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You searched for subject:(C glycosides). Showing records 1 – 17 of 17 total matches.

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1. Fleury, Adeline. Synthèse de c-glycosides et daminoacides glycosyles trifluoromethyles : C-glycosides synthesis and SYNTHESIS OF TRIFLUOROMETHYL GROUP CONTAINING GLYCOSIDES AND GLYCOPEPTIDES.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2011, Cergy-Pontoise

L’objectif de nos travaux consiste en la préparation de C-glycosides et d’aminoacides glycosylés trifluorométhylés dans le but d'obtenir des structures biologiquement actives stabilisées. L'intérêt des… (more)

Subjects/Keywords: C-glycosides; Trifluorométhyl glycosides; Trifluoromethyl glycopeptides; C-glycosides; Trifluoromethyl glycosides; Trifluoromethyl glycopeptides

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APA (6th Edition):

Fleury, A. (2011). Synthèse de c-glycosides et daminoacides glycosyles trifluoromethyles : C-glycosides synthesis and SYNTHESIS OF TRIFLUOROMETHYL GROUP CONTAINING GLYCOSIDES AND GLYCOPEPTIDES. (Doctoral Dissertation). Cergy-Pontoise. Retrieved from http://www.theses.fr/2011CERG0509

Chicago Manual of Style (16th Edition):

Fleury, Adeline. “Synthèse de c-glycosides et daminoacides glycosyles trifluoromethyles : C-glycosides synthesis and SYNTHESIS OF TRIFLUOROMETHYL GROUP CONTAINING GLYCOSIDES AND GLYCOPEPTIDES.” 2011. Doctoral Dissertation, Cergy-Pontoise. Accessed September 18, 2019. http://www.theses.fr/2011CERG0509.

MLA Handbook (7th Edition):

Fleury, Adeline. “Synthèse de c-glycosides et daminoacides glycosyles trifluoromethyles : C-glycosides synthesis and SYNTHESIS OF TRIFLUOROMETHYL GROUP CONTAINING GLYCOSIDES AND GLYCOPEPTIDES.” 2011. Web. 18 Sep 2019.

Vancouver:

Fleury A. Synthèse de c-glycosides et daminoacides glycosyles trifluoromethyles : C-glycosides synthesis and SYNTHESIS OF TRIFLUOROMETHYL GROUP CONTAINING GLYCOSIDES AND GLYCOPEPTIDES. [Internet] [Doctoral dissertation]. Cergy-Pontoise; 2011. [cited 2019 Sep 18]. Available from: http://www.theses.fr/2011CERG0509.

Council of Science Editors:

Fleury A. Synthèse de c-glycosides et daminoacides glycosyles trifluoromethyles : C-glycosides synthesis and SYNTHESIS OF TRIFLUOROMETHYL GROUP CONTAINING GLYCOSIDES AND GLYCOPEPTIDES. [Doctoral Dissertation]. Cergy-Pontoise; 2011. Available from: http://www.theses.fr/2011CERG0509

2. Gonzalez, Simon. Galactosides et peptides de fusion pour l'amélioration de l'activité anti-VHC d'un C-nucléoside : C-nucleoside anti-HCV activity enhanced by conjugation to galactosides and HCV fusion peptides.

Degree: Docteur es, Chimie - Cergy, 2017, Cergy-Pontoise

Le virus de l’hépatite C (VHC) est, encore aujourd’hui, un problème de santé mondiale majeur entraînant dans certains cas des cirrhoses et des hépatocarcinomes. De… (more)

Subjects/Keywords: C-Nucléosides; Adressage; Peptides Fusion; Glycosides; Hepatite C; C-Nucleosides; Targeted Delivery; Fusion Peptides; Glycosides; Hepatitis C

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APA (6th Edition):

Gonzalez, S. (2017). Galactosides et peptides de fusion pour l'amélioration de l'activité anti-VHC d'un C-nucléoside : C-nucleoside anti-HCV activity enhanced by conjugation to galactosides and HCV fusion peptides. (Doctoral Dissertation). Cergy-Pontoise. Retrieved from http://www.theses.fr/2017CERG0900

Chicago Manual of Style (16th Edition):

Gonzalez, Simon. “Galactosides et peptides de fusion pour l'amélioration de l'activité anti-VHC d'un C-nucléoside : C-nucleoside anti-HCV activity enhanced by conjugation to galactosides and HCV fusion peptides.” 2017. Doctoral Dissertation, Cergy-Pontoise. Accessed September 18, 2019. http://www.theses.fr/2017CERG0900.

MLA Handbook (7th Edition):

Gonzalez, Simon. “Galactosides et peptides de fusion pour l'amélioration de l'activité anti-VHC d'un C-nucléoside : C-nucleoside anti-HCV activity enhanced by conjugation to galactosides and HCV fusion peptides.” 2017. Web. 18 Sep 2019.

Vancouver:

Gonzalez S. Galactosides et peptides de fusion pour l'amélioration de l'activité anti-VHC d'un C-nucléoside : C-nucleoside anti-HCV activity enhanced by conjugation to galactosides and HCV fusion peptides. [Internet] [Doctoral dissertation]. Cergy-Pontoise; 2017. [cited 2019 Sep 18]. Available from: http://www.theses.fr/2017CERG0900.

