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You searched for subject:(Cascade Reactions). Showing records 1 – 18 of 18 total matches.

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University of Saskatchewan

1. Wang, Li. NHC-catalyzed ring expansions and cascade reactions.

Degree: 2009, University of Saskatchewan

 In recent years, N-hetereocyclic carbenes (NHCs) have received considerable attention as organocatalysts due to their unusual ability to induce a reversal of reactivity (Umpolung) in… (more)

Subjects/Keywords: Cascade Reactions; Lactams; Ring expansions; Lactones; Organocatalysis; N-Heterocyclic Carbene

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APA (6th Edition):

Wang, L. (2009). NHC-catalyzed ring expansions and cascade reactions. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-12252009-082204

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):

Wang, Li. “NHC-catalyzed ring expansions and cascade reactions.” 2009. Thesis, University of Saskatchewan. Accessed October 23, 2019. http://hdl.handle.net/10388/etd-12252009-082204.

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

MLA Handbook (7th Edition):

Wang, Li. “NHC-catalyzed ring expansions and cascade reactions.” 2009. Web. 23 Oct 2019.

Vancouver:

Wang L. NHC-catalyzed ring expansions and cascade reactions. [Internet] [Thesis]. University of Saskatchewan; 2009. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10388/etd-12252009-082204.

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

Council of Science Editors:

Wang L. NHC-catalyzed ring expansions and cascade reactions. [Thesis]. University of Saskatchewan; 2009. Available from: http://hdl.handle.net/10388/etd-12252009-082204

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

2. Boudhar, Aicha. Fenestranes, cyclooctatriènes et leurs dérivés comme châssis moléculaires innovants pour le développement de plateformes modulables : Fenestranes, cyclooctatrienes and their derivates as innovative scaffolds for the development of tunable platforms.

Degree: Docteur es, Chimie, 2012, Université de Strasbourg

Ces travaux de thèse nous ont permis de mettre en évidence un accès à un large nombre de composés polycycliques. Les étendues des méthodes employant… (more)

Subjects/Keywords: Fenestranes; Cyclooctatriènes; Cascades réactionnelles; Hétéroatomes; Fenestranes; Cyclooctatrienes; Cascade reactions; Heteroatoms; 547.2

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APA (6th Edition):

Boudhar, A. (2012). Fenestranes, cyclooctatriènes et leurs dérivés comme châssis moléculaires innovants pour le développement de plateformes modulables : Fenestranes, cyclooctatrienes and their derivates as innovative scaffolds for the development of tunable platforms. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAF022

Chicago Manual of Style (16th Edition):

Boudhar, Aicha. “Fenestranes, cyclooctatriènes et leurs dérivés comme châssis moléculaires innovants pour le développement de plateformes modulables : Fenestranes, cyclooctatrienes and their derivates as innovative scaffolds for the development of tunable platforms.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed October 23, 2019. http://www.theses.fr/2012STRAF022.

MLA Handbook (7th Edition):

Boudhar, Aicha. “Fenestranes, cyclooctatriènes et leurs dérivés comme châssis moléculaires innovants pour le développement de plateformes modulables : Fenestranes, cyclooctatrienes and their derivates as innovative scaffolds for the development of tunable platforms.” 2012. Web. 23 Oct 2019.

Vancouver:

Boudhar A. Fenestranes, cyclooctatriènes et leurs dérivés comme châssis moléculaires innovants pour le développement de plateformes modulables : Fenestranes, cyclooctatrienes and their derivates as innovative scaffolds for the development of tunable platforms. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2012STRAF022.

Council of Science Editors:

Boudhar A. Fenestranes, cyclooctatriènes et leurs dérivés comme châssis moléculaires innovants pour le développement de plateformes modulables : Fenestranes, cyclooctatrienes and their derivates as innovative scaffolds for the development of tunable platforms. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAF022


University of Michigan

3. White, Derick. Palladium Catalyzed Alkene Difunctionalization Reactions for the Synthesis of Polycyclic Nitrogen Heterocycles and Functionalized Carbocycles.

Degree: PhD, Chemistry, 2017, University of Michigan

 Saturated heterocycles are structures commonly found in pharmaceutically relevant compounds and natural products. From a synthetic perspective, controllable and efficient syntheses of such motifs are… (more)

Subjects/Keywords: synthetic methods; palladium catalysis; alkene difunctionalization; stereoselective synthesis; carboheterofunctionalization; cascade reactions; Chemistry; Science

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APA (6th Edition):

White, D. (2017). Palladium Catalyzed Alkene Difunctionalization Reactions for the Synthesis of Polycyclic Nitrogen Heterocycles and Functionalized Carbocycles. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/138747

Chicago Manual of Style (16th Edition):

White, Derick. “Palladium Catalyzed Alkene Difunctionalization Reactions for the Synthesis of Polycyclic Nitrogen Heterocycles and Functionalized Carbocycles.” 2017. Doctoral Dissertation, University of Michigan. Accessed October 23, 2019. http://hdl.handle.net/2027.42/138747.

