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You searched for subject:(Organische Synthese). Showing records 1 – 30 of 379 total matches.

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Ruhr Universität Bochum

1. Mönninghoff, Sven. Dendritische Polythioetherliganden zur Synthese von Goldnanopartikel-Oligonucleotid-Monokonjugaten.

Degree: 2009, Ruhr Universität Bochum

 Basierend auf der Entwicklung des Rubigoldes als thermostabilem Marker für Biomoleküle wurden in dieser Arbeit Polythioether-Liganden zur Synthese von monofunktionalen Cluster-Oligonucleotid-Konjugaten (COK) entwickelt. Zum Aufbau… (more)

Subjects/Keywords: Cluster; Organische Sulfide; Nanotechnologie; DNS-Synthese; Temperaturbeständigkeit

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

APA (6th Edition):

Mönninghoff, S. (2009). Dendritische Polythioetherliganden zur Synthese von Goldnanopartikel-Oligonucleotid-Monokonjugaten. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-26229

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):

Mönninghoff, Sven. “Dendritische Polythioetherliganden zur Synthese von Goldnanopartikel-Oligonucleotid-Monokonjugaten.” 2009. Thesis, Ruhr Universität Bochum. Accessed May 08, 2021. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-26229.

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

MLA Handbook (7th Edition):

Mönninghoff, Sven. “Dendritische Polythioetherliganden zur Synthese von Goldnanopartikel-Oligonucleotid-Monokonjugaten.” 2009. Web. 08 May 2021.

Vancouver:

Mönninghoff S. Dendritische Polythioetherliganden zur Synthese von Goldnanopartikel-Oligonucleotid-Monokonjugaten. [Internet] [Thesis]. Ruhr Universität Bochum; 2009. [cited 2021 May 08]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-26229.

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

Council of Science Editors:

Mönninghoff S. Dendritische Polythioetherliganden zur Synthese von Goldnanopartikel-Oligonucleotid-Monokonjugaten. [Thesis]. Ruhr Universität Bochum; 2009. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-26229

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


Ruhr Universität Bochum

2. Bischof, Caroline. Building blocks for multinuclear near-IR luminescent lanthanide complexes.

Degree: 2013, Ruhr Universität Bochum

 Ziel dieser Arbeit war die Entwicklung eines binuklearen Liganden für einen lanthanoidbasierten Upconversionkomplex. Leitstruktur dafür waren Trisbipyridin-Kryptate, welche stabile, lumineszente Lanthanoidkomplexe bilden, das Metall effektiv… (more)

Subjects/Keywords: Lanthanoide; Bipyridine; Supramolekulare Chemie; Organische Synthese; Lumineszenz

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APA (6th Edition):

Bischof, C. (2013). Building blocks for multinuclear near-IR luminescent lanthanide complexes. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-37295

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):

Bischof, Caroline. “Building blocks for multinuclear near-IR luminescent lanthanide complexes.” 2013. Thesis, Ruhr Universität Bochum. Accessed May 08, 2021. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-37295.

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

MLA Handbook (7th Edition):

Bischof, Caroline. “Building blocks for multinuclear near-IR luminescent lanthanide complexes.” 2013. Web. 08 May 2021.

Vancouver:

Bischof C. Building blocks for multinuclear near-IR luminescent lanthanide complexes. [Internet] [Thesis]. Ruhr Universität Bochum; 2013. [cited 2021 May 08]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-37295.

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

Council of Science Editors:

Bischof C. Building blocks for multinuclear near-IR luminescent lanthanide complexes. [Thesis]. Ruhr Universität Bochum; 2013. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-37295

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

3. Nöcker, Christina. Synthese von Naturstoff-basierten Substanzbibliotheken.

Degree: 2017, Technische Universität Dortmund

 The following thesis describes the synthesis of natural product inspired compound libraries. The synthesis of depsipeptides Chondramid C and analogues was conducted. The synthesis strategy… (more)

Subjects/Keywords: Cyclodepsipeptide; Sec14p; Cycloaddition; Organische Synthese; 570; 540

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APA (6th Edition):

Nöcker, C. (2017). Synthese von Naturstoff-basierten Substanzbibliotheken. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-17961

Chicago Manual of Style (16th Edition):

Nöcker, Christina. “Synthese von Naturstoff-basierten Substanzbibliotheken.” 2017. Doctoral Dissertation, Technische Universität Dortmund. Accessed May 08, 2021. http://dx.doi.org/10.17877/DE290R-17961.

MLA Handbook (7th Edition):

Nöcker, Christina. “Synthese von Naturstoff-basierten Substanzbibliotheken.” 2017. Web. 08 May 2021.

Vancouver:

Nöcker C. Synthese von Naturstoff-basierten Substanzbibliotheken. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2017. [cited 2021 May 08]. Available from: http://dx.doi.org/10.17877/DE290R-17961.

Council of Science Editors:

Nöcker C. Synthese von Naturstoff-basierten Substanzbibliotheken. [Doctoral Dissertation]. Technische Universität Dortmund; 2017. Available from: http://dx.doi.org/10.17877/DE290R-17961

4. Deck, Patrick Hugo. Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1.

Degree: 2002, Universität Dortmund

Different covalently lipidated proteins play decisive roles in biological signal transduction. The lipid modifications of the proteins are usually essential for their correct biological function.… (more)

Subjects/Keywords: Biologie; Organische Synthese; Signaltransduktion; 540

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APA (6th Edition):

Deck, P. H. (2002). Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1. (Thesis). Universität Dortmund. Retrieved from http://hdl.handle.net/2003/5549

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):

Deck, Patrick Hugo. “Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1.” 2002. Thesis, Universität Dortmund. Accessed May 08, 2021. http://hdl.handle.net/2003/5549.

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

MLA Handbook (7th Edition):

Deck, Patrick Hugo. “Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1.” 2002. Web. 08 May 2021.

Vancouver:

Deck PH. Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1. [Internet] [Thesis]. Universität Dortmund; 2002. [cited 2021 May 08]. Available from: http://hdl.handle.net/2003/5549.

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

Council of Science Editors:

Deck PH. Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1. [Thesis]. Universität Dortmund; 2002. Available from: http://hdl.handle.net/2003/5549

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

5. Deck, Patrick Hugo. Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1.

Degree: 2002, Technische Universität Dortmund

 Different covalently lipidated proteins play decisive roles in biological signal transduction. The lipid modifications of the proteins are usually essential for their correct biological function.… (more)

Subjects/Keywords: Organische Synthese; Biologie; Signaltransduktion; 540

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

APA (6th Edition):

Deck, P. H. (2002). Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-15325

Chicago Manual of Style (16th Edition):

Deck, Patrick Hugo. “Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1.” 2002. Doctoral Dissertation, Technische Universität Dortmund. Accessed May 08, 2021. http://dx.doi.org/10.17877/DE290R-15325.

MLA Handbook (7th Edition):

Deck, Patrick Hugo. “Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1.” 2002. Web. 08 May 2021.

Vancouver:

Deck PH. Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2002. [cited 2021 May 08]. Available from: http://dx.doi.org/10.17877/DE290R-15325.

Council of Science Editors:

Deck PH. Synthese und biologische Evaluierung von Inhibitoren der Acyl-Protein-Thioesterase 1. [Doctoral Dissertation]. Technische Universität Dortmund; 2002. Available from: http://dx.doi.org/10.17877/DE290R-15325

6. Kaul, Sandra. Synthese hochsubstituierter Thiazolidinone, Pyrrole und Benzo[h]chinoline für elektrochemische und mikrobiologische Anwendungen.

Degree: 2018, Technische Universität Dortmund

Als chemischer Grundbaustein in dieser Arbeit diente das 1,1,3,4,4-Pentachlor-2-nitrobuta- 1,3-dien (PCNiB), welches mit unterschiedlichen Mercaptanen umgesetzt werden kann. Ausgehend von den derart zugänglichen Sulfanyl-substituierten Butadienen… (more)

Subjects/Keywords: Abschlussarbeit; doctoral thesis; ddc:540; Organische Synthese  – Pyrrole  – Benzo[h]chinoline

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APA (6th Edition):

Kaul, S. (2018). Synthese hochsubstituierter Thiazolidinone, Pyrrole und Benzo[h]chinoline für elektrochemische und mikrobiologische Anwendungen. (Thesis). Technische Universität Dortmund. Retrieved from https://doi.org/10.21268/20180722-200854 ; https://nbn-resolving.org/urn:nbn:de:gbv:104-20180904-082933-5 ; https://dokumente.ub.tu-clausthal.de/receive/clausthal_mods_00000627 ; https://dokumente.ub.tu-clausthal.de/servlets/MCRFileNodeServlet/clausthal_derivate_00000412/Db113695.pdf

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):

Kaul, Sandra. “Synthese hochsubstituierter Thiazolidinone, Pyrrole und Benzo[h]chinoline für elektrochemische und mikrobiologische Anwendungen.” 2018. Thesis, Technische Universität Dortmund. Accessed May 08, 2021. https://doi.org/10.21268/20180722-200854 ; https://nbn-resolving.org/urn:nbn:de:gbv:104-20180904-082933-5 ; https://dokumente.ub.tu-clausthal.de/receive/clausthal_mods_00000627 ; https://dokumente.ub.tu-clausthal.de/servlets/MCRFileNodeServlet/clausthal_derivate_00000412/Db113695.pdf.

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

MLA Handbook (7th Edition):

Kaul, Sandra. “Synthese hochsubstituierter Thiazolidinone, Pyrrole und Benzo[h]chinoline für elektrochemische und mikrobiologische Anwendungen.” 2018. Web. 08 May 2021.

Vancouver:

Kaul S. Synthese hochsubstituierter Thiazolidinone, Pyrrole und Benzo[h]chinoline für elektrochemische und mikrobiologische Anwendungen. [Internet] [Thesis]. Technische Universität Dortmund; 2018. [cited 2021 May 08]. Available from: https://doi.org/10.21268/20180722-200854 ; https://nbn-resolving.org/urn:nbn:de:gbv:104-20180904-082933-5 ; https://dokumente.ub.tu-clausthal.de/receive/clausthal_mods_00000627 ; https://dokumente.ub.tu-clausthal.de/servlets/MCRFileNodeServlet/clausthal_derivate_00000412/Db113695.pdf.

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

Council of Science Editors:

Kaul S. Synthese hochsubstituierter Thiazolidinone, Pyrrole und Benzo[h]chinoline für elektrochemische und mikrobiologische Anwendungen. [Thesis]. Technische Universität Dortmund; 2018. Available from: https://doi.org/10.21268/20180722-200854 ; https://nbn-resolving.org/urn:nbn:de:gbv:104-20180904-082933-5 ; https://dokumente.ub.tu-clausthal.de/receive/clausthal_mods_00000627 ; https://dokumente.ub.tu-clausthal.de/servlets/MCRFileNodeServlet/clausthal_derivate_00000412/Db113695.pdf

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


Ruhr Universität Bochum

7. Schulz, Frank. Monooxygenases : experiments to turn a class of enzymes into a toolbox for biocatalysis.

Degree: 2007, Ruhr Universität Bochum

 Biocatalysis, the use of natural catalysts (enzymes) for the selective and environmentally friendly conversion of synthetic chemicals for pharmaceutical, agrochemical or fine chemical applications has… (more)

Subjects/Keywords: Biokatalyse; Organische Synthese; Biochemie; Enzymkatalyse; Asymmetrische Synthese

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APA (6th Edition):

Schulz, F. (2007). Monooxygenases : experiments to turn a class of enzymes into a toolbox for biocatalysis. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-22582

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):

Schulz, Frank. “Monooxygenases : experiments to turn a class of enzymes into a toolbox for biocatalysis.” 2007. Thesis, Ruhr Universität Bochum. Accessed May 08, 2021. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-22582.

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

MLA Handbook (7th Edition):

Schulz, Frank. “Monooxygenases : experiments to turn a class of enzymes into a toolbox for biocatalysis.” 2007. Web. 08 May 2021.

Vancouver:

Schulz F. Monooxygenases : experiments to turn a class of enzymes into a toolbox for biocatalysis. [Internet] [Thesis]. Ruhr Universität Bochum; 2007. [cited 2021 May 08]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-22582.

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

Council of Science Editors:

Schulz F. Monooxygenases : experiments to turn a class of enzymes into a toolbox for biocatalysis. [Thesis]. Ruhr Universität Bochum; 2007. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-22582

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


University of Vienna

8. Dank, Christian. Synthesis of novel antimalarials.

Degree: 2015, University of Vienna

Die Tropenkrankheit Malaria spielte eine große und einflussreiche Rolle in der Geschichte der Menschheit. Noch am heutigen Tag ist beinahe die halbe Weltbevölkerung gefährdet, mit… (more)

Subjects/Keywords: 35.50 Organische Chemie: Allgemeines; 44.42 Pharmazeutische Chemie; 35.51 Organische Reaktionen, Stereochemie; Malaria / Synthese / Wirkstoff / Konformationsaufklärung; Malaria / Synthesis / antimalarial / configurational analysis

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APA (6th Edition):

Dank, C. (2015). Synthesis of novel antimalarials. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/39301/

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):

Dank, Christian. “Synthesis of novel antimalarials.” 2015. Thesis, University of Vienna. Accessed May 08, 2021. http://othes.univie.ac.at/39301/.

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

MLA Handbook (7th Edition):

Dank, Christian. “Synthesis of novel antimalarials.” 2015. Web. 08 May 2021.

Vancouver:

Dank C. Synthesis of novel antimalarials. [Internet] [Thesis]. University of Vienna; 2015. [cited 2021 May 08]. Available from: http://othes.univie.ac.at/39301/.

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

Council of Science Editors:

Dank C. Synthesis of novel antimalarials. [Thesis]. University of Vienna; 2015. Available from: http://othes.univie.ac.at/39301/

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


University of Vienna

9. Kiesenhofer, Gabriel. Synthetic studies toward molecules for protein NMR.

Degree: 2020, University of Vienna

 Proteine und Peptide stellen ein zentrales Element des menschlichen wie auch jedes anderen Organismus dar. Ihre Aufgaben umfassen das Aufrechterhalten von Strukturen, die Funktion als… (more)

Subjects/Keywords: 35.52 Präparative Organische Chemie; 35.62 Aminosäuren, Peptide, Eiweiße; Protein NMR / Prolin / organische Synthese / Fluor / Fluor NMR / PhenoFluor

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APA (6th Edition):

Kiesenhofer, G. (2020). Synthetic studies toward molecules for protein NMR. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/62694/

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):

Kiesenhofer, Gabriel. “Synthetic studies toward molecules for protein NMR.” 2020. Thesis, University of Vienna. Accessed May 08, 2021. http://othes.univie.ac.at/62694/.

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

MLA Handbook (7th Edition):

Kiesenhofer, Gabriel. “Synthetic studies toward molecules for protein NMR.” 2020. Web. 08 May 2021.

Vancouver:

Kiesenhofer G. Synthetic studies toward molecules for protein NMR. [Internet] [Thesis]. University of Vienna; 2020. [cited 2021 May 08]. Available from: http://othes.univie.ac.at/62694/.

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

Council of Science Editors:

Kiesenhofer G. Synthetic studies toward molecules for protein NMR. [Thesis]. University of Vienna; 2020. Available from: http://othes.univie.ac.at/62694/

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

10. Leßmann, Torben. Stereoselektive Synthese von α, β -ungesättigten δ-Laktonen an der festen Phase und Protein-Modifikation durch Palladium-Katalyse.

Degree: 2007, Technische Universität Dortmund

 Die Arbeit beschreibt die Synthese naturstoffabgeleiteter Verbindungen am polymeren Träger und Palladium-katalysierte Kreuzkupplungsreaktionen an Peptiden und Proteinen. Naturstoffe mit einer α,β-ungesättigten -Lakton-Einheit weisen eine Vielzahl… (more)

Subjects/Keywords: Asymmetrische Synthese; Chemische Biologie; Kombinatorische Chemie; Naturstoffe; Organische Chemie; Sonogashira-Reaktion; 610

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APA (6th Edition):

Leßmann, T. (2007). Stereoselektive Synthese von α, β -ungesättigten δ-Laktonen an der festen Phase und Protein-Modifikation durch Palladium-Katalyse. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/23302

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):

Leßmann, Torben. “Stereoselektive Synthese von α, β -ungesättigten δ-Laktonen an der festen Phase und Protein-Modifikation durch Palladium-Katalyse.” 2007. Thesis, Technische Universität Dortmund. Accessed May 08, 2021. http://hdl.handle.net/2003/23302.

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

MLA Handbook (7th Edition):

Leßmann, Torben. “Stereoselektive Synthese von α, β -ungesättigten δ-Laktonen an der festen Phase und Protein-Modifikation durch Palladium-Katalyse.” 2007. Web. 08 May 2021.

Vancouver:

Leßmann T. Stereoselektive Synthese von α, β -ungesättigten δ-Laktonen an der festen Phase und Protein-Modifikation durch Palladium-Katalyse. [Internet] [Thesis]. Technische Universität Dortmund; 2007. [cited 2021 May 08]. Available from: http://hdl.handle.net/2003/23302.

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

Council of Science Editors:

Leßmann T. Stereoselektive Synthese von α, β -ungesättigten δ-Laktonen an der festen Phase und Protein-Modifikation durch Palladium-Katalyse. [Thesis]. Technische Universität Dortmund; 2007. Available from: http://hdl.handle.net/2003/23302

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


University of Vienna

11. Jahandideh, Saadi Zahra. Synthese von primären (Thio)amiden aus silylierten Iso(thio)cyanaten.

Degree: 2017, University of Vienna

 Im Rahmen der vorliegenden Arbeit konnte gezeigt werden, dass die nukleophile Addition von Organolithiumreagenzien an Silylisothiocyanaten eine effiziente Methode zur Herstellung von primären Thioamiden darstellt,… (more)

Subjects/Keywords: 35.00 Chemie: Allgemeines; 35.50 Organische Chemie: Allgemeines; Synthese von primären (Thio)amiden

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APA (6th Edition):

Jahandideh, S. Z. (2017). Synthese von primären (Thio)amiden aus silylierten Iso(thio)cyanaten. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/46701/

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):

Jahandideh, Saadi Zahra. “Synthese von primären (Thio)amiden aus silylierten Iso(thio)cyanaten.” 2017. Thesis, University of Vienna. Accessed May 08, 2021. http://othes.univie.ac.at/46701/.

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

MLA Handbook (7th Edition):

Jahandideh, Saadi Zahra. “Synthese von primären (Thio)amiden aus silylierten Iso(thio)cyanaten.” 2017. Web. 08 May 2021.

Vancouver:

Jahandideh SZ. Synthese von primären (Thio)amiden aus silylierten Iso(thio)cyanaten. [Internet] [Thesis]. University of Vienna; 2017. [cited 2021 May 08]. Available from: http://othes.univie.ac.at/46701/.

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

Council of Science Editors:

Jahandideh SZ. Synthese von primären (Thio)amiden aus silylierten Iso(thio)cyanaten. [Thesis]. University of Vienna; 2017. Available from: http://othes.univie.ac.at/46701/

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


University of Vienna

12. Riedl, Bettina. Contributions toward the synthesis of bioactive compounds.

Degree: 2018, University of Vienna

Diese Dissertation setzt sich aus zwei Projekten zusammen. Das erste Projekt umfasst einen flexiblen, synthetischen Zugang zu N-Acetylgalaktosamin (GalNAc) and N-Acetylidosamin (IdoNAc). GalNAc, als Teil… (more)

Subjects/Keywords: 35.07 Chemisches Labor, chemische Methoden; Organische Chemie / Asymmetrische Synthese / Kohlenhydrate; Organic Chemistry / Asymmetric Synthesis / Carbohydrates

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APA (6th Edition):

Riedl, B. (2018). Contributions toward the synthesis of bioactive compounds. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/51280/

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):

Riedl, Bettina. “Contributions toward the synthesis of bioactive compounds.” 2018. Thesis, University of Vienna. Accessed May 08, 2021. http://othes.univie.ac.at/51280/.

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

MLA Handbook (7th Edition):

Riedl, Bettina. “Contributions toward the synthesis of bioactive compounds.” 2018. Web. 08 May 2021.

Vancouver:

Riedl B. Contributions toward the synthesis of bioactive compounds. [Internet] [Thesis]. University of Vienna; 2018. [cited 2021 May 08]. Available from: http://othes.univie.ac.at/51280/.

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

Council of Science Editors:

Riedl B. Contributions toward the synthesis of bioactive compounds. [Thesis]. University of Vienna; 2018. Available from: http://othes.univie.ac.at/51280/

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


University of Vienna

13. Dimov, Konstantin. New Perspectives in Asymmetric Organolithium Chemistry: Weinreb Amides Acylations en route to Chiral α-Substituted Ketones.

Degree: 2018, University of Vienna

 Diese Diplomarbeit berichtet von einem Protokoll zur asymmetrishen Lithiierung von N-BocPyrrolidin 1 bei -78 °C für 30 Minuten unter Verwendung des Lösungsmittels CPME, das zwei… (more)

Subjects/Keywords: 35.51 Organische Reaktionen, Stereochemie; N-Boc-Pyrrolidin / CPME / (-)-Spartein / Weinreb Amide / asymmetrische Synthese

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APA (6th Edition):

Dimov, K. (2018). New Perspectives in Asymmetric Organolithium Chemistry: Weinreb Amides Acylations en route to Chiral α-Substituted Ketones. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/55655/

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):

Dimov, Konstantin. “New Perspectives in Asymmetric Organolithium Chemistry: Weinreb Amides Acylations en route to Chiral α-Substituted Ketones.” 2018. Thesis, University of Vienna. Accessed May 08, 2021. http://othes.univie.ac.at/55655/.

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

MLA Handbook (7th Edition):

Dimov, Konstantin. “New Perspectives in Asymmetric Organolithium Chemistry: Weinreb Amides Acylations en route to Chiral α-Substituted Ketones.” 2018. Web. 08 May 2021.

Vancouver:

Dimov K. New Perspectives in Asymmetric Organolithium Chemistry: Weinreb Amides Acylations en route to Chiral α-Substituted Ketones. [Internet] [Thesis]. University of Vienna; 2018. [cited 2021 May 08]. Available from: http://othes.univie.ac.at/55655/.

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

Council of Science Editors:

Dimov K. New Perspectives in Asymmetric Organolithium Chemistry: Weinreb Amides Acylations en route to Chiral α-Substituted Ketones. [Thesis]. University of Vienna; 2018. Available from: http://othes.univie.ac.at/55655/

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


Radboud University Nijmegen

14. Smeets, Frans Leo Maria. Synthese van pyrenophorine.

Degree: 2007, Radboud University Nijmegen

Subjects/Keywords: Pyrenophorine; Epoxydiazomethylketonen; Synthese (chemie); organische synthesen

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APA (6th Edition):

Smeets, F. L. M. (2007). Synthese van pyrenophorine. (Doctoral Dissertation). Radboud University Nijmegen. Retrieved from http://hdl.handle.net/2066/30070

Chicago Manual of Style (16th Edition):

Smeets, Frans Leo Maria. “Synthese van pyrenophorine.” 2007. Doctoral Dissertation, Radboud University Nijmegen. Accessed May 08, 2021. http://hdl.handle.net/2066/30070.

MLA Handbook (7th Edition):

Smeets, Frans Leo Maria. “Synthese van pyrenophorine.” 2007. Web. 08 May 2021.

Vancouver:

Smeets FLM. Synthese van pyrenophorine. [Internet] [Doctoral dissertation]. Radboud University Nijmegen; 2007. [cited 2021 May 08]. Available from: http://hdl.handle.net/2066/30070.

Council of Science Editors:

Smeets FLM. Synthese van pyrenophorine. [Doctoral Dissertation]. Radboud University Nijmegen; 2007. Available from: http://hdl.handle.net/2066/30070


Radboud University Nijmegen

15. Rewinkel, Johannes Bernardus Maria. Synthesis and reactions of oxo sulfines and oxo sulfoxides.

Degree: 2007, Radboud University Nijmegen

Subjects/Keywords: Sulfoxyden; Sulfinen; Synthese (chemie); organische synthesen

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APA (6th Edition):

Rewinkel, J. B. M. (2007). Synthesis and reactions of oxo sulfines and oxo sulfoxides. (Doctoral Dissertation). Radboud University Nijmegen. Retrieved from http://hdl.handle.net/2066/30075

Chicago Manual of Style (16th Edition):

Rewinkel, Johannes Bernardus Maria. “Synthesis and reactions of oxo sulfines and oxo sulfoxides.” 2007. Doctoral Dissertation, Radboud University Nijmegen. Accessed May 08, 2021. http://hdl.handle.net/2066/30075.

MLA Handbook (7th Edition):

Rewinkel, Johannes Bernardus Maria. “Synthesis and reactions of oxo sulfines and oxo sulfoxides.” 2007. Web. 08 May 2021.

Vancouver:

Rewinkel JBM. Synthesis and reactions of oxo sulfines and oxo sulfoxides. [Internet] [Doctoral dissertation]. Radboud University Nijmegen; 2007. [cited 2021 May 08]. Available from: http://hdl.handle.net/2066/30075.

Council of Science Editors:

Rewinkel JBM. Synthesis and reactions of oxo sulfines and oxo sulfoxides. [Doctoral Dissertation]. Radboud University Nijmegen; 2007. Available from: http://hdl.handle.net/2066/30075


Radboud University Nijmegen

16. Legters, Johan. Synthesis and reactions of aziridine-2-carboxylic esters.

Degree: 2007, Radboud University Nijmegen

Subjects/Keywords: Synthese (chemie); Carbonzuren; Esters; organische synthesen

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APA (6th Edition):

Legters, J. (2007). Synthesis and reactions of aziridine-2-carboxylic esters. (Doctoral Dissertation). Radboud University Nijmegen. Retrieved from http://hdl.handle.net/2066/30085

Chicago Manual of Style (16th Edition):

Legters, Johan. “Synthesis and reactions of aziridine-2-carboxylic esters.” 2007. Doctoral Dissertation, Radboud University Nijmegen. Accessed May 08, 2021. http://hdl.handle.net/2066/30085.

MLA Handbook (7th Edition):

Legters, Johan. “Synthesis and reactions of aziridine-2-carboxylic esters.” 2007. Web. 08 May 2021.

Vancouver:

Legters J. Synthesis and reactions of aziridine-2-carboxylic esters. [Internet] [Doctoral dissertation]. Radboud University Nijmegen; 2007. [cited 2021 May 08]. Available from: http://hdl.handle.net/2066/30085.

Council of Science Editors:

Legters J. Synthesis and reactions of aziridine-2-carboxylic esters. [Doctoral Dissertation]. Radboud University Nijmegen; 2007. Available from: http://hdl.handle.net/2066/30085

17. Dittrich, Jan Christoph. Peptid-funktionalisierte Gold(III)-Komplexe als Substrat für Matrix-Metalloprotease 2.

Degree: 2013, Ruhr Universität Bochum

 Es sind viele antiproliferative Gold(I)- und Gold(III)-Komplexe bekannt, die großes Potential als Anti-Tumor-Wirkstoff haben. Jedoch sind diese Verbindungen nicht selektiv gegen karzinogene Zellen. Zur Verbesserung… (more)

Subjects/Keywords: Gold; Peptidsynthese; Festphasentechnik; Komplexe; Organische Synthese

…Inhaltsverzeichnis Synthese von 2-Phenylpyridin-3´-propansäuremethylester-1-gold(III… …x29;trichorid 12 ...... 107 Synthese von 4-Brom-2-Phenylpyridin 14… …108 Synthese von 4-Brom-2-Phenylpyridin-1-gold(III)trichorid 15… …110 Synthese von 2-Phenylquinolin-4-methylcarboxylat-1´-chloromercury 17… …111 Synthese von Methyl-6,6´-dimethyl-[2,2´-bipyridin]-4-carboxylat-1-gold(… 

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APA (6th Edition):

Dittrich, J. C. (2013). Peptid-funktionalisierte Gold(III)-Komplexe als Substrat für Matrix-Metalloprotease 2. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-39390

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):

Dittrich, Jan Christoph. “Peptid-funktionalisierte Gold(III)-Komplexe als Substrat für Matrix-Metalloprotease 2.” 2013. Thesis, Ruhr Universität Bochum. Accessed May 08, 2021. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-39390.

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

MLA Handbook (7th Edition):

Dittrich, Jan Christoph. “Peptid-funktionalisierte Gold(III)-Komplexe als Substrat für Matrix-Metalloprotease 2.” 2013. Web. 08 May 2021.

Vancouver:

Dittrich JC. Peptid-funktionalisierte Gold(III)-Komplexe als Substrat für Matrix-Metalloprotease 2. [Internet] [Thesis]. Ruhr Universität Bochum; 2013. [cited 2021 May 08]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-39390.

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

Council of Science Editors:

Dittrich JC. Peptid-funktionalisierte Gold(III)-Komplexe als Substrat für Matrix-Metalloprotease 2. [Thesis]. Ruhr Universität Bochum; 2013. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-39390

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


Ruhr Universität Bochum

18. Mastalerz, Michael. Funktionalisierte Calix[4]arene : Synthese und supramolekulare Eigenschaften.

Degree: 2005, Ruhr Universität Bochum

 Die Dissertation behandelt zum einen die gezielte Palladium-vermittelte Synthese von π-elektronenreichen Calixarenen, welche z. T. als potentielle Wirtmoleküle zur Komplexierung organischer Kationen getestet wurden. Über… (more)

Subjects/Keywords: Organische Chemie / Synthese; Supramolekulare Chemie; Metacyclophane; Photochemie; Kristallstrukturanalyse

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APA (6th Edition):

Mastalerz, M. (2005). Funktionalisierte Calix[4]arene : Synthese und supramolekulare Eigenschaften. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-14611

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):

Mastalerz, Michael. “Funktionalisierte Calix[4]arene : Synthese und supramolekulare Eigenschaften.” 2005. Thesis, Ruhr Universität Bochum. Accessed May 08, 2021. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-14611.

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

MLA Handbook (7th Edition):

Mastalerz, Michael. “Funktionalisierte Calix[4]arene : Synthese und supramolekulare Eigenschaften.” 2005. Web. 08 May 2021.

Vancouver:

Mastalerz M. Funktionalisierte Calix[4]arene : Synthese und supramolekulare Eigenschaften. [Internet] [Thesis]. Ruhr Universität Bochum; 2005. [cited 2021 May 08]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-14611.

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

Council of Science Editors:

Mastalerz M. Funktionalisierte Calix[4]arene : Synthese und supramolekulare Eigenschaften. [Thesis]. Ruhr Universität Bochum; 2005. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-14611

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


Ruhr Universität Bochum

19. Eipper, Andreas. Neue Methoden für die gerichtete Evolution von Enzymen.

Degree: 2002, Ruhr Universität Bochum

 Thema der vorliegenden Arbeit war die Entwicklung von effizienten Strategien sowie neuen, wirkungsvollen Werkzeugen für die Gerichtete Evolution von Enzymen. Die Etablierung neuer Mutagenesestrategien und… (more)

Subjects/Keywords: Organische Chemie; Asymmetrische Synthese; Enzym; Mutagenese; Heubacillus

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APA (6th Edition):

Eipper, A. (2002). Neue Methoden für die gerichtete Evolution von Enzymen. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-6166

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):

Eipper, Andreas. “Neue Methoden für die gerichtete Evolution von Enzymen.” 2002. Thesis, Ruhr Universität Bochum. Accessed May 08, 2021. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-6166.

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

MLA Handbook (7th Edition):

Eipper, Andreas. “Neue Methoden für die gerichtete Evolution von Enzymen.” 2002. Web. 08 May 2021.

Vancouver:

Eipper A. Neue Methoden für die gerichtete Evolution von Enzymen. [Internet] [Thesis]. Ruhr Universität Bochum; 2002. [cited 2021 May 08]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-6166.

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

Council of Science Editors:

Eipper A. Neue Methoden für die gerichtete Evolution von Enzymen. [Thesis]. Ruhr Universität Bochum; 2002. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-6166

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


Ruhr Universität Bochum

20. Maywald, Matthias. Methodenentwicklung zur Anwendung genetischer Optimierungsstrategien auf semisynthetische Enzyme.

Degree: 2005, Ruhr Universität Bochum

 Die vorliegende Arbeit befasst sich mit semisynthetischen Enzymen, das heißt Enzymen, deren katalytisch aktives Zentrum zuvor in einem chemischen Modifikationsschritt in ein Protein eingebaut wurde.… (more)

Subjects/Keywords: Übergangsmetall; Streptavidin; Enzyminhibitor; Asymmetrische Synthese / Katalyse; Automation / Organische Chemie

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APA (6th Edition):

Maywald, M. (2005). Methodenentwicklung zur Anwendung genetischer Optimierungsstrategien auf semisynthetische Enzyme. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-14107

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):

Maywald, Matthias. “Methodenentwicklung zur Anwendung genetischer Optimierungsstrategien auf semisynthetische Enzyme.” 2005. Thesis, Ruhr Universität Bochum. Accessed May 08, 2021. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-14107.

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

MLA Handbook (7th Edition):

Maywald, Matthias. “Methodenentwicklung zur Anwendung genetischer Optimierungsstrategