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You searched for subject:(Umpolung). Showing records 1 – 30 of 32 total matches.

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1. Ryzhakov, Dmytro. Désaromatisation radicalaire d'indoles pour la synthèse de spiroindolines trifluorométhylées ou phosphorées : Radical desaromatisation of indoles for the synthesis of trifluoromethylated or phosphorus spiroindolines.

Degree: Docteur es, Chimie, 2019, Université Paris-Saclay (ComUE)

Les spirooxindoles se retrouvent fréquemment dans les produits naturels et les composés biologiquement actifs. Certains principes actifs pharmaceutiques contenant un motif spirooxindole ont également été… (more)

Subjects/Keywords: Indole; Umpolung; Radicaux; Indole; Umpolung; Radicals

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APA (6th Edition):

Ryzhakov, D. (2019). Désaromatisation radicalaire d'indoles pour la synthèse de spiroindolines trifluorométhylées ou phosphorées : Radical desaromatisation of indoles for the synthesis of trifluoromethylated or phosphorus spiroindolines. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS366

Chicago Manual of Style (16th Edition):

Ryzhakov, Dmytro. “Désaromatisation radicalaire d'indoles pour la synthèse de spiroindolines trifluorométhylées ou phosphorées : Radical desaromatisation of indoles for the synthesis of trifluoromethylated or phosphorus spiroindolines.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed September 20, 2020. http://www.theses.fr/2019SACLS366.

MLA Handbook (7th Edition):

Ryzhakov, Dmytro. “Désaromatisation radicalaire d'indoles pour la synthèse de spiroindolines trifluorométhylées ou phosphorées : Radical desaromatisation of indoles for the synthesis of trifluoromethylated or phosphorus spiroindolines.” 2019. Web. 20 Sep 2020.

Vancouver:

Ryzhakov D. Désaromatisation radicalaire d'indoles pour la synthèse de spiroindolines trifluorométhylées ou phosphorées : Radical desaromatisation of indoles for the synthesis of trifluoromethylated or phosphorus spiroindolines. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Sep 20]. Available from: http://www.theses.fr/2019SACLS366.

Council of Science Editors:

Ryzhakov D. Désaromatisation radicalaire d'indoles pour la synthèse de spiroindolines trifluorométhylées ou phosphorées : Radical desaromatisation of indoles for the synthesis of trifluoromethylated or phosphorus spiroindolines. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS366


Vanderbilt University

2. Witt, Jonathan Okrent. Umpolung Amide Synthesis Using Free Amino Acids.

Degree: MS, Chemistry, 2014, Vanderbilt University

 Traditional amide synthesis employs a nucleophilic amine, which is reacted with an electrophilic activated carboxylic acid or carboxylic acid surrogate. Recently, colleagues in the Johnston… (more)

Subjects/Keywords: amide; nitroalkane; umpolung amide synthesis

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APA (6th Edition):

Witt, J. O. (2014). Umpolung Amide Synthesis Using Free Amino Acids. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13196

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):

Witt, Jonathan Okrent. “Umpolung Amide Synthesis Using Free Amino Acids.” 2014. Thesis, Vanderbilt University. Accessed September 20, 2020. http://hdl.handle.net/1803/13196.

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

MLA Handbook (7th Edition):

Witt, Jonathan Okrent. “Umpolung Amide Synthesis Using Free Amino Acids.” 2014. Web. 20 Sep 2020.

Vancouver:

Witt JO. Umpolung Amide Synthesis Using Free Amino Acids. [Internet] [Thesis]. Vanderbilt University; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1803/13196.

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

Council of Science Editors:

Witt JO. Umpolung Amide Synthesis Using Free Amino Acids. [Thesis]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/13196

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


Vanderbilt University

3. Beezer, Dain Bridgeon. The application of umpolung amide synthesis to the enantioselective synthesis of dihydroxyamides.

Degree: MS, Chemistry, 2013, Vanderbilt University

 The amide bond is one of the most important linkages in organic chemistry and constitutes the key functional group in peptides, polymers, and many natural… (more)

Subjects/Keywords: cross metathesis; dihydroxyamides; umpolung amide synthesis; dihydroxylation

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APA (6th Edition):

Beezer, D. B. (2013). The application of umpolung amide synthesis to the enantioselective synthesis of dihydroxyamides. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13974

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):

Beezer, Dain Bridgeon. “The application of umpolung amide synthesis to the enantioselective synthesis of dihydroxyamides.” 2013. Thesis, Vanderbilt University. Accessed September 20, 2020. http://hdl.handle.net/1803/13974.

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

MLA Handbook (7th Edition):

Beezer, Dain Bridgeon. “The application of umpolung amide synthesis to the enantioselective synthesis of dihydroxyamides.” 2013. Web. 20 Sep 2020.

Vancouver:

Beezer DB. The application of umpolung amide synthesis to the enantioselective synthesis of dihydroxyamides. [Internet] [Thesis]. Vanderbilt University; 2013. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1803/13974.

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

Council of Science Editors:

Beezer DB. The application of umpolung amide synthesis to the enantioselective synthesis of dihydroxyamides. [Thesis]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/13974

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


Vanderbilt University

4. Shackleford, Jessica Paige. A Mechanistic Study of Umpolung Amide Synthesis, the Straightforward Synthesis of 18O-Labeled Amides, and the Development of Catalytic Umpolung Amide Synthesis.

Degree: MS, Chemistry, 2012, Vanderbilt University

 Johnston and coworkers recently reported a novel amide bond forming reaction wherein the amine acts as the electrophile and the carbon donor acts as the… (more)

Subjects/Keywords: umpolung; peptides; amide synthesis; 18O; isotope

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APA (6th Edition):

Shackleford, J. P. (2012). A Mechanistic Study of Umpolung Amide Synthesis, the Straightforward Synthesis of 18O-Labeled Amides, and the Development of Catalytic Umpolung Amide Synthesis. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11294

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):

Shackleford, Jessica Paige. “A Mechanistic Study of Umpolung Amide Synthesis, the Straightforward Synthesis of 18O-Labeled Amides, and the Development of Catalytic Umpolung Amide Synthesis.” 2012. Thesis, Vanderbilt University. Accessed September 20, 2020. http://hdl.handle.net/1803/11294.

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

MLA Handbook (7th Edition):

Shackleford, Jessica Paige. “A Mechanistic Study of Umpolung Amide Synthesis, the Straightforward Synthesis of 18O-Labeled Amides, and the Development of Catalytic Umpolung Amide Synthesis.” 2012. Web. 20 Sep 2020.

Vancouver:

Shackleford JP. A Mechanistic Study of Umpolung Amide Synthesis, the Straightforward Synthesis of 18O-Labeled Amides, and the Development of Catalytic Umpolung Amide Synthesis. [Internet] [Thesis]. Vanderbilt University; 2012. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1803/11294.