Council of Science Editors:

Gonzalez S. Galactosides et peptides de fusion pour l'amélioration de l'activité anti-VHC d'un C-nucléoside : C-nucleoside anti-HCV activity enhanced by conjugation to galactosides and HCV fusion peptides. [Doctoral Dissertation]. Cergy-Pontoise; 2017. Available from: http://www.theses.fr/2017CERG0900


Université de Lorraine

3. Richard, Mylène. Les exo-glycals activés pour la synthèse de dérivés saccharidiques complexes : application à la préparation de glycoamino acides et de peptidomimétiques : Acyivated exo-glycals for the synthesis of carbohydrate derivatives : application for the preparation of glycoaminoacids and peptidomimetics.

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

Ces travaux s’articulent autour de dérivés saccharidiques de type exo-glycals ou C-glycosides pour lesquels de nouvelles méthodologies synthétiques ainsi que des applications dans le domaine… (more)

Subjects/Keywords: Exo-Glycals; C-Glycosides; Addition de Michael; Oligomères; Peptidomimétiques; NRP-1; Exo-Glycals; C-Glycosides; Michael addition; Oligomers; Peptidomimetics; NRP-1

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APA (6th Edition):

Richard, M. (2015). Les exo-glycals activés pour la synthèse de dérivés saccharidiques complexes : application à la préparation de glycoamino acides et de peptidomimétiques : Acyivated exo-glycals for the synthesis of carbohydrate derivatives : application for the preparation of glycoaminoacids and peptidomimetics. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2015LORR0133

Chicago Manual of Style (16th Edition):

Richard, Mylène. “Les exo-glycals activés pour la synthèse de dérivés saccharidiques complexes : application à la préparation de glycoamino acides et de peptidomimétiques : Acyivated exo-glycals for the synthesis of carbohydrate derivatives : application for the preparation of glycoaminoacids and peptidomimetics.” 2015. Doctoral Dissertation, Université de Lorraine. Accessed September 18, 2019. http://www.theses.fr/2015LORR0133.

MLA Handbook (7th Edition):

Richard, Mylène. “Les exo-glycals activés pour la synthèse de dérivés saccharidiques complexes : application à la préparation de glycoamino acides et de peptidomimétiques : Acyivated exo-glycals for the synthesis of carbohydrate derivatives : application for the preparation of glycoaminoacids and peptidomimetics.” 2015. Web. 18 Sep 2019.

Vancouver:

Richard M. Les exo-glycals activés pour la synthèse de dérivés saccharidiques complexes : application à la préparation de glycoamino acides et de peptidomimétiques : Acyivated exo-glycals for the synthesis of carbohydrate derivatives : application for the preparation of glycoaminoacids and peptidomimetics. [Internet] [Doctoral dissertation]. Université de Lorraine; 2015. [cited 2019 Sep 18]. Available from: http://www.theses.fr/2015LORR0133.

Council of Science Editors:

Richard M. Les exo-glycals activés pour la synthèse de dérivés saccharidiques complexes : application à la préparation de glycoamino acides et de peptidomimétiques : Acyivated exo-glycals for the synthesis of carbohydrate derivatives : application for the preparation of glycoaminoacids and peptidomimetics. [Doctoral Dissertation]. Université de Lorraine; 2015. Available from: http://www.theses.fr/2015LORR0133


National University of Ireland – Galway

4. Moynihan, Lorna. Synthesis of Iminosugar C-Glycosides via Tandem Allylic Azide Rearrangement - Huisgen Cycloaddition.

Degree: 2014, National University of Ireland – Galway

Iminosugars are naturally occurring polyhydroxylated alkaloids. These natural mimics of carbohydrates have found clinical use with their biological activity mainly attributed to their inhibition of… (more)

Subjects/Keywords: Iminosugar C-Glycosides; 1,3-Dipolar; Cycloaddition; Allylic azide rearrangement; Chemistry

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APA (6th Edition):

Moynihan, L. (2014). Synthesis of Iminosugar C-Glycosides via Tandem Allylic Azide Rearrangement - Huisgen Cycloaddition. (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/4253

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):

Moynihan, Lorna. “Synthesis of Iminosugar C-Glycosides via Tandem Allylic Azide Rearrangement - Huisgen Cycloaddition.” 2014. Thesis, National University of Ireland – Galway. Accessed September 18, 2019. http://hdl.handle.net/10379/4253.

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

MLA Handbook (7th Edition):

Moynihan, Lorna. “Synthesis of Iminosugar C-Glycosides via Tandem Allylic Azide Rearrangement - Huisgen Cycloaddition.” 2014. Web. 18 Sep 2019.

Vancouver:

Moynihan L. Synthesis of Iminosugar C-Glycosides via Tandem Allylic Azide Rearrangement - Huisgen Cycloaddition. [Internet] [Thesis]. National University of Ireland – Galway; 2014. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/10379/4253.