MLA Handbook (7th Edition):

White, Derick. “Palladium Catalyzed Alkene Difunctionalization Reactions for the Synthesis of Polycyclic Nitrogen Heterocycles and Functionalized Carbocycles.” 2017. Web. 23 Oct 2019.

Vancouver:

White D. Palladium Catalyzed Alkene Difunctionalization Reactions for the Synthesis of Polycyclic Nitrogen Heterocycles and Functionalized Carbocycles. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2027.42/138747.

Council of Science Editors:

White D. Palladium Catalyzed Alkene Difunctionalization Reactions for the Synthesis of Polycyclic Nitrogen Heterocycles and Functionalized Carbocycles. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/138747

4. Joussot, Jessie. Stratégies de synthèse d’un nouvel antipsychotique potentiel : cascades réactionnelles palladocatalysées : un outil puissant pour la synthèse de structures polycycliques complexes et hautement fonctionnalisées : Synthetic strategies of a new potential antipsychotic drug : palladium-catalyzed cascade reactions : a powerful tool for the synthesis of highly functionalized and complex polycyclic structures.

Degree: Docteur es, Chimie, 2015, Université de Strasbourg

Ces travaux de thèse ont permis dans un premier temps, d'aborder différentes voies de synthèse d'un nouvel antipsychotique potentiel (F17464) proposé par les laboratoires Pierre… (more)

Subjects/Keywords: Antipsychotique; Chromone; Naphtalène; Cycle à sept atomes de carbone; Fenestradiène; Cyclooctatriène; Cascade réactionnelle palladocatalysée; Cyclocarbopalladation; Antipsychotic; Chromone; Naphthalene; Seven-membered carbocycle; Fenestradiene; Cyclooctatriene; Palladium-catalyzed cascade reactions; Cyclocarbopalladation; 547.2; 615.19

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APA (6th Edition):

Joussot, J. (2015). Stratégies de synthèse d’un nouvel antipsychotique potentiel : cascades réactionnelles palladocatalysées : un outil puissant pour la synthèse de structures polycycliques complexes et hautement fonctionnalisées : Synthetic strategies of a new potential antipsychotic drug : palladium-catalyzed cascade reactions : a powerful tool for the synthesis of highly functionalized and complex polycyclic structures. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2015STRAF016

Chicago Manual of Style (16th Edition):

Joussot, Jessie. “Stratégies de synthèse d’un nouvel antipsychotique potentiel : cascades réactionnelles palladocatalysées : un outil puissant pour la synthèse de structures polycycliques complexes et hautement fonctionnalisées : Synthetic strategies of a new potential antipsychotic drug : palladium-catalyzed cascade reactions : a powerful tool for the synthesis of highly functionalized and complex polycyclic structures.” 2015. Doctoral Dissertation, Université de Strasbourg. Accessed October 23, 2019. http://www.theses.fr/2015STRAF016.

MLA Handbook (7th Edition):

Joussot, Jessie. “Stratégies de synthèse d’un nouvel antipsychotique potentiel : cascades réactionnelles palladocatalysées : un outil puissant pour la synthèse de structures polycycliques complexes et hautement fonctionnalisées : Synthetic strategies of a new potential antipsychotic drug : palladium-catalyzed cascade reactions : a powerful tool for the synthesis of highly functionalized and complex polycyclic structures.” 2015. Web. 23 Oct 2019.

Vancouver:

Joussot J. Stratégies de synthèse d’un nouvel antipsychotique potentiel : cascades réactionnelles palladocatalysées : un outil puissant pour la synthèse de structures polycycliques complexes et hautement fonctionnalisées : Synthetic strategies of a new potential antipsychotic drug : palladium-catalyzed cascade reactions : a powerful tool for the synthesis of highly functionalized and complex polycyclic structures. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2015. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2015STRAF016.

