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You searched for subject:(547 2). Showing records 1 – 26 of 26 total matches.

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University of Edinburgh

1. Pecharman, Anne-Frederique. Reductive functionalisation of the uranyl dication.

Degree: PhD, 2013, University of Edinburgh

 This thesis describes the synthesis and reactivity studies of the actinyl dications [AnO2]2+ in a variety of oxidation states. Chapter one introduces the importance of… (more)

Subjects/Keywords: 547; actinyl dications [AnO2]2+; oxidation

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APA (6th Edition):

Pecharman, A. (2013). Reductive functionalisation of the uranyl dication. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9472

Chicago Manual of Style (16th Edition):

Pecharman, Anne-Frederique. “Reductive functionalisation of the uranyl dication.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed October 31, 2020. http://hdl.handle.net/1842/9472.

MLA Handbook (7th Edition):

Pecharman, Anne-Frederique. “Reductive functionalisation of the uranyl dication.” 2013. Web. 31 Oct 2020.

Vancouver:

Pecharman A. Reductive functionalisation of the uranyl dication. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1842/9472.

Council of Science Editors:

Pecharman A. Reductive functionalisation of the uranyl dication. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/9472

2. Guelen, Simon. Approche des squelettes ladderanes par photocycloaddition [2+2] multiples : Ladderane skeleton approach by multiple [2+2] photocycloaddition.

Degree: Docteur es, Chimie Organique, 2016, Université Pierre et Marie Curie – Paris VI

Ces travaux de thèse ont pour but de synthétiser des squelettes ladderanes en une seule étape de photocycloaddition [2+2] multiple. Le produit naturel acide pentacycloanammoxique… (more)

Subjects/Keywords: Photocycloaddition [2+2]; Ladderanes; Acide pentacycloanammoxique; Photoredox; Encapsulation supramoléculaire; Cycloisomérisation; [2+2] photocycloaddition; Ladderanes; Supramolecular encapsulation; 547

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APA (6th Edition):

Guelen, S. (2016). Approche des squelettes ladderanes par photocycloaddition [2+2] multiples : Ladderane skeleton approach by multiple [2+2] photocycloaddition. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066269

Chicago Manual of Style (16th Edition):

Guelen, Simon. “Approche des squelettes ladderanes par photocycloaddition [2+2] multiples : Ladderane skeleton approach by multiple [2+2] photocycloaddition.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 31, 2020. http://www.theses.fr/2016PA066269.

MLA Handbook (7th Edition):

Guelen, Simon. “Approche des squelettes ladderanes par photocycloaddition [2+2] multiples : Ladderane skeleton approach by multiple [2+2] photocycloaddition.” 2016. Web. 31 Oct 2020.

Vancouver:

Guelen S. Approche des squelettes ladderanes par photocycloaddition [2+2] multiples : Ladderane skeleton approach by multiple [2+2] photocycloaddition. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2016PA066269.

Council of Science Editors:

Guelen S. Approche des squelettes ladderanes par photocycloaddition [2+2] multiples : Ladderane skeleton approach by multiple [2+2] photocycloaddition. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066269

3. Ye, Fei. Ru- and Rh-catalyzed [2+2+2] cycloadditions : an access to fluorenone, 2-aminopyridine, and 1,3-dihydroisobenzofuran derivatives : Réactions de cycloadditions [2+2+2] catalysées par des complexes de ruthénium et de rhodium : une voie d’accès aux fluorénones, 2-aminopyridines et dihydroisobenzofuranes fonctionnalisés.

Degree: Docteur es, Chimie organique, 2017, Université Pierre et Marie Curie – Paris VI

Ce manuscrit traite de la mise au point d’une méthode d’accès éco-compatible à des squelettes carbocycliques et hétérocycliques, présents dans de nombreux composés d’intérêt biologique.… (more)

Subjects/Keywords: Réactions sans solvant; Ruthénium; Rhodium; Cycloadditions [2+2+2]; Fluorénones; 2-Aminopyridines; 1,3-Dihydroisobenzofuranes; Solvent-free reactions; Ruthenium; Rhodium; 547

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APA (6th Edition):

Ye, F. (2017). Ru- and Rh-catalyzed [2+2+2] cycloadditions : an access to fluorenone, 2-aminopyridine, and 1,3-dihydroisobenzofuran derivatives : Réactions de cycloadditions [2+2+2] catalysées par des complexes de ruthénium et de rhodium : une voie d’accès aux fluorénones, 2-aminopyridines et dihydroisobenzofuranes fonctionnalisés. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066347

Chicago Manual of Style (16th Edition):

Ye, Fei. “Ru- and Rh-catalyzed [2+2+2] cycloadditions : an access to fluorenone, 2-aminopyridine, and 1,3-dihydroisobenzofuran derivatives : Réactions de cycloadditions [2+2+2] catalysées par des complexes de ruthénium et de rhodium : une voie d’accès aux fluorénones, 2-aminopyridines et dihydroisobenzofuranes fonctionnalisés.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 31, 2020. http://www.theses.fr/2017PA066347.

MLA Handbook (7th Edition):

Ye, Fei. “Ru- and Rh-catalyzed [2+2+2] cycloadditions : an access to fluorenone, 2-aminopyridine, and 1,3-dihydroisobenzofuran derivatives : Réactions de cycloadditions [2+2+2] catalysées par des complexes de ruthénium et de rhodium : une voie d’accès aux fluorénones, 2-aminopyridines et dihydroisobenzofuranes fonctionnalisés.” 2017. Web. 31 Oct 2020.

Vancouver:

Ye F. Ru- and Rh-catalyzed [2+2+2] cycloadditions : an access to fluorenone, 2-aminopyridine, and 1,3-dihydroisobenzofuran derivatives : Réactions de cycloadditions [2+2+2] catalysées par des complexes de ruthénium et de rhodium : une voie d’accès aux fluorénones, 2-aminopyridines et dihydroisobenzofuranes fonctionnalisés. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2017PA066347.

Council of Science Editors:

Ye F. Ru- and Rh-catalyzed [2+2+2] cycloadditions : an access to fluorenone, 2-aminopyridine, and 1,3-dihydroisobenzofuran derivatives : Réactions de cycloadditions [2+2+2] catalysées par des complexes de ruthénium et de rhodium : une voie d’accès aux fluorénones, 2-aminopyridines et dihydroisobenzofuranes fonctionnalisés. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066347

4. Li, Quan. Integrated motions of light driven molecular motors at macroscopic scale : Mouvements macroscopiques intégrés de moteurs moléculaires activés par la lumière.

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

Dans la nature, des moteurs moléculaires tells que l'ATP synthase ou la kinésine peuvent consommer de l'énergie pour générer du mouvement et ainsi assurer des… (more)

Subjects/Keywords: Moteurs moléculaires; Gels; Molecular motor; Integrated motion; Smart gel; 547..2

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APA (6th Edition):

Li, Q. (2015). Integrated motions of light driven molecular motors at macroscopic scale : Mouvements macroscopiques intégrés de moteurs moléculaires activés par la lumière. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2015STRAF001

Chicago Manual of Style (16th Edition):

Li, Quan. “Integrated motions of light driven molecular motors at macroscopic scale : Mouvements macroscopiques intégrés de moteurs moléculaires activés par la lumière.” 2015. Doctoral Dissertation, Université de Strasbourg. Accessed October 31, 2020. http://www.theses.fr/2015STRAF001.

