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You searched for subject:(Isoxazolidine). Showing records 1 – 9 of 9 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: MS, Chemistry, 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. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82

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. Masters Thesis, Texas A&M University. Accessed April 15, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82.

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. 15 Apr 2021.

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] [Masters thesis]. Texas A&M University; 2010. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82.

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. [Masters Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82


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 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 April 15, 2021. http://hdl.handle.net/2134/13907.

MLA Handbook (7th Edition):

Lee, Darren S. “Advances in palladium catalysed Wacker-type oxidative transformations.” 2013. Web. 15 Apr 2021.

Vancouver:

Lee DS. Advances in palladium catalysed Wacker-type oxidative transformations. [Internet] [Doctoral dissertation]. Loughborough University; 2013. [cited 2021 Apr 15]. 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

3. 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 April 15, 2021. 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. 15 Apr 2021.

Vancouver:

Varrica MGS. Sintesi di isossazolidinil-ipa ad arrività antineoplastica. [Internet] [Thesis]. Università degli Studi di Catania; 2014. [cited 2021 Apr 15]. 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

4. 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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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


University of Michigan

5. Rowe, Steven P. Characteristics of activation domains that control potency and permissiveness of activation domain binding sites.

Degree: PhD, Pure Sciences, 2009, University of Michigan

 The regulation of transcription levels of specific genes is one of the fundamental processes that underlie human physiology. Nearly every human disease is caused by… (more)

Subjects/Keywords: Activation Domains; Binding; Characteristics; Control; Domain; Isoxazolidine; Peptidomimetics; Permissiveness; Potency; Sites

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APA (6th Edition):

Rowe, S. P. (2009). Characteristics of activation domains that control potency and permissiveness of activation domain binding sites. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/127101

Chicago Manual of Style (16th Edition):

Rowe, Steven P. “Characteristics of activation domains that control potency and permissiveness of activation domain binding sites.” 2009. Doctoral Dissertation, University of Michigan. Accessed April 15, 2021. http://hdl.handle.net/2027.42/127101.

MLA Handbook (7th Edition):

Rowe, Steven P. “Characteristics of activation domains that control potency and permissiveness of activation domain binding sites.” 2009. Web. 15 Apr 2021.

Vancouver:

Rowe SP. Characteristics of activation domains that control potency and permissiveness of activation domain binding sites. [Internet] [Doctoral dissertation]. University of Michigan; 2009. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2027.42/127101.

Council of Science Editors:

Rowe SP. Characteristics of activation domains that control potency and permissiveness of activation domain binding sites. [Doctoral Dissertation]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/127101

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 April 15, 2021. 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. 15 Apr 2021.

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 2021 Apr 15]. 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. Hamdi, Abdelrahman. Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique.

Degree: Docteur es, Chimie organique, 2020, Le Mans; Université de Mansoura

L’’ infection par le virus de l’ hépatite C (HCV) est considérée comme un des défis majeurs de santé publique en Egypte où la prévalence… (more)

Subjects/Keywords: Hépatite C; Ether vinylique; Nitrone; Réaction 1,3-dipolaire; Isoxazolidine; Allylation; Analogues de l’asunaprévir; HCV NS 3/4A; Hepatitis C; Vinyl ether; 1,3-DC reaction; Asunaprevir analogues; 547.59

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APA (6th Edition):

Hamdi, A. (2020). Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique. (Doctoral Dissertation). Le Mans; Université de Mansoura. Retrieved from http://www.theses.fr/2020LEMA1020

Chicago Manual of Style (16th Edition):

Hamdi, Abdelrahman. “Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique.” 2020. Doctoral Dissertation, Le Mans; Université de Mansoura. Accessed April 15, 2021. http://www.theses.fr/2020LEMA1020.

MLA Handbook (7th Edition):

Hamdi, Abdelrahman. “Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique.” 2020. Web. 15 Apr 2021.

Vancouver:

Hamdi A. Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique. [Internet] [Doctoral dissertation]. Le Mans; Université de Mansoura; 2020. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2020LEMA1020.

Council of Science Editors:

Hamdi A. Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique. [Doctoral Dissertation]. Le Mans; Université de Mansoura; 2020. Available from: http://www.theses.fr/2020LEMA1020

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 April 15, 2021. 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. 15 Apr 2021.

Vancouver:

Lemen GS. Carboamination Methodology to the Synthesis of 2,5-trans-Pyrrolidines and Isoxazolidines. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2021 Apr 15]. 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

9. 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 https://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 April 15, 2021. https://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. 15 Apr 2021.

Vancouver:

Wang W. Asymmetric Syntheses of Analogs of Kainic Acid. [Internet] [Doctoral dissertation]. Florida International University; 2012. [cited 2021 Apr 15]. Available from: https://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: https://digitalcommons.fiu.edu/etd/756 ; 10.25148/etd.FI12113007 ; FI12113007

.