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

Council of Science Editors:

Shackleford JP. A Mechanistic Study of Umpolung Amide Synthesis, the Straightforward Synthesis of 18O-Labeled Amides, and the Development of Catalytic Umpolung Amide Synthesis. [Thesis]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/11294

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

5. Esgulian, Mathieu. Oxyhomologation diastéréosélective de la sérine : développement de la méthodologie MAC : Diastereoselective oxyhomologation of serine : MAC methodology development.

Degree: Docteur es, Chimie, 2017, Université Paris-Saclay (ComUE)

La méthodologie MAC consiste à employer des réactifs umpolung pour permettre l’insertion formelle d’une fonction carbonyle entre un électrophile et un nucléophile. Cette thèse est… (more)

Subjects/Keywords: Réaction multicomposés; One-pot; Oxyhomologation; Aminoacide; Hétérocycle; Umpolung; Multicomponent reaction; One-pot; Oxyhomologation; Aminoacid; Heterocycle; Umpolung

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APA (6th Edition):

Esgulian, M. (2017). Oxyhomologation diastéréosélective de la sérine : développement de la méthodologie MAC : Diastereoselective oxyhomologation of serine : MAC methodology development. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2017SACLS392

Chicago Manual of Style (16th Edition):

Esgulian, Mathieu. “Oxyhomologation diastéréosélective de la sérine : développement de la méthodologie MAC : Diastereoselective oxyhomologation of serine : MAC methodology development.” 2017. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed September 20, 2020. http://www.theses.fr/2017SACLS392.

MLA Handbook (7th Edition):

Esgulian, Mathieu. “Oxyhomologation diastéréosélective de la sérine : développement de la méthodologie MAC : Diastereoselective oxyhomologation of serine : MAC methodology development.” 2017. Web. 20 Sep 2020.

Vancouver:

Esgulian M. Oxyhomologation diastéréosélective de la sérine : développement de la méthodologie MAC : Diastereoselective oxyhomologation of serine : MAC methodology development. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2017. [cited 2020 Sep 20]. Available from: http://www.theses.fr/2017SACLS392.

Council of Science Editors:

Esgulian M. Oxyhomologation diastéréosélective de la sérine : développement de la méthodologie MAC : Diastereoselective oxyhomologation of serine : MAC methodology development. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2017. Available from: http://www.theses.fr/2017SACLS392


Vanderbilt University

6. Schwieter, Kenneth Edward. Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides.

Degree: PhD, Chemistry, 2016, Vanderbilt University

 Unnatural amino acid derived fragments are present in a multitude of pharmaceuticals and biologically relevant molecules including complex peptides. Current preparative methods focus almost entirely… (more)

Subjects/Keywords: peptide synthesis; umpolung; amide synthesis; amino acids; aza-Henry; organocatalysis

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APA (6th Edition):

Schwieter, K. E. (2016). Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14372

Chicago Manual of Style (16th Edition):

Schwieter, Kenneth Edward. “Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed September 20, 2020. http://hdl.handle.net/1803/14372.

MLA Handbook (7th Edition):

Schwieter, Kenneth Edward. “Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides.” 2016. Web. 20 Sep 2020.

Vancouver:

Schwieter KE. Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1803/14372.

Council of Science Editors:

Schwieter KE. Toward On-Demand Peptide Synthesis: Development and Application of Enantioselective Syntheses of Unnatural α-Amino Amides. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/14372


Vanderbilt University

7. Doody, Amanda Blane. Synthetic Pursuit of the Tridecapeptide Feglymycin and the Manzamine Alkaloid Kauluamine.

Degree: PhD, Chemistry, 2014, Vanderbilt University

 Feglymycin is a tridecapeptide that has been shown to act as an inhibitor of the formation of HIV syncytia as well as the cell-to-cell transmission… (more)

Subjects/Keywords: Umpolung Amide Synthesis; UmAS; Feglymycin; Kauluamine; aryl glycine; arylglycine

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APA (6th Edition):

Doody, A. B. (2014). Synthetic Pursuit of the Tridecapeptide Feglymycin and the Manzamine Alkaloid Kauluamine. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10892

Chicago Manual of Style (16th Edition):

Doody, Amanda Blane. “Synthetic Pursuit of the Tridecapeptide Feglymycin and the Manzamine Alkaloid Kauluamine.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed September 20, 2020. http://hdl.handle.net/1803/10892.

MLA Handbook (7th Edition):

Doody, Amanda Blane. “Synthetic Pursuit of the Tridecapeptide Feglymycin and the Manzamine Alkaloid Kauluamine.” 2014. Web. 20 Sep 2020.

Vancouver:

Doody AB. Synthetic Pursuit of the Tridecapeptide Feglymycin and the Manzamine Alkaloid Kauluamine. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1803/10892.

Council of Science Editors:

Doody AB. Synthetic Pursuit of the Tridecapeptide Feglymycin and the Manzamine Alkaloid Kauluamine. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/10892


Penn State University

8. Witek, Jason Anthony. Nitrosoalkene Alkylation and Stereochemical Studies.

Degree: 2013, Penn State University

 Novel synthetic methodology involving intermolecular conjugate additions to nitrosoalkenes has been developed (Tables 2-4). The reactivity of various soft nucleophiles with both cyclic and acyclic… (more)

Subjects/Keywords: nitrosoalkenes; michael additions; oximes; deoximation; enolonium ion; umpolung

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APA (6th Edition):

Witek, J. A. (2013). Nitrosoalkene Alkylation and Stereochemical Studies. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/18377

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):

Witek, Jason Anthony. “Nitrosoalkene Alkylation and Stereochemical Studies.” 2013. Thesis, Penn State University. Accessed September 20, 2020. https://submit-etda.libraries.psu.edu/catalog/18377.

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

MLA Handbook (7th Edition):

Witek, Jason Anthony. “Nitrosoalkene Alkylation and Stereochemical Studies.” 2013. Web. 20 Sep 2020.

Vancouver:

Witek JA. Nitrosoalkene Alkylation and Stereochemical Studies. [Internet] [Thesis]. Penn State University; 2013. [cited 2020 Sep 20]. Available from: https://submit-etda.libraries.psu.edu/catalog/18377.

