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:(asymmetric). Showing records 1 – 30 of 1750 total matches.

[1] [2] [3] [4] [5] … [59]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters

1. Khumsubdee, Sakunchai. Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations.

Degree: 2013, Texas Digital Library

 N-Heterocyclic carbene and phosphorus ligands have been synthesized and used for many catalytic reactions including chiral analogs of Crabtree???s catalyst for asymmetric hydrogenation. These catalysts… (more)

Subjects/Keywords: Asymmetric Hydrogenation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Khumsubdee, S. (2013). Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations. (Thesis). Texas Digital Library. Retrieved from http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66618

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):

Khumsubdee, Sakunchai. “Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations.” 2013. Thesis, Texas Digital Library. Accessed February 24, 2020. http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66618.

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

MLA Handbook (7th Edition):

Khumsubdee, Sakunchai. “Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations.” 2013. Web. 24 Feb 2020.

Vancouver:

Khumsubdee S. Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations. [Internet] [Thesis]. Texas Digital Library; 2013. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66618.

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

Council of Science Editors:

Khumsubdee S. Synthesis and Application of New Ligands Derived from N-Heterocyclic Carbenes, Phosphines and Phosphites for Asymmetric Hydrogenations. [Thesis]. Texas Digital Library; 2013. Available from: http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66618

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

2. Al-Taie, Zahraa. Amino acid substituted guanidines as organocatalysts.

Degree: PhD, 2019, Bangor University

 A series of amino acid substituted guanidines of general structure I and II (AA = L-Proline, L-alanine and L-phenylalanine derivatives; (R, R1, R2 = H,… (more)

Subjects/Keywords: asymmetric orhganocatalysts

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Al-Taie, Z. (2019). Amino acid substituted guanidines as organocatalysts. (Doctoral Dissertation). Bangor University. Retrieved from https://research.bangor.ac.uk/portal/en/theses/amino-acid-substituted-guanidines-as-organocatalysts(38a784b4-e5cc-45a9-96d5-ef206987304b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.787506

Chicago Manual of Style (16th Edition):

Al-Taie, Zahraa. “Amino acid substituted guanidines as organocatalysts.” 2019. Doctoral Dissertation, Bangor University. Accessed February 24, 2020. https://research.bangor.ac.uk/portal/en/theses/amino-acid-substituted-guanidines-as-organocatalysts(38a784b4-e5cc-45a9-96d5-ef206987304b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.787506.

MLA Handbook (7th Edition):

Al-Taie, Zahraa. “Amino acid substituted guanidines as organocatalysts.” 2019. Web. 24 Feb 2020.

Vancouver:

Al-Taie Z. Amino acid substituted guanidines as organocatalysts. [Internet] [Doctoral dissertation]. Bangor University; 2019. [cited 2020 Feb 24]. Available from: https://research.bangor.ac.uk/portal/en/theses/amino-acid-substituted-guanidines-as-organocatalysts(38a784b4-e5cc-45a9-96d5-ef206987304b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.787506.

Council of Science Editors:

Al-Taie Z. Amino acid substituted guanidines as organocatalysts. [Doctoral Dissertation]. Bangor University; 2019. Available from: https://research.bangor.ac.uk/portal/en/theses/amino-acid-substituted-guanidines-as-organocatalysts(38a784b4-e5cc-45a9-96d5-ef206987304b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.787506


Queens University

3. de Winter, Tamara. Asymmetric Homogeneous Hydrogenation of Prochiral Substrates Mediated Through Carboxylic Acid and Carbamic Acid Metal-Binding Functional Groups .

Degree: Chemistry, 2016, Queens University

 The need for enantiopure chiral compounds has driven the development of asymmetric synthesis, and more specifically asymmetric catalysis. The ability to selectively produce one enantiomer… (more)

Subjects/Keywords: Hydrogenation; Asymmetric

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

de Winter, T. (2016). Asymmetric Homogeneous Hydrogenation of Prochiral Substrates Mediated Through Carboxylic Acid and Carbamic Acid Metal-Binding Functional Groups . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13922

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):

de Winter, Tamara. “Asymmetric Homogeneous Hydrogenation of Prochiral Substrates Mediated Through Carboxylic Acid and Carbamic Acid Metal-Binding Functional Groups .” 2016. Thesis, Queens University. Accessed February 24, 2020. http://hdl.handle.net/1974/13922.

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

MLA Handbook (7th Edition):

de Winter, Tamara. “Asymmetric Homogeneous Hydrogenation of Prochiral Substrates Mediated Through Carboxylic Acid and Carbamic Acid Metal-Binding Functional Groups .” 2016. Web. 24 Feb 2020.

Vancouver:

de Winter T. Asymmetric Homogeneous Hydrogenation of Prochiral Substrates Mediated Through Carboxylic Acid and Carbamic Acid Metal-Binding Functional Groups . [Internet] [Thesis]. Queens University; 2016. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/1974/13922.

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

Council of Science Editors:

de Winter T. Asymmetric Homogeneous Hydrogenation of Prochiral Substrates Mediated Through Carboxylic Acid and Carbamic Acid Metal-Binding Functional Groups . [Thesis]. Queens University; 2016. Available from: http://hdl.handle.net/1974/13922

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


University of Oxford

4. Maciver, Eleanor E. Asymmetric electrocyclic reactions.

Degree: PhD, 2013, University of Oxford

 Pericyclic reactions are a class of transformations that comprise sigmatropic rearrangements, group transfer reactions, cycloadditions and electrocyclic reactions. Since Woodward and Hoffmann rationalized the mechanism… (more)

Subjects/Keywords: 547; Asymmetric catalysis; Electrocyclization; Asymmetric; Catalysis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Maciver, E. E. (2013). Asymmetric electrocyclic reactions. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:17ba3cb0-0c62-406a-bed4-14c410a45918 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588436

Chicago Manual of Style (16th Edition):

Maciver, Eleanor E. “Asymmetric electrocyclic reactions.” 2013. Doctoral Dissertation, University of Oxford. Accessed February 24, 2020. http://ora.ox.ac.uk/objects/uuid:17ba3cb0-0c62-406a-bed4-14c410a45918 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588436.

MLA Handbook (7th Edition):

Maciver, Eleanor E. “Asymmetric electrocyclic reactions.” 2013. Web. 24 Feb 2020.

Vancouver:

Maciver EE. Asymmetric electrocyclic reactions. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Feb 24]. Available from: http://ora.ox.ac.uk/objects/uuid:17ba3cb0-0c62-406a-bed4-14c410a45918 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588436.

Council of Science Editors:

Maciver EE. Asymmetric electrocyclic reactions. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:17ba3cb0-0c62-406a-bed4-14c410a45918 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.588436


Brock University

5. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 February 24, 2020. 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. 24 Feb 2020.

Vancouver:

Zaifman JD. Stereoselective synthesis of substituted hexahydro-3a,4a-diazacyclopentaphenanthren-4-ones and aminoferrocenes . [Internet] [Thesis]. Brock University; 2011. [cited 2020 Feb 24]. 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 Notre Dame

6. Eric C. Hansen. Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>.

Degree: PhD, Chemistry and Biochemistry, 2017, University of Notre Dame

Asymmetric synthesis is a major focus in modern organic chemistry. Experimentally screening for selective ligands is a cumbersome process, and provides only indirect insight… (more)

Subjects/Keywords: Chemistry; Asymmetric catalysis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hansen, E. C. (2017). Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/wd375t37h4h

Chicago Manual of Style (16th Edition):

Hansen, Eric C.. “Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>.” 2017. Doctoral Dissertation, University of Notre Dame. Accessed February 24, 2020. https://curate.nd.edu/show/wd375t37h4h.

MLA Handbook (7th Edition):

Hansen, Eric C.. “Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>.” 2017. Web. 24 Feb 2020.

Vancouver:

Hansen EC. Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2017. [cited 2020 Feb 24]. Available from: https://curate.nd.edu/show/wd375t37h4h.

Council of Science Editors:

Hansen EC. Development and Applications of Quantum to Molecular Mechanics (Q2MM)</h1>. [Doctoral Dissertation]. University of Notre Dame; 2017. Available from: https://curate.nd.edu/show/wd375t37h4h


Penn State University

7. Miller, Eric Jacob. Development of a Phosphorus (III)-Mediated Asymmetric Reductive C-N and C-O Bond Forming Method.

Degree: MS, Chemistry, 2012, Penn State University

 Synthetic methods leading to the formation of carbonyl derivatives with α- heterofunctionality are valuable for the synthesis of important molecular targets. The research described in… (more)

Subjects/Keywords: Asymmetric; Phosphorus; Ramirez

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Miller, E. J. (2012). Development of a Phosphorus (III)-Mediated Asymmetric Reductive C-N and C-O Bond Forming Method. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/27609

Chicago Manual of Style (16th Edition):

Miller, Eric Jacob. “Development of a Phosphorus (III)-Mediated Asymmetric Reductive C-N and C-O Bond Forming Method.” 2012. Masters Thesis, Penn State University. Accessed February 24, 2020. https://etda.libraries.psu.edu/catalog/27609.

MLA Handbook (7th Edition):

Miller, Eric Jacob. “Development of a Phosphorus (III)-Mediated Asymmetric Reductive C-N and C-O Bond Forming Method.” 2012. Web. 24 Feb 2020.

Vancouver:

Miller EJ. Development of a Phosphorus (III)-Mediated Asymmetric Reductive C-N and C-O Bond Forming Method. [Internet] [Masters thesis]. Penn State University; 2012. [cited 2020 Feb 24]. Available from: https://etda.libraries.psu.edu/catalog/27609.

Council of Science Editors:

Miller EJ. Development of a Phosphorus (III)-Mediated Asymmetric Reductive C-N and C-O Bond Forming Method. [Masters Thesis]. Penn State University; 2012. Available from: https://etda.libraries.psu.edu/catalog/27609


Osaka University

8. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 February 24, 2020. 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. 24 Feb 2020.

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 2020 Feb 24]. 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


University of Debrecen

9. Kovács, Győző. Asymmetric synthesis of an AmpC analog boronic acid .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Kémiai Intézet, 2012, University of Debrecen

 The aim of this thesis is to synthetize a boronic acid analog of ampicillin. Ampicillin is a widely emloyed antibiotic in clinical use (for instance,… (more)

Subjects/Keywords: boronic acid; asymmetric

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kovács, G. (2012). Asymmetric synthesis of an AmpC analog boronic acid . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/128983

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):

Kovács, Győző. “Asymmetric synthesis of an AmpC analog boronic acid .” 2012. Thesis, University of Debrecen. Accessed February 24, 2020. http://hdl.handle.net/2437/128983.

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

MLA Handbook (7th Edition):

Kovács, Győző. “Asymmetric synthesis of an AmpC analog boronic acid .” 2012. Web. 24 Feb 2020.

Vancouver:

Kovács G. Asymmetric synthesis of an AmpC analog boronic acid . [Internet] [Thesis]. University of Debrecen; 2012. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2437/128983.

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

Council of Science Editors:

Kovács G. Asymmetric synthesis of an AmpC analog boronic acid . [Thesis]. University of Debrecen; 2012. Available from: http://hdl.handle.net/2437/128983

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


University of Arizona

10. Lu, Chin-Wei. Synthesis of Asymmetric Phthalocyanine Derivatives .

Degree: 2013, University of Arizona

 The work in this dissertation describes improved methods of asymmetrically substituted Pc derivative synthesis addressing some currently encountered problems including: (1) the need for facile… (more)

Subjects/Keywords: Phthalocyanine; Chemistry; Asymmetric

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lu, C. (2013). Synthesis of Asymmetric Phthalocyanine Derivatives . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/312651

Chicago Manual of Style (16th Edition):

Lu, Chin-Wei. “Synthesis of Asymmetric Phthalocyanine Derivatives .” 2013. Doctoral Dissertation, University of Arizona. Accessed February 24, 2020. http://hdl.handle.net/10150/312651.

MLA Handbook (7th Edition):

Lu, Chin-Wei. “Synthesis of Asymmetric Phthalocyanine Derivatives .” 2013. Web. 24 Feb 2020.

Vancouver:

Lu C. Synthesis of Asymmetric Phthalocyanine Derivatives . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/10150/312651.

Council of Science Editors:

Lu C. Synthesis of Asymmetric Phthalocyanine Derivatives . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/312651


University of Oxford

11. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 February 24, 2020. 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. 24 Feb 2020.

Vancouver:

You H. Non-stabilized nucleophiles in Cu-catalyzed asymmetric synthesis. [Internet] [Doctoral dissertation]. University of Oxford; 2016. [cited 2020 Feb 24]. 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


University of Alberta

12. Bhakta, Urmi Bhusan. Investigation of Neglected Areas of Asymmetric Carbonyl Allylboration Chemistry.

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

Asymmetric allylboration is a very useful and potent method for the synthesis of chiral homoallylic alcohols, a structural motif present in many natural products and… (more)

Subjects/Keywords: Imine allylboration; Asymmetric allylboration; Fluorination

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bhakta, U. B. (2015). Investigation of Neglected Areas of Asymmetric Carbonyl Allylboration Chemistry. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/h702q904v

Chicago Manual of Style (16th Edition):

Bhakta, Urmi Bhusan. “Investigation of Neglected Areas of Asymmetric Carbonyl Allylboration Chemistry.” 2015. Doctoral Dissertation, University of Alberta. Accessed February 24, 2020. https://era.library.ualberta.ca/files/h702q904v.

MLA Handbook (7th Edition):

Bhakta, Urmi Bhusan. “Investigation of Neglected Areas of Asymmetric Carbonyl Allylboration Chemistry.” 2015. Web. 24 Feb 2020.

Vancouver:

Bhakta UB. Investigation of Neglected Areas of Asymmetric Carbonyl Allylboration Chemistry. [Internet] [Doctoral dissertation]. University of Alberta; 2015. [cited 2020 Feb 24]. Available from: https://era.library.ualberta.ca/files/h702q904v.

Council of Science Editors:

Bhakta UB. Investigation of Neglected Areas of Asymmetric Carbonyl Allylboration Chemistry. [Doctoral Dissertation]. University of Alberta; 2015. Available from: https://era.library.ualberta.ca/files/h702q904v


Baylor University

13. Bell, Jason R. Synthesis and application of C₂ asymmetric phosphinines via their pyrylium salt precursors.

Degree: Chemistry and Biochemistry., 2010, Baylor University

 The development of new chiral ligands for asymmetric catalysis is an increasingly important area of research. Though many ligands are phosphorus based, one class of… (more)

Subjects/Keywords: Organic chemistry.; Asymmetric catalysis.; Phosphinines.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bell, J. R. (2010). Synthesis and application of C₂ asymmetric phosphinines via their pyrylium salt precursors. (Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/7925

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):

Bell, Jason R. “Synthesis and application of C₂ asymmetric phosphinines via their pyrylium salt precursors. ” 2010. Thesis, Baylor University. Accessed February 24, 2020. http://hdl.handle.net/2104/7925.

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

MLA Handbook (7th Edition):

Bell, Jason R. “Synthesis and application of C₂ asymmetric phosphinines via their pyrylium salt precursors. ” 2010. Web. 24 Feb 2020.

Vancouver:

Bell JR. Synthesis and application of C₂ asymmetric phosphinines via their pyrylium salt precursors. [Internet] [Thesis]. Baylor University; 2010. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2104/7925.

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

Council of Science Editors:

Bell JR. Synthesis and application of C₂ asymmetric phosphinines via their pyrylium salt precursors. [Thesis]. Baylor University; 2010. Available from: http://hdl.handle.net/2104/7925

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


University of KwaZulu-Natal

14. [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.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 February 24, 2020. 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. 24 Feb 2020.

Vancouver:

author] [. Synthesis of camphor derived ligands for applications in asymmetric catalysis. [Internet] [Thesis]. University of KwaZulu-Natal; 2009. [cited 2020 Feb 24]. 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

15. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 February 24, 2020. 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. 24 Feb 2020.

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 2020 Feb 24]. 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


University of Rochester

16. Rabinowitz, Jeremy S. (1982 - ). Centrosome-mediated RNA segregation : a novel patterning mechanism in Ilyanassa.

Degree: PhD, 2010, University of Rochester

 All multicellular organisms require asymmetric cell divisions for normal patterning during embryogenesis. Spiralian embryos are thought to be particularly reliant on autonomous cues for embryonic… (more)

Subjects/Keywords: Asymmetric cell division; Spiralia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rabinowitz, J. S. (. -. ). (2010). Centrosome-mediated RNA segregation : a novel patterning mechanism in Ilyanassa. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/12775

Chicago Manual of Style (16th Edition):

Rabinowitz, Jeremy S (1982 - ). “Centrosome-mediated RNA segregation : a novel patterning mechanism in Ilyanassa.” 2010. Doctoral Dissertation, University of Rochester. Accessed February 24, 2020. http://hdl.handle.net/1802/12775.

MLA Handbook (7th Edition):

Rabinowitz, Jeremy S (1982 - ). “Centrosome-mediated RNA segregation : a novel patterning mechanism in Ilyanassa.” 2010. Web. 24 Feb 2020.

Vancouver:

Rabinowitz JS(-). Centrosome-mediated RNA segregation : a novel patterning mechanism in Ilyanassa. [Internet] [Doctoral dissertation]. University of Rochester; 2010. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/1802/12775.

Council of Science Editors:

Rabinowitz JS(-). Centrosome-mediated RNA segregation : a novel patterning mechanism in Ilyanassa. [Doctoral Dissertation]. University of Rochester; 2010. Available from: http://hdl.handle.net/1802/12775


University of Southern California

17. Kelsom, Corey Sayuri Kauai. Asymmetric cell division during neurogenesis, and the mechanisms behind GABAergic cortical interneuron development and specification.

Degree: MS, Biochemistry and Molecular Biology, 2012, University of Southern California

 On the most basic level, an asymmetric division is a developmental process that produces two daughter cells, each possessing a different identity or fate. Progenitor… (more)

Subjects/Keywords: neuroblast; asymmetric; GABA; cortical; interneuron

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kelsom, C. S. K. (2012). Asymmetric cell division during neurogenesis, and the mechanisms behind GABAergic cortical interneuron development and specification. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/116106/rec/975

Chicago Manual of Style (16th Edition):

Kelsom, Corey Sayuri Kauai. “Asymmetric cell division during neurogenesis, and the mechanisms behind GABAergic cortical interneuron development and specification.” 2012. Masters Thesis, University of Southern California. Accessed February 24, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/116106/rec/975.

MLA Handbook (7th Edition):

Kelsom, Corey Sayuri Kauai. “Asymmetric cell division during neurogenesis, and the mechanisms behind GABAergic cortical interneuron development and specification.” 2012. Web. 24 Feb 2020.

Vancouver:

Kelsom CSK. Asymmetric cell division during neurogenesis, and the mechanisms behind GABAergic cortical interneuron development and specification. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2020 Feb 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/116106/rec/975.

Council of Science Editors:

Kelsom CSK. Asymmetric cell division during neurogenesis, and the mechanisms behind GABAergic cortical interneuron development and specification. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/116106/rec/975


Addis Ababa University

18. YIBEKAL, KASSA. TRANSPORT DRIVEN BY A RANDOM TELEGRAPH FORCE IN AN ASYMMETRIC MEMBRANE CHANNEL .

Degree: 2013, Addis Ababa University

 Channel proteins that selectively conduct molecules across the cell membrane often exhibit an asymmetric structure. By means of a stochastic model the channel asymmetry in… (more)

Subjects/Keywords: ASYMMETRIC MEMBRANE CHANNEL; TELEGRAPH FORCE

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

YIBEKAL, K. (2013). TRANSPORT DRIVEN BY A RANDOM TELEGRAPH FORCE IN AN ASYMMETRIC MEMBRANE CHANNEL . (Thesis). Addis Ababa University. Retrieved from http://etd.aau.edu.et/dspace/handle/123456789/1317

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):

YIBEKAL, KASSA. “TRANSPORT DRIVEN BY A RANDOM TELEGRAPH FORCE IN AN ASYMMETRIC MEMBRANE CHANNEL .” 2013. Thesis, Addis Ababa University. Accessed February 24, 2020. http://etd.aau.edu.et/dspace/handle/123456789/1317.

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

MLA Handbook (7th Edition):

YIBEKAL, KASSA. “TRANSPORT DRIVEN BY A RANDOM TELEGRAPH FORCE IN AN ASYMMETRIC MEMBRANE CHANNEL .” 2013. Web. 24 Feb 2020.

Vancouver:

YIBEKAL K. TRANSPORT DRIVEN BY A RANDOM TELEGRAPH FORCE IN AN ASYMMETRIC MEMBRANE CHANNEL . [Internet] [Thesis]. Addis Ababa University; 2013. [cited 2020 Feb 24]. Available from: http://etd.aau.edu.et/dspace/handle/123456789/1317.

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

Council of Science Editors:

YIBEKAL K. TRANSPORT DRIVEN BY A RANDOM TELEGRAPH FORCE IN AN ASYMMETRIC MEMBRANE CHANNEL . [Thesis]. Addis Ababa University; 2013. Available from: http://etd.aau.edu.et/dspace/handle/123456789/1317

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


Nelson Mandela Metropolitan University

19. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 February 24, 2020. 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. 24 Feb 2020.

Vancouver:

Pohl PL. Tetrol and derivatives: synthesis, host-guest properties and racemate resolutions. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2015. [cited 2020 Feb 24]. 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


Penn State University

20. SUN, XIANFENG. HIGHLY ENANTIOSELECTIVE TRANSITION METAL-CATALYZED HYDROGENATION EACTIONS: AN EFFICIENT TOOL FOR THE.

Degree: PhD, Chemistry, 2008, Penn State University

 Catalytic asymmetric synthesis is a significant component in modern organic chemistry. Transition metal enantioselective catalysis is certainly among the most challenging and widely investigated areas… (more)

Subjects/Keywords: asymmetric hydrogenation; chiral ligand

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

SUN, X. (2008). HIGHLY ENANTIOSELECTIVE TRANSITION METAL-CATALYZED HYDROGENATION EACTIONS: AN EFFICIENT TOOL FOR THE. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8172

Chicago Manual of Style (16th Edition):

SUN, XIANFENG. “HIGHLY ENANTIOSELECTIVE TRANSITION METAL-CATALYZED HYDROGENATION EACTIONS: AN EFFICIENT TOOL FOR THE.” 2008. Doctoral Dissertation, Penn State University. Accessed February 24, 2020. https://etda.libraries.psu.edu/catalog/8172.

