the publishing process, such… (more)

Subjects/Keywords: Puthenium; Asymmetric Synthesis

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APA (6th Edition):

Kanbayashi, Naoya; 神林, . (2013). Studies on Novel Asymmetric Allylic Substitution and Asymmetric Polymerization Catalyzed by Planar-Chiral Cyclopentadienyl-Ruthenium Complex : 面不斉シクロペンタジエニルルテニウム錯体を用いた新規不斉アリル位置換反応と不斉重合反応に関する研究; メン フセイ シクロペンタジエニルルテニウム サクタイ ヲ モチイタ シンキ フセイ アリル イチカン ハンノウ ト フセイ ジュウゴウ ハンノウ 二 カンスル ケンキュウ. (Thesis). Osaka University. Retrieved from http://hdl.handle.net/11094/51372

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):

Kanbayashi, Naoya; 神林, 直哉. “Studies on Novel Asymmetric Allylic Substitution and Asymmetric Polymerization Catalyzed by Planar-Chiral Cyclopentadienyl-Ruthenium Complex : 面不斉シクロペンタジエニルルテニウム錯体を用いた新規不斉アリル位置換反応と不斉重合反応に関する研究; メン フセイ シクロペンタジエニルルテニウム サクタイ ヲ モチイタ シンキ フセイ アリル イチカン ハンノウ ト フセイ ジュウゴウ ハンノウ 二 カンスル ケンキュウ.” 2013. Thesis, Osaka University. Accessed November 22, 2019. http://hdl.handle.net/11094/51372.

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

MLA Handbook (7th Edition):

Kanbayashi, Naoya; 神林, 直哉. “Studies on Novel Asymmetric Allylic Substitution and Asymmetric Polymerization Catalyzed by Planar-Chiral Cyclopentadienyl-Ruthenium Complex : 面不斉シクロペンタジエニルルテニウム錯体を用いた新規不斉アリル位置換反応と不斉重合反応に関する研究; メン フセイ シクロペンタジエニルルテニウム サクタイ ヲ モチイタ シンキ フセイ アリル イチカン ハンノウ ト フセイ ジュウゴウ ハンノウ 二 カンスル ケンキュウ.” 2013. Web. 22 Nov 2019.

Vancouver:

Kanbayashi, Naoya; 神林 . Studies on Novel Asymmetric Allylic Substitution and Asymmetric Polymerization Catalyzed by Planar-Chiral Cyclopentadienyl-Ruthenium Complex : 面不斉シクロペンタジエニルルテニウム錯体を用いた新規不斉アリル位置換反応と不斉重合反応に関する研究; メン フセイ シクロペンタジエニルルテニウム サクタイ ヲ モチイタ シンキ フセイ アリル イチカン ハンノウ ト フセイ ジュウゴウ ハンノウ 二 カンスル ケンキュウ. [Internet] [Thesis]. Osaka University; 2013. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/11094/51372.

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

Council of Science Editors:

Kanbayashi, Naoya; 神林 . Studies on Novel Asymmetric Allylic Substitution and Asymmetric Polymerization Catalyzed by Planar-Chiral Cyclopentadienyl-Ruthenium Complex : 面不斉シクロペンタジエニルルテニウム錯体を用いた新規不斉アリル位置換反応と不斉重合反応に関する研究; メン フセイ シクロペンタジエニルルテニウム サクタイ ヲ モチイタ シンキ フセイ アリル イチカン ハンノウ ト フセイ ジュウゴウ ハンノウ 二 カンスル ケンキュウ. [Thesis]. Osaka University; 2013. Available from: http://hdl.handle.net/11094/51372

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


Brock University

2. Zaifman, Joshua David. Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes .

Degree: Department of Chemistry, 2011, Brock University

 This thesis explored the development of several methodologies for the stereoselective construction of ligand frameworks and some of their applications. The first segment concerns the… (more)

Subjects/Keywords: Asymmetric synthesis; Catalysis

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APA (6th Edition):

Zaifman, J. D. (2011). Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/3383

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):

Zaifman, Joshua David. “Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes .” 2011. Thesis, Brock University. Accessed November 22, 2019. http://hdl.handle.net/10464/3383.

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

MLA Handbook (7th Edition):

Zaifman, Joshua David. “Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes .” 2011. Web. 22 Nov 2019.

Vancouver:

Zaifman JD. Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes . [Internet] [Thesis]. Brock University; 2011. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10464/3383.

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

Council of Science Editors:

Zaifman JD. Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes . [Thesis]. Brock University; 2011. Available from: http://hdl.handle.net/10464/3383

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


University of Oxford

3. You, Hengzhi. Non-stabilized nucleophiles in Cu-catalyzed asymmetric synthesis.

Degree: PhD, 2016, University of Oxford

 This thesis describes the study of organozirconium reagents used in copper-catalyzed asymmetric synthesis. Explorations on the asymmetric allylic alkylation of linear substrates, the cyclic substrates… (more)

Subjects/Keywords: 547; Asymmetric synthesis

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APA (6th Edition):

You, H. (2016). Non-stabilized nucleophiles in Cu-catalyzed asymmetric synthesis. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:765cdc58-75a9-490b-b879-38b95b7b79ec ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730049

Chicago Manual of Style (16th Edition):

You, Hengzhi. “Non-stabilized nucleophiles in Cu-catalyzed asymmetric synthesis.” 2016. Doctoral Dissertation, University of Oxford. Accessed November 22, 2019. http://ora.ox.ac.uk/objects/uuid:765cdc58-75a9-490b-b879-38b95b7b79ec ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730049.

MLA Handbook (7th Edition):

You, Hengzhi. “Non-stabilized nucleophiles in Cu-catalyzed asymmetric synthesis.” 2016. Web. 22 Nov 2019.

Vancouver:

You H. Non-stabilized nucleophiles in Cu-catalyzed asymmetric synthesis. [Internet] [Doctoral dissertation]. University of Oxford; 2016. [cited 2019 Nov 22]. Available from: http://ora.ox.ac.uk/objects/uuid:765cdc58-75a9-490b-b879-38b95b7b79ec ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730049.