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

Council of Science Editors:

Moynihan L. Synthesis of Iminosugar C-Glycosides via Tandem Allylic Azide Rearrangement - Huisgen Cycloaddition. [Thesis]. National University of Ireland – Galway; 2014. Available from: http://hdl.handle.net/10379/4253

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

5. Novoa, Alexandre. Synthèse et fonctionnalisation d'exo-glycals : application à la préparation d'anti-tumoraux : Synthesis and functionnalization of exo-glycals : toward potential anti-cancer compounds.

Degree: Docteur es, Chimie, 2010, Université Henri Poincaré – Nancy I

Ce travail est une contribution à la synthèse et à la fonctionnalisation d'exo-glycals en vue d'accéder à des composés à activité anti-tumorale potentielle. Les objectifs… (more)

Subjects/Keywords: Exo-glycals; C-glycosides; Couplage pallado-catalysé; Peptidomimétiques; Antitumoraux

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APA (6th Edition):

Novoa, A. (2010). Synthèse et fonctionnalisation d'exo-glycals : application à la préparation d'anti-tumoraux : Synthesis and functionnalization of exo-glycals : toward potential anti-cancer compounds. (Doctoral Dissertation). Université Henri Poincaré – Nancy I. Retrieved from http://www.theses.fr/2010NAN10006

Chicago Manual of Style (16th Edition):

Novoa, Alexandre. “Synthèse et fonctionnalisation d'exo-glycals : application à la préparation d'anti-tumoraux : Synthesis and functionnalization of exo-glycals : toward potential anti-cancer compounds.” 2010. Doctoral Dissertation, Université Henri Poincaré – Nancy I. Accessed September 18, 2019. http://www.theses.fr/2010NAN10006.

MLA Handbook (7th Edition):

Novoa, Alexandre. “Synthèse et fonctionnalisation d'exo-glycals : application à la préparation d'anti-tumoraux : Synthesis and functionnalization of exo-glycals : toward potential anti-cancer compounds.” 2010. Web. 18 Sep 2019.

Vancouver:

Novoa A. Synthèse et fonctionnalisation d'exo-glycals : application à la préparation d'anti-tumoraux : Synthesis and functionnalization of exo-glycals : toward potential anti-cancer compounds. [Internet] [Doctoral dissertation]. Université Henri Poincaré – Nancy I; 2010. [cited 2019 Sep 18]. Available from: http://www.theses.fr/2010NAN10006.

Council of Science Editors:

Novoa A. Synthèse et fonctionnalisation d'exo-glycals : application à la préparation d'anti-tumoraux : Synthesis and functionnalization of exo-glycals : toward potential anti-cancer compounds. [Doctoral Dissertation]. Université Henri Poincaré – Nancy I; 2010. Available from: http://www.theses.fr/2010NAN10006


Johannes Gutenberg Universität Mainz

6. Weiß, Torsten. Übergangsmetallvermittelte [2+2+2]-Zyklotrimerisierungsreaktionen zum Aufbau anellierter Phthalide : Intermediate zur Synthese von Anguzyklinonen.

Degree: 2011, Johannes Gutenberg Universität Mainz

Anguzykline sind eine große Gruppe von Naturstoffen. Ihnen ist gemein, dass sie eine Benz[a]anthracen-Struktur besitzen oder dass sie in der Biosynthese aus einer Verbindung mit… (more)

Subjects/Keywords: Zyklotrimerisierung; Anguzyklinone; Phthalide; C-Glykoside; cyclotrimerisation; angucyclinones; phthalides; C-glycosides; Chemistry and allied sciences

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APA (6th Edition):

Weiß, T. (2011). Übergangsmetallvermittelte [2+2+2]-Zyklotrimerisierungsreaktionen zum Aufbau anellierter Phthalide : Intermediate zur Synthese von Anguzyklinonen. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3537/

Chicago Manual of Style (16th Edition):

Weiß, Torsten. “Übergangsmetallvermittelte [2+2+2]-Zyklotrimerisierungsreaktionen zum Aufbau anellierter Phthalide : Intermediate zur Synthese von Anguzyklinonen.” 2011. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 18, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2013/3537/.

MLA Handbook (7th Edition):

Weiß, Torsten. “Übergangsmetallvermittelte [2+2+2]-Zyklotrimerisierungsreaktionen zum Aufbau anellierter Phthalide : Intermediate zur Synthese von Anguzyklinonen.” 2011. Web. 18 Sep 2019.

Vancouver:

Weiß T. Übergangsmetallvermittelte [2+2+2]-Zyklotrimerisierungsreaktionen zum Aufbau anellierter Phthalide : Intermediate zur Synthese von Anguzyklinonen. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2011. [cited 2019 Sep 18]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3537/.

Council of Science Editors:

Weiß T. Übergangsmetallvermittelte [2+2+2]-Zyklotrimerisierungsreaktionen zum Aufbau anellierter Phthalide : Intermediate zur Synthese von Anguzyklinonen. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2011. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3537/

7. Bruneau, Alexandre. Développement de nouvelles réactions métallo-catalysées pour la création de liaisons C-C et C-hétéroatomes : Application à la synthèse d’inhibiteurs de la Hsp90 et aux ligands de la lectine A. : New metal-catalyzed methodologies for C-C and C-heteroatom bond-forming reactions : Application to the synthesis of Hsp90 inhibitors and Lectine A ligands.

Degree: Docteur es, Chimie thérapeutique, 2015, Paris Saclay

Les travaux rapportés dans ce mémoire concernent le développement de nouvelles réactions métallo-catalysées pour la création de liaison carbone-hétéroatome et carbone-carbone ainsi que leurs applications… (more)

Subjects/Keywords: Catalyse organométallique; Liaison C-Hétéroatome; Hétérosides; Liaison C-C; Hsp90; Lectine A; Organometallic catalysis; C-Heteroatom bond; Glycosides; C-C bond; Hsp90; Lectin A

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APA (6th Edition):

Bruneau, A. (2015). Développement de nouvelles réactions métallo-catalysées pour la création de liaisons C-C et C-hétéroatomes : Application à la synthèse d’inhibiteurs de la Hsp90 et aux ligands de la lectine A. : New metal-catalyzed methodologies for C-C and C-heteroatom bond-forming reactions : Application to the synthesis of Hsp90 inhibitors and Lectine A ligands. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2015SACLS138

Chicago Manual of Style (16th Edition):

Bruneau, Alexandre. “Développement de nouvelles réactions métallo-catalysées pour la création de liaisons C-C et C-hétéroatomes : Application à la synthèse d’inhibiteurs de la Hsp90 et aux ligands de la lectine A. : New metal-catalyzed methodologies for C-C and C-heteroatom bond-forming reactions : Application to the synthesis of Hsp90 inhibitors and Lectine A ligands.” 2015. Doctoral Dissertation, Paris Saclay. Accessed September 18, 2019. http://www.theses.fr/2015SACLS138.

MLA Handbook (7th Edition):

Bruneau, Alexandre. “Développement de nouvelles réactions métallo-catalysées pour la création de liaisons C-C et C-hétéroatomes : Application à la synthèse d’inhibiteurs de la Hsp90 et aux ligands de la lectine A. : New metal-catalyzed methodologies for C-C and C-heteroatom bond-forming reactions : Application to the synthesis of Hsp90 inhibitors and Lectine A ligands.” 2015. Web. 18 Sep 2019.

Vancouver:

Bruneau A. Développement de nouvelles réactions métallo-catalysées pour la création de liaisons C-C et C-hétéroatomes : Application à la synthèse d’inhibiteurs de la Hsp90 et aux ligands de la lectine A. : New metal-catalyzed methodologies for C-C and C-heteroatom bond-forming reactions : Application to the synthesis of Hsp90 inhibitors and Lectine A ligands. [Internet] [Doctoral dissertation]. Paris Saclay; 2015. [cited 2019 Sep 18]. Available from: http://www.theses.fr/2015SACLS138.

Council of Science Editors:

Bruneau A. Développement de nouvelles réactions métallo-catalysées pour la création de liaisons C-C et C-hétéroatomes : Application à la synthèse d’inhibiteurs de la Hsp90 et aux ligands de la lectine A. : New metal-catalyzed methodologies for C-C and C-heteroatom bond-forming reactions : Application to the synthesis of Hsp90 inhibitors and Lectine A ligands. [Doctoral Dissertation]. Paris Saclay; 2015. Available from: http://www.theses.fr/2015SACLS138

8. Cocaud, Chloé. Nouvelles méthodologies de synthèse et évaluation biologique d’analogues de glycosides et de glycosyl phosphates en série iminosucre : New methods of synthesis and biological evaluation of glycosides and glycosyl phosphates analogs in the iminosugar series.

Degree: Docteur es, Chimie organique, 2016, Université d'Orléans

Les glycosylamines sont des précurseurs très utiles pour préparer une grande diversité de produits naturels et leurs analogues d’intérêts biologiques. Elles ont été particulièrement utilisées… (more)

Subjects/Keywords: Imino-C-glycosides; Sulfinylglycosylamines; Réactifs organométalliques; Aglycone fluoré; Mimes de glycosyl phosphates; GafT2; Imino-C-glycosides; Sulfinylglycosylamines; Organometallic reagents; Fluorinated aglycon; Glycosyl phosphate mimics; GafT2; 547

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APA (6th Edition):

Cocaud, C. (2016). Nouvelles méthodologies de synthèse et évaluation biologique d’analogues de glycosides et de glycosyl phosphates en série iminosucre : New methods of synthesis and biological evaluation of glycosides and glycosyl phosphates analogs in the iminosugar series. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2016ORLE2044

Chicago Manual of Style (16th Edition):

Cocaud, Chloé. “Nouvelles méthodologies de synthèse et évaluation biologique d’analogues de glycosides et de glycosyl phosphates en série iminosucre : New methods of synthesis and biological evaluation of glycosides and glycosyl phosphates analogs in the iminosugar series.” 2016. Doctoral Dissertation, Université d'Orléans. Accessed September 18, 2019. http://www.theses.fr/2016ORLE2044.

MLA Handbook (7th Edition):

Cocaud, Chloé. “Nouvelles méthodologies de synthèse et évaluation biologique d’analogues de glycosides et de glycosyl phosphates en série iminosucre : New methods of synthesis and biological evaluation of glycosides and glycosyl phosphates analogs in the iminosugar series.” 2016. Web. 18 Sep 2019.