MLA Handbook (7th Edition):

Li, Quan. “Integrated motions of light driven molecular motors at macroscopic scale : Mouvements macroscopiques intégrés de moteurs moléculaires activés par la lumière.” 2015. Web. 31 Oct 2020.

Vancouver:

Li Q. Integrated motions of light driven molecular motors at macroscopic scale : Mouvements macroscopiques intégrés de moteurs moléculaires activés par la lumière. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2015. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2015STRAF001.

Council of Science Editors:

Li Q. Integrated motions of light driven molecular motors at macroscopic scale : Mouvements macroscopiques intégrés de moteurs moléculaires activés par la lumière. [Doctoral Dissertation]. Université de Strasbourg; 2015. Available from: http://www.theses.fr/2015STRAF001


University of Edinburgh

5. Kujawa, Szymon. Rapid generation of molecular complexity under Pd(II) and Rh(III) catalysis.

Degree: PhD, 2015, University of Edinburgh

 1. Enantioselective Pd(II)-Catalysed Nucleophilic Additions of 2- Alkylazaarenes The first project deals with enantio- and diastereoselective palladium(II)-catalysed nucleophilic additions of 2-alkylazaarenes to N-Boc imines and… (more)

Subjects/Keywords: 547; enantioselective synthesis; 2-(ß-aminoalkyl)azaarenes; spirocyclic enones; synthesis

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APA (6th Edition):

Kujawa, S. (2015). Rapid generation of molecular complexity under Pd(II) and Rh(III) catalysis. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/11697

Chicago Manual of Style (16th Edition):

Kujawa, Szymon. “Rapid generation of molecular complexity under Pd(II) and Rh(III) catalysis.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed October 31, 2020. http://hdl.handle.net/1842/11697.

MLA Handbook (7th Edition):

Kujawa, Szymon. “Rapid generation of molecular complexity under Pd(II) and Rh(III) catalysis.” 2015. Web. 31 Oct 2020.

Vancouver:

Kujawa S. Rapid generation of molecular complexity under Pd(II) and Rh(III) catalysis. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1842/11697.

Council of Science Editors:

Kujawa S. Rapid generation of molecular complexity under Pd(II) and Rh(III) catalysis. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/11697


Freie Universität Berlin

6. Faghani, Abbas. Synthese und kontrollierte zerstörungsfreie kovalente Funktionalisierung von niedrigdimensionalen Kohlenstoff-Nanomaterialien.

Degree: 2020, Freie Universität Berlin

 Carbon materials have shown a great potential in the academic field and have been employed for plenty of applications. Graphene, a natural two dimensional polymer,… (more)

Subjects/Keywords: Triazine; 2 D synthesis; carbon based nanomaterials; ddc:547

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APA (6th Edition):

Faghani, A. (2020). Synthese und kontrollierte zerstörungsfreie kovalente Funktionalisierung von niedrigdimensionalen Kohlenstoff-Nanomaterialien. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-26965

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):

Faghani, Abbas. “Synthese und kontrollierte zerstörungsfreie kovalente Funktionalisierung von niedrigdimensionalen Kohlenstoff-Nanomaterialien.” 2020. Thesis, Freie Universität Berlin. Accessed October 31, 2020. http://dx.doi.org/10.17169/refubium-26965.

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

MLA Handbook (7th Edition):

Faghani, Abbas. “Synthese und kontrollierte zerstörungsfreie kovalente Funktionalisierung von niedrigdimensionalen Kohlenstoff-Nanomaterialien.” 2020. Web. 31 Oct 2020.

Vancouver:

Faghani A. Synthese und kontrollierte zerstörungsfreie kovalente Funktionalisierung von niedrigdimensionalen Kohlenstoff-Nanomaterialien. [Internet] [Thesis]. Freie Universität Berlin; 2020. [cited 2020 Oct 31]. Available from: http://dx.doi.org/10.17169/refubium-26965.

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

Council of Science Editors:

Faghani A. Synthese und kontrollierte zerstörungsfreie kovalente Funktionalisierung von niedrigdimensionalen Kohlenstoff-Nanomaterialien. [Thesis]. Freie Universität Berlin; 2020. Available from: http://dx.doi.org/10.17169/refubium-26965

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

7. Medena, Caleb. Synthèses d’hélicènes énantioenrichis et application en catalyse asymétrique : Synthesis of enantioenriched helicenes and application in asymmetric catalysis.

Degree: Docteur es, Chimie organique, 2017, Université Pierre et Marie Curie – Paris VI

De nouveaux phosphinites énantiopurs à la structure hélicoïdale ont été synthétisés et utilisés en catalyse asymétrique. Les plateformes 2,15-dihydroxyhélicènes ciblées pour l’étude ont été synthétisées… (more)

Subjects/Keywords: Hélicènes; Chiralité; Photocyclisation; Cycloaddition [2+2+2]; Phosphinites; Catalyse asymétrique homogène; Ligand; Or; Palladium; Helicenes; Chirality; Biophospinites; 547

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APA (6th Edition):

Medena, C. (2017). Synthèses d’hélicènes énantioenrichis et application en catalyse asymétrique : Synthesis of enantioenriched helicenes and application in asymmetric catalysis. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066430

Chicago Manual of Style (16th Edition):

Medena, Caleb. “Synthèses d’hélicènes énantioenrichis et application en catalyse asymétrique : Synthesis of enantioenriched helicenes and application in asymmetric catalysis.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 31, 2020. http://www.theses.fr/2017PA066430.

MLA Handbook (7th Edition):

Medena, Caleb. “Synthèses d’hélicènes énantioenrichis et application en catalyse asymétrique : Synthesis of enantioenriched helicenes and application in asymmetric catalysis.” 2017. Web. 31 Oct 2020.

Vancouver:

Medena C. Synthèses d’hélicènes énantioenrichis et application en catalyse asymétrique : Synthesis of enantioenriched helicenes and application in asymmetric catalysis. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2017PA066430.

Council of Science Editors:

Medena C. Synthèses d’hélicènes énantioenrichis et application en catalyse asymétrique : Synthesis of enantioenriched helicenes and application in asymmetric catalysis. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066430


Universitat de Barcelona

8. León Serrano, Thierry. Síntesi estereoselectiva de fosfines amb quiralitat al fòsfor. Aplicacions en catàlisis.

Degree: Departament de Química Orgànica, 2012, Universitat de Barcelona

 The synthesis of efficient and easily affordable chiral ligands are one of the main goals in catalysis. Bulky stereogenic phosphine have demonstrated to be excellent… (more)

Subjects/Keywords: Oxazofosfolidinas; Fosforo esterogénico; Pauson-Khand; Aminofosfinas quirales; Ligandos fosfinosulfonamida; Cicloadición [2+2+2] intramolecular; Ligandos ThaxPHOS; Ciències Experimentals i Matemàtiques; 547

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APA (6th Edition):

León Serrano, T. (2012). Síntesi estereoselectiva de fosfines amb quiralitat al fòsfor. Aplicacions en catàlisis. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/53534

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):

León Serrano, Thierry. “Síntesi estereoselectiva de fosfines amb quiralitat al fòsfor. Aplicacions en catàlisis.” 2012. Thesis, Universitat de Barcelona. Accessed October 31, 2020. http://hdl.handle.net/10803/53534.

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

MLA Handbook (7th Edition):

León Serrano, Thierry. “Síntesi estereoselectiva de fosfines amb quiralitat al fòsfor. Aplicacions en catàlisis.” 2012. Web. 31 Oct 2020.

Vancouver:

León Serrano T. Síntesi estereoselectiva de fosfines amb quiralitat al fòsfor. Aplicacions en catàlisis. [Internet] [Thesis]. Universitat de Barcelona; 2012. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10803/53534.

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

Council of Science Editors:

León Serrano T. Síntesi estereoselectiva de fosfines amb quiralitat al fòsfor. Aplicacions en catàlisis. [Thesis]. Universitat de Barcelona; 2012. Available from: http://hdl.handle.net/10803/53534

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


Universitat Autònoma de Barcelona

9. Alibés Arqués, Ramon. Síntesi total de (+)-i(-)-grandisol. Fotocicloaddició (2+2) diastereoselectiva de 2(5H)-furanones a alquens.

Degree: Departament de Química, 1993, Universitat Autònoma de Barcelona

Pendent Advisors/Committee Members: [email protected] (authoremail), false (authoremailshow), Font i Cierco, Josep (director), Bourdelande, J. L. (José Luis) (director), true (authorsendemail).

Subjects/Keywords: (+)-grandisol; Compostos ciclobutànics; (2+2)-fotocicloaddicions; Ciències Experimentals; 547

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APA (6th Edition):

Alibés Arqués, R. (1993). Síntesi total de (+)-i(-)-grandisol. Fotocicloaddició (2+2) diastereoselectiva de 2(5H)-furanones a alquens. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/32150

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):

Alibés Arqués, Ramon. “Síntesi total de (+)-i(-)-grandisol. Fotocicloaddició (2+2) diastereoselectiva de 2(5H)-furanones a alquens.” 1993. Thesis, Universitat Autònoma de Barcelona. Accessed October 31, 2020. http://hdl.handle.net/10803/32150.

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

MLA Handbook (7th Edition):

Alibés Arqués, Ramon. “Síntesi total de (+)-i(-)-grandisol. Fotocicloaddició (2+2) diastereoselectiva de 2(5H)-furanones a alquens.” 1993. Web. 31 Oct 2020.

Vancouver:

Alibés Arqués R. Síntesi total de (+)-i(-)-grandisol. Fotocicloaddició (2+2) diastereoselectiva de 2(5H)-furanones a alquens. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 1993. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10803/32150.

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

Council of Science Editors:

Alibés Arqués R. Síntesi total de (+)-i(-)-grandisol. Fotocicloaddició (2+2) diastereoselectiva de 2(5H)-furanones a alquens. [Thesis]. Universitat Autònoma de Barcelona; 1993. Available from: http://hdl.handle.net/10803/32150

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

10. Rioton, Sarah. Agrandissement de cycle : synthèse de pipéridines et d'azépanes α-trifluorométhylés : Ring expansion : synthesis of α-trifluoromethyl piperidines and azepanes.

Degree: Docteur es, Chimie Organique, 2017, Université Pierre et Marie Curie – Paris VI

L'introduction d'atomes de fluor sur des composés organiques peut avoir une forte influence sur les propriétés physico-chimiques, ainsi que sur l'activité biologique de ces composés.… (more)

Subjects/Keywords: 2-(trifluorométhyl)pipéridines; 2-(trifluorométhyl)azépanes; Agrandissement de cycle; Aziridinium; Azétidinium; Trifluorométhyle; Trifluoromethyl; Aziridinium; Azetidinium; 547

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APA (6th Edition):

Rioton, S. (2017). Agrandissement de cycle : synthèse de pipéridines et d'azépanes α-trifluorométhylés : Ring expansion : synthesis of α-trifluoromethyl piperidines and azepanes. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066173

Chicago Manual of Style (16th Edition):

Rioton, Sarah. “Agrandissement de cycle : synthèse de pipéridines et d'azépanes α-trifluorométhylés : Ring expansion : synthesis of α-trifluoromethyl piperidines and azepanes.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 31, 2020. http://www.theses.fr/2017PA066173.

MLA Handbook (7th Edition):

Rioton, Sarah. “Agrandissement de cycle : synthèse de pipéridines et d'azépanes α-trifluorométhylés : Ring expansion : synthesis of α-trifluoromethyl piperidines and azepanes.” 2017. Web. 31 Oct 2020.

Vancouver:

Rioton S. Agrandissement de cycle : synthèse de pipéridines et d'azépanes α-trifluorométhylés : Ring expansion : synthesis of α-trifluoromethyl piperidines and azepanes. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2017PA066173.

Council of Science Editors:

Rioton S. Agrandissement de cycle : synthèse de pipéridines et d'azépanes α-trifluorométhylés : Ring expansion : synthesis of α-trifluoromethyl piperidines and azepanes. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066173


Loughborough University

11. Fernandez, Beatriz. New functionalisation chemistry of 2- and 4-pyridones and related heterocycles.

Degree: PhD, 2016, Loughborough University

 New methodology for the synthesis of several 4H-pyrido[1,2-a]pyrimidin-4-ones has been developed from commercially available 2-aminopyridines and β-oxo esters catalysed by Montmorillonite under solvent-free conditions in… (more)

Subjects/Keywords: 547; Pyridone; Quinolizinone; 4H-pyrido[1]; 2-[a]pyrimidin-4-ones; 4H-pyrimido[1]; 2-[a]pyrimidin-4-one

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APA (6th Edition):

Fernandez, B. (2016). New functionalisation chemistry of 2- and 4-pyridones and related heterocycles. (Doctoral Dissertation). Loughborough University. Retrieved from http://hdl.handle.net/2134/21685

Chicago Manual of Style (16th Edition):

Fernandez, Beatriz. “New functionalisation chemistry of 2- and 4-pyridones and related heterocycles.” 2016. Doctoral Dissertation, Loughborough University. Accessed October 31, 2020. http://hdl.handle.net/2134/21685.

MLA Handbook (7th Edition):

Fernandez, Beatriz. “New functionalisation chemistry of 2- and 4-pyridones and related heterocycles.” 2016. Web. 31 Oct 2020.

Vancouver:

Fernandez B. New functionalisation chemistry of 2- and 4-pyridones and related heterocycles. [Internet] [Doctoral dissertation]. Loughborough University; 2016. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/2134/21685.

Council of Science Editors:

Fernandez B. New functionalisation chemistry of 2- and 4-pyridones and related heterocycles. [Doctoral Dissertation]. Loughborough University; 2016. Available from: http://hdl.handle.net/2134/21685

12. Rkein, Batoul. Désaromatisation d'arènes électro-appauvris par des réactions de cycloadition (4+2) : Dearomatization of electron-poor arenes by (4+2) cycloaddition reactions.