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

Council of Science Editors:

Witek JA. Nitrosoalkene Alkylation and Stereochemical Studies. [Thesis]. Penn State University; 2013. Available from: https://submit-etda.libraries.psu.edu/catalog/18377

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

9. Thai, Karen. NHC-catalyzed transformations: Stetter, benzoin, and ring expansion reactions.

Degree: 2012, University of Saskatchewan

 N-Hetereocyclic carbenes (NHC) have been intensively investigated since Ukai et al had reported the first NHC-catalyzed coupling of two equivalents of benzaldehyde, to form what… (more)

Subjects/Keywords: organocatalysis; carbenes; umpolung

…15 Extended Umpolung Transformations… …Umpolung Reactivity of Aldehydes through the Generation of Dithiane and Cyanohydrin Compounds… …coupling of two components with the same polarity. The inversion of polarity (umpolung… …Scheme 1.1 Umpolung Reactivity of Aldehydes through the Generation of Dithiane and Cyanohydrin… …Benzoin Reaction Proposed by 4 In addition to the reversal of reactivity (umpolung)… 

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APA (6th Edition):

Thai, K. (2012). NHC-catalyzed transformations: Stetter, benzoin, and ring expansion reactions. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2012-06-489

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):

Thai, Karen. “NHC-catalyzed transformations: Stetter, benzoin, and ring expansion reactions.” 2012. Thesis, University of Saskatchewan. Accessed September 20, 2020. http://hdl.handle.net/10388/ETD-2012-06-489.

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

MLA Handbook (7th Edition):

Thai, Karen. “NHC-catalyzed transformations: Stetter, benzoin, and ring expansion reactions.” 2012. Web. 20 Sep 2020.

Vancouver:

Thai K. NHC-catalyzed transformations: Stetter, benzoin, and ring expansion reactions. [Internet] [Thesis]. University of Saskatchewan; 2012. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10388/ETD-2012-06-489.

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

Council of Science Editors:

Thai K. NHC-catalyzed transformations: Stetter, benzoin, and ring expansion reactions. [Thesis]. University of Saskatchewan; 2012. Available from: http://hdl.handle.net/10388/ETD-2012-06-489

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


University of Pennsylvania

10. Struble, Justin R. N-HETEROCYCLIC CARBENES: FROM DESIGN TO SYNTHESIS AND THEIR APPLICATION AS NUCLEOPHILIC CATALYSTS.

Degree: 2009, University of Pennsylvania

 Our group has pioneered novel internal redox process of aldehydes possessing an internal α-reducible functionality mediated by N-heterocyclic carbenes (NHCs). Two discrete discoveries have been… (more)

Subjects/Keywords: N-Heterocyclic Carbenes; NHCs; organocatalysis; nucleophilic catalysis; umpolung; Organic Chemistry

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APA (6th Edition):

Struble, J. R. (2009). N-HETEROCYCLIC CARBENES: FROM DESIGN TO SYNTHESIS AND THEIR APPLICATION AS NUCLEOPHILIC CATALYSTS. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/49

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):

Struble, Justin R. “N-HETEROCYCLIC CARBENES: FROM DESIGN TO SYNTHESIS AND THEIR APPLICATION AS NUCLEOPHILIC CATALYSTS.” 2009. Thesis, University of Pennsylvania. Accessed September 20, 2020. https://repository.upenn.edu/edissertations/49.

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

MLA Handbook (7th Edition):

Struble, Justin R. “N-HETEROCYCLIC CARBENES: FROM DESIGN TO SYNTHESIS AND THEIR APPLICATION AS NUCLEOPHILIC CATALYSTS.” 2009. Web. 20 Sep 2020.

Vancouver:

Struble JR. N-HETEROCYCLIC CARBENES: FROM DESIGN TO SYNTHESIS AND THEIR APPLICATION AS NUCLEOPHILIC CATALYSTS. [Internet] [Thesis]. University of Pennsylvania; 2009. [cited 2020 Sep 20]. Available from: https://repository.upenn.edu/edissertations/49.

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

Council of Science Editors:

Struble JR. N-HETEROCYCLIC CARBENES: FROM DESIGN TO SYNTHESIS AND THEIR APPLICATION AS NUCLEOPHILIC CATALYSTS. [Thesis]. University of Pennsylvania; 2009. Available from: https://repository.upenn.edu/edissertations/49

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


University of Adelaide

11. Alexander, Sean Geoffrey. NHC-supported mixed halohydrides of aluminium and related studies.

Degree: 2011, University of Adelaide

 Chapter 1. General introduction This chapter comprises a comprehensive overview of group 13 chemistry, including the elements of group 13, the trihydrides of aluminium and… (more)

Subjects/Keywords: group 13; aluminium; gallium; triazeide; hydrometallation; amidinate; umpolung

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APA (6th Edition):

Alexander, S. G. (2011). NHC-supported mixed halohydrides of aluminium and related studies. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/103164

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):

Alexander, Sean Geoffrey. “NHC-supported mixed halohydrides of aluminium and related studies.” 2011. Thesis, University of Adelaide. Accessed September 20, 2020. http://hdl.handle.net/2440/103164.

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

MLA Handbook (7th Edition):

Alexander, Sean Geoffrey. “NHC-supported mixed halohydrides of aluminium and related studies.” 2011. Web. 20 Sep 2020.

Vancouver:

Alexander SG. NHC-supported mixed halohydrides of aluminium and related studies. [Internet] [Thesis]. University of Adelaide; 2011. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/2440/103164.

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

Council of Science Editors:

Alexander SG. NHC-supported mixed halohydrides of aluminium and related studies. [Thesis]. University of Adelaide; 2011. Available from: http://hdl.handle.net/2440/103164

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

12. Nikolaev, Andrei. Synthesis and Reactivity of Umpolung Reagents Through Transition Metal Catalysis.

Degree: PhD, Chemistry, 2019, York University

 The cyclopropanol-derived palladium-homoenolates have previously been exploited as a unique class of cross-coupling partners in our group. The major advantage of using cyclopropanols as the… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Organic Synthesis; Catalysis; Organometallics; Umpolung

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APA (6th Edition):

Nikolaev, A. (2019). Synthesis and Reactivity of Umpolung Reagents Through Transition Metal Catalysis. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/35919

Chicago Manual of Style (16th Edition):

Nikolaev, Andrei. “Synthesis and Reactivity of Umpolung Reagents Through Transition Metal Catalysis.” 2019. Doctoral Dissertation, York University. Accessed September 20, 2020. http://hdl.handle.net/10315/35919.

MLA Handbook (7th Edition):

Nikolaev, Andrei. “Synthesis and Reactivity of Umpolung Reagents Through Transition Metal Catalysis.” 2019. Web. 20 Sep 2020.

Vancouver:

Nikolaev A. Synthesis and Reactivity of Umpolung Reagents Through Transition Metal Catalysis. [Internet] [Doctoral dissertation]. York University; 2019. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10315/35919.

Council of Science Editors:

Nikolaev A. Synthesis and Reactivity of Umpolung Reagents Through Transition Metal Catalysis. [Doctoral Dissertation]. York University; 2019. Available from: http://hdl.handle.net/10315/35919

13. Vander Wal, Mark Nicholas. The Development of Novel Methods for the α-Functionalization of Carbonyl Compounds to Generate High-Value Intermediates .

