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You searched for subject:(isoxazolidine). Showing records 1 – 8 of 8 total matches.

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Texas A&M University

1. Kang, Jun Yong. Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene.

Degree: 2010, Texas A&M University

 A new synthetic method toward 5-substituted isoxazolidines by [3 plus 2] cycloaddition of nitrones generated from nitrosobenzene and styrene was discovered. The formation of nitrones… (more)

Subjects/Keywords: [3+2] dipolar cycloaddition; isoxazolidine; nitrone

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APA (6th Edition):

Kang, J. Y. (2010). Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82

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):

Kang, Jun Yong. “Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene.” 2010. Thesis, Texas A&M University. Accessed October 19, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82.

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

MLA Handbook (7th Edition):

Kang, Jun Yong. “Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene.” 2010. Web. 19 Oct 2019.

Vancouver:

Kang JY. Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene. [Internet] [Thesis]. Texas A&M University; 2010. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82.

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

Council of Science Editors:

Kang JY. Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene. [Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82

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


Loughborough University

2. Lee, Darren S. Advances in palladium catalysed Wacker-type oxidative transformations.

Degree: PhD, 2013, Loughborough University

 The development and optimisation of conditions for oxidative Wacker-type cyclisations followed by establishing the reaction scope are reported. Building upon the achievements in the field… (more)

Subjects/Keywords: 547; Organic chemistry; Catalysis; Palladium; Amination; Isoxazolidine; Pyrazolidine; Diastereoselective; Amino alcohols; Diamines

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APA (6th Edition):

Lee, D. S. (2013). Advances in palladium catalysed Wacker-type oxidative transformations. (Doctoral Dissertation). Loughborough University. Retrieved from https://dspace.lboro.ac.uk/2134/13907 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.594448

Chicago Manual of Style (16th Edition):

Lee, Darren S. “Advances in palladium catalysed Wacker-type oxidative transformations.” 2013. Doctoral Dissertation, Loughborough University. Accessed October 19, 2019. https://dspace.lboro.ac.uk/2134/13907 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.594448.

MLA Handbook (7th Edition):

Lee, Darren S. “Advances in palladium catalysed Wacker-type oxidative transformations.” 2013. Web. 19 Oct 2019.

Vancouver:

Lee DS. Advances in palladium catalysed Wacker-type oxidative transformations. [Internet] [Doctoral dissertation]. Loughborough University; 2013. [cited 2019 Oct 19]. Available from: https://dspace.lboro.ac.uk/2134/13907 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.594448.

Council of Science Editors:

Lee DS. Advances in palladium catalysed Wacker-type oxidative transformations. [Doctoral Dissertation]. Loughborough University; 2013. Available from: https://dspace.lboro.ac.uk/2134/13907 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.594448


Loughborough University

3. Lee, Darren S. Advances in palladium catalysed Wacker-type oxidative transformations.

Degree: PhD, 2013, Loughborough University

 The development and optimisation of conditions for oxidative Wacker-type cyclisations followed by establishing the reaction scope are reported. Building upon the achievements in the field… (more)

Subjects/Keywords: 547; Organic chemistry; Catalysis; Palladium; Amination; Isoxazolidine; Pyrazolidine; Diastereoselective; Amino alcohols; Diamines

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

APA (6th Edition):

Lee, D. S. (2013). Advances in palladium catalysed Wacker-type oxidative transformations. (Doctoral Dissertation). Loughborough University. Retrieved from http://hdl.handle.net/2134/13907

Chicago Manual of Style (16th Edition):

Lee, Darren S. “Advances in palladium catalysed Wacker-type oxidative transformations.” 2013. Doctoral Dissertation, Loughborough University. Accessed October 19, 2019. http://hdl.handle.net/2134/13907.

MLA Handbook (7th Edition):

Lee, Darren S. “Advances in palladium catalysed Wacker-type oxidative transformations.” 2013. Web. 19 Oct 2019.

Vancouver:

Lee DS. Advances in palladium catalysed Wacker-type oxidative transformations. [Internet] [Doctoral dissertation]. Loughborough University; 2013. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/2134/13907.

Council of Science Editors:

Lee DS. Advances in palladium catalysed Wacker-type oxidative transformations. [Doctoral Dissertation]. Loughborough University; 2013. Available from: http://hdl.handle.net/2134/13907

4. Varrica, Maria Giulia Sara. Sintesi di isossazolidinil-ipa ad arrività antineoplastica.

Degree: 2014, Università degli Studi di Catania

 Nel lavoro oggetto della tesi di dottorato viene riportata la sintesi e l attività antineoplastica di una serie di idrocarburi policiclici aromatici (IPA) a core… (more)

Subjects/Keywords: Area 03 - Scienze chimiche; DNA intercalation, Antitumor agent, Docking, Polycyclic aromatic hydrocarbons, Isoxazolidine, 1,3-Dipolar cycloaddition

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APA (6th Edition):

Varrica, M. G. S. (2014). Sintesi di isossazolidinil-ipa ad arrività antineoplastica. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/1546

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):

Varrica, Maria Giulia Sara. “Sintesi di isossazolidinil-ipa ad arrività antineoplastica.” 2014. Thesis, Università degli Studi di Catania. Accessed October 19, 2019. http://hdl.handle.net/10761/1546.

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

MLA Handbook (7th Edition):

Varrica, Maria Giulia Sara. “Sintesi di isossazolidinil-ipa ad arrività antineoplastica.” 2014. Web. 19 Oct 2019.

Vancouver:

Varrica MGS. Sintesi di isossazolidinil-ipa ad arrività antineoplastica. [Internet] [Thesis]. Università degli Studi di Catania; 2014. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/10761/1546.

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

Council of Science Editors:

Varrica MGS. Sintesi di isossazolidinil-ipa ad arrività antineoplastica. [Thesis]. Università degli Studi di Catania; 2014. Available from: http://hdl.handle.net/10761/1546

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

5. Shpak-Kraievskyi, Pavlo. Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition.

Degree: Docteur es, Chimie fine, 2013, Le Mans

Les peptides aldéhydes sont connus comme inhibiteurs de protéases et précurseurs de différentes classes de composés biologiquement actifs. Les méthodes pour leur synthèse impliquent classiquement… (more)

Subjects/Keywords: Β-aminoaldéhyde; Épimérisation; Synthèse peptidique; Oxazinone; 6-ATO; Transacétalisation; Cycloaddition dipolaire-1,3; Nitrone; Isoxazolidine; Stéréosélective; Organocatalyseur; Couplage peptidique encombré; Β-aminoaldehyde; Epimerisation; Peptide synthesis; Oxazinone; 6-ATO; Transacetalisation; 1,3-dipolar cycloaddition; Nitrone; Isoxazolidine; Stereoselective; Organocatalyst; Hindered peptide coupling

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APA (6th Edition):

Shpak-Kraievskyi, P. (2013). Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition. (Doctoral Dissertation). Le Mans. Retrieved from http://www.theses.fr/2013LEMA1002

Chicago Manual of Style (16th Edition):

Shpak-Kraievskyi, Pavlo. “Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition.” 2013. Doctoral Dissertation, Le Mans. Accessed October 19, 2019. http://www.theses.fr/2013LEMA1002.

MLA Handbook (7th Edition):

Shpak-Kraievskyi, Pavlo. “Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition.” 2013. Web. 19 Oct 2019.

Vancouver:

Shpak-Kraievskyi P. Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition. [Internet] [Doctoral dissertation]. Le Mans; 2013. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2013LEMA1002.

Council of Science Editors:

Shpak-Kraievskyi P. Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition. [Doctoral Dissertation]. Le Mans; 2013. Available from: http://www.theses.fr/2013LEMA1002

6. Ben Ayed Achich, Kawther. Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones.

Degree: Docteur es, Chimie organique, 2016, Le Mans; Université de Sfax (Tunisie)

Lors de ces travaux de thèse, nous nous sommes intéressés au développement de deux voies différentes de cycloaddition dipolaire-1,3 (CD-1,3) asymétrique pour accéder à des… (more)

Subjects/Keywords: Synthèse asymétrique; Cycloaddition dipolaire 1,3; Nitrone; Isoxazolidine; Dipolarophile; Ether vinylique chiral; Enal; Isoxazoline; Asymmetric synthesis; Cycloaddition 1,3 dipolar; Chiral vinyl ether; 547.037

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APA (6th Edition):

Ben Ayed Achich, K. (2016). Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones. (Doctoral Dissertation). Le Mans; Université de Sfax (Tunisie). Retrieved from http://www.theses.fr/2016LEMA1013

Chicago Manual of Style (16th Edition):

Ben Ayed Achich, Kawther. “Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones.” 2016. Doctoral Dissertation, Le Mans; Université de Sfax (Tunisie). Accessed October 19, 2019. http://www.theses.fr/2016LEMA1013.

MLA Handbook (7th Edition):

Ben Ayed Achich, Kawther. “Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones.” 2016. Web. 19 Oct 2019.

Vancouver:

Ben Ayed Achich K. Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones. [Internet] [Doctoral dissertation]. Le Mans; Université de Sfax (Tunisie); 2016. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2016LEMA1013.