Degree: Docteur es, Chimie, 2019, Normandie

Les composés aromatiques sont largement accessibles, que ce soit à partir de la pétrochimie, ou de molécules naturelles. Ainsi, des efforts importants ont été faits… (more)

Subjects/Keywords: Désaromatisation; Réactions de cycloaddition (4 + 2); Silyloxydiènes; Enolate de lithium; Dearomatization; (4 + 2) cycloaddition; Silyloxydiènes; Lithium enolate; 547

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APA (6th Edition):

Rkein, B. (2019). Désaromatisation d'arènes électro-appauvris par des réactions de cycloadition (4+2) : Dearomatization of electron-poor arenes by (4+2) cycloaddition reactions. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2019NORMR092

Chicago Manual of Style (16th Edition):

Rkein, Batoul. “Désaromatisation d'arènes électro-appauvris par des réactions de cycloadition (4+2) : Dearomatization of electron-poor arenes by (4+2) cycloaddition reactions.” 2019. Doctoral Dissertation, Normandie. Accessed October 31, 2020. http://www.theses.fr/2019NORMR092.

MLA Handbook (7th Edition):

Rkein, Batoul. “Désaromatisation d'arènes électro-appauvris par des réactions de cycloadition (4+2) : Dearomatization of electron-poor arenes by (4+2) cycloaddition reactions.” 2019. Web. 31 Oct 2020.

Vancouver:

Rkein B. Désaromatisation d'arènes électro-appauvris par des réactions de cycloadition (4+2) : Dearomatization of electron-poor arenes by (4+2) cycloaddition reactions. [Internet] [Doctoral dissertation]. Normandie; 2019. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2019NORMR092.

Council of Science Editors:

Rkein B. Désaromatisation d'arènes électro-appauvris par des réactions de cycloadition (4+2) : Dearomatization of electron-poor arenes by (4+2) cycloaddition reactions. [Doctoral Dissertation]. Normandie; 2019. Available from: http://www.theses.fr/2019NORMR092

13. Laugeois, Maxime. Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis.

Degree: Docteur es, Chimie organique, 2017, Université Pierre et Marie Curie – Paris VI

Ce manuscrit présente le développement de nouvelles réactions de cycloaddition [3+2] palladocatalysées entre des vinylcyclopropanes électro-appauvris et diverses espèces dipolarophiles. La première partie de ces… (more)

Subjects/Keywords: Cycloaddition [3+2]; Palladium; Vinylcyclopropanes; Désaromatisation; Métallo-organocatalyse; Catalyse asymétrique; Palladium; Asymmetric catalysis; Vinylcyclopropanes; 547

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

APA (6th Edition):

Laugeois, M. (2017). Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066353

Chicago Manual of Style (16th Edition):

Laugeois, Maxime. “Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 31, 2020. http://www.theses.fr/2017PA066353.

MLA Handbook (7th Edition):

Laugeois, Maxime. “Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis.” 2017. Web. 31 Oct 2020.

Vancouver:

Laugeois M. Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2017PA066353.

Council of Science Editors:

Laugeois M. Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066353


Universitat Rovira i Virgili

14. Rodríguez Gómez, Miguel Angel. Stereoselective Synthesis of 2-Deoxy-glycosides. Approach to the Synthesis of Digitoxine.

Degree: Departament de Química Analítica i Química Orgànica, 2007, Universitat Rovira i Virgili

 Informe Preceptiu sobre la Tesi doctoral "Estereoselective Synthesis of 2 Deoxyglycosides. Approach to the síntesis of Digitoxine" presentada per Miguel Àngel Rodríguez Gómez. La tesi… (more)

Subjects/Keywords: 2-Desoxiglicosidos; Sintesis Esteroselectiva; Digitoxina; 547; 6

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APA (6th Edition):

Rodríguez Gómez, M. A. (2007). Stereoselective Synthesis of 2-Deoxy-glycosides. Approach to the Synthesis of Digitoxine. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/9010

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):

Rodríguez Gómez, Miguel Angel. “Stereoselective Synthesis of 2-Deoxy-glycosides. Approach to the Synthesis of Digitoxine.” 2007. Thesis, Universitat Rovira i Virgili. Accessed October 31, 2020. http://hdl.handle.net/10803/9010.

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

MLA Handbook (7th Edition):

Rodríguez Gómez, Miguel Angel. “Stereoselective Synthesis of 2-Deoxy-glycosides. Approach to the Synthesis of Digitoxine.” 2007. Web. 31 Oct 2020.

Vancouver:

Rodríguez Gómez MA. Stereoselective Synthesis of 2-Deoxy-glycosides. Approach to the Synthesis of Digitoxine. [Internet] [Thesis]. Universitat Rovira i Virgili; 2007. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10803/9010.

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

Council of Science Editors:

Rodríguez Gómez MA. Stereoselective Synthesis of 2-Deoxy-glycosides. Approach to the Synthesis of Digitoxine. [Thesis]. Universitat Rovira i Virgili; 2007. Available from: http://hdl.handle.net/10803/9010

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


Universitat Rovira i Virgili

15. Boutureira Martin, Omar. Stereoselective synthesis of 2-deoxoligosaccharides.

Degree: Departament de Química Analítica i Química Orgànica, 2007, Universitat Rovira i Virgili

 Stereoselective Synthesis of 2-Deoxyoliogosaccharides Autor: Omar Boutureira Martín The research described in this thesis aims to investigate a new method for the stereoselective synthesis of… (more)

Subjects/Keywords: 2-desoxi-oligosacarias; ciclacions; 2-desoxi-glicosias; síntesi estereoselectiva; 54; 542; 547

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

APA (6th Edition):

Boutureira Martin, O. (2007). Stereoselective synthesis of 2-deoxoligosaccharides. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/9017

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):

Boutureira Martin, Omar. “Stereoselective synthesis of 2-deoxoligosaccharides.” 2007. Thesis, Universitat Rovira i Virgili. Accessed October 31, 2020. http://hdl.handle.net/10803/9017.

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

MLA Handbook (7th Edition):

Boutureira Martin, Omar. “Stereoselective synthesis of 2-deoxoligosaccharides.” 2007. Web. 31 Oct 2020.

Vancouver:

Boutureira Martin O. Stereoselective synthesis of 2-deoxoligosaccharides. [Internet] [Thesis]. Universitat Rovira i Virgili; 2007. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10803/9017.

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

Council of Science Editors:

Boutureira Martin O. Stereoselective synthesis of 2-deoxoligosaccharides. [Thesis]. Universitat Rovira i Virgili; 2007. Available from: http://hdl.handle.net/10803/9017

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


Universitat Rovira i Virgili

16. Ojeda Montes, María José. Computational approaches for the characterization of the Dipeptidyl Peptidase IV inhibition: Applications to drug discovery, drug design and binding site similarity.

Degree: Departament de Bioquímica i Biotecnologia, 2017, Universitat Rovira i Virgili

 The inhibition of dipeptidyl peptidase-IV (DPP-IV) enzyme has emerged over the last decade as one of the most effective treatments for type II diabetes mellitus… (more)

Subjects/Keywords: Dipeptidil peptidasa IV; Cribratge virtual; Receptor adrenèrgic beta 2; cribado virtual; Receptor adrenérgico beta 2; Dipeptidyl peptidase IV; Virtual screening; beta 2 adrenergic receptor; Ciències de la salut; 004; 547; 577; 663/664

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APA (6th Edition):

Ojeda Montes, M. J. (2017). Computational approaches for the characterization of the Dipeptidyl Peptidase IV inhibition: Applications to drug discovery, drug design and binding site similarity. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/456381

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):

Ojeda Montes, María José. “Computational approaches for the characterization of the Dipeptidyl Peptidase IV inhibition: Applications to drug discovery, drug design and binding site similarity.” 2017. Thesis, Universitat Rovira i Virgili. Accessed October 31, 2020. http://hdl.handle.net/10803/456381.

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

MLA Handbook (7th Edition):

Ojeda Montes, María José. “Computational approaches for the characterization of the Dipeptidyl Peptidase IV inhibition: Applications to drug discovery, drug design and binding site similarity.” 2017. Web. 31 Oct 2020.

Vancouver:

Ojeda Montes MJ. Computational approaches for the characterization of the Dipeptidyl Peptidase IV inhibition: Applications to drug discovery, drug design and binding site similarity. [Internet] [Thesis]. Universitat Rovira i Virgili; 2017. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10803/456381.

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

Council of Science Editors:

Ojeda Montes MJ. Computational approaches for the characterization of the Dipeptidyl Peptidase IV inhibition: Applications to drug discovery, drug design and binding site similarity. [Thesis]. Universitat Rovira i Virgili; 2017. Available from: http://hdl.handle.net/10803/456381

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

17. Ella Obame, Idriss. Réactivité des glyconitriles vis-à-vis d’organométalliques : accès à des céto-C-glycosides précurseurs de C-glycoconjugés : Reactivity of glyconitriles towards organométallics : acces to C-glycosides precursors of C-glycoconjugates.

Degree: Docteur es, Chimie fine. Chimie organique, 2016, Le Mans

Les glycoconjugués constituent une classe de molécules organiques importante car ils sont impliqués dans de nombreux processus biologiques à savoir l'inflammation, la transmission du signal,… (more)

Subjects/Keywords: C-glycoconjugués; Glyconitriles; Céto-C-glycosides; Organométalliques; Analogues C-glycoconjugués; SGLT-2; Glycogène phosphorylase; C-glycoconjuguated; Keto-C-glycosides; Organometallics; C-glycosidic analogues; Glycogen phosphorylase; 547

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APA (6th Edition):

Ella Obame, I. (2016). Réactivité des glyconitriles vis-à-vis d’organométalliques : accès à des céto-C-glycosides précurseurs de C-glycoconjugés : Reactivity of glyconitriles towards organométallics : acces to C-glycosides precursors of C-glycoconjugates. (Doctoral Dissertation). Le Mans. Retrieved from http://www.theses.fr/2016LEMA1042

Chicago Manual of Style (16th Edition):

Ella Obame, Idriss. “Réactivité des glyconitriles vis-à-vis d’organométalliques : accès à des céto-C-glycosides précurseurs de C-glycoconjugés : Reactivity of glyconitriles towards organométallics : acces to C-glycosides precursors of C-glycoconjugates.” 2016. Doctoral Dissertation, Le Mans. Accessed October 31, 2020. http://www.theses.fr/2016LEMA1042.

MLA Handbook (7th Edition):

Ella Obame, Idriss. “Réactivité des glyconitriles vis-à-vis d’organométalliques : accès à des céto-C-glycosides précurseurs de C-glycoconjugés : Reactivity of glyconitriles towards organométallics : acces to C-glycosides precursors of C-glycoconjugates.” 2016. Web. 31 Oct 2020.

Vancouver:

Ella Obame I. Réactivité des glyconitriles vis-à-vis d’organométalliques : accès à des céto-C-glycosides précurseurs de C-glycoconjugés : Reactivity of glyconitriles towards organométallics : acces to C-glycosides precursors of C-glycoconjugates. [Internet] [Doctoral dissertation]. Le Mans; 2016. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2016LEMA1042.

Council of Science Editors:

Ella Obame I. Réactivité des glyconitriles vis-à-vis d’organométalliques : accès à des céto-C-glycosides précurseurs de C-glycoconjugés : Reactivity of glyconitriles towards organométallics : acces to C-glycosides precursors of C-glycoconjugates. [Doctoral Dissertation]. Le Mans; 2016. Available from: http://www.theses.fr/2016LEMA1042


Brunel University

18. Yeadon, Alan. A study of the polymorphism of 4-methyl-2-nitroacetanilide and related compounds.

Degree: PhD, 1985, Brunel University

 The full crystal structures of three polymorphs of 4-methyl-2-nitroacetanilide (MNA) are described. The white form (MNA-l), is the most stable form. The least stable form… (more)

Subjects/Keywords: 547; Polymorphism : 4-methyl-2-nitroacetanilide : Topotactic phase change : MNA polymorphs

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APA (6th Edition):

Yeadon, A. (1985). A study of the polymorphism of 4-methyl-2-nitroacetanilide and related compounds. (Doctoral Dissertation). Brunel University. Retrieved from http://bura.brunel.ac.uk/handle/2438/7880 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.353748

Chicago Manual of Style (16th Edition):

Yeadon, Alan. “A study of the polymorphism of 4-methyl-2-nitroacetanilide and related compounds.” 1985. Doctoral Dissertation, Brunel University. Accessed October 31, 2020. http://bura.brunel.ac.uk/handle/2438/7880 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.353748.

MLA Handbook (7th Edition):

Yeadon, Alan. “A study of the polymorphism of 4-methyl-2-nitroacetanilide and related compounds.” 1985. Web. 31 Oct 2020.

Vancouver:

Yeadon A. A study of the polymorphism of 4-methyl-2-nitroacetanilide and related compounds. [Internet] [Doctoral dissertation]. Brunel University; 1985. [cited 2020 Oct 31]. Available from: http://bura.brunel.ac.uk/handle/2438/7880 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.353748.

Council of Science Editors:

Yeadon A. A study of the polymorphism of 4-methyl-2-nitroacetanilide and related compounds. [Doctoral Dissertation]. Brunel University; 1985. Available from: http://bura.brunel.ac.uk/handle/2438/7880 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.353748

19. Toulot, Stephanie. Utilisation de complexes de titane pour la formation de dérivés azotés : synthèses d'homoallylamines et d'amidines : Titanium complexes for the formation of nitrogen compounds : synthesis of homoallylamines and amidines.