Degree: PhD, 2012, Princeton University

 Photoredox organocatalysis has led to the development of several new catalytic asymmetric reactions within the MacMillan group. The reactive intermediates used in this process have… (more)

Subjects/Keywords: Benzylation; Carbonyls; Catalysis; Umpolung

…83 x Chapter 4: Development of an Umpolung Strategy for the Generic Nucleophilic α… …Substitution of Ketones I. Carbonyls and Umpolung Reactivity… …82 xii Chapter 4: Development of an Umpolung Strategy for the Generic Nucleophilic α… …81 Chapter 4: Development of an Umpolung Strategy for the Generic Nucleophilic α… …34 Chapter 4: Development of an Umpolung Strategy for the Generic Nucleophilic α… 

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APA (6th Edition):

Vander Wal, M. N. (2012). The Development of Novel Methods for the α-Functionalization of Carbonyl Compounds to Generate High-Value Intermediates . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01qv33rw697

Chicago Manual of Style (16th Edition):

Vander Wal, Mark Nicholas. “The Development of Novel Methods for the α-Functionalization of Carbonyl Compounds to Generate High-Value Intermediates .” 2012. Doctoral Dissertation, Princeton University. Accessed September 20, 2020. http://arks.princeton.edu/ark:/88435/dsp01qv33rw697.

MLA Handbook (7th Edition):

Vander Wal, Mark Nicholas. “The Development of Novel Methods for the α-Functionalization of Carbonyl Compounds to Generate High-Value Intermediates .” 2012. Web. 20 Sep 2020.

Vancouver:

Vander Wal MN. The Development of Novel Methods for the α-Functionalization of Carbonyl Compounds to Generate High-Value Intermediates . [Internet] [Doctoral dissertation]. Princeton University; 2012. [cited 2020 Sep 20]. Available from: http://arks.princeton.edu/ark:/88435/dsp01qv33rw697.

Council of Science Editors:

Vander Wal MN. The Development of Novel Methods for the α-Functionalization of Carbonyl Compounds to Generate High-Value Intermediates . [Doctoral Dissertation]. Princeton University; 2012. Available from: http://arks.princeton.edu/ark:/88435/dsp01qv33rw697


Vanderbilt University

14. Makley, Dawn Marie. Umpolung amide synthesis: applications in enantioselective peptide synthesis.

Degree: PhD, Chemistry, 2012, Vanderbilt University

UMPOLUNG AMIDE SYNTHESIS: APPLICATIONS IN ENANTIOSELECTIVE PEPTIDE SYNTHESISDAWN M. MAKLEYDissertation under the direction of Professor Jeffrey N. JohnstonThe development and application of the novel Umpolung(more)

Subjects/Keywords: silyl imines; n-halo amines; natural product synthesis; peptide synthesis; amide synthesis; umpolung; methodology development; chemistry; aza-Henry; umpolung amide synthesis; UmAS

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

APA (6th Edition):

Makley, D. M. (2012). Umpolung amide synthesis: applications in enantioselective peptide synthesis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14598

Chicago Manual of Style (16th Edition):

Makley, Dawn Marie. “Umpolung amide synthesis: applications in enantioselective peptide synthesis.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed September 20, 2020. http://hdl.handle.net/1803/14598.

MLA Handbook (7th Edition):

Makley, Dawn Marie. “Umpolung amide synthesis: applications in enantioselective peptide synthesis.” 2012. Web. 20 Sep 2020.

Vancouver:

Makley DM. Umpolung amide synthesis: applications in enantioselective peptide synthesis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1803/14598.

Council of Science Editors:

Makley DM. Umpolung amide synthesis: applications in enantioselective peptide synthesis. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/14598


Johannes Gutenberg Universität Mainz

15. Meyer, Nino. Synthese hochsubstituierter Pyrrolidine aus alpha-Aminonitrilen und alpha-(Alkylidenamino)-nitrilen.

Degree: 2006, Johannes Gutenberg Universität Mainz

Viele substituierte Pyrrolidine zeigen eine hohe Affinität zu biologischen Makromolekülen wie zu G-Protein-gekoppelten Rezeptoren, Ionenkanälen oder Enzymen. Eine synthetische Route zur Darstellung von Pyrrolidinen mit… (more)

Subjects/Keywords: Umpolung, Heterocyclen, Naturstoffe; Umpolung, heterocycles, natural products; Chemistry and allied sciences

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APA (6th Edition):

Meyer, N. (2006). Synthese hochsubstituierter Pyrrolidine aus alpha-Aminonitrilen und alpha-(Alkylidenamino)-nitrilen. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2006/999/

Chicago Manual of Style (16th Edition):

Meyer, Nino. “Synthese hochsubstituierter Pyrrolidine aus alpha-Aminonitrilen und alpha-(Alkylidenamino)-nitrilen.” 2006. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 20, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2006/999/.

MLA Handbook (7th Edition):

Meyer, Nino. “Synthese hochsubstituierter Pyrrolidine aus alpha-Aminonitrilen und alpha-(Alkylidenamino)-nitrilen.” 2006. Web. 20 Sep 2020.

Vancouver:

Meyer N. Synthese hochsubstituierter Pyrrolidine aus alpha-Aminonitrilen und alpha-(Alkylidenamino)-nitrilen. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2006. [cited 2020 Sep 20]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2006/999/.

Council of Science Editors:

Meyer N. Synthese hochsubstituierter Pyrrolidine aus alpha-Aminonitrilen und alpha-(Alkylidenamino)-nitrilen. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2006. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2006/999/


Université Paris-Sud – Paris XI

16. Le, Xuan-Tien. Nouvelles réactions d’allylations induites par le samarium divalent. Application à la modification contrôlée de dérivés de l’acide sialique : Novel samarium(II) - induced allylation reactions. Application to the controlled modification of sialic acid derivatives.

Degree: Docteur es, Chimie, 2014, Université Paris-Sud – Paris XI

Le couplage croisé entre les esters allyliques et les composés carbonylés promu par le diiodure de samarium est une méthode efficace pour la formation de… (more)

Subjects/Keywords: Diiodure de samarium; Réaction d’allylation; Couplage réducteur; D-glycal; Acide sialique; Umpolung; Samarium diiodide; Carbonyl allylation; Reductive coupling; D-glycal; Sialic acid; Umpolung

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APA (6th Edition):

Le, X. (2014). Nouvelles réactions d’allylations induites par le samarium divalent. Application à la modification contrôlée de dérivés de l’acide sialique : Novel samarium(II) - induced allylation reactions. Application to the controlled modification of sialic acid derivatives. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA112073

Chicago Manual of Style (16th Edition):

Le, Xuan-Tien. “Nouvelles réactions d’allylations induites par le samarium divalent. Application à la modification contrôlée de dérivés de l’acide sialique : Novel samarium(II) - induced allylation reactions. Application to the controlled modification of sialic acid derivatives.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed September 20, 2020. http://www.theses.fr/2014PA112073.

MLA Handbook (7th Edition):

Le, Xuan-Tien. “Nouvelles réactions d’allylations induites par le samarium divalent. Application à la modification contrôlée de dérivés de l’acide sialique : Novel samarium(II) - induced allylation reactions. Application to the controlled modification of sialic acid derivatives.” 2014. Web. 20 Sep 2020.

Vancouver:

Le X. Nouvelles réactions d’allylations induites par le samarium divalent. Application à la modification contrôlée de dérivés de l’acide sialique : Novel samarium(II) - induced allylation reactions. Application to the controlled modification of sialic acid derivatives. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2020 Sep 20]. Available from: http://www.theses.fr/2014PA112073.

Council of Science Editors:

Le X. Nouvelles réactions d’allylations induites par le samarium divalent. Application à la modification contrôlée de dérivés de l’acide sialique : Novel samarium(II) - induced allylation reactions. Application to the controlled modification of sialic acid derivatives. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA112073


Université du Québec à Montréal

17. Desjardins, Samuel. Polycyclisation oxydative et son application en synthèse asymétrique.

Degree: 2013, Université du Québec à Montréal

 L'activation par voie oxydative de dérivés phénoliques contenant une chaine latérale insaturée avec un réactif d'iode hypervalent permet la formation de produits bicycliques et tricycliques… (more)

Subjects/Keywords: Cyclisation (Chimie); Phénol; Synthèse asymétrique; Déaromatisation; Iode hypervalent; Prins; Réaction de Polonovski; Umpolung

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APA (6th Edition):

Desjardins, S. (2013). Polycyclisation oxydative et son application en synthèse asymétrique. (Thesis). Université du Québec à Montréal. Retrieved from http://www.archipel.uqam.ca/5812/1/M12777.pdf

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):

Desjardins, Samuel. “Polycyclisation oxydative et son application en synthèse asymétrique.” 2013. Thesis, Université du Québec à Montréal. Accessed September 20, 2020. http://www.archipel.uqam.ca/5812/1/M12777.pdf.

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

MLA Handbook (7th Edition):

Desjardins, Samuel. “Polycyclisation oxydative et son application en synthèse asymétrique.” 2013. Web. 20 Sep 2020.

Vancouver:

Desjardins S. Polycyclisation oxydative et son application en synthèse asymétrique. [Internet] [Thesis]. Université du Québec à Montréal; 2013. [cited 2020 Sep 20]. Available from: http://www.archipel.uqam.ca/5812/1/M12777.pdf.

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

Council of Science Editors:

Desjardins S. Polycyclisation oxydative et son application en synthèse asymétrique. [Thesis]. Université du Québec à Montréal; 2013. Available from: http://www.archipel.uqam.ca/5812/1/M12777.pdf

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


University of Alberta

18. Wu, Yen-Ku. Exploring New Aspects of the Nazarov Cyclization.

Degree: PhD, Department of Chemistry, 2013, University of Alberta

 The five-membered carbocyclic framework is a prevailing structural motif found in natural products and bioactive compounds. Over the years, the Nazarov reaction has been continuously… (more)

Subjects/Keywords: Nazarov reaction; Domino; Umpolung; vinylallene; Interrupted Nazarov reaction; Alternative Nazarov reaction; allenamide

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APA (6th Edition):

Wu, Y. (2013). Exploring New Aspects of the Nazarov Cyclization. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/x633f270d

Chicago Manual of Style (16th Edition):

Wu, Yen-Ku. “Exploring New Aspects of the Nazarov Cyclization.” 2013. Doctoral Dissertation, University of Alberta. Accessed September 20, 2020. https://era.library.ualberta.ca/files/x633f270d.

MLA Handbook (7th Edition):

Wu, Yen-Ku. “Exploring New Aspects of the Nazarov Cyclization.” 2013. Web. 20 Sep 2020.

Vancouver:

Wu Y. Exploring New Aspects of the Nazarov Cyclization. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2020 Sep 20]. Available from: https://era.library.ualberta.ca/files/x633f270d.

Council of Science Editors:

Wu Y. Exploring New Aspects of the Nazarov Cyclization. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/x633f270d


University of Saskatchewan

19. Wilde, Myron 1986-. Preparation of Novel Carbenes and their Catalytic Application to the Cross-Benzoin, Aza-Benzoin and Stetter Reactions.

Degree: 2016, University of Saskatchewan

 N-Heterocyclic carbenes (NHCs) derived from bicyclic triazolium salts possessing a fused 6 membered ring were found to induce chemoselectivity in the cross-benzoin between aromatic and… (more)

Subjects/Keywords: Stetter; benzoin; aza-benzoin, NHC; carbene bis(amino)cyclopropenium; bis(amino)cyclopropenylidene; umpolung

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APA (6th Edition):

Wilde, M. 1. (2016). Preparation of Novel Carbenes and their Catalytic Application to the Cross-Benzoin, Aza-Benzoin and Stetter Reactions. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12590

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):

Wilde, Myron 1986-. “Preparation of Novel Carbenes and their Catalytic Application to the Cross-Benzoin, Aza-Benzoin and Stetter Reactions.” 2016. Thesis, University of Saskatchewan. Accessed September 20, 2020. http://hdl.handle.net/10388/12590.

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

MLA Handbook (7th Edition):

Wilde, Myron 1986-. “Preparation of Novel Carbenes and their Catalytic Application to the Cross-Benzoin, Aza-Benzoin and Stetter Reactions.” 2016. Web. 20 Sep 2020.

Vancouver:

Wilde M1. Preparation of Novel Carbenes and their Catalytic Application to the Cross-Benzoin, Aza-Benzoin and Stetter Reactions. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10388/12590.

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

Council of Science Editors:

Wilde M1. Preparation of Novel Carbenes and their Catalytic Application to the Cross-Benzoin, Aza-Benzoin and Stetter Reactions. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/12590

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


Université du Québec à Montréal

20. Desjardins, Samuel. Polycyclisation oxydative et son application en synthèse asymétrique.

Degree: 2013, Université du Québec à Montréal

 L'activation par voie oxydative de dérivés phénoliques contenant une chaine latérale insaturée avec un réactif d'iode hypervalent permet la formation de produits bicycliques et tricycliques… (more)

Subjects/Keywords: Cyclisation (Chimie); Phénol; Synthèse asymétrique; Déaromatisation; Iode hypervalent; Prins; Réaction de Polonovski; Umpolung

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

APA (6th Edition):

Desjardins, S. (2013). Polycyclisation oxydative et son application en synthèse asymétrique. (Thesis). Université du Québec à Montréal. Retrieved from http://archipel.uqam.ca/5812/1/M12777.pdf

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):

Desjardins, Samuel. “Polycyclisation oxydative et son application en synthèse asymétrique.” 2013. Thesis, Université du Québec à Montréal. Accessed September 20, 2020. http://archipel.uqam.ca/5812/1/M12777.pdf.

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

MLA Handbook (7th Edition):

Desjardins, Samuel. “Polycyclisation oxydative et son application en synthèse asymétrique.” 2013. Web. 20 Sep 2020.

Vancouver:

Desjardins S. Polycyclisation oxydative et son application en synthèse asymétrique. [Internet] [Thesis]. Université du Québec à Montréal; 2013. [cited 2020 Sep 20]. Available from: http://archipel.uqam.ca/5812/1/M12777.pdf.

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

Council of Science Editors:

Desjardins S. Polycyclisation oxydative et son application en synthèse asymétrique. [Thesis]. Université du Québec à Montréal; 2013. Available from: http://archipel.uqam.ca/5812/1/M12777.pdf

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

21. McFarlane, Michael Thomas. Metal-catalyzed cross-coupling reactions with dithiolanes and dithianes.

Degree: Chemistry, 2012, University of Manitoba

 Creating new carbon-carbon bonds is one of the most important and challenging reactions in organic synthesis. Metal-catalyzed cross-coupling reactions have emerged as one of the… (more)

Subjects/Keywords: cross-coupling; thioacetal; organohalide; Umpolung

…phenyl)methanol. 89 viii List of Schemes Scheme 1.1. Example of Umpolung chemistry… …creates a reversal of polarity for the carbonyl group and is referred to as “umpolung” chemistry… …of Umpolung chemistry with benzaldehyde using 1,3-propanedithiol. 1,3-Dithianes are… …carbonyl groups with dithiols is an excellent approach for umpolung chemistry and the acyl anion… …help to stabilize carbanions – an acyl anion equivalent. This is an example of umpolung… 

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APA (6th Edition):

McFarlane, M. T. (2012). Metal-catalyzed cross-coupling reactions with dithiolanes and dithianes. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/13706

Chicago Manual of Style (16th Edition):

McFarlane, Michael Thomas. “Metal-catalyzed cross-coupling reactions with dithiolanes and dithianes.” 2012. Masters Thesis, University of Manitoba. Accessed September 20, 2020. http://hdl.handle.net/1993/13706.

MLA Handbook (7th Edition):

McFarlane, Michael Thomas. “Metal-catalyzed cross-coupling reactions with dithiolanes and dithianes.” 2012. Web. 20 Sep 2020.

Vancouver:

McFarlane MT. Metal-catalyzed cross-coupling reactions with dithiolanes and dithianes. [Internet] [Masters thesis]. University of Manitoba; 2012. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1993/13706.

Council of Science Editors:

McFarlane MT. Metal-catalyzed cross-coupling reactions with dithiolanes and dithianes. [Masters Thesis]. University of Manitoba; 2012. Available from: http://hdl.handle.net/1993/13706

22. Holmes, Janice. The Stetter reaction : synthesis of complex spiro Bis-indanes and studies on quaternary centre formation.

Degree: 2012, University of Saskatchewan

 This work covers recent advances in the Stetter reaction, including two novel domino Stetter reactions and preliminary studies on quaternary center formation via the intermolecular… (more)

Subjects/Keywords: Stetter reaction; carbenes; organocatalysis; umpolung; domino reactions

Umpolung. ..............................................1 Figure 2-1 Structures of Spiro Bis… …Catalysis of Aldehydes Umpolung, the reversal of a functional group’s innate reactivity, is a… …reactivity, the umpolung of a formal acceptor permits the formation of a carboncarbon bond between… …Reactivity Products FG FG FG Umpolung Products Figure 1-1 Products of Classical Reactivity and… …Umpolung. A class of organic catalysts, known as N-heterocyclic carbenes (NHCs), has… 

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APA (6th Edition):

Holmes, J. (2012). The Stetter reaction : synthesis of complex spiro Bis-indanes and studies on quaternary centre formation. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2012-09-523

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):

Holmes, Janice. “The Stetter reaction : synthesis of complex spiro Bis-indanes and studies on quaternary centre formation.” 2012. Thesis, University of Saskatchewan. Accessed September 20, 2020. http://hdl.handle.net/10388/ETD-2012-09-523.

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

MLA Handbook (7th Edition):

Holmes, Janice. “The Stetter reaction : synthesis of complex spiro Bis-indanes and studies on quaternary centre formation.” 2012. Web. 20 Sep 2020.

Vancouver:

Holmes J. The Stetter reaction : synthesis of complex spiro Bis-indanes and studies on quaternary centre formation. [Internet] [Thesis]. University of Saskatchewan; 2012. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10388/ETD-2012-09-523.

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

Council of Science Editors:

Holmes J. The Stetter reaction : synthesis of complex spiro Bis-indanes and studies on quaternary centre formation. [Thesis]. University of Saskatchewan; 2012. Available from: http://hdl.handle.net/10388/ETD-2012-09-523

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

23. Tomakinian, Terry. Nouvelles méthodes de synthèse de benzofuroindolines. Vers la synthèse de la phalarine : New methodologies for the synthesis of benzofuroindolines.Towards the synthesis of phalarine.

Degree: Docteur es, Chimie, 2015, Université Paris-Saclay (ComUE)

Les benzofuroindolines forment une famille de composés qui se retrouvent sous deux formes : les benzofuro[2,3-b]indolines ou les benzofuro[3,2-b]indolines. Ce motif se retrouve dans de… (more)

Subjects/Keywords: Benzofuroindolines; Indoles; Phénols; Umpolung; O-arylation/réarrangement sigmatropique [3,3]; Couplage pallado-catalysé; Réaction de Fischer interrompue; Benzofuroindolines; Indoles; Phenols; Umpolung; O-arylation/[3,3] sigmatropic rearrangement; Pallado-catalyzed coupling; Interrupted Fischer indolization reaction

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APA (6th Edition):

Tomakinian, T. (2015). Nouvelles méthodes de synthèse de benzofuroindolines. Vers la synthèse de la phalarine : New methodologies for the synthesis of benzofuroindolines.Towards the synthesis of phalarine. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2015SACLS031

Chicago Manual of Style (16th Edition):

Tomakinian, Terry. “Nouvelles méthodes de synthèse de benzofuroindolines. Vers la synthèse de la phalarine : New methodologies for the synthesis of benzofuroindolines.Towards the synthesis of phalarine.” 2015. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed September 20, 2020. http://www.theses.fr/2015SACLS031.

MLA Handbook (7th Edition):

Tomakinian, Terry. “Nouvelles méthodes de synthèse de benzofuroindolines. Vers la synthèse de la phalarine : New methodologies for the synthesis of benzofuroindolines.Towards the synthesis of phalarine.” 2015. Web. 20 Sep 2020.

Vancouver:

Tomakinian T. Nouvelles méthodes de synthèse de benzofuroindolines. Vers la synthèse de la phalarine : New methodologies for the synthesis of benzofuroindolines.Towards the synthesis of phalarine. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2015. [cited 2020 Sep 20]. Available from: http://www.theses.fr/2015SACLS031.

Council of Science Editors:

Tomakinian T. Nouvelles méthodes de synthèse de benzofuroindolines. Vers la synthèse de la phalarine : New methodologies for the synthesis of benzofuroindolines.Towards the synthesis of phalarine. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2015. Available from: http://www.theses.fr/2015SACLS031

24. Lemmerer, Miran. Chemoselective nucleophilic α-amination of amides.

Degree: 2018, University of Vienna

Carbonsäureamide sind in lebenden Organismen omnipräsent. Die Amidbindung spielt eine zentrale Rolle in Proteinenstrukturen, um nur ein Beispiel zu nennen. Wegen ihrer geringen Reaktivität ist… (more)

Subjects/Keywords: 35.52 Präparative Organische Chemie; 35.51 Organische Reaktionen, Stereochemie; Chemoselektive Umpolung / Amide; chemoselective Umpolung / amides

…Deprotection can be achieved under acidic conditions. Scheme 2 a) Umpolung of aldehydes via… …dithiols: The Corey-Seebach reaction. b) Umpolung of aldehydes via tBu-hydrazine: The… …Seebach or the Baldwin reactions. A more atom-economical approach is the Umpolung by cyanide… …Umpolung of aldehydes: a) The benzoin condensation, b) N-heterocyclic carbene catalysis… …While Umpolung at the carbonyl carbon is now a well-established concept, with many methods… 

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APA (6th Edition):

Lemmerer, M. (2018). Chemoselective nucleophilic α-amination of amides. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/52890/

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):

Lemmerer, Miran. “Chemoselective nucleophilic α-amination of amides.” 2018. Thesis, University of Vienna. Accessed September 20, 2020. http://othes.univie.ac.at/52890/.

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

MLA Handbook (7th Edition):

Lemmerer, Miran. “Chemoselective nucleophilic α-amination of amides.” 2018. Web. 20 Sep 2020.

Vancouver:

Lemmerer M. Chemoselective nucleophilic α-amination of amides. [Internet] [Thesis]. University of Vienna; 2018. [cited 2020 Sep 20]. Available from: http://othes.univie.ac.at/52890/.

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

Council of Science Editors:

Lemmerer M. Chemoselective nucleophilic α-amination of amides. [Thesis]. University of Vienna; 2018. Available from: http://othes.univie.ac.at/52890/

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

25. Sanchez-Larios, Jose. Enantioselective and Domino Intermolecular Stetter Reactions.

Degree: 2011, University of Saskatchewan

 This thesis describes three advances in the field of NHC-catalyzed reactions. In particular, a complementary method for the enantioselective intermolecular Stetter reaction as well as… (more)

Subjects/Keywords: Organocatalysis; N-Heterocyclic carbenes; Umpolung; acyl anion equivalents; Stetter reaction

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APA (6th Edition):

Sanchez-Larios, J. (2011). Enantioselective and Domino Intermolecular Stetter Reactions. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2011-12-238

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):

Sanchez-Larios, Jose. “Enantioselective and Domino Intermolecular Stetter Reactions.” 2011. Thesis, University of Saskatchewan. Accessed September 20, 2020. http://hdl.handle.net/10388/ETD-2011-12-238.

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

MLA Handbook (7th Edition):

Sanchez-Larios, Jose. “Enantioselective and Domino Intermolecular Stetter Reactions.” 2011. Web. 20 Sep 2020.

Vancouver:

Sanchez-Larios J. Enantioselective and Domino Intermolecular Stetter Reactions. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10388/ETD-2011-12-238.

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

Council of Science Editors:

Sanchez-Larios J. Enantioselective and Domino Intermolecular Stetter Reactions. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/ETD-2011-12-238

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


University of Manitoba

26. Sharma, Maya. Synthesis of a fluorous benzodithiol support and its utility in the construction of diverse ring systems.

Degree: Chemistry, 2008, University of Manitoba

 A method for the synthesis of a symmetrical fluorous tagged benzodithiol support has been developed through a seven-step synthetic pathway. The Wittig olefination and catalytic… (more)

Subjects/Keywords: Fluorous; Fluorous Solid-Phase Extractions; Tagging; Traceless Linkers; Umpolung; Metathesis

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APA (6th Edition):

Sharma, M. (2008). Synthesis of a fluorous benzodithiol support and its utility in the construction of diverse ring systems. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/3063

Chicago Manual of Style (16th Edition):

Sharma, Maya. “Synthesis of a fluorous benzodithiol support and its utility in the construction of diverse ring systems.” 2008. Masters Thesis, University of Manitoba. Accessed September 20, 2020. http://hdl.handle.net/1993/3063.

MLA Handbook (7th Edition):

Sharma, Maya. “Synthesis of a fluorous benzodithiol support and its utility in the construction of diverse ring systems.” 2008. Web. 20 Sep 2020.

Vancouver:

Sharma M. Synthesis of a fluorous benzodithiol support and its utility in the construction of diverse ring systems. [Internet] [Masters thesis]. University of Manitoba; 2008. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1993/3063.

Council of Science Editors:

Sharma M. Synthesis of a fluorous benzodithiol support and its utility in the construction of diverse ring systems. [Masters Thesis]. University of Manitoba; 2008. Available from: http://hdl.handle.net/1993/3063

27. Giraldo Perez , Daniel. Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) .

Degree: 2014, Universidad de los Andes

 El 5Z-7-Oxozeaenol pertenece a una familia de moléculas conocidas como lactonas del ácido resolcilico (RALs), las cuales presentan una gran variedad de propiedades como potenciales… (more)

Subjects/Keywords: Reaccion de Grignard; Tiamichael; Reacción de Michael; RAL; 5Z-7-oxozeaenol; Borohidruro de Sodio; Síntesis Total; Umpolung; Mitsunobu; Knoevenagel; Heck

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APA (6th Edition):

Giraldo Perez , D. (2014). Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) . (Thesis). Universidad de los Andes. Retrieved from http://documentodegrado.uniandes.edu.co/documentos/200911848_fecha_2014_01_21_hora_09_52_47_parte_1.pdf

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):

Giraldo Perez , Daniel. “Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) .” 2014. Thesis, Universidad de los Andes. Accessed September 20, 2020. http://documentodegrado.uniandes.edu.co/documentos/200911848_fecha_2014_01_21_hora_09_52_47_parte_1.pdf.