Council of Science Editors:

Ben Ayed Achich K. Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones. [Doctoral Dissertation]. Le Mans; Université de Sfax (Tunisie); 2016. Available from: http://www.theses.fr/2016LEMA1013

7. Wang, Wentian. Asymmetric Syntheses of Analogs of Kainic Acid.

Degree: PhD, Chemistry, 2012, Florida International University

  Kainic acid has been used for nearly 50 years as a tool in neuroscience due to its pronounced neuroexcitatory properties. However, the significant price… (more)

Subjects/Keywords: Kainic Acid; Pyrrolidine; Dipolar cycloaddition; Asymmetric; Exo/Endo; Isoxazolidine; Mosher method

…Another potential functional mimic of kainic acid is isoxazolidine analogs of kainoids… …43 3. Synthesis of isoxazolidine analog of kainic acid… …preparing isoxazolidine analogs of kainic acid 28 ..88 4. Conclusion… …Revised synthetic plan of isoxazolidine analog 28… …isoxazolidine 68… 

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APA (6th Edition):

Wang, W. (2012). Asymmetric Syntheses of Analogs of Kainic Acid. (Doctoral Dissertation). Florida International University. Retrieved from http://digitalcommons.fiu.edu/etd/756 ; 10.25148/etd.FI12113007 ; FI12113007

Chicago Manual of Style (16th Edition):

Wang, Wentian. “Asymmetric Syntheses of Analogs of Kainic Acid.” 2012. Doctoral Dissertation, Florida International University. Accessed October 19, 2019. http://digitalcommons.fiu.edu/etd/756 ; 10.25148/etd.FI12113007 ; FI12113007.

MLA Handbook (7th Edition):

Wang, Wentian. “Asymmetric Syntheses of Analogs of Kainic Acid.” 2012. Web. 19 Oct 2019.

Vancouver:

Wang W. Asymmetric Syntheses of Analogs of Kainic Acid. [Internet] [Doctoral dissertation]. Florida International University; 2012. [cited 2019 Oct 19]. Available from: http://digitalcommons.fiu.edu/etd/756 ; 10.25148/etd.FI12113007 ; FI12113007.

Council of Science Editors:

Wang W. Asymmetric Syntheses of Analogs of Kainic Acid. [Doctoral Dissertation]. Florida International University; 2012. Available from: http://digitalcommons.fiu.edu/etd/756 ; 10.25148/etd.FI12113007 ; FI12113007

8. Lemen, Georgia S. Carboamination Methodology to the Synthesis of 2,5-trans-Pyrrolidines and Isoxazolidines.

Degree: PhD, Chemistry, 2011, University of Michigan

 This thesis details the development of new methods for the synthesis of four classes of biologically relevant heterocycles: 2,5-trans-pyrrolidines, benzofused 1-azabicyclo[3.3.0]octanes, benzofused 1-azabicyclo[4.3.0]nonanes, and 3,5-cis… (more)

Subjects/Keywords: Palladium Catalyzed Carboamination; Pyrrolidine Synthesis; Isoxazolidine Synthesis; Hetereocycles; Tandem Reaction; Palladium Catalysis; Chemistry; Science

…78 Scheme 6-1: Synthesis of Bis-Fused Alkaloids from Isoxazolidine Intermediates… …generates an isoxazolidine with the same aryl bromide added to both the nitrogen and the C1'… …Isoxazolidine Formation O R Ar N O 1. Pd2(dba)3 (1.5 mol%) (o-biphenyl)… …an isoxazolidine with a methyl ester side chain (Scheme 1-7). While this method… …works well for adding a methyl ester side chain to the isoxazolidine, it does require a… 

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APA (6th Edition):

Lemen, G. S. (2011). Carboamination Methodology to the Synthesis of 2,5-trans-Pyrrolidines and Isoxazolidines. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/86479

Chicago Manual of Style (16th Edition):

Lemen, Georgia S. “Carboamination Methodology to the Synthesis of 2,5-trans-Pyrrolidines and Isoxazolidines.” 2011. Doctoral Dissertation, University of Michigan. Accessed October 19, 2019. http://hdl.handle.net/2027.42/86479.

MLA Handbook (7th Edition):

Lemen, Georgia S. “Carboamination Methodology to the Synthesis of 2,5-trans-Pyrrolidines and Isoxazolidines.” 2011. Web. 19 Oct 2019.

Vancouver:

Lemen GS. Carboamination Methodology to the Synthesis of 2,5-trans-Pyrrolidines and Isoxazolidines. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/2027.42/86479.

Council of Science Editors:

Lemen GS. Carboamination Methodology to the Synthesis of 2,5-trans-Pyrrolidines and Isoxazolidines. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/86479

.