MLA Handbook (7th Edition):

SUN, XIANFENG. “HIGHLY ENANTIOSELECTIVE TRANSITION METAL-CATALYZED HYDROGENATION EACTIONS: AN EFFICIENT TOOL FOR THE.” 2008. Web. 24 Feb 2020.

Vancouver:

SUN X. HIGHLY ENANTIOSELECTIVE TRANSITION METAL-CATALYZED HYDROGENATION EACTIONS: AN EFFICIENT TOOL FOR THE. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2020 Feb 24]. Available from: https://etda.libraries.psu.edu/catalog/8172.

Council of Science Editors:

SUN X. HIGHLY ENANTIOSELECTIVE TRANSITION METAL-CATALYZED HYDROGENATION EACTIONS: AN EFFICIENT TOOL FOR THE. [Doctoral Dissertation]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8172


Penn State University

21. Zhang, Weicheng. DEVELOPMENT OF EFFECTIVE CHIRAL LIGANDS FOR CATALYTIC ASYMMETRIC HYDROGENATION.

Degree: PhD, Chemistry, 2009, Penn State University

 This thesis summarizes the author’s graduate research on catalytic asymmetric hydrogenation at Penn State. The first chapter gives a brief review of ligand development in… (more)

Subjects/Keywords: hydrogenation; asymmetric; catalysis; ligand; rhodium

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zhang, W. (2009). DEVELOPMENT OF EFFECTIVE CHIRAL LIGANDS FOR CATALYTIC ASYMMETRIC HYDROGENATION. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/9308

Chicago Manual of Style (16th Edition):

Zhang, Weicheng. “DEVELOPMENT OF EFFECTIVE CHIRAL LIGANDS FOR CATALYTIC ASYMMETRIC HYDROGENATION.” 2009. Doctoral Dissertation, Penn State University. Accessed February 24, 2020. https://etda.libraries.psu.edu/catalog/9308.

MLA Handbook (7th Edition):

Zhang, Weicheng. “DEVELOPMENT OF EFFECTIVE CHIRAL LIGANDS FOR CATALYTIC ASYMMETRIC HYDROGENATION.” 2009. Web. 24 Feb 2020.

Vancouver:

Zhang W. DEVELOPMENT OF EFFECTIVE CHIRAL LIGANDS FOR CATALYTIC ASYMMETRIC HYDROGENATION. [Internet] [Doctoral dissertation]. Penn State University; 2009. [cited 2020 Feb 24]. Available from: https://etda.libraries.psu.edu/catalog/9308.

Council of Science Editors:

Zhang W. DEVELOPMENT OF EFFECTIVE CHIRAL LIGANDS FOR CATALYTIC ASYMMETRIC HYDROGENATION. [Doctoral Dissertation]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/9308


Penn State University

22. Zou, Yaping. SYNTHESIS OF NEW PHOSPHORUS LIGANDS FOR ASYMMETRIC CATALYSIS.

Degree: MS, Chemistry, 2009, Penn State University

Asymmetric hydroformylation is one of the most challenging transformations because it requires both high enantioselectivities and regioselectivies with high activity. Also, there are few effective… (more)

Subjects/Keywords: hydrogenation; asymmetric; phosphorus ligands; hydroformylation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zou, Y. (2009). SYNTHESIS OF NEW PHOSPHORUS LIGANDS FOR ASYMMETRIC CATALYSIS. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/9392

Chicago Manual of Style (16th Edition):

Zou, Yaping. “SYNTHESIS OF NEW PHOSPHORUS LIGANDS FOR ASYMMETRIC CATALYSIS.” 2009. Masters Thesis, Penn State University. Accessed February 24, 2020. https://etda.libraries.psu.edu/catalog/9392.

MLA Handbook (7th Edition):

Zou, Yaping. “SYNTHESIS OF NEW PHOSPHORUS LIGANDS FOR ASYMMETRIC CATALYSIS.” 2009. Web. 24 Feb 2020.

Vancouver:

Zou Y. SYNTHESIS OF NEW PHOSPHORUS LIGANDS FOR ASYMMETRIC CATALYSIS. [Internet] [Masters thesis]. Penn State University; 2009. [cited 2020 Feb 24]. Available from: https://etda.libraries.psu.edu/catalog/9392.

Council of Science Editors:

Zou Y. SYNTHESIS OF NEW PHOSPHORUS LIGANDS FOR ASYMMETRIC CATALYSIS. [Masters Thesis]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/9392


University of California – Berkeley

23. Brown, Casey Jameson. Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host.

Degree: Chemistry, 2011, University of California – Berkeley

 Chapter 1. An overview of supramolecular catalysis is presented with attention to the diverse strategies used in developing these materials. Different strategies for the design… (more)

Subjects/Keywords: Chemistry; asymmetric; catalysis; organometallic; supramolecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Brown, C. J. (2011). Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7jv7m4wh

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):

Brown, Casey Jameson. “Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host.” 2011. Thesis, University of California – Berkeley. Accessed February 24, 2020. http://www.escholarship.org/uc/item/7jv7m4wh.

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

MLA Handbook (7th Edition):

Brown, Casey Jameson. “Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host.” 2011. Web. 24 Feb 2020.

Vancouver:

Brown CJ. Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2020 Feb 24]. Available from: http://www.escholarship.org/uc/item/7jv7m4wh.

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

Council of Science Editors:

Brown CJ. Asymmetric and Organometallic Catalysis Mediated by a Chiral Supramolecular Host. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/7jv7m4wh

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


Montana Tech

24. Guo, Lilu. Exploring the interaction between asymmetric phosphonates and acetylcholinesterase. Probing the gorge and P-site via customized covalent modification.

Degree: PhD, 2008, Montana Tech

  Organophosphates (OPs) react with acetylcholinesterases (AChEs) to form a covalent bond at a specific serine residue in the active gorge, thereby providing a highly… (more)

Subjects/Keywords: asymmetric phosphonates

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Guo, L. (2008). Exploring the interaction between asymmetric phosphonates and acetylcholinesterase. Probing the gorge and P-site via customized covalent modification. (Doctoral Dissertation). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/421

Chicago Manual of Style (16th Edition):

Guo, Lilu. “Exploring the interaction between asymmetric phosphonates and acetylcholinesterase. Probing the gorge and P-site via customized covalent modification.” 2008. Doctoral Dissertation, Montana Tech. Accessed February 24, 2020. https://scholarworks.umt.edu/etd/421.

MLA Handbook (7th Edition):

Guo, Lilu. “Exploring the interaction between asymmetric phosphonates and acetylcholinesterase. Probing the gorge and P-site via customized covalent modification.” 2008. Web. 24 Feb 2020.

Vancouver:

Guo L. Exploring the interaction between asymmetric phosphonates and acetylcholinesterase. Probing the gorge and P-site via customized covalent modification. [Internet] [Doctoral dissertation]. Montana Tech; 2008. [cited 2020 Feb 24]. Available from: https://scholarworks.umt.edu/etd/421.

Council of Science Editors:

Guo L. Exploring the interaction between asymmetric phosphonates and acetylcholinesterase. Probing the gorge and P-site via customized covalent modification. [Doctoral Dissertation]. Montana Tech; 2008. Available from: https://scholarworks.umt.edu/etd/421


Stellenbosch University

25. Andrade, Julio Anthony. The possibility of sacrifice: a Levinasian reconceptualisation of supererogation.

Degree: PhD, Philosophy, 2018, Stellenbosch University

ENGLISH ABSTRACT: This study offers a reconceptualisation of supererogation based on the ethics of Emmanuel Levinas. The study comprises two parts. In Part I, a… (more)

Subjects/Keywords: UCTD; Autonomy; Supererogation; Asymmetric information

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Andrade, J. A. (2018). The possibility of sacrifice: a Levinasian reconceptualisation of supererogation. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/104857

Chicago Manual of Style (16th Edition):

Andrade, Julio Anthony. “The possibility of sacrifice: a Levinasian reconceptualisation of supererogation.” 2018. Doctoral Dissertation, Stellenbosch University. Accessed February 24, 2020. http://hdl.handle.net/10019.1/104857.

MLA Handbook (7th Edition):

Andrade, Julio Anthony. “The possibility of sacrifice: a Levinasian reconceptualisation of supererogation.” 2018. Web. 24 Feb 2020.

Vancouver:

Andrade JA. The possibility of sacrifice: a Levinasian reconceptualisation of supererogation. [Internet] [Doctoral dissertation]. Stellenbosch University; 2018. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/10019.1/104857.