Degree: Docteur es, Chimie, 2011, Université de Bourgogne

Les amines homoallyliques sont des synthons clés pour la construction de nombreuses molécules d’intérêt biologique. Du fait de la double liaison carbone-carbone du fragment allylique,… (more)

Subjects/Keywords: Amines homoallyliques; Homoallylamines; Titane; Allyltitanation; Réarrangement cationique 2-Aza-Cope; Homocrotylamines; Dérivés benzotriazole; Dérivés bis(benzotriazole); Homoallyl-(E)-homocrotylamines; Dioxocyclames; Diamidines macrocyliques; Homoallylic amines; Homoallylamines; Titanium; Allyltitanation; Cationic 2-Aza- Cope rearrangement; Homocrotylamines; Benzotriazole derivatives; Bis(benzotriazole) derivatives; Homoallyl-(E)-homocrotylamines; Dioxocyclams; Macrocyclic diamidines; 541.39; 547

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APA (6th Edition):

Toulot, S. (2011). Utilisation de complexes de titane pour la formation de dérivés azotés : synthèses d'homoallylamines et d'amidines : Titanium complexes for the formation of nitrogen compounds : synthesis of homoallylamines and amidines. (Doctoral Dissertation). Université de Bourgogne. Retrieved from http://www.theses.fr/2011DIJOS026

Chicago Manual of Style (16th Edition):

Toulot, Stephanie. “Utilisation de complexes de titane pour la formation de dérivés azotés : synthèses d'homoallylamines et d'amidines : Titanium complexes for the formation of nitrogen compounds : synthesis of homoallylamines and amidines.” 2011. Doctoral Dissertation, Université de Bourgogne. Accessed October 31, 2020. http://www.theses.fr/2011DIJOS026.

MLA Handbook (7th Edition):

Toulot, Stephanie. “Utilisation de complexes de titane pour la formation de dérivés azotés : synthèses d'homoallylamines et d'amidines : Titanium complexes for the formation of nitrogen compounds : synthesis of homoallylamines and amidines.” 2011. Web. 31 Oct 2020.

Vancouver:

Toulot S. Utilisation de complexes de titane pour la formation de dérivés azotés : synthèses d'homoallylamines et d'amidines : Titanium complexes for the formation of nitrogen compounds : synthesis of homoallylamines and amidines. [Internet] [Doctoral dissertation]. Université de Bourgogne; 2011. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2011DIJOS026.

Council of Science Editors:

Toulot S. Utilisation de complexes de titane pour la formation de dérivés azotés : synthèses d'homoallylamines et d'amidines : Titanium complexes for the formation of nitrogen compounds : synthesis of homoallylamines and amidines. [Doctoral Dissertation]. Université de Bourgogne; 2011. Available from: http://www.theses.fr/2011DIJOS026

20. D'Attoma, Joseph. Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.

Degree: Docteur es, Chimie, 2013, Université Claude Bernard – Lyon I

Les lymphomes à grandes cellules anaplasiques ou ALCL (Anaplastic Large-Cell Lymphoma) sont des cancers appartenant à la famille des lymphomes de type non-Hodgkin. La majorité… (more)

Subjects/Keywords: 2-acylaminothiazoles; Restriction calorique; ALCL; NPM-ALK; Réaction de Suzuki- Miyaura; Réaction de Buchwald-Hartwig; Réaction de Sonogashira; 2-acylaminothiazols; Caloric restriction; ALCL; NPM-ALK; Suzuki-Miyaura crosscoupling reaction; Buchwald-Hartwig cross-coupling reaction; Sonogashira cross-coupling reaction; 547

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APA (6th Edition):

D'Attoma, J. (2013). Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2013LYO10243

Chicago Manual of Style (16th Edition):

D'Attoma, Joseph. “Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.” 2013. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed October 31, 2020. http://www.theses.fr/2013LYO10243.

MLA Handbook (7th Edition):

D'Attoma, Joseph. “Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.” 2013. Web. 31 Oct 2020.

Vancouver:

D'Attoma J. Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2013. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2013LYO10243.

Council of Science Editors:

D'Attoma J. Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2013. Available from: http://www.theses.fr/2013LYO10243


Universitat Ramon Llull

21. Berzosa Rodríguez, Xavier. Diseño y síntesis de una quimioteca de sistemas 5,6-dihidropirido[2,3-d]pirimidin-7(8H)-ona no sustituidos en C4 como inhibidores potenciales de tirosina quinasas.

Degree: 2010, Universitat Ramon Llull

 Tyrosine Kinases (TKs) are a group of Protein Kinases key in cell signaling. These kinases are involved in tumor growth processes, so the search for… (more)

Subjects/Keywords: guanidine; 4-cyanopentanoic esters; 4-cyanopentenoic esters; Michael addition; 3. 3-dimethoxypropanenitrile; pyrido[2. 3-d]pyrimidines; TK inhibitors; guanidina; ésteres 4-cianopentenoicos; ésteres 4-cianopentanoicos; adición de Michael; 3. 3-dimetoxipropionitrilo; pirido[2. 3-d]pirimidinas; inhibidores de TKs; guanidina; èsters 4-cianopentenoics; èsters 4-cianopentanoics; addició de Michael; 3. 3-dimetoxipropionitril; pirido[2. 3-d]pirimidinas; inhibidors de TKs; Química i Enginyeria Química; 547

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APA (6th Edition):

Berzosa Rodríguez, X. (2010). Diseño y síntesis de una quimioteca de sistemas 5,6-dihidropirido[2,3-d]pirimidin-7(8H)-ona no sustituidos en C4 como inhibidores potenciales de tirosina quinasas. (Thesis). Universitat Ramon Llull. Retrieved from http://hdl.handle.net/10803/9299

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):

Berzosa Rodríguez, Xavier. “Diseño y síntesis de una quimioteca de sistemas 5,6-dihidropirido[2,3-d]pirimidin-7(8H)-ona no sustituidos en C4 como inhibidores potenciales de tirosina quinasas.” 2010. Thesis, Universitat Ramon Llull. Accessed October 31, 2020. http://hdl.handle.net/10803/9299.

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

MLA Handbook (7th Edition):

Berzosa Rodríguez, Xavier. “Diseño y síntesis de una quimioteca de sistemas 5,6-dihidropirido[2,3-d]pirimidin-7(8H)-ona no sustituidos en C4 como inhibidores potenciales de tirosina quinasas.” 2010. Web. 31 Oct 2020.

Vancouver:

Berzosa Rodríguez X. Diseño y síntesis de una quimioteca de sistemas 5,6-dihidropirido[2,3-d]pirimidin-7(8H)-ona no sustituidos en C4 como inhibidores potenciales de tirosina quinasas. [Internet] [Thesis]. Universitat Ramon Llull; 2010. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10803/9299.

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

Council of Science Editors:

Berzosa Rodríguez X. Diseño y síntesis de una quimioteca de sistemas 5,6-dihidropirido[2,3-d]pirimidin-7(8H)-ona no sustituidos en C4 como inhibidores potenciales de tirosina quinasas. [Thesis]. Universitat Ramon Llull; 2010. Available from: http://hdl.handle.net/10803/9299

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

22. Cobo Cardenete, Isidro Felipe. Glycolipids: synthesis and multivalent systems.

Degree: Departament de Química Analítica i Química Orgànica, 2012, Universitat Rovira i Virgili

 Glycolipids such as glycosphingolipids are interesting compounds because they can interact with biofactors by inhibiting or interfering in physiological processes on cells. For instance, the… (more)

Subjects/Keywords: Glycolipid; glycosphingolipid; 2-deoxy-glycolipid; galactosylceramide; 2-iodoglycal; 2-C-arylglycal; suzuki-miyaura coupling; glycocluster; hyperbranched polymers; Cholera Toxin; 54; 547

…tetramethyluronium hexafluorophosphate HCCA: α-Cyano-4-hydroxycinnamic acid HFIP: 1,1,1,3,3,3-Hexafluoro-2… …32 Chapter 2. Synthesis of β-Galceramide analogues: Glycosylation of amidoalcohols using… …66 Chapter 3. Synthesis of 2-deoxygalactosyl ceramides… …84 3.2.1. Synthesis of 2-deoxy-β-GalCer analogue… …84 3.2.2. Synthesis of 2-deoxy-2-iodo-α-TalCer analogue… 

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

APA (6th Edition):

Cobo Cardenete, I. F. (2012). Glycolipids: synthesis and multivalent systems. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/284152

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):

Cobo Cardenete, Isidro Felipe. “Glycolipids: synthesis and multivalent systems.” 2012. Thesis, Universitat Rovira i Virgili. Accessed October 31, 2020. http://hdl.handle.net/10803/284152.

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

MLA Handbook (7th Edition):

Cobo Cardenete, Isidro Felipe. “Glycolipids: synthesis and multivalent systems.” 2012. Web. 31 Oct 2020.

Vancouver:

Cobo Cardenete IF. Glycolipids: synthesis and multivalent systems. [Internet] [Thesis]. Universitat Rovira i Virgili; 2012. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10803/284152.

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

Council of Science Editors:

Cobo Cardenete IF. Glycolipids: synthesis and multivalent systems. [Thesis]. Universitat Rovira i Virgili; 2012. Available from: http://hdl.handle.net/10803/284152

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

23. Subirós Funosas, Ramon. Nous reactius d’acoblament per a la síntesi de pèptids basats en 2-ciano-2-hidroxiimino acetat d’etil (Oxyma) com a additiu.

Degree: Departament de Química Orgànica, 2011, Universitat de Barcelona

 Peptides are naturally-ocurring biopolymers that exert essential functions in the human body. Moreover, many applications of peptides have been found recently in cosmetics, biotechnology, drug… (more)

Subjects/Keywords: Síntesi de pèptids; Síntesis de péptidos; Peptide synthesis; Oxyma; Formació enllaç peptídic; Reactius d'acoblament; Additiu; 2-ciano-2-hidroxiimino acetat d’etil; Ciències Experimentals i Matemàtiques; 547

…synthesis CAPÍTOL 2: Oxyma com a additiu per carbodiimides. Publicació II. Oxyma: An Efficient… …used in the prevention of base-driven side reactions and its effect on 2-chlorotrityl… …Ciano-2-etoxi-2-oxoetilidenaminooxi) iii Abreviatures, acrònims i annexos HCTU HDMA… …HOPO veure HOPy HOPy N-òxid de 2-hidroxipiridina HOSu N-hidroxisuccinimida HOTU… …d’alta resolució acoblat a espectrometría de masses J constant d’acoblament 2-MBT 2… 

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APA (6th Edition):

Subirós Funosas, R. (2011). Nous reactius d’acoblament per a la síntesi de pèptids basats en 2-ciano-2-hidroxiimino acetat d’etil (Oxyma) com a additiu. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/51298

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):

Subirós Funosas, Ramon. “Nous reactius d’acoblament per a la síntesi de pèptids basats en 2-ciano-2-hidroxiimino acetat d’etil (Oxyma) com a additiu.” 2011. Thesis, Universitat de Barcelona. Accessed October 31, 2020. http://hdl.handle.net/10803/51298.

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

MLA Handbook (7th Edition):

Subirós Funosas, Ramon. “Nous reactius d’acoblament per a la síntesi de pèptids basats en 2-ciano-2-hidroxiimino acetat d’etil (Oxyma) com a additiu.” 2011. Web. 31 Oct 2020.

Vancouver:

Subirós Funosas R. Nous reactius d’acoblament per a la síntesi de pèptids basats en 2-ciano-2-hidroxiimino acetat d’etil (Oxyma) com a additiu. [Internet] [Thesis]. Universitat de Barcelona; 2011. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10803/51298.

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

Council of Science Editors:

Subirós Funosas R. Nous reactius d’acoblament per a la síntesi de pèptids basats en 2-ciano-2-hidroxiimino acetat d’etil (Oxyma) com a additiu. [Thesis]. Universitat de Barcelona; 2011. Available from: http://hdl.handle.net/10803/51298

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


Freie Universität Berlin

24. Gorzynski, Marek. Synthesis of kahweofuran or 2,3-dihydro-6-methylthieno[2,3-c]furan or 2-methyl-3-oxa-8-thiabicyclo[3,3,0]octa-1,4-diene and its derivatives, aroma compounds of coffee.

Degree: 1985, Freie Universität Berlin

 A new synthesis was developed to manufacture the unsubstituted 3-oxa-8-thiabicyclo[3,3,0]octa-1,4-diene (1), 2-methyl- (kahweofuran, 2), 2-ethyl- (3), 4-methyl- (4), 7-methyl-(5), 2,4-dimethyl- (6), 2,4-diethyl- (7), 2,7-dimethyl- (8)… (more)

Subjects/Keywords: Eintopf-Synthese; Kahweofuran; 2-Methyl-3-oxa-8-thiabicyclo[3,3,0]octa-1,4-dien; kahweofuran; 2,3-dihydro-6-methylthieno[2,3-c]furan; 2-methyl-3-oxa-8-thiabicyclo[3,3,0]octa-1,4-diene; one-pot-synthesis; synthesis; 500 Natural sciences and mathematics::540 Chemistry and allied sciences::547 Organic chemistry

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

APA (6th Edition):

Gorzynski, M. (1985). Synthesis of kahweofuran or 2,3-dihydro-6-methylthieno[2,3-c]furan or 2-methyl-3-oxa-8-thiabicyclo[3,3,0]octa-1,4-diene and its derivatives, aroma compounds of coffee. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-884

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):

Gorzynski, Marek. “Synthesis of kahweofuran or 2,3-dihydro-6-methylthieno[2,3-c]furan or 2-methyl-3-oxa-8-thiabicyclo[3,3,0]octa-1,4-diene and its derivatives, aroma compounds of coffee.” 1985. Thesis, Freie Universität Berlin. Accessed October 31, 2020. http://dx.doi.org/10.17169/refubium-884.

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

MLA Handbook (7th Edition):

Gorzynski, Marek. “Synthesis of kahweofuran or 2,3-dihydro-6-methylthieno[2,3-c]furan or 2-methyl-3-oxa-8-thiabicyclo[3,3,0]octa-1,4-diene and its derivatives, aroma compounds of coffee.” 1985. Web. 31 Oct 2020.

Vancouver:

Gorzynski M. Synthesis of kahweofuran or 2,3-dihydro-6-methylthieno[2,3-c]furan or 2-methyl-3-oxa-8-thiabicyclo[3,3,0]octa-1,4-diene and its derivatives, aroma compounds of coffee. [Internet] [Thesis]. Freie Universität Berlin; 1985. [cited 2020 Oct 31]. Available from: http://dx.doi.org/10.17169/refubium-884.