Council of Science Editors:

You H. Non-stabilized nucleophiles in Cu-catalyzed asymmetric synthesis. [Doctoral Dissertation]. University of Oxford; 2016. Available from: http://ora.ox.ac.uk/objects/uuid:765cdc58-75a9-490b-b879-38b95b7b79ec ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730049


Hong Kong University of Science and Technology

4. Sun, Lijie. Synthesis of atropisomeric 1-Naphthamide-Derived phosphines and application for asymmetric heck and Suzuki-Miyaura reactions.

Degree: 2009, Hong Kong University of Science and Technology

Asymmetric carbon–carbon bond formation reactions are some of the most important processes, which enable key steps in building of complex molecules. The palladium-catalyzed asymmetric carbon–carbon… (more)

Subjects/Keywords: Phosphine  – Synthesis; Asymmetric synthesis

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APA (6th Edition):

Sun, L. (2009). Synthesis of atropisomeric 1-Naphthamide-Derived phosphines and application for asymmetric heck and Suzuki-Miyaura reactions. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1070295 ; http://repository.ust.hk/ir/bitstream/1783.1-6215/1/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):

Sun, Lijie. “Synthesis of atropisomeric 1-Naphthamide-Derived phosphines and application for asymmetric heck and Suzuki-Miyaura reactions.” 2009. Thesis, Hong Kong University of Science and Technology. Accessed November 22, 2019. https://doi.org/10.14711/thesis-b1070295 ; http://repository.ust.hk/ir/bitstream/1783.1-6215/1/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):

Sun, Lijie. “Synthesis of atropisomeric 1-Naphthamide-Derived phosphines and application for asymmetric heck and Suzuki-Miyaura reactions.” 2009. Web. 22 Nov 2019.

Vancouver:

Sun L. Synthesis of atropisomeric 1-Naphthamide-Derived phosphines and application for asymmetric heck and Suzuki-Miyaura reactions. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2009. [cited 2019 Nov 22]. Available from: https://doi.org/10.14711/thesis-b1070295 ; http://repository.ust.hk/ir/bitstream/1783.1-6215/1/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:

Sun L. Synthesis of atropisomeric 1-Naphthamide-Derived phosphines and application for asymmetric heck and Suzuki-Miyaura reactions. [Thesis]. Hong Kong University of Science and Technology; 2009. Available from: https://doi.org/10.14711/thesis-b1070295 ; http://repository.ust.hk/ir/bitstream/1783.1-6215/1/th_redirect.html

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


University of North Carolina – Greensboro

5. Benavides, Amanda Rache. Facile synthesis of enantioenriched hydroxy esters via Brønsted acid catalyzed kinetic resolution.

Degree: 2014, University of North Carolina – Greensboro

 The synthesis of natural products is a growing area of research within the field of chemistry. Compounds are extracted from sources such as fungi, plants,… (more)

Subjects/Keywords: Asymmetric synthesis; Natural products – Synthesis

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APA (6th Edition):

Benavides, A. R. (2014). Facile synthesis of enantioenriched hydroxy esters via Brønsted acid catalyzed kinetic resolution. (Masters Thesis). University of North Carolina – Greensboro. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16552

Chicago Manual of Style (16th Edition):

Benavides, Amanda Rache. “Facile synthesis of enantioenriched hydroxy esters via Brønsted acid catalyzed kinetic resolution.” 2014. Masters Thesis, University of North Carolina – Greensboro. Accessed November 22, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16552.

MLA Handbook (7th Edition):

Benavides, Amanda Rache. “Facile synthesis of enantioenriched hydroxy esters via Brønsted acid catalyzed kinetic resolution.” 2014. Web. 22 Nov 2019.

Vancouver:

Benavides AR. Facile synthesis of enantioenriched hydroxy esters via Brønsted acid catalyzed kinetic resolution. [Internet] [Masters thesis]. University of North Carolina – Greensboro; 2014. [cited 2019 Nov 22]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16552.

Council of Science Editors:

Benavides AR. Facile synthesis of enantioenriched hydroxy esters via Brønsted acid catalyzed kinetic resolution. [Masters Thesis]. University of North Carolina – Greensboro; 2014. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16552


University of KwaZulu-Natal

6. [No author]. Synthesis of camphor derived ligands for applications in asymmetric catalysis.

Degree: Chemistry, 2009, University of KwaZulu-Natal

 Chiral monoterpenes such as camphor have been widely used in the development of asymmetric catalysts with varying degrees of success. Pyridyl N-donor ligands derived from… (more)

Subjects/Keywords: Camphor.; Asymmetric synthesis.; Chemistry.

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APA (6th Edition):

author], [. (2009). Synthesis of camphor derived ligands for applications in asymmetric catalysis. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/7870

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):

author], [No. “Synthesis of camphor derived ligands for applications in asymmetric catalysis. ” 2009. Thesis, University of KwaZulu-Natal. Accessed November 22, 2019. http://hdl.handle.net/10413/7870.

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

MLA Handbook (7th Edition):

author], [No. “Synthesis of camphor derived ligands for applications in asymmetric catalysis. ” 2009. Web. 22 Nov 2019.

Vancouver:

author] [. Synthesis of camphor derived ligands for applications in asymmetric catalysis. [Internet] [Thesis]. University of KwaZulu-Natal; 2009. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10413/7870.

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

Council of Science Editors:

author] [. Synthesis of camphor derived ligands for applications in asymmetric catalysis. [Thesis]. University of KwaZulu-Natal; 2009. Available from: http://hdl.handle.net/10413/7870

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


Nelson Mandela Metropolitan University

7. Saku, Duduetsang. Synthesis and characterization of symmetrical and unsymmetrical ferrocenyl ligands for use in the preparation of Redox Active Ruthenium Alkylidene Complexes.

Degree: MSc, Faculty of Science, 2007, Nelson Mandela Metropolitan University

 Oxidation of a ferrocenyl group in conjugation to another metal centre can alter the electron density at that metal centre and lead to a change… (more)

Subjects/Keywords: Ferrocene; Ligands; Asymmetric synthesis

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APA (6th Edition):

Saku, D. (2007). Synthesis and characterization of symmetrical and unsymmetrical ferrocenyl ligands for use in the preparation of Redox Active Ruthenium Alkylidene Complexes. (Masters Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/701

Chicago Manual of Style (16th Edition):

Saku, Duduetsang. “Synthesis and characterization of symmetrical and unsymmetrical ferrocenyl ligands for use in the preparation of Redox Active Ruthenium Alkylidene Complexes.” 2007. Masters Thesis, Nelson Mandela Metropolitan University. Accessed November 22, 2019. http://hdl.handle.net/10948/701.

MLA Handbook (7th Edition):

Saku, Duduetsang. “Synthesis and characterization of symmetrical and unsymmetrical ferrocenyl ligands for use in the preparation of Redox Active Ruthenium Alkylidene Complexes.” 2007. Web. 22 Nov 2019.

Vancouver:

Saku D. Synthesis and characterization of symmetrical and unsymmetrical ferrocenyl ligands for use in the preparation of Redox Active Ruthenium Alkylidene Complexes. [Internet] [Masters thesis]. Nelson Mandela Metropolitan University; 2007. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10948/701.

Council of Science Editors:

Saku D. Synthesis and characterization of symmetrical and unsymmetrical ferrocenyl ligands for use in the preparation of Redox Active Ruthenium Alkylidene Complexes. [Masters Thesis]. Nelson Mandela Metropolitan University; 2007. Available from: http://hdl.handle.net/10948/701


Nelson Mandela Metropolitan University

8. Pohl, Pieter Lourens. Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions.

Degree: Faculty of Science, 2015, Nelson Mandela Metropolitan University

 In this study, we investigated the potential of a novel chiral host compound (+)-(2R,3R)-1,1,4,4-tetraphenylbutane-1,2,3,4-tetraol (TETROL) and its derivatives for use in racemate resolution using host-guest… (more)

Subjects/Keywords: Chemistry, Organic; Chirality; Asymmetric synthesis

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APA (6th Edition):

Pohl, P. L. (2015). Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions. (Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/2879

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):

Pohl, Pieter Lourens. “Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions.” 2015. Thesis, Nelson Mandela Metropolitan University. Accessed November 22, 2019. http://hdl.handle.net/10948/2879.

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

MLA Handbook (7th Edition):

Pohl, Pieter Lourens. “Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions.” 2015. Web. 22 Nov 2019.

Vancouver:

Pohl PL. Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2015. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10948/2879.

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

Council of Science Editors:

Pohl PL. Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions. [Thesis]. Nelson Mandela Metropolitan University; 2015. Available from: http://hdl.handle.net/10948/2879

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


Oregon State University

9. Sephton, Mark Alan. Synthesis of novel ambifunctional atropisomeric 2,2',6,6'-tetrasubstituted biphenyls and investigation of their properties and organocatalytic activity.

Degree: PhD, Chemistry, 2008, Oregon State University

 Ambifunctional axially chiral 2,2',6,6'-tetrasubstituted biphenyls containing nucleophilic (or basic) functional groups juxtaposed with hydrogen-bond donors were synthesized and their properties studied. Applications for the prepared… (more)

Subjects/Keywords: Asymmetric; Biphenyl compounds  – Synthesis

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APA (6th Edition):

Sephton, M. A. (2008). Synthesis of novel ambifunctional atropisomeric 2,2',6,6'-tetrasubstituted biphenyls and investigation of their properties and organocatalytic activity. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/8905

Chicago Manual of Style (16th Edition):

Sephton, Mark Alan. “Synthesis of novel ambifunctional atropisomeric 2,2',6,6'-tetrasubstituted biphenyls and investigation of their properties and organocatalytic activity.” 2008. Doctoral Dissertation, Oregon State University. Accessed November 22, 2019. http://hdl.handle.net/1957/8905.

MLA Handbook (7th Edition):

Sephton, Mark Alan. “Synthesis of novel ambifunctional atropisomeric 2,2',6,6'-tetrasubstituted biphenyls and investigation of their properties and organocatalytic activity.” 2008. Web. 22 Nov 2019.

Vancouver:

Sephton MA. Synthesis of novel ambifunctional atropisomeric 2,2',6,6'-tetrasubstituted biphenyls and investigation of their properties and organocatalytic activity. [Internet] [Doctoral dissertation]. Oregon State University; 2008. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1957/8905.

Council of Science Editors:

Sephton MA. Synthesis of novel ambifunctional atropisomeric 2,2',6,6'-tetrasubstituted biphenyls and investigation of their properties and organocatalytic activity. [Doctoral Dissertation]. Oregon State University; 2008. Available from: http://hdl.handle.net/1957/8905


University of Adelaide

10. Christie, Hamish S. Synthesis and effectiveness of a new cyclohexyl chiral auxiliary and studies towards the systhesis of bicyclo[4.4.4]tetradeca-3,8,12-triyne.

Degree: 1999, University of Adelaide

Subjects/Keywords: Asymmetric synthesis

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APA (6th Edition):

Christie, H. S. (1999). Synthesis and effectiveness of a new cyclohexyl chiral auxiliary and studies towards the systhesis of bicyclo[4.4.4]tetradeca-3,8,12-triyne. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/110297

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):

Christie, Hamish S. “Synthesis and effectiveness of a new cyclohexyl chiral auxiliary and studies towards the systhesis of bicyclo[4.4.4]tetradeca-3,8,12-triyne.” 1999. Thesis, University of Adelaide. Accessed November 22, 2019. http://hdl.handle.net/2440/110297.

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

MLA Handbook (7th Edition):

Christie, Hamish S. “Synthesis and effectiveness of a new cyclohexyl chiral auxiliary and studies towards the systhesis of bicyclo[4.4.4]tetradeca-3,8,12-triyne.” 1999. Web. 22 Nov 2019.

Vancouver:

Christie HS. Synthesis and effectiveness of a new cyclohexyl chiral auxiliary and studies towards the systhesis of bicyclo[4.4.4]tetradeca-3,8,12-triyne. [Internet] [Thesis]. University of Adelaide; 1999. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/2440/110297.

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

Council of Science Editors:

Christie HS. Synthesis and effectiveness of a new cyclohexyl chiral auxiliary and studies towards the systhesis of bicyclo[4.4.4]tetradeca-3,8,12-triyne. [Thesis]. University of Adelaide; 1999. Available from: http://hdl.handle.net/2440/110297

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


University of Oxford

11. Yang, Jinchao. Development and application of bifunctional iminophosphorane organocatalysts.

Degree: PhD, 2016, University of Oxford

 This thesis presents the development and application of bifunctional iminophosphorane (BIMP) organocatalysts, incorporating a triaryl-substituted iminophosphorane organosuperbase for organocatalytic enantioselective reactions. Chapter 2 describes the… (more)

Subjects/Keywords: 547; Organic chemistry; Asymmetric synthesis

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APA (6th Edition):

Yang, J. (2016). Development and application of bifunctional iminophosphorane organocatalysts. (Doctoral Dissertation). University of Oxford. Retrieved from https://ora.ox.ac.uk/objects/uuid:fa250f43-ab91-4aec-9fa3-f6ccdb444bb5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728891

Chicago Manual of Style (16th Edition):

Yang, Jinchao. “Development and application of bifunctional iminophosphorane organocatalysts.” 2016. Doctoral Dissertation, University of Oxford. Accessed November 22, 2019. https://ora.ox.ac.uk/objects/uuid:fa250f43-ab91-4aec-9fa3-f6ccdb444bb5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728891.

MLA Handbook (7th Edition):

Yang, Jinchao. “Development and application of bifunctional iminophosphorane organocatalysts.” 2016. Web. 22 Nov 2019.

Vancouver:

Yang J. Development and application of bifunctional iminophosphorane organocatalysts. [Internet] [Doctoral dissertation]. University of Oxford; 2016. [cited 2019 Nov 22]. Available from: https://ora.ox.ac.uk/objects/uuid:fa250f43-ab91-4aec-9fa3-f6ccdb444bb5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728891.

Council of Science Editors:

Yang J. Development and application of bifunctional iminophosphorane organocatalysts. [Doctoral Dissertation]. University of Oxford; 2016. Available from: https://ora.ox.ac.uk/objects/uuid:fa250f43-ab91-4aec-9fa3-f6ccdb444bb5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728891


University of Guelph

12. Findlay, Joseph. Chiral beta-Amino Sulfenates: Synthetic Access and Diastereoselective Alkylation .

Degree: 2019, University of Guelph

 Research into a new family of chiral sulfenates containing a β-substituted, N-protected β- amino functionality, derived from amino acids, has been extended in this investigation… (more)

Subjects/Keywords: Sulfenates; Sulfoxides; Asymmetric; Synthesis; Sulfur

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APA (6th Edition):

Findlay, J. (2019). Chiral beta-Amino Sulfenates: Synthetic Access and Diastereoselective Alkylation . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16084

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):

Findlay, Joseph. “Chiral beta-Amino Sulfenates: Synthetic Access and Diastereoselective Alkylation .” 2019. Thesis, University of Guelph. Accessed November 22, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16084.

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

MLA Handbook (7th Edition):

Findlay, Joseph. “Chiral beta-Amino Sulfenates: Synthetic Access and Diastereoselective Alkylation .” 2019. Web. 22 Nov 2019.

Vancouver:

Findlay J. Chiral beta-Amino Sulfenates: Synthetic Access and Diastereoselective Alkylation . [Internet] [Thesis]. University of Guelph; 2019. [cited 2019 Nov 22]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16084.

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

Council of Science Editors:

Findlay J. Chiral beta-Amino Sulfenates: Synthetic Access and Diastereoselective Alkylation . [Thesis]. University of Guelph; 2019. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16084

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


Michigan State University

13. Valles, Luis. A study of some factors that influence asymmetric induction in additions to 3-phenyl-2-pentanone-1,1,1,3-d₄̲ and 2-phenylbutanal-2-d₁̲.

Degree: MS, Dept. of Chemistry, 1970, Michigan State University

Subjects/Keywords: Asymmetric synthesis

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APA (6th Edition):

Valles, L. (1970). A study of some factors that influence asymmetric induction in additions to 3-phenyl-2-pentanone-1,1,1,3-d₄̲ and 2-phenylbutanal-2-d₁̲. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:9007

Chicago Manual of Style (16th Edition):

Valles, Luis. “A study of some factors that influence asymmetric induction in additions to 3-phenyl-2-pentanone-1,1,1,3-d₄̲ and 2-phenylbutanal-2-d₁̲.” 1970. Masters Thesis, Michigan State University. Accessed November 22, 2019. http://etd.lib.msu.edu/islandora/object/etd:9007.

MLA Handbook (7th Edition):

Valles, Luis. “A study of some factors that influence asymmetric induction in additions to 3-phenyl-2-pentanone-1,1,1,3-d₄̲ and 2-phenylbutanal-2-d₁̲.” 1970. Web. 22 Nov 2019.

Vancouver:

Valles L. A study of some factors that influence asymmetric induction in additions to 3-phenyl-2-pentanone-1,1,1,3-d₄̲ and 2-phenylbutanal-2-d₁̲. [Internet] [Masters thesis]. Michigan State University; 1970. [cited 2019 Nov 22]. Available from: http://etd.lib.msu.edu/islandora/object/etd:9007.

Council of Science Editors:

Valles L. A study of some factors that influence asymmetric induction in additions to 3-phenyl-2-pentanone-1,1,1,3-d₄̲ and 2-phenylbutanal-2-d₁̲. [Masters Thesis]. Michigan State University; 1970. Available from: http://etd.lib.msu.edu/islandora/object/etd:9007


University of Hong Kong

14. 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 November 22, 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. 22 Nov 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 Nov 22]. 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


Hong Kong University of Science and Technology

15. Chen, Zhilong. Development of new asymmetric desymmetrization reactions catalyzed by chiral phosphoric acids.

Degree: 2013, Hong Kong University of Science and Technology

 This thesis mainly involves CPA-catalyzed desymmetrization of symmetrical oxetanes and acetals. Several interesting and useful catalytic asymmetric reactions have been developed for the synthesis of… (more)

Subjects/Keywords: Asymmetric synthesis; Tetrahydrofuran; Heterocyclic compounds; Synthesis

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APA (6th Edition):

Chen, Z. (2013). Development of new asymmetric desymmetrization reactions catalyzed by chiral phosphoric acids. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1254344 ; http://repository.ust.hk/ir/bitstream/1783.1-62235/1/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):

Chen, Zhilong. “Development of new asymmetric desymmetrization reactions catalyzed by chiral phosphoric acids.” 2013. Thesis, Hong Kong University of Science and Technology. Accessed November 22, 2019. https://doi.org/10.14711/thesis-b1254344 ; http://repository.ust.hk/ir/bitstream/1783.1-62235/1/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):

Chen, Zhilong. “Development of new asymmetric desymmetrization reactions catalyzed by chiral phosphoric acids.” 2013. Web. 22 Nov 2019.

Vancouver:

Chen Z. Development of new asymmetric desymmetrization reactions catalyzed by chiral phosphoric acids. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2013. [cited 2019 Nov 22]. Available from: https://doi.org/10.14711/thesis-b1254344 ; http://repository.ust.hk/ir/bitstream/1783.1-62235/1/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:

Chen Z. Development of new asymmetric desymmetrization reactions catalyzed by chiral phosphoric acids. [Thesis]. Hong Kong University of Science and Technology; 2013. Available from: https://doi.org/10.14711/thesis-b1254344 ; http://repository.ust.hk/ir/bitstream/1783.1-62235/1/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

16. Hermeke, Julia. Chiral phosphonium ion tagged and spiroindane-based organocatalysts.

Degree: M. Phil., 2011, University of Hong Kong

The research on asymmetric organocatalysis has been intensifying since the beginning of 2000. The growing interest in this research area is driven by the importance… (more)

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

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APA (6th Edition):

Hermeke, J. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Masters Thesis). University of Hong Kong. Retrieved from Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871

Chicago Manual of Style (16th Edition):

Hermeke, Julia. “Chiral phosphonium ion tagged and spiroindane-based organocatalysts.” 2011. Masters Thesis, University of Hong Kong. Accessed November 22, 2019. Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871.

MLA Handbook (7th Edition):

Hermeke, Julia. “Chiral phosphonium ion tagged and spiroindane-based organocatalysts.” 2011. Web. 22 Nov 2019.

Vancouver:

Hermeke J. Chiral phosphonium ion tagged and spiroindane-based organocatalysts. [Internet] [Masters thesis]. University of Hong Kong; 2011. [cited 2019 Nov 22]. Available from: Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871.

Council of Science Editors:

Hermeke J. Chiral phosphonium ion tagged and spiroindane-based organocatalysts. [Masters Thesis]. University of Hong Kong; 2011. Available from: Hermeke, J.. (2011). Chiral phosphonium ion tagged and spiroindane-based organocatalysts. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4729568 ; http://dx.doi.org/10.5353/th_b4729568 ; http://hdl.handle.net/10722/205871


University of Hong Kong

17. 汪子玉; Wang, Ziyu. Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes.

Degree: PhD, 2012, University of Hong Kong

The synthesis of useful chiral skeletons from simple achiral starting materials is always the dream of organic chemists. In the past decades, organocatalysis has been… (more)

Subjects/Keywords: Nitroalkenes; Asymmetric synthesis; Dibenzofurans; Organic compounds - Synthesis

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APA (6th Edition):

汪子玉; Wang, Z. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388

Chicago Manual of Style (16th Edition):

汪子玉; Wang, Ziyu. “Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed November 22, 2019. Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388.

MLA Handbook (7th Edition):

汪子玉; Wang, Ziyu. “Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes.” 2012. Web. 22 Nov 2019.

Vancouver:

汪子玉; Wang Z. Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2019 Nov 22]. Available from: Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388.

Council of Science Editors:

汪子玉; Wang Z. Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Wang, Z. [汪子玉]. (2012). Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979914 ; http://dx.doi.org/10.5353/th_b4979914 ; http://hdl.handle.net/10722/193388


University of Oxford

18. Zammit, Charlotte Maria. Asymmetric synthesis of β- and γ- amino acids.

Degree: PhD, 2015, University of Oxford

 This thesis is concerned with the development of new synthetic routes for the asymmetric syntheses of a range of β- and γ-amino acids. Chapter 1… (more)

Subjects/Keywords: 547; Asymmetric synthesis; Amino acids – Synthesis

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APA (6th Edition):

Zammit, C. M. (2015). Asymmetric synthesis of β- and γ- amino acids. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:35138286-c217-4d28-990b-941149b5daa5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692875

Chicago Manual of Style (16th Edition):

Zammit, Charlotte Maria. “Asymmetric synthesis of β- and γ- amino acids.” 2015. Doctoral Dissertation, University of Oxford. Accessed November 22, 2019. http://ora.ox.ac.uk/objects/uuid:35138286-c217-4d28-990b-941149b5daa5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692875.

MLA Handbook (7th Edition):

Zammit, Charlotte Maria. “Asymmetric synthesis of β- and γ- amino acids.” 2015. Web. 22 Nov 2019.

Vancouver:

Zammit CM. Asymmetric synthesis of β- and γ- amino acids. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2019 Nov 22]. Available from: http://ora.ox.ac.uk/objects/uuid:35138286-c217-4d28-990b-941149b5daa5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692875.

Council of Science Editors:

Zammit CM. Asymmetric synthesis of β- and γ- amino acids. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:35138286-c217-4d28-990b-941149b5daa5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692875

19. Shaw, Subrata. Cis-2,5-diaminobicyclo[2.2.2]octane : a novel C₂-symmetric scaffold for asymmetric catalysis.

Degree: PhD, Chemistry, 2014, Oregon State University

 This thesis describes the development of a new enantioselective synthetic method employing chiral cis-2,5-diaminobicyclo[2.2.2]octane-based organometallic catalysts. The significance of this new method to organic synthesis(more)

Subjects/Keywords: Asymmetric Synthesis; Asymmetric synthesis

…catalyst loading and reaction temperature .86 5.3 Asymmetric synthesis of I3-nitro alcohols… …asymmetric synthesis, the rational design of chiral ligands is still in its infancy and it is not… …x28;a) Asymmetric Catalysis in Organic Synthesis; Noyori, R., Ed.; Wiley: New York… …1994. (b) Catalytic Asymmetric Synthesis, 2nd ed.; Ojima, I., Ed.; Wiley-VCH: New… …for a chiral template that would have broad utility as a catalyst in asymmetric synthesis… 

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APA (6th Edition):

Shaw, S. (2014). Cis-2,5-diaminobicyclo[2.2.2]octane : a novel C₂-symmetric scaffold for asymmetric catalysis. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/46034

Chicago Manual of Style (16th Edition):

Shaw, Subrata. “Cis-2,5-diaminobicyclo[2.2.2]octane : a novel C₂-symmetric scaffold for asymmetric catalysis.” 2014. Doctoral Dissertation, Oregon State University. Accessed November 22, 2019. http://hdl.handle.net/1957/46034.

MLA Handbook (7th Edition):

Shaw, Subrata. “Cis-2,5-diaminobicyclo[2.2.2]octane : a novel C₂-symmetric scaffold for asymmetric catalysis.” 2014. Web. 22 Nov 2019.

Vancouver:

Shaw S. Cis-2,5-diaminobicyclo[2.2.2]octane : a novel C₂-symmetric scaffold for asymmetric catalysis. [Internet] [Doctoral dissertation]. Oregon State University; 2014. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1957/46034.

Council of Science Editors:

Shaw S. Cis-2,5-diaminobicyclo[2.2.2]octane : a novel C₂-symmetric scaffold for asymmetric catalysis. [Doctoral Dissertation]. Oregon State University; 2014. Available from: http://hdl.handle.net/1957/46034


Northeastern University

20. Blechman, Scotty. Synthesis Of Racemic And Enantiopure Samples Of Zearalenone.

Degree: MS, Department of Chemistry and Chemical Biology, 2019, Northeastern University

 Herein, synthesis of the resorcylic acid lactone (RAL) zearalenone is investigated. As an excellent model compound, zearalenone has been synthesized over 20 times, but the… (more)

Subjects/Keywords: asymmetric catalysis; asymmetric synthesis; de novo synthesis; macrolactone; organic synthesis; zearalenone; Organic chemistry; Chemistry

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APA (6th Edition):

Blechman, S. (2019). Synthesis Of Racemic And Enantiopure Samples Of Zearalenone. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20317958

Chicago Manual of Style (16th Edition):

Blechman, Scotty. “Synthesis Of Racemic And Enantiopure Samples Of Zearalenone.” 2019. Masters Thesis, Northeastern University. Accessed November 22, 2019. http://hdl.handle.net/2047/D20317958.

MLA Handbook (7th Edition):

Blechman, Scotty. “Synthesis Of Racemic And Enantiopure Samples Of Zearalenone.” 2019. Web. 22 Nov 2019.

Vancouver:

Blechman S. Synthesis Of Racemic And Enantiopure Samples Of Zearalenone. [Internet] [Masters thesis]. Northeastern University; 2019. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/2047/D20317958.

Council of Science Editors:

Blechman S. Synthesis Of Racemic And Enantiopure Samples Of Zearalenone. [Masters Thesis]. Northeastern University; 2019. Available from: http://hdl.handle.net/2047/D20317958


University of North Carolina – Greensboro

21. Wilent, Jennifer E. Enantioselective cyclization of symmetric diesters.

Degree: 2016, University of North Carolina – Greensboro

 Two important facets that are found in many biologically active compounds and complex natural products are chirality and heterocyclic motifs, in particular lactones and lactams.… (more)

Subjects/Keywords: Lactones – Synthesis; Lactams – Synthesis; Asymmetric synthesis; Enantioselective catalysis

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APA (6th Edition):

Wilent, J. E. (2016). Enantioselective cyclization of symmetric diesters. (Doctoral Dissertation). University of North Carolina – Greensboro. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=19824

Chicago Manual of Style (16th Edition):

Wilent, Jennifer E. “Enantioselective cyclization of symmetric diesters.” 2016. Doctoral Dissertation, University of North Carolina – Greensboro. Accessed November 22, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=19824.

MLA Handbook (7th Edition):

Wilent, Jennifer E. “Enantioselective cyclization of symmetric diesters.” 2016. Web. 22 Nov 2019.

Vancouver:

Wilent JE. Enantioselective cyclization of symmetric diesters. [Internet] [Doctoral dissertation]. University of North Carolina – Greensboro; 2016. [cited 2019 Nov 22]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=19824.

Council of Science Editors:

Wilent JE. Enantioselective cyclization of symmetric diesters. [Doctoral Dissertation]. University of North Carolina – Greensboro; 2016. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=19824


University of Illinois – Urbana-Champaign

22. Macor, Joseph Alexander. On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 The work described herein details the synthesis of a variety of pentavalent organophosphorus compounds and their applications as ligands to address important problems in coordination… (more)

Subjects/Keywords: Asymmetric Synthesis; Minor Actinide Separations; Heterogeneous Asymmetric Catalysis

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APA (6th Edition):

Macor, J. A. (2015). On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78615

Chicago Manual of Style (16th Edition):

Macor, Joseph Alexander. “On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 22, 2019. http://hdl.handle.net/2142/78615.

MLA Handbook (7th Edition):

Macor, Joseph Alexander. “On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds.” 2015. Web. 22 Nov 2019.

Vancouver:

Macor JA. On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/2142/78615.

Council of Science Editors:

Macor JA. On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78615


University of St Andrews

23. Noonan, Gary M. Asymmetric hydroformylation : a powerful tool for the synthesis of pharmaceutical intermediates.

Degree: PhD, 2011, University of St Andrews

 The hydroformylation of unfunctionalised olefins (such as prop-1-ene and oct-1-ene) is an extremely valuable process and is practised on a massive scale industrially in the… (more)

Subjects/Keywords: 660; Catalysis; Asymmetric hydroformylation; Asymmetric synthesis; Green chemistry

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APA (6th Edition):

Noonan, G. M. (2011). Asymmetric hydroformylation : a powerful tool for the synthesis of pharmaceutical intermediates. (Doctoral Dissertation). University of St Andrews. Retrieved from http://hdl.handle.net/10023/3105

Chicago Manual of Style (16th Edition):

Noonan, Gary M. “Asymmetric hydroformylation : a powerful tool for the synthesis of pharmaceutical intermediates.” 2011. Doctoral Dissertation, University of St Andrews. Accessed November 22, 2019. http://hdl.handle.net/10023/3105.

MLA Handbook (7th Edition):

Noonan, Gary M. “Asymmetric hydroformylation : a powerful tool for the synthesis of pharmaceutical intermediates.” 2011. Web. 22 Nov 2019.

Vancouver:

Noonan GM. Asymmetric hydroformylation : a powerful tool for the synthesis of pharmaceutical intermediates. [Internet] [Doctoral dissertation]. University of St Andrews; 2011. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10023/3105.

Council of Science Editors:

Noonan GM. Asymmetric hydroformylation : a powerful tool for the synthesis of pharmaceutical intermediates. [Doctoral Dissertation]. University of St Andrews; 2011. Available from: http://hdl.handle.net/10023/3105

24. Jamsheera, A. Synthesis and characterization of new asymmetric metal based potential chemotherapeutic agents and their in vitro DNA binding studies; -.

Degree: Chemistry, 2002, Aligarh Muslim University

Abstract available newline

Bibliography p.145-162

Advisors/Committee Members: Arjmand, farukh.

Subjects/Keywords: Synthesis; asymmetric; chemotherapeutic

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APA (6th Edition):

Jamsheera, A. (2002). Synthesis and characterization of new asymmetric metal based potential chemotherapeutic agents and their in vitro DNA binding studies; -. (Thesis). Aligarh Muslim University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/28513

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):

Jamsheera, A. “Synthesis and characterization of new asymmetric metal based potential chemotherapeutic agents and their in vitro DNA binding studies; -.” 2002. Thesis, Aligarh Muslim University. Accessed November 22, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/28513.

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

MLA Handbook (7th Edition):

Jamsheera, A. “Synthesis and characterization of new asymmetric metal based potential chemotherapeutic agents and their in vitro DNA binding studies; -.” 2002. Web. 22 Nov 2019.

Vancouver:

Jamsheera A. Synthesis and characterization of new asymmetric metal based potential chemotherapeutic agents and their in vitro DNA binding studies; -. [Internet] [Thesis]. Aligarh Muslim University; 2002. [cited 2019 Nov 22]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/28513.

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

Council of Science Editors:

Jamsheera A. Synthesis and characterization of new asymmetric metal based potential chemotherapeutic agents and their in vitro DNA binding studies; -. [Thesis]. Aligarh Muslim University; 2002. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/28513

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

25. Bena, Luvuyo Clifford. Investigations into the asymmetric reduction of ketones.

Degree: Faculty of Science, 2003, University of Port Elizabeth

 A six-step synthesis of salbutamol from methyl salicylate with an overall yield of 17% has been completed, although the yield was not optimised. In the… (more)

Subjects/Keywords: Ketones; Asymmetric synthesis

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APA (6th Edition):

Bena, L. C. (2003). Investigations into the asymmetric reduction of ketones. (Thesis). University of Port Elizabeth. Retrieved from http://hdl.handle.net/10948/323

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):

Bena, Luvuyo Clifford. “Investigations into the asymmetric reduction of ketones.” 2003. Thesis, University of Port Elizabeth. Accessed November 22, 2019. http://hdl.handle.net/10948/323.

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

MLA Handbook (7th Edition):

Bena, Luvuyo Clifford. “Investigations into the asymmetric reduction of ketones.” 2003. Web. 22 Nov 2019.

Vancouver:

Bena LC. Investigations into the asymmetric reduction of ketones. [Internet] [Thesis]. University of Port Elizabeth; 2003. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10948/323.

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

Council of Science Editors:

Bena LC. Investigations into the asymmetric reduction of ketones. [Thesis]. University of Port Elizabeth; 2003. Available from: http://hdl.handle.net/10948/323

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

26. Wouters, Ana Dionéia. Carboidratos como matéria-prima para a preparação de substratos quirais: aplicações em catálise enantiosseletiva e processos diastereosseletivos.

Degree: PhD, Insumos Farmacêuticos, 2013, University of São Paulo

O presente trabalho descreve o uso de carboidratos como materiais de partida para a preparação de catalisadores quirais e também de substratos quirais. Primeiramente estudos… (more)

Subjects/Keywords: Asymmetric synthesis; Carbohydrates; Carboidratos; Síntese assimétrica

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APA (6th Edition):

Wouters, A. D. (2013). Carboidratos como matéria-prima para a preparação de substratos quirais: aplicações em catálise enantiosseletiva e processos diastereosseletivos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/9/9138/tde-01102013-151136/ ;

Chicago Manual of Style (16th Edition):

Wouters, Ana Dionéia. “Carboidratos como matéria-prima para a preparação de substratos quirais: aplicações em catálise enantiosseletiva e processos diastereosseletivos.” 2013. Doctoral Dissertation, University of São Paulo. Accessed November 22, 2019. http://www.teses.usp.br/teses/disponiveis/9/9138/tde-01102013-151136/ ;.

MLA Handbook (7th Edition):

Wouters, Ana Dionéia. “Carboidratos como matéria-prima para a preparação de substratos quirais: aplicações em catálise enantiosseletiva e processos diastereosseletivos.” 2013. Web. 22 Nov 2019.

Vancouver:

Wouters AD. Carboidratos como matéria-prima para a preparação de substratos quirais: aplicações em catálise enantiosseletiva e processos diastereosseletivos. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2019 Nov 22]. Available from: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-01102013-151136/ ;.

Council of Science Editors:

Wouters AD. Carboidratos como matéria-prima para a preparação de substratos quirais: aplicações em catálise enantiosseletiva e processos diastereosseletivos. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-01102013-151136/ ;

27. Laxmi Narasimhulu, G. Asymmetric Synthesis of Amines by the Applications of (S) or (R) Tert-Butanesulfinamide and Study on Synthesis of 2-Haloalkyl-1, 2-Benzisoxazoles; -.