Vancouver:

Cocaud C. Nouvelles méthodologies de synthèse et évaluation biologique d’analogues de glycosides et de glycosyl phosphates en série iminosucre : New methods of synthesis and biological evaluation of glycosides and glycosyl phosphates analogs in the iminosugar series. [Internet] [Doctoral dissertation]. Université d'Orléans; 2016. [cited 2019 Sep 18]. Available from: http://www.theses.fr/2016ORLE2044.

Council of Science Editors:

Cocaud C. Nouvelles méthodologies de synthèse et évaluation biologique d’analogues de glycosides et de glycosyl phosphates en série iminosucre : New methods of synthesis and biological evaluation of glycosides and glycosyl phosphates analogs in the iminosugar series. [Doctoral Dissertation]. Université d'Orléans; 2016. Available from: http://www.theses.fr/2016ORLE2044

9. Fontelle, Nathalie. Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2013, Poitiers

Les iminosucres, analogues de sucres dont l'oxygène intracyclique a été remplacé par un azote, constituent une classe importante de mimes de sucres. Introduire une chaîne… (more)

Subjects/Keywords: Iminosucres C-Glycosides; Iminosucres-Aza-Couronne; N-Acétyl-D-Glucosamine; Contraction de cycle; Glycosidases; Iminosugars C-Glycosides; Iminosugars-Aza-Crown; N-Acetyl-D-Glucosamine; Ring contraction; Glycosidases; 547

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APA (6th Edition):

Fontelle, N. (2013). Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine. (Doctoral Dissertation). Poitiers. Retrieved from http://www.theses.fr/2013POIT2334

Chicago Manual of Style (16th Edition):

Fontelle, Nathalie. “Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine.” 2013. Doctoral Dissertation, Poitiers. Accessed September 18, 2019. http://www.theses.fr/2013POIT2334.

MLA Handbook (7th Edition):

Fontelle, Nathalie. “Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine.” 2013. Web. 18 Sep 2019.

Vancouver:

Fontelle N. Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine. [Internet] [Doctoral dissertation]. Poitiers; 2013. [cited 2019 Sep 18]. Available from: http://www.theses.fr/2013POIT2334.

Council of Science Editors:

Fontelle N. Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine. [Doctoral Dissertation]. Poitiers; 2013. Available from: http://www.theses.fr/2013POIT2334


Johannes Gutenberg Universität Mainz

10. Weck, Stefan. Synthese von Sialyl-Lewis-X-Mimetika durch stereoselektive ortho-C-Glycosylierung von Phenolen.

Degree: 2011, Johannes Gutenberg Universität Mainz

Ziel der Arbeit war es, Sialyl-LewisX-Mimetika auf Basis ortho-C-glycosylierter Phenole als Inhibitoren für die Selektin-Ligand-Wechselwirkungen zu synthetisieren. Dazu wurde zunächst die Stereoselektivität der ortho-C-Mannosylierung untersucht.… (more)

Subjects/Keywords: Sialyl-Lewisx; Mimetika; Glycosylierung; C-Glycoside; Anomer; sialyl-Lewisx; mimetics; glycosylation; C-glycosides; anomer; Chemistry and allied sciences

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APA (6th Edition):

Weck, S. (2011). Synthese von Sialyl-Lewis-X-Mimetika durch stereoselektive ortho-C-Glycosylierung von Phenolen. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2012/2986/

Chicago Manual of Style (16th Edition):

Weck, Stefan. “Synthese von Sialyl-Lewis-X-Mimetika durch stereoselektive ortho-C-Glycosylierung von Phenolen.” 2011. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 18, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2012/2986/.

MLA Handbook (7th Edition):

Weck, Stefan. “Synthese von Sialyl-Lewis-X-Mimetika durch stereoselektive ortho-C-Glycosylierung von Phenolen.” 2011. Web. 18 Sep 2019.

Vancouver:

Weck S. Synthese von Sialyl-Lewis-X-Mimetika durch stereoselektive ortho-C-Glycosylierung von Phenolen. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2011. [cited 2019 Sep 18]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/2986/.

Council of Science Editors:

Weck S. Synthese von Sialyl-Lewis-X-Mimetika durch stereoselektive ortho-C-Glycosylierung von Phenolen. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2011. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/2986/


University of Debrecen

11. Okonkwo, Victor Awele. Study of the protecting group manipulation and C-C bond formation reactions of 1-C substituted glycals.

Degree: DE – Természettudományi és Technológiai Kar – Kémiai Intézet, University of Debrecen

The goal of this thesis was to study the protecting groups manipulation of 1-C substituted glucals and galactals possessing electron withdrawing substituents at the anomeric centre. These compounds can be used to study the cross coupling reaction of these molecules in details. Advisors/Committee Members: Juhasz, Laszlo (advisor).

Subjects/Keywords: protecting groups; C-C bond formation; C-glycosides; 1-C substituted glycal.

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

APA (6th Edition):

Okonkwo, V. A. (n.d.). Study of the protecting group manipulation and C-C bond formation reactions of 1-C substituted glycals. (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/232467

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Okonkwo, Victor Awele. “Study of the protecting group manipulation and C-C bond formation reactions of 1-C substituted glycals. ” Thesis, University of Debrecen. Accessed September 18, 2019. http://hdl.handle.net/2437/232467.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Okonkwo, Victor Awele. “Study of the protecting group manipulation and C-C bond formation reactions of 1-C substituted glycals. ” Web. 18 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Okonkwo VA. Study of the protecting group manipulation and C-C bond formation reactions of 1-C substituted glycals. [Internet] [Thesis]. University of Debrecen; [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2437/232467.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Okonkwo VA. Study of the protecting group manipulation and C-C bond formation reactions of 1-C substituted glycals. [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/232467

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Indian Institute of Science

12. Paul, Somak. Synthesis Of 2-Deoxy-1-Thioglycosides And Establishing Their Efficient Glycosyl Donor Properties To Prepare Aryl 2-Deoxy Glycosides And 2-Deoxy Oligosaccharides.

Degree: 2008, Indian Institute of Science

 Carbohydrates are a family of polyfunctional natural products and can be chemically modified in numerous ways. The primary significance of carbohydrates rests in their importance… (more)

Subjects/Keywords: Glycosides; 2-Deoxy-1-Thioglycosides; Oligosaccharides; C-2 Modified Sugars; Carbohydrates- Synthesis; Disaccharides; 2-Deoxy Oligosaccharides; Aryl 2-Deoxy Glycosides; Organic Chemistry

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APA (6th Edition):

Paul, S. (2008). Synthesis Of 2-Deoxy-1-Thioglycosides And Establishing Their Efficient Glycosyl Donor Properties To Prepare Aryl 2-Deoxy Glycosides And 2-Deoxy Oligosaccharides. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/737

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):

Paul, Somak. “Synthesis Of 2-Deoxy-1-Thioglycosides And Establishing Their Efficient Glycosyl Donor Properties To Prepare Aryl 2-Deoxy Glycosides And 2-Deoxy Oligosaccharides.” 2008. Thesis, Indian Institute of Science. Accessed September 18, 2019. http://hdl.handle.net/2005/737.

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

MLA Handbook (7th Edition):

Paul, Somak. “Synthesis Of 2-Deoxy-1-Thioglycosides And Establishing Their Efficient Glycosyl Donor Properties To Prepare Aryl 2-Deoxy Glycosides And 2-Deoxy Oligosaccharides.” 2008. Web. 18 Sep 2019.

Vancouver:

Paul S. Synthesis Of 2-Deoxy-1-Thioglycosides And Establishing Their Efficient Glycosyl Donor Properties To Prepare Aryl 2-Deoxy Glycosides And 2-Deoxy Oligosaccharides. [Internet] [Thesis]. Indian Institute of Science; 2008. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2005/737.

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

Council of Science Editors:

Paul S. Synthesis Of 2-Deoxy-1-Thioglycosides And Establishing Their Efficient Glycosyl Donor Properties To Prepare Aryl 2-Deoxy Glycosides And 2-Deoxy Oligosaccharides. [Thesis]. Indian Institute of Science; 2008. Available from: http://hdl.handle.net/2005/737

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


University of Alabama

13. Martinez, Dionicio Solorio. Syntheses of C-glycoside natural products via oxocarbenium cationic intermediates.

Degree: 2011, University of Alabama

 This dissertation highlights studies into the total synthesis of C-glycoside natural products via oxocarbenium cationic intermediates with a brief introduction given in the first chapter.… (more)

Subjects/Keywords: Electronic Thesis or Dissertation;  – thesis; Organic Chemistry; Chemistry; C-glycosides; natural products; oxocarbenium; polyketides; synthetic chemistry

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

APA (6th Edition):

Martinez, D. S. (2011). Syntheses of C-glycoside natural products via oxocarbenium cationic intermediates. (Thesis). University of Alabama. Retrieved from http://purl.lib.ua.edu/34918

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):

Martinez, Dionicio Solorio. “Syntheses of C-glycoside natural products via oxocarbenium cationic intermediates.” 2011. Thesis, University of Alabama. Accessed September 18, 2019. http://purl.lib.ua.edu/34918.

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

MLA Handbook (7th Edition):

Martinez, Dionicio Solorio. “Syntheses of C-glycoside natural products via oxocarbenium cationic intermediates.” 2011. Web. 18 Sep 2019.

Vancouver:

Martinez DS. Syntheses of C-glycoside natural products via oxocarbenium cationic intermediates. [Internet] [Thesis]. University of Alabama; 2011. [cited 2019 Sep 18]. Available from: http://purl.lib.ua.edu/34918.

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

Council of Science Editors:

Martinez DS. Syntheses of C-glycoside natural products via oxocarbenium cationic intermediates. [Thesis]. University of Alabama; 2011. Available from: http://purl.lib.ua.edu/34918

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

14. Bordes, Alexandra. Conception de nouveaux inhibiteurs d'enzymes et de chélatants de métaux à base d'iminosucres : Iminosugars-based macrocycles to deliver new sweet azacrowns.

Degree: Docteur es, Chimie organique, minérale et industrielle, 2016, Poitiers

Les iminosucres, analogues de sucres dans lesquels l'oxygène endocyclique a été remplacé par un atome d'azote, constitue une classe importante de mimes de sucres. Aujourd'hui,… (more)

Subjects/Keywords: Iminosucres C-Glycosides; Iminosucres aza-Couronnes; Propriétés de chélation; Macrocycles; Fonctionnalisation diastéréosélectives et stéréocontrollées; Récepteurs moléculaires; Chélation; Iminosugars C-Glycosides; Iminosugars aza-Crown; Therapeutic properties; Macrocycles; Diastereoselective and stereocontrolled functionalization; Molecular receptors; Chelation; 547.2

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APA (6th Edition):

Bordes, A. (2016). Conception de nouveaux inhibiteurs d'enzymes et de chélatants de métaux à base d'iminosucres : Iminosugars-based macrocycles to deliver new sweet azacrowns. (Doctoral Dissertation). Poitiers. Retrieved from http://www.theses.fr/2016POIT2301

Chicago Manual of Style (16th Edition):

Bordes, Alexandra. “Conception de nouveaux inhibiteurs d'enzymes et de chélatants de métaux à base d'iminosucres : Iminosugars-based macrocycles to deliver new sweet azacrowns.” 2016. Doctoral Dissertation, Poitiers. Accessed September 18, 2019. http://www.theses.fr/2016POIT2301.

MLA Handbook (7th Edition):

Bordes, Alexandra. “Conception de nouveaux inhibiteurs d'enzymes et de chélatants de métaux à base d'iminosucres : Iminosugars-based macrocycles to deliver new sweet azacrowns.” 2016. Web. 18 Sep 2019.

Vancouver:

Bordes A. Conception de nouveaux inhibiteurs d'enzymes et de chélatants de métaux à base d'iminosucres : Iminosugars-based macrocycles to deliver new sweet azacrowns. [Internet] [Doctoral dissertation]. Poitiers; 2016. [cited 2019 Sep 18]. Available from: http://www.theses.fr/2016POIT2301.

Council of Science Editors:

Bordes A. Conception de nouveaux inhibiteurs d'enzymes et de chélatants de métaux à base d'iminosucres : Iminosugars-based macrocycles to deliver new sweet azacrowns. [Doctoral Dissertation]. Poitiers; 2016. Available from: http://www.theses.fr/2016POIT2301

15. Dimirjian, Christine. Towards the Synthesis of Diandraflavone.

Degree: MS, Department of Chemistry and Biochemistry, 2015, California State University – Northridge

 Diandraflavone is a natural product isolated and characterized from the Drymaria diandra plant native to Taiwan. It has been used in traditional medicine to treat… (more)

Subjects/Keywords: C-glycosides; Dissertations, Academic  – CSUN  – Chemistry and Biochemistry  – Chemistry.

C-Aryl Glycosides Scheme 2.8 Regioselective Cycloadducts Using Silicon Tether Scheme… …TABLES Table 1.1 Classification of C-Aryl Glycosides Table 4.1 Reaction Conditions for… …chromophore can occur. xv Chapter 1: Chemical and Biological Significance of C-Aryl Glycosides… …new class of structures called C-glycosides (Figure 1.1). C-glycosides have been… …8 1.3 C-Aryl Glycosides 1.3.1 Classification As previously mentioned, flavones occur… 

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APA (6th Edition):

Dimirjian, C. (2015). Towards the Synthesis of Diandraflavone. (Masters Thesis). California State University – Northridge. Retrieved from http://hdl.handle.net/10211.3/147594

Chicago Manual of Style (16th Edition):

Dimirjian, Christine. “Towards the Synthesis of Diandraflavone.” 2015. Masters Thesis, California State University – Northridge. Accessed September 18, 2019. http://hdl.handle.net/10211.3/147594.

MLA Handbook (7th Edition):

Dimirjian, Christine. “Towards the Synthesis of Diandraflavone.” 2015. Web. 18 Sep 2019.

Vancouver:

Dimirjian C. Towards the Synthesis of Diandraflavone. [Internet] [Masters thesis]. California State University – Northridge; 2015. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/10211.3/147594.

Council of Science Editors:

Dimirjian C. Towards the Synthesis of Diandraflavone. [Masters Thesis]. California State University – Northridge; 2015. Available from: http://hdl.handle.net/10211.3/147594

16. Gossan, Apie Diane Patricia. Etude phytochimique de plantes médicinales issues de la flore de la Côte d’Ivoire : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) et Glyphaea brevis (Malvaceae) : Phytochemical study of medicinal plants used in traditional medicine in Ivory Coast : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) and Glyphaea brevis (Malvaceae).

Degree: Docteur es, Sciences - STS, 2013, Reims; Université de Cocody-Abidjan

L'étude phytochimique de plantes médicinales suscite depuis toujours beaucoup d'intérêt à cause de la variété de métabolites secondaires à activités biologiques intéressantes fabriqués par les… (more)

Subjects/Keywords: Rhamnaceae; Combretaceae; Malvaceae; Saponosides; Squelette dammarane; Hétérosides flavoniques; Rhamnocitrin; Triterpènes; Cinnamide; Phenyl alkyle C-Glycoside; Iminosucre; Rhamnaceae; Combretaceae; Malvaceae; Saponosides; Dammarane skeleton; Flavonoid glycosides

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APA (6th Edition):

Gossan, A. D. P. (2013). Etude phytochimique de plantes médicinales issues de la flore de la Côte d’Ivoire : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) et Glyphaea brevis (Malvaceae) : Phytochemical study of medicinal plants used in traditional medicine in Ivory Coast : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) and Glyphaea brevis (Malvaceae). (Doctoral Dissertation). Reims; Université de Cocody-Abidjan. Retrieved from http://www.theses.fr/2013REIMS040

Chicago Manual of Style (16th Edition):

Gossan, Apie Diane Patricia. “Etude phytochimique de plantes médicinales issues de la flore de la Côte d’Ivoire : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) et Glyphaea brevis (Malvaceae) : Phytochemical study of medicinal plants used in traditional medicine in Ivory Coast : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) and Glyphaea brevis (Malvaceae).” 2013. Doctoral Dissertation, Reims; Université de Cocody-Abidjan. Accessed September 18, 2019. http://www.theses.fr/2013REIMS040.

MLA Handbook (7th Edition):

Gossan, Apie Diane Patricia. “Etude phytochimique de plantes médicinales issues de la flore de la Côte d’Ivoire : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) et Glyphaea brevis (Malvaceae) : Phytochemical study of medicinal plants used in traditional medicine in Ivory Coast : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) and Glyphaea brevis (Malvaceae).” 2013. Web. 18 Sep 2019.

Vancouver:

Gossan ADP. Etude phytochimique de plantes médicinales issues de la flore de la Côte d’Ivoire : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) et Glyphaea brevis (Malvaceae) : Phytochemical study of medicinal plants used in traditional medicine in Ivory Coast : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) and Glyphaea brevis (Malvaceae). [Internet] [Doctoral dissertation]. Reims; Université de Cocody-Abidjan; 2013. [cited 2019 Sep 18]. Available from: http://www.theses.fr/2013REIMS040.

Council of Science Editors:

Gossan ADP. Etude phytochimique de plantes médicinales issues de la flore de la Côte d’Ivoire : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) et Glyphaea brevis (Malvaceae) : Phytochemical study of medicinal plants used in traditional medicine in Ivory Coast : Gouania longipetala, Ventilago africana (Rhamnaceae), Combretum racemosum (Combretaceae) and Glyphaea brevis (Malvaceae). [Doctoral Dissertation]. Reims; Université de Cocody-Abidjan; 2013. Available from: http://www.theses.fr/2013REIMS040


Johannes Gutenberg Universität Mainz

17. Buba, Annette. Synthese C-glycosidischer und N-methylierter Glycosylaminosäuren für den Aufbau von Mimetika tumorassoziierter MUC1-Glycopeptidantigene unter Verwendung mikrostrukturierter Reaktoren.

Degree: 2015, Johannes Gutenberg Universität Mainz

Zur Synthese hydrolysestabiler MUC1-Antitumorvakzine wurde im Rahmen dieser Arbeit zunächst ein Verfahren zur effizienten N Methylierung von Fmoc-Aminosäuren entwickelt. Die Synthese erfolgte in einer zweistufigen… (more)

Subjects/Keywords: Tube-in-Tube-Reaktor; N-Methylaminosäuren; N-Methylglycosylaminosäuren; N-Methylpeptid; C-Glycoside; Tube-in-tube-reactor; N-methyl amino acids; N-methyl glycosyl amino acids; N-methyl peptide; C-glycosides; Chemistry and allied sciences

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APA (6th Edition):

Buba, A. (2015). Synthese C-glycosidischer und N-methylierter Glycosylaminosäuren für den Aufbau von Mimetika tumorassoziierter MUC1-Glycopeptidantigene unter Verwendung mikrostrukturierter Reaktoren. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2015/4076/

Chicago Manual of Style (16th Edition):

Buba, Annette. “Synthese C-glycosidischer und N-methylierter Glycosylaminosäuren für den Aufbau von Mimetika tumorassoziierter MUC1-Glycopeptidantigene unter Verwendung mikrostrukturierter Reaktoren.” 2015. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 18, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2015/4076/.

MLA Handbook (7th Edition):

Buba, Annette. “Synthese C-glycosidischer und N-methylierter Glycosylaminosäuren für den Aufbau von Mimetika tumorassoziierter MUC1-Glycopeptidantigene unter Verwendung mikrostrukturierter Reaktoren.” 2015. Web. 18 Sep 2019.

Vancouver:

Buba A. Synthese C-glycosidischer und N-methylierter Glycosylaminosäuren für den Aufbau von Mimetika tumorassoziierter MUC1-Glycopeptidantigene unter Verwendung mikrostrukturierter Reaktoren. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2015. [cited 2019 Sep 18]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4076/.

Council of Science Editors:

Buba A. Synthese C-glycosidischer und N-methylierter Glycosylaminosäuren für den Aufbau von Mimetika tumorassoziierter MUC1-Glycopeptidantigene unter Verwendung mikrostrukturierter Reaktoren. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2015. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4076/

.