Council of Science Editors:

Andrade JA. The possibility of sacrifice: a Levinasian reconceptualisation of supererogation. [Doctoral Dissertation]. Stellenbosch University; 2018. Available from: http://hdl.handle.net/10019.1/104857


Clemson University

26. Kemmann, Guy Maximilian. An Experimental Investigation of Combined Symmetric Asymmetric Composite Laminates.

Degree: MS, Mechanical Engineering, 2018, Clemson University

 It has been found that certain asymmetric composite laminates exhibit bistability, and are thus called bistable composite laminates. A bistable composite laminate is a composite… (more)

Subjects/Keywords: asymmetric; Bistable; Composite; Laminates; symmetric

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kemmann, G. M. (2018). An Experimental Investigation of Combined Symmetric Asymmetric Composite Laminates. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/2991

Chicago Manual of Style (16th Edition):

Kemmann, Guy Maximilian. “An Experimental Investigation of Combined Symmetric Asymmetric Composite Laminates.” 2018. Masters Thesis, Clemson University. Accessed February 24, 2020. https://tigerprints.clemson.edu/all_theses/2991.

MLA Handbook (7th Edition):

Kemmann, Guy Maximilian. “An Experimental Investigation of Combined Symmetric Asymmetric Composite Laminates.” 2018. Web. 24 Feb 2020.

Vancouver:

Kemmann GM. An Experimental Investigation of Combined Symmetric Asymmetric Composite Laminates. [Internet] [Masters thesis]. Clemson University; 2018. [cited 2020 Feb 24]. Available from: https://tigerprints.clemson.edu/all_theses/2991.

Council of Science Editors:

Kemmann GM. An Experimental Investigation of Combined Symmetric Asymmetric Composite Laminates. [Masters Thesis]. Clemson University; 2018. Available from: https://tigerprints.clemson.edu/all_theses/2991


Oregon State University

27. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 February 24, 2020. 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. 24 Feb 2020.

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 2020 Feb 24]. 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


Colorado State University

28. White, Nicholas Andrew. Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis.

Degree: PhD, Chemistry, 2016, Colorado State University

 A series of δ-nitroesters were synthesized through the N-heterocyclic carbene catalyzed coupling of enals and nitroalkenes. The asymmetric coupling of these substrates via the homoenolate… (more)

Subjects/Keywords: asymmetric; carbene; catalysis; organic

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

White, N. A. (2016). Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/170358

Chicago Manual of Style (16th Edition):

White, Nicholas Andrew. “Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis.” 2016. Doctoral Dissertation, Colorado State University. Accessed February 24, 2020. http://hdl.handle.net/10217/170358.

MLA Handbook (7th Edition):

White, Nicholas Andrew. “Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis.” 2016. Web. 24 Feb 2020.

Vancouver:

White NA. Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis. [Internet] [Doctoral dissertation]. Colorado State University; 2016. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/10217/170358.

Council of Science Editors:

White NA. Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis. [Doctoral Dissertation]. Colorado State University; 2016. Available from: http://hdl.handle.net/10217/170358


University of St. Andrews

29. Widegren, Magnus Benkt. Manganese catalysed hydrogenation of carbonyl compounds .

Degree: 2019, University of St. Andrews

 The use of manganese catalysts represents a new area of research in the field of catalytic homogenous hydrogenation. This thesis covers the work on the… (more)

Subjects/Keywords: Manganese; Hydrogenation; Asymmetric; Carbonyl compounds

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Widegren, M. B. (2019). Manganese catalysed hydrogenation of carbonyl compounds . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/18705

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):

Widegren, Magnus Benkt. “Manganese catalysed hydrogenation of carbonyl compounds .” 2019. Thesis, University of St. Andrews. Accessed February 24, 2020. http://hdl.handle.net/10023/18705.

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

MLA Handbook (7th Edition):

Widegren, Magnus Benkt. “Manganese catalysed hydrogenation of carbonyl compounds .” 2019. Web. 24 Feb 2020.

Vancouver:

Widegren MB. Manganese catalysed hydrogenation of carbonyl compounds . [Internet] [Thesis]. University of St. Andrews; 2019. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/10023/18705.

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

Council of Science Editors:

Widegren MB. Manganese catalysed hydrogenation of carbonyl compounds . [Thesis]. University of St. Andrews; 2019. Available from: http://hdl.handle.net/10023/18705

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


University of Adelaide

30. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 February 24, 2020. 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. 24 Feb 2020.

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 2020 Feb 24]. 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

[1] [2] [3] [4] [5] … [59]

.