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

The thesis entitled Asymmetric Synthesis of amines by the applications of (S) or (R) tert -butanesulfinamide and study on synthesis of 3-haloalkyl-1,2-benzisoxazoles has been divided… (more)

Subjects/Keywords: Amines; Applications; Asymmetric; Benzisoxazoles; Haloalky; Synthesis

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APA (6th Edition):

Laxmi Narasimhulu, G. (2013). Asymmetric Synthesis of Amines by the Applications of (S) or (R) Tert-Butanesulfinamide and Study on Synthesis of 2-Haloalkyl-1, 2-Benzisoxazoles; -. (Thesis). Jawaharlal Nehru Technological University, Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19553

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):

Laxmi Narasimhulu, G. “Asymmetric Synthesis of Amines by the Applications of (S) or (R) Tert-Butanesulfinamide and Study on Synthesis of 2-Haloalkyl-1, 2-Benzisoxazoles; -.” 2013. Thesis, Jawaharlal Nehru Technological University, Hyderabad. Accessed November 22, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/19553.

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

MLA Handbook (7th Edition):

Laxmi Narasimhulu, G. “Asymmetric Synthesis of Amines by the Applications of (S) or (R) Tert-Butanesulfinamide and Study on Synthesis of 2-Haloalkyl-1, 2-Benzisoxazoles; -.” 2013. Web. 22 Nov 2019.

Vancouver:

Laxmi Narasimhulu G. Asymmetric Synthesis of Amines by the Applications of (S) or (R) Tert-Butanesulfinamide and Study on Synthesis of 2-Haloalkyl-1, 2-Benzisoxazoles; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. [cited 2019 Nov 22]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19553.

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

Council of Science Editors:

Laxmi Narasimhulu G. Asymmetric Synthesis of Amines by the Applications of (S) or (R) Tert-Butanesulfinamide and Study on Synthesis of 2-Haloalkyl-1, 2-Benzisoxazoles; -. [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19553

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


University of California – Berkeley

28. Neel, Andrew James. Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements.

Degree: Chemistry, 2016, University of California – Berkeley

 Throughout my doctoral studies, I have endeavored to address the question of how to rationally design chiral catalysts to control enantioselectivity in a predictable fashion.… (more)

Subjects/Keywords: Chemistry; Asymmetric Catalysis; Organic Synthesis; Organocatalysis

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APA (6th Edition):

Neel, A. J. (2016). Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/34d2396n

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):

Neel, Andrew James. “Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements.” 2016. Thesis, University of California – Berkeley. Accessed November 22, 2019. http://www.escholarship.org/uc/item/34d2396n.

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

MLA Handbook (7th Edition):

Neel, Andrew James. “Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements.” 2016. Web. 22 Nov 2019.

Vancouver:

Neel AJ. Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Nov 22]. Available from: http://www.escholarship.org/uc/item/34d2396n.

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

Council of Science Editors:

Neel AJ. Toward the Rational Design of Asymmetric Catalysts using Attractive Non-Covalent Interactions and Design Elements. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/34d2396n

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


National University of Ireland – Galway

29. Mc Cleary, Nadine. Design, synthesis and catalytic activity of novel oxazoline based ligands.

Degree: 2015, National University of Ireland – Galway

This thesis can be viewed as two separate studies. Firstly, the design, synthesis and catalytic activity of novel 2-pyridyl mono(oxazoline). A family of mono(oxazoline) ligands… (more)

Subjects/Keywords: Asymmetric catalysis; Organic synthesis; School of Chemistry

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APA (6th Edition):

Mc Cleary, N. (2015). Design, synthesis and catalytic activity of novel oxazoline based ligands. (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/5210

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):

Mc Cleary, Nadine. “Design, synthesis and catalytic activity of novel oxazoline based ligands.” 2015. Thesis, National University of Ireland – Galway. Accessed November 22, 2019. http://hdl.handle.net/10379/5210.

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

MLA Handbook (7th Edition):

Mc Cleary, Nadine. “Design, synthesis and catalytic activity of novel oxazoline based ligands.” 2015. Web. 22 Nov 2019.

Vancouver:

Mc Cleary N. Design, synthesis and catalytic activity of novel oxazoline based ligands. [Internet] [Thesis]. National University of Ireland – Galway; 2015. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10379/5210.

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

Council of Science Editors:

Mc Cleary N. Design, synthesis and catalytic activity of novel oxazoline based ligands. [Thesis]. National University of Ireland – Galway; 2015. Available from: http://hdl.handle.net/10379/5210

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


Mississippi State University

30. Chakraborty, Amarraj. The method development for synthesizing chiral CCC-NHC Zr pincer complexes.

Degree: MS, Chemistry, 2015, Mississippi State University

  There are numerous classes of N-heterocyclic carbenes (NHCs) that have been synthesized since the discovery of stable NHCs in 1988. Their application as ligands… (more)

Subjects/Keywords: synthesis; Zr chemistry; organometallic chemistry; asymmetric catalysis

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APA (6th Edition):

Chakraborty, A. (2015). The method development for synthesizing chiral CCC-NHC Zr pincer complexes. (Masters Thesis). Mississippi State University. Retrieved from http://sun.library.msstate.edu/ETD-db/theses/available/etd-08062015-162047/ ;

Chicago Manual of Style (16th Edition):

Chakraborty, Amarraj. “The method development for synthesizing chiral CCC-NHC Zr pincer complexes.” 2015. Masters Thesis, Mississippi State University. Accessed November 22, 2019. http://sun.library.msstate.edu/ETD-db/theses/available/etd-08062015-162047/ ;.

MLA Handbook (7th Edition):

Chakraborty, Amarraj. “The method development for synthesizing chiral CCC-NHC Zr pincer complexes.” 2015. Web. 22 Nov 2019.

Vancouver:

Chakraborty A. The method development for synthesizing chiral CCC-NHC Zr pincer complexes. [Internet] [Masters thesis]. Mississippi State University; 2015. [cited 2019 Nov 22]. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-08062015-162047/ ;.

Council of Science Editors:

Chakraborty A. The method development for synthesizing chiral CCC-NHC Zr pincer complexes. [Masters Thesis]. Mississippi State University; 2015. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-08062015-162047/ ;

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