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

MLA Handbook (7th Edition):

Giraldo Perez , Daniel. “Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) .” 2014. Web. 20 Sep 2020.

Vancouver:

Giraldo Perez D. Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) . [Internet] [Thesis]. Universidad de los Andes; 2014. [cited 2020 Sep 20]. Available from: http://documentodegrado.uniandes.edu.co/documentos/200911848_fecha_2014_01_21_hora_09_52_47_parte_1.pdf.

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

Council of Science Editors:

Giraldo Perez D. Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) . [Thesis]. Universidad de los Andes; 2014. Available from: http://documentodegrado.uniandes.edu.co/documentos/200911848_fecha_2014_01_21_hora_09_52_47_parte_1.pdf

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

28. Gamba Sanchez , Diego Alexander. Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) .

Degree: 2015, Universidad de los Andes

 El 5Z-7-Oxozeaenol pertenece a una familia de moléculas conocidas como lactonas del ácido resolcilico (RALs), las cuales presentan una gran variedad de propiedades como potenciales… (more)

Subjects/Keywords: Reaccion de Grignard; Tiamichael; Reacción de Michael; RAL; 5Z-7-oxozeaenol; Borohidruro de Sodio; Síntesis Total; Umpolung; Mitsunobu; Knoevenagel; Heck

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

APA (6th Edition):

Gamba Sanchez , D. A. (2015). Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) . (Thesis). Universidad de los Andes. Retrieved from http://documentodegrado.uniandes.edu.co/documentos/200911848_fecha_2014_01_21_hora_09_52_47_parte_1.pdf

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):

Gamba Sanchez , Diego Alexander. “Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) .” 2015. Thesis, Universidad de los Andes. Accessed September 20, 2020. http://documentodegrado.uniandes.edu.co/documentos/200911848_fecha_2014_01_21_hora_09_52_47_parte_1.pdf.

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

MLA Handbook (7th Edition):

Gamba Sanchez , Diego Alexander. “Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) .” 2015. Web. 20 Sep 2020.

Vancouver:

Gamba Sanchez DA. Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) . [Internet] [Thesis]. Universidad de los Andes; 2015. [cited 2020 Sep 20]. Available from: http://documentodegrado.uniandes.edu.co/documentos/200911848_fecha_2014_01_21_hora_09_52_47_parte_1.pdf.

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

Council of Science Editors:

Gamba Sanchez DA. Síntesis de Precursores del 5Z-7-Oxozeaenol (LL-Z1640-2) . [Thesis]. Universidad de los Andes; 2015. Available from: http://documentodegrado.uniandes.edu.co/documentos/200911848_fecha_2014_01_21_hora_09_52_47_parte_1.pdf

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

29. Zhang, Kui. Phosphine-Mediated Multi-Component γ-Umpolung/Aldol/Wittig Cascade Reaction for the Synthesis of Functionalized Naphthalenes.

Degree: Chemistry, 2013, UCLA

 This study describes an efficient and convenient triphenylphosphine-mediated γ-umpolung/aldol/Wittig cascade reaction. This is the first time that phosphine has been used to mediate a multi-component… (more)

Subjects/Keywords: Chemistry; γ; -umpolung; multi-component reaction; naphthalene; phosphine-mediated; Wittig reaction

…phosphine catalysis reactions include the γ-umpolung addition,15 the β’-umpolung addition,16 the… …γ-umpolung-Michael [n + 2] annulation,17 the double-Michael [4 + 1]… …annulation,18 and the γ-umpolung-SN2’ [4 + n] annulation (Schemes 14–18).19… …Scheme 14. γ-Umpolung addition. Scheme 15. β’-Umpolung addition. 4 Scheme 16. γ-Umpolung… …Scheme 18. γ-Umpolung-SN2’ [4 + n] annulation. Functionalized naphthalene compounds… 

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APA (6th Edition):

Zhang, K. (2013). Phosphine-Mediated Multi-Component γ-Umpolung/Aldol/Wittig Cascade Reaction for the Synthesis of Functionalized Naphthalenes. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/77m3r61j

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):

Zhang, Kui. “Phosphine-Mediated Multi-Component γ-Umpolung/Aldol/Wittig Cascade Reaction for the Synthesis of Functionalized Naphthalenes.” 2013. Thesis, UCLA. Accessed September 20, 2020. http://www.escholarship.org/uc/item/77m3r61j.

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

MLA Handbook (7th Edition):

Zhang, Kui. “Phosphine-Mediated Multi-Component γ-Umpolung/Aldol/Wittig Cascade Reaction for the Synthesis of Functionalized Naphthalenes.” 2013. Web. 20 Sep 2020.

Vancouver:

Zhang K. Phosphine-Mediated Multi-Component γ-Umpolung/Aldol/Wittig Cascade Reaction for the Synthesis of Functionalized Naphthalenes. [Internet] [Thesis]. UCLA; 2013. [cited 2020 Sep 20]. Available from: http://www.escholarship.org/uc/item/77m3r61j.

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

Council of Science Editors:

Zhang K. Phosphine-Mediated Multi-Component γ-Umpolung/Aldol/Wittig Cascade Reaction for the Synthesis of Functionalized Naphthalenes. [Thesis]. UCLA; 2013. Available from: http://www.escholarship.org/uc/item/77m3r61j

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

30. Morra, Nicholas A. Progress Towards the Total Synthesis of Amphidinolide C.

Degree: 2012, University of Western Ontario

 A second generation catalyst for the Mukaiyama oxidative cyclization for the formation of trans-THF rings is described. Co(nmp)2, displays increased stability to the reaction conditions,… (more)

Subjects/Keywords: Natural Product Synthesis; trans-THF; Amphidinolide; Mukaiyama Oxidative Cyclization; Macrocycle; Umpolung Chemistry; Organic Chemistry

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APA (6th Edition):

Morra, N. A. (2012). Progress Towards the Total Synthesis of Amphidinolide C. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/502

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):

Morra, Nicholas A. “Progress Towards the Total Synthesis of Amphidinolide C.” 2012. Thesis, University of Western Ontario. Accessed September 20, 2020. https://ir.lib.uwo.ca/etd/502.

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

MLA Handbook (7th Edition):

Morra, Nicholas A. “Progress Towards the Total Synthesis of Amphidinolide C.” 2012. Web. 20 Sep 2020.

Vancouver:

Morra NA. Progress Towards the Total Synthesis of Amphidinolide C. [Internet] [Thesis]. University of Western Ontario; 2012. [cited 2020 Sep 20]. Available from: https://ir.lib.uwo.ca/etd/502.

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

Council of Science Editors:

Morra NA. Progress Towards the Total Synthesis of Amphidinolide C. [Thesis]. University of Western Ontario; 2012. Available from: https://ir.lib.uwo.ca/etd/502

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

[1] [2]

.