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

Council of Science Editors:

Gorzynski M. Synthesis of kahweofuran or 2,3-dihydro-6-methylthieno[2,3-c]furan or 2-methyl-3-oxa-8-thiabicyclo[3,3,0]octa-1,4-diene and its derivatives, aroma compounds of coffee. [Thesis]. Freie Universität Berlin; 1985. Available from: http://dx.doi.org/10.17169/refubium-884

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

25. Adidou, Ouissam. Ligands dérivés de saccharides et, ou supportés par un bras poly(éthylène) glycol : synthèse et applications en catalyse organométallique : Ligands derived from saccharides and, or supported on poly(ethylene) glycol arm : synthesis and applications in organometallic catalysis.

Degree: Docteur es, Chimie, 2009, Université Claude Bernard – Lyon I

La synthèse de deux familles de ligands a été envisagée. La première famille de ligands concerne la préparation de nouveaux ligands dérivés de la D-glucosamine… (more)

Subjects/Keywords: D-glucosamine; D-glucose; Di-(2-pyridyl)méthylamine; Poly(éthylène) glycol; Ligands hydrosolubles; Substitution allylique de type Tsuji-Trost; Réaction de couplage-croisé de type Suzuki-Miyaura; D-glucosamine; D-glucose; Di-(2-pyridyl)methylamine; Poly(ethylene) glycol; Hydrosoluble ligands; Allylic substitution of Tsuji-Trost; Cross-coupling Suzuki-Miyaura reaction; 547

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APA (6th Edition):

Adidou, O. (2009). Ligands dérivés de saccharides et, ou supportés par un bras poly(éthylène) glycol : synthèse et applications en catalyse organométallique : Ligands derived from saccharides and, or supported on poly(ethylene) glycol arm : synthesis and applications in organometallic catalysis. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2009LYO10171

Chicago Manual of Style (16th Edition):

Adidou, Ouissam. “Ligands dérivés de saccharides et, ou supportés par un bras poly(éthylène) glycol : synthèse et applications en catalyse organométallique : Ligands derived from saccharides and, or supported on poly(ethylene) glycol arm : synthesis and applications in organometallic catalysis.” 2009. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed October 31, 2020. http://www.theses.fr/2009LYO10171.

MLA Handbook (7th Edition):

Adidou, Ouissam. “Ligands dérivés de saccharides et, ou supportés par un bras poly(éthylène) glycol : synthèse et applications en catalyse organométallique : Ligands derived from saccharides and, or supported on poly(ethylene) glycol arm : synthesis and applications in organometallic catalysis.” 2009. Web. 31 Oct 2020.

Vancouver:

Adidou O. Ligands dérivés de saccharides et, ou supportés par un bras poly(éthylène) glycol : synthèse et applications en catalyse organométallique : Ligands derived from saccharides and, or supported on poly(ethylene) glycol arm : synthesis and applications in organometallic catalysis. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2009. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2009LYO10171.

Council of Science Editors:

Adidou O. Ligands dérivés de saccharides et, ou supportés par un bras poly(éthylène) glycol : synthèse et applications en catalyse organométallique : Ligands derived from saccharides and, or supported on poly(ethylene) glycol arm : synthesis and applications in organometallic catalysis. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2009. Available from: http://www.theses.fr/2009LYO10171

26. Galve Murillo, Iñaki. Síntesis de pirido[2,3-d]pirimidin-7(8H)-onas 2-arilamino sustituidas y derivados.

Degree: 2013, Universitat Ramon Llull

 Protein Kinases (PKs) are involved in basic cellular cycle regulatory mechanisms. Deregulation of those has been found on cells of different tissues with cancer, immunological… (more)

Subjects/Keywords: Cinases de proteïna; cinases de tirosina; inhibidors selectius; estratègies de síntesi massiva; guanidinació d’amines; bromació de pirido[2,3-d]pirimidines; intermedi de Wheland bicíclic; diazotació de 4-aminopirido[2,3-d]pirimidines; obtenció de 4-oxopirido[2,3-d]pirimidines; 2-amino-3-aril-4-iminopirido[2,3-d]pirimidines; transposició de Dimroth; Quinasas de proteína; quinasas de tirosina; inhibidores selectivos; estrategias de síntesis masiva; guanidinación de aminas; bromación de pirido[2,3-d]pirimidinas; intermedio de Wheland bicíclico; diazotación de 4-aminopirido[2,3-d]pirimidinas; obtención de 4-oxopirido[2,3-d]pirimidinas; 2-amino-3-aril-4-iminopirido[2,3-d]pirimidinas; transposición de Dimroth; Protein kinases; tyrosine kinases; selective inhibitors; strategies for massive synthesis; amine guanidination; pyrido[2,3-d]pyrimidines bromination; Wheland intermediate; 4-aminopyrido[2,3-d]pyrimidines diazotation; 4-oxopyrido[2,3-d]pyrimidines synthesis; 2-amino-3-aryl-4-iminopyrido[2,3-d]pyrimidines; Dimroth rearrangement; Química i Enginyeria Química; 54; 547

…47 1. CAPÍTULO 1: Síntesis de 2-amino-4-arilamino-pirido[2,3-d]pirimidinas… …100 1.5. Obtención de 2-arilamino-4-aminopirido[2,3-d]pirimidinas a partir de 3… …160 2. CAPÍTULO 2: Propuesta y estudio de una nueva estrategia sintética orientada a… …comunes y conocidos son SH2 (Src -la primera Tyr-quinasa descubierta- homologo tipo 2)… …estímulo. 2. Hormonal: se establece un loop de autoseñalización celular que promociona la acción… 

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

APA (6th Edition):

Galve Murillo, I. (2013). Síntesis de pirido[2,3-d]pirimidin-7(8H)-onas 2-arilamino sustituidas y derivados. (Thesis). Universitat Ramon Llull. Retrieved from http://hdl.handle.net/10803/101403

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):

Galve Murillo, Iñaki. “Síntesis de pirido[2,3-d]pirimidin-7(8H)-onas 2-arilamino sustituidas y derivados.” 2013. Thesis, Universitat Ramon Llull. Accessed October 31, 2020. http://hdl.handle.net/10803/101403.

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

MLA Handbook (7th Edition):

Galve Murillo, Iñaki. “Síntesis de pirido[2,3-d]pirimidin-7(8H)-onas 2-arilamino sustituidas y derivados.” 2013. Web. 31 Oct 2020.

Vancouver:

Galve Murillo I. Síntesis de pirido[2,3-d]pirimidin-7(8H)-onas 2-arilamino sustituidas y derivados. [Internet] [Thesis]. Universitat Ramon Llull; 2013. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10803/101403.

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

Council of Science Editors:

Galve Murillo I. Síntesis de pirido[2,3-d]pirimidin-7(8H)-onas 2-arilamino sustituidas y derivados. [Thesis]. Universitat Ramon Llull; 2013. Available from: http://hdl.handle.net/10803/101403

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

.