Council of Science Editors:

Joussot J. Stratégies de synthèse d’un nouvel antipsychotique potentiel : cascades réactionnelles palladocatalysées : un outil puissant pour la synthèse de structures polycycliques complexes et hautement fonctionnalisées : Synthetic strategies of a new potential antipsychotic drug : palladium-catalyzed cascade reactions : a powerful tool for the synthesis of highly functionalized and complex polycyclic structures. [Doctoral Dissertation]. Université de Strasbourg; 2015. Available from: http://www.theses.fr/2015STRAF016

5. Blouin, Sarah. Synthèse de cyclooctatétraènes par réactions en cascade palladocatalysées : Synthesis of cyclooctatetraenes through palladium-catalyzed cascade reactions.

Degree: Docteur es, Chimie organique, 2016, Université de Strasbourg

Ces travaux de thèse ont permis de développer une voie d’accès à des systèmes polycycliques complexes contenant un cyclooctatétraène par réactions en cascade palladocatalysées à… (more)

Subjects/Keywords: Cyclooctatétraène; Réactions en cascade; Cyclocarbopalladation; Palladium; Electrocyclisation 8pi; Electrocyclisation 6pi; Cyclooctadiènallène; Beta-carbo élimination; Cyclooctatetraene; Cascade reactions; Cyclocarbopalladation; Palladium; Electrocyclization 8pi; Electrocyclization 6pi; Cyclooctadienallene; Beta-carbo-elimination; 547.2

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APA (6th Edition):

Blouin, S. (2016). Synthèse de cyclooctatétraènes par réactions en cascade palladocatalysées : Synthesis of cyclooctatetraenes through palladium-catalyzed cascade reactions. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2016STRAF048

Chicago Manual of Style (16th Edition):

Blouin, Sarah. “Synthèse de cyclooctatétraènes par réactions en cascade palladocatalysées : Synthesis of cyclooctatetraenes through palladium-catalyzed cascade reactions.” 2016. Doctoral Dissertation, Université de Strasbourg. Accessed October 23, 2019. http://www.theses.fr/2016STRAF048.

MLA Handbook (7th Edition):

Blouin, Sarah. “Synthèse de cyclooctatétraènes par réactions en cascade palladocatalysées : Synthesis of cyclooctatetraenes through palladium-catalyzed cascade reactions.” 2016. Web. 23 Oct 2019.

Vancouver:

Blouin S. Synthèse de cyclooctatétraènes par réactions en cascade palladocatalysées : Synthesis of cyclooctatetraenes through palladium-catalyzed cascade reactions. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2016. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2016STRAF048.

Council of Science Editors:

Blouin S. Synthèse de cyclooctatétraènes par réactions en cascade palladocatalysées : Synthesis of cyclooctatetraenes through palladium-catalyzed cascade reactions. [Doctoral Dissertation]. Université de Strasbourg; 2016. Available from: http://www.theses.fr/2016STRAF048

6. Salacz, Laura. Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis.

Degree: Docteur es, Chimie, 2018, Université de Strasbourg

Ces travaux de thèse ont permis, au cours de deux projets, de s’attacher à la synthèse de structures complexes au moyen de réaction en cascade(more)

Subjects/Keywords: Tropone; Cycloaddition carbonylative; Cyclohydrocarbonylation; Réaction en cascade; Rhodium; Hydroformylation désymétrisante; Aspidosperma; Tropone; Carbonylative cycloaddition; Cyclohydrocarbonylation; Cascade reactions; Rhodium; Dessymmetrising hydroformylation; Aspidosperma; 541.3

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APA (6th Edition):

Salacz, L. (2018). Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2018STRAF034

Chicago Manual of Style (16th Edition):

Salacz, Laura. “Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis.” 2018. Doctoral Dissertation, Université de Strasbourg. Accessed October 23, 2019. http://www.theses.fr/2018STRAF034.

MLA Handbook (7th Edition):

Salacz, Laura. “Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis.” 2018. Web. 23 Oct 2019.

Vancouver:

Salacz L. Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2018. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2018STRAF034.

Council of Science Editors:

Salacz L. Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis. [Doctoral Dissertation]. Université de Strasbourg; 2018. Available from: http://www.theses.fr/2018STRAF034

7. Buttard, Floris. 3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis.

Degree: Docteur es, Chimie Organique, 2018, Université d'Orléans

Le développement de nouvelles méthodes de synthèse de molécules hétérocycliques originales représente un enjeu actuel majeur en chimie organique. L’objectif est de fournir de nouveaux… (more)

Subjects/Keywords: Chimie hétéroaromatique; Réaction en cascade; Organocatalyse; Addition conjuguée; Cycloaddition; Heteroaromatic chemistry; Domino reactions; Organocatalysis; Conjugate addition; Cycloaddition; 547

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APA (6th Edition):

Buttard, F. (2018). 3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2018ORLE2032

Chicago Manual of Style (16th Edition):

Buttard, Floris. “3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis.” 2018. Doctoral Dissertation, Université d'Orléans. Accessed October 23, 2019. http://www.theses.fr/2018ORLE2032.

MLA Handbook (7th Edition):

Buttard, Floris. “3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis.” 2018. Web. 23 Oct 2019.

Vancouver:

Buttard F. 3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis. [Internet] [Doctoral dissertation]. Université d'Orléans; 2018. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2018ORLE2032.

Council of Science Editors:

Buttard F. 3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis. [Doctoral Dissertation]. Université d'Orléans; 2018. Available from: http://www.theses.fr/2018ORLE2032


Colorado State University

8. Lathrop, Stephen Paul. N-Heterocyclic carbene catalysis : application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions.

Degree: PhD, Chemistry, 2007, Colorado State University

 Application of the N-Heterocyclic carbene catalyzed Stetter reaction to the total synthesis of 9-epi-cephalimysin A has been realized. The approach centers on the use of… (more)

Subjects/Keywords: carbenes; Stetter reaction; cephalimysin A; cascade reactions; benzoin reaction

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APA (6th Edition):

Lathrop, S. P. (2007). N-Heterocyclic carbene catalysis : application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/47287

Chicago Manual of Style (16th Edition):

Lathrop, Stephen Paul. “N-Heterocyclic carbene catalysis : application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions.” 2007. Doctoral Dissertation, Colorado State University. Accessed October 23, 2019. http://hdl.handle.net/10217/47287.

MLA Handbook (7th Edition):

Lathrop, Stephen Paul. “N-Heterocyclic carbene catalysis : application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions.” 2007. Web. 23 Oct 2019.

Vancouver:

Lathrop SP. N-Heterocyclic carbene catalysis : application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10217/47287.

Council of Science Editors:

Lathrop SP. N-Heterocyclic carbene catalysis : application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions. [Doctoral Dissertation]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/47287

9. Maury, Julien. Nouveaux développements en chimie radicalaire des dialkylzincs : études mécanistiques et applications en synthèse : New development in dialkylzincs radical chemistry : mechanistic studies and synthetic applications.

Degree: Docteur es, Chimie organique, 2012, Aix Marseille Université

Le travail présenté dans ce mémoire de thèse concerne pour l'essentiel, l'utilisation des dialkylzincs en tant que médiateurs de réactions radicalaires. La particularité de ces… (more)

Subjects/Keywords: Dialkylzincs; Oxydation; Réactions radicalaires et polaires en cascade; Réactions multi-composés; Étude mécanistique par RPE; Spin trapping; Pyrrolizidines; Dérivés fumariques; Azoture d’alkyle; Lactones; Dialkylzincs; Multicomponent reactions; Mechanistic study by EPR; Spin-trapping; Lactones; Pyrrolizidines; Fumaric derivatives; Alkyl azides; Oxidation; Radical-polar cascade reactions

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APA (6th Edition):

Maury, J. (2012). Nouveaux développements en chimie radicalaire des dialkylzincs : études mécanistiques et applications en synthèse : New development in dialkylzincs radical chemistry : mechanistic studies and synthetic applications. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2012AIXM4351

Chicago Manual of Style (16th Edition):

Maury, Julien. “Nouveaux développements en chimie radicalaire des dialkylzincs : études mécanistiques et applications en synthèse : New development in dialkylzincs radical chemistry : mechanistic studies and synthetic applications.” 2012. Doctoral Dissertation, Aix Marseille Université. Accessed October 23, 2019. http://www.theses.fr/2012AIXM4351.

MLA Handbook (7th Edition):

Maury, Julien. “Nouveaux développements en chimie radicalaire des dialkylzincs : études mécanistiques et applications en synthèse : New development in dialkylzincs radical chemistry : mechanistic studies and synthetic applications.” 2012. Web. 23 Oct 2019.

Vancouver:

Maury J. Nouveaux développements en chimie radicalaire des dialkylzincs : études mécanistiques et applications en synthèse : New development in dialkylzincs radical chemistry : mechanistic studies and synthetic applications. [Internet] [Doctoral dissertation]. Aix Marseille Université 2012. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2012AIXM4351.

Council of Science Editors:

Maury J. Nouveaux développements en chimie radicalaire des dialkylzincs : études mécanistiques et applications en synthèse : New development in dialkylzincs radical chemistry : mechanistic studies and synthetic applications. [Doctoral Dissertation]. Aix Marseille Université 2012. Available from: http://www.theses.fr/2012AIXM4351

10. E. Massolo. NOVEL SYNTHETIC ORGANOCATALYTIC METHODOLOGIES.

Degree: 2015, Università degli Studi di Milano

 The objective of this PhD study was to apply organocatalytic synthetic methods for the regio- and stereoselective synthesis of highly functionalized compounds. We exploited different… (more)

Subjects/Keywords: stereoselective organocatalysis; aminocatalysis; nitroacrylates; bifunctional organocatlysts; cascade reactions; fluorinated compounds; deep eutectic solvents; photocatalysis; acyl anion mimic; Settore CHIM/06 - Chimica Organica

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APA (6th Edition):

Massolo, E. (2015). NOVEL SYNTHETIC ORGANOCATALYTIC METHODOLOGIES. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/330262

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):

Massolo, E.. “NOVEL SYNTHETIC ORGANOCATALYTIC METHODOLOGIES.” 2015. Thesis, Università degli Studi di Milano. Accessed October 23, 2019. http://hdl.handle.net/2434/330262.

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

MLA Handbook (7th Edition):

Massolo, E.. “NOVEL SYNTHETIC ORGANOCATALYTIC METHODOLOGIES.” 2015. Web. 23 Oct 2019.

Vancouver:

Massolo E. NOVEL SYNTHETIC ORGANOCATALYTIC METHODOLOGIES. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2434/330262.

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

Council of Science Editors:

Massolo E. NOVEL SYNTHETIC ORGANOCATALYTIC METHODOLOGIES. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/330262

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

11. Loiseau, Francis. Cope-type Hydroamination of Alkenes with Hydroxylamines and Hydrazines - Scope and Mechanism .

Degree: 2013, University of Ottawa

 Hydroamination stands as a desirable approach to nitrogen-containing molecules, which have important applications ranging from pharmaceuticals (fine chemicals) to paints, coatings, insecticides and agrochemicals (bulk… (more)

Subjects/Keywords: Synthesis; Hydroamination; Hydrohydrazination; Hydroxylamine; Hydrazine; Catalysis; Nitrogen; Cascade Reactions; Alkaloids

…20 2 Cope-type Hydroamination with Hydroxylamines – Cascade Reactions… …27 2.1.3 Concept of Cascade Reactions… …28 2.1.4 Planned Cascade Reactions… …concerted or catalyzed reaction on the reaction, vs. the use of cascade reactions. 29 Figure… …cascade reactions. Tested in standard conditions, 100 °C for 42 h, with excess alkene (2-5… 

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APA (6th Edition):

Loiseau, F. (2013). Cope-type Hydroamination of Alkenes with Hydroxylamines and Hydrazines - Scope and Mechanism . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/23794

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):

Loiseau, Francis. “Cope-type Hydroamination of Alkenes with Hydroxylamines and Hydrazines - Scope and Mechanism .” 2013. Thesis, University of Ottawa. Accessed October 23, 2019. http://hdl.handle.net/10393/23794.

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

MLA Handbook (7th Edition):

Loiseau, Francis. “Cope-type Hydroamination of Alkenes with Hydroxylamines and Hydrazines - Scope and Mechanism .” 2013. Web. 23 Oct 2019.

Vancouver:

Loiseau F. Cope-type Hydroamination of Alkenes with Hydroxylamines and Hydrazines - Scope and Mechanism . [Internet] [Thesis]. University of Ottawa; 2013. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10393/23794.

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

Council of Science Editors:

Loiseau F. Cope-type Hydroamination of Alkenes with Hydroxylamines and Hydrazines - Scope and Mechanism . [Thesis]. University of Ottawa; 2013. Available from: http://hdl.handle.net/10393/23794

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

12. Pantaine, Loïc. Aminocatalyse et Réactions en Cascade pour la Synthèse de Polycycles Tridimensionnels : Aminocatalysis and Cascade Reactions for the Synthesis of Tridimensional Polycycles.

Degree: Docteur es, Chimie, 2016, Paris Saclay

Les travaux exposés dans ce manuscrit ont pour objectif d’étudier des séquences réactionnelles organocatalysées permettant la formation stéréosélective de liaisons carbone-carbone ou carbone-hétéroatome. Plusieurs stratégies… (more)

Subjects/Keywords: Aminocatalyse asymétrique; Synthèse énantiosélective; Cascade réactionelle; Polycycles chiraux; Composés azotés; Asymmetric aminocatalysis; Enantioselective synthesis; One-Pot reactions; Chiral polycycles; Nitrogen-Containing compounds; 547

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APA (6th Edition):

Pantaine, L. (2016). Aminocatalyse et Réactions en Cascade pour la Synthèse de Polycycles Tridimensionnels : Aminocatalysis and Cascade Reactions for the Synthesis of Tridimensional Polycycles. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2016SACLV084

Chicago Manual of Style (16th Edition):

Pantaine, Loïc. “Aminocatalyse et Réactions en Cascade pour la Synthèse de Polycycles Tridimensionnels : Aminocatalysis and Cascade Reactions for the Synthesis of Tridimensional Polycycles.” 2016. Doctoral Dissertation, Paris Saclay. Accessed October 23, 2019. http://www.theses.fr/2016SACLV084.

MLA Handbook (7th Edition):

Pantaine, Loïc. “Aminocatalyse et Réactions en Cascade pour la Synthèse de Polycycles Tridimensionnels : Aminocatalysis and Cascade Reactions for the Synthesis of Tridimensional Polycycles.” 2016. Web. 23 Oct 2019.

Vancouver:

Pantaine L. Aminocatalyse et Réactions en Cascade pour la Synthèse de Polycycles Tridimensionnels : Aminocatalysis and Cascade Reactions for the Synthesis of Tridimensional Polycycles. [Internet] [Doctoral dissertation]. Paris Saclay; 2016. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2016SACLV084.

Council of Science Editors:

Pantaine L. Aminocatalyse et Réactions en Cascade pour la Synthèse de Polycycles Tridimensionnels : Aminocatalysis and Cascade Reactions for the Synthesis of Tridimensional Polycycles. [Doctoral Dissertation]. Paris Saclay; 2016. Available from: http://www.theses.fr/2016SACLV084

13. Jewett, Ivan Tucker. Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules.

Degree: PhD, Chemistry, 2010, University of Texas – Austin

 In the interests of synthetic efficiency several cascade reactions involving iminium ion intermediates have developed to allow for the rapid assembly of complex molecules from… (more)

Subjects/Keywords: Iminium ion; Cascade reactions; Quinolizidine; Alkaloid; Actinophyllic acid

…xv 1. Cascade Reactions… …22 1.2 Cascade Reactions as a tool for synthetic efficiency ...........................22… …63 Figure 2.3. Cascade reactions: ketal vs. acetal… …181 xxi 1. 1.1. Cascade Reactions INTRODUCTION Over millions of years, organisms have… …economy.7 1.2 CASCADE REACTIONS AS A TOOL FOR SYNTHETIC EFFICIENCY One of the simplest ways to… 

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APA (6th Edition):

Jewett, I. T. (2010). Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30932

Chicago Manual of Style (16th Edition):

Jewett, Ivan Tucker. “Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed October 23, 2019. http://hdl.handle.net/2152/30932.

MLA Handbook (7th Edition):

Jewett, Ivan Tucker. “Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules.” 2010. Web. 23 Oct 2019.

Vancouver:

Jewett IT. Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2152/30932.

Council of Science Editors:

Jewett IT. Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/30932

14. Gigant, Nicolas. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.

Degree: Docteur es, Chimie organique, 2012, Université d'Orléans

La nécessité grandissante de disposer d’une large librairie de diverses petites molécules pour le screening biologique constitue une puissante force motrice pour les chimistes organiciens… (more)

Subjects/Keywords: Enamide; Diversité moléculaire; Synthèse orientée vers la diversité; Phosphates vinyliques; Additions d’aza-Michaël; Nitrènes; Réactions de couplage pallado-catalysées; Réactions en cascades; Enamides; Molecular diversity; Diversity-oriented synthesis; Vinylphosphates; Aza-Michael additions; Nitrenes; Palladium-catalyzed cross-coupling reactions; Cascade reactions

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APA (6th Edition):

Gigant, N. (2012). Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2012ORLE2039

Chicago Manual of Style (16th Edition):

Gigant, Nicolas. “Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.” 2012. Doctoral Dissertation, Université d'Orléans. Accessed October 23, 2019. http://www.theses.fr/2012ORLE2039.

MLA Handbook (7th Edition):

Gigant, Nicolas. “Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.” 2012. Web. 23 Oct 2019.

Vancouver:

Gigant N. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. [Internet] [Doctoral dissertation]. Université d'Orléans; 2012. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2012ORLE2039.

Council of Science Editors:

Gigant N. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. [Doctoral Dissertation]. Université d'Orléans; 2012. Available from: http://www.theses.fr/2012ORLE2039


Kyoto University

15. NGUYEN, MINH THANG. Arranging multiple types of enzymes in defined space by modular adaptors .

Degree: 2019, Kyoto University

Subjects/Keywords: DNA origami; DNA binding proteins; Self-ligating protein tags; Enzyme cascade; Orthogonal reactions; Modular adaptors; Atomic force microscopy

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APA (6th Edition):

NGUYEN, M. T. (2019). Arranging multiple types of enzymes in defined space by modular adaptors . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/242324

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):

NGUYEN, MINH THANG. “Arranging multiple types of enzymes in defined space by modular adaptors .” 2019. Thesis, Kyoto University. Accessed October 23, 2019. http://hdl.handle.net/2433/242324.

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

MLA Handbook (7th Edition):

NGUYEN, MINH THANG. “Arranging multiple types of enzymes in defined space by modular adaptors .” 2019. Web. 23 Oct 2019.

Vancouver:

NGUYEN MT. Arranging multiple types of enzymes in defined space by modular adaptors . [Internet] [Thesis]. Kyoto University; 2019. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2433/242324.

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

Council of Science Editors:

NGUYEN MT. Arranging multiple types of enzymes in defined space by modular adaptors . [Thesis]. Kyoto University; 2019. Available from: http://hdl.handle.net/2433/242324

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

16. Ioannou, Georgios. Ανάπτυξη και εφαρμογή βιώσιμων συνθετικών τεχνολογιών του διεγερμένου οξυγόνου: φωτοξειδώσεις συνεχούς ροής σε εκνέφωμα.

Degree: 2017, University of Crete (UOC); Πανεπιστήμιο Κρήτης

In Chapter 1 of this dissertation, an introduction to the chemistry of singlet oxygen (1O2) and continuous flow photochemistry in micro- and macroreactors is presented.… (more)

Subjects/Keywords: Διεγερμένο μοριακό οξυγόνο; Φωτοχημεία συνεχούς ροής; Φωτοαντιδραστήρας συνεχούς ροής; Αερόλυμα; Πνευματικός εκνεφωτής; Φωτοξείδωση φουρανίων; Bιώσιμη χημεία; Διαδοχικές αντιδράσεις; N-ακυλοϊμινικό ιόν; Pictet-Spengler; Glochidine; Glochidicine; γ-Λακτάμες; Attenol A; Attenol B; Singlet oxygen; Continuous flow photochemistry; Continuous flow photoreactor; Aerosol; Pneumatic nebulizer; Furan photooxidation; Sustainable chemistry; Cascade reactions; N-acyliminium; Pictet-Spengler; Glochidine; Glochidicine; γ-Lactams; Attenol A; Attenol B

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

APA (6th Edition):

Ioannou, G. (2017). Ανάπτυξη και εφαρμογή βιώσιμων συνθετικών τεχνολογιών του διεγερμένου οξυγόνου: φωτοξειδώσεις συνεχούς ροής σε εκνέφωμα. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/42217

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):

Ioannou, Georgios. “Ανάπτυξη και εφαρμογή βιώσιμων συνθετικών τεχνολογιών του διεγερμένου οξυγόνου: φωτοξειδώσεις συνεχούς ροής σε εκνέφωμα.” 2017. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed October 23, 2019. http://hdl.handle.net/10442/hedi/42217.

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

MLA Handbook (7th Edition):

Ioannou, Georgios. “Ανάπτυξη και εφαρμογή βιώσιμων συνθετικών τεχνολογιών του διεγερμένου οξυγόνου: φωτοξειδώσεις συνεχούς ροής σε εκνέφωμα.” 2017. Web. 23 Oct 2019.

Vancouver:

Ioannou G. Ανάπτυξη και εφαρμογή βιώσιμων συνθετικών τεχνολογιών του διεγερμένου οξυγόνου: φωτοξειδώσεις συνεχούς ροής σε εκνέφωμα. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2017. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10442/hedi/42217.

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

Council of Science Editors:

Ioannou G. Ανάπτυξη και εφαρμογή βιώσιμων συνθετικών τεχνολογιών του διεγερμένου οξυγόνου: φωτοξειδώσεις συνεχούς ροής σε εκνέφωμα. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2017. Available from: http://hdl.handle.net/10442/hedi/42217

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

17. Rodrigues, Tulio Eduardo. O modelo de cascata intranuclear MCMC e aplicações para o mecanismo do quase-dêuteron e a fotoprodução de pions em energias intermediárias e altas.

Degree: PhD, Física, 2005, University of São Paulo

O Presente trabalho propôs o estudo de reações fotonucleares e fotoprodução de pions em energias intermediárias e altas usando o modelo de cascata intranuclear MCMC… (more)

Subjects/Keywords: Cascade Model; Emissões de Pré-equilíbrio; Evaporação Nuclear; Fotoprodução de mesons; Meson Photoproduction; Modelo de Cascata; Modelo de Regge; Nuclear Evaporation; Photonuclear Reactions; Pre-equilibrium emissions; Quase-dêuteron; Quasi-Deuteron; Reações Fotonucleares; Regge Model

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APA (6th Edition):

Rodrigues, T. E. (2005). O modelo de cascata intranuclear MCMC e aplicações para o mecanismo do quase-dêuteron e a fotoprodução de pions em energias intermediárias e altas. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/43/43134/tde-27042009-114231/ ;

Chicago Manual of Style (16th Edition):

Rodrigues, Tulio Eduardo. “O modelo de cascata intranuclear MCMC e aplicações para o mecanismo do quase-dêuteron e a fotoprodução de pions em energias intermediárias e altas.” 2005. Doctoral Dissertation, University of São Paulo. Accessed October 23, 2019. http://www.teses.usp.br/teses/disponiveis/43/43134/tde-27042009-114231/ ;.

MLA Handbook (7th Edition):

Rodrigues, Tulio Eduardo. “O modelo de cascata intranuclear MCMC e aplicações para o mecanismo do quase-dêuteron e a fotoprodução de pions em energias intermediárias e altas.” 2005. Web. 23 Oct 2019.

Vancouver:

Rodrigues TE. O modelo de cascata intranuclear MCMC e aplicações para o mecanismo do quase-dêuteron e a fotoprodução de pions em energias intermediárias e altas. [Internet] [Doctoral dissertation]. University of São Paulo; 2005. [cited 2019 Oct 23]. Available from: http://www.teses.usp.br/teses/disponiveis/43/43134/tde-27042009-114231/ ;.

Council of Science Editors:

Rodrigues TE. O modelo de cascata intranuclear MCMC e aplicações para o mecanismo do quase-dêuteron e a fotoprodução de pions em energias intermediárias e altas. [Doctoral Dissertation]. University of São Paulo; 2005. Available from: http://www.teses.usp.br/teses/disponiveis/43/43134/tde-27042009-114231/ ;

18. Μαργαρός, Ιωάννης. Ολική σύνθεση των φυσικών προϊόντων zerumin B, chinensines A-E και premnalane A στη βάση βιομιμητικών φωτοχημικών μετασχηματισμών του μοριακού οξυγόνου.

Degree: 2008, University of Crete (UOC); Πανεπιστήμιο Κρήτης

Subjects/Keywords: Ολική σύνθεση; Φυσικά προϊόντα; Βιομιμητική σύνθεση; Οξυγόνο απλής κατάστασης; Φωτοοξείδωση φουρανίων; [4+2] κυκλοπροσθήκη; Τοποεκλεκτική σύνθεση; Pomino αντιδράσεις; Total synthesis; Natural products; Biomimetic synthesis; Singlet oxygen; Furons photooxygenation; [4+2] cycloaddition; Regioselective synthesis; Cascade reactions; Zerumin B; Chinensine A; Chinensine B; Chinensine C; Chinensine D; Chinensine E; Premnalene A

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APA (6th Edition):

Μαργαρός, . . (2008). Ολική σύνθεση των φυσικών προϊόντων zerumin B, chinensines A-E και premnalane A στη βάση βιομιμητικών φωτοχημικών μετασχηματισμών του μοριακού οξυγόνου. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/15746

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):

Μαργαρός, Ιωάννης. “Ολική σύνθεση των φυσικών προϊόντων zerumin B, chinensines A-E και premnalane A στη βάση βιομιμητικών φωτοχημικών μετασχηματισμών του μοριακού οξυγόνου.” 2008. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed October 23, 2019. http://hdl.handle.net/10442/hedi/15746.

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

MLA Handbook (7th Edition):

Μαργαρός, Ιωάννης. “Ολική σύνθεση των φυσικών προϊόντων zerumin B, chinensines A-E και premnalane A στη βάση βιομιμητικών φωτοχημικών μετασχηματισμών του μοριακού οξυγόνου.” 2008. Web. 23 Oct 2019.

Vancouver:

Μαργαρός . Ολική σύνθεση των φυσικών προϊόντων zerumin B, chinensines A-E και premnalane A στη βάση βιομιμητικών φωτοχημικών μετασχηματισμών του μοριακού οξυγόνου. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2008. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10442/hedi/15746.

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

Council of Science Editors:

Μαργαρός . Ολική σύνθεση των φυσικών προϊόντων zerumin B, chinensines A-E και premnalane A στη βάση βιομιμητικών φωτοχημικών μετασχηματισμών του μοριακού οξυγόνου. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2008. Available from: http://hdl.handle.net/10442/hedi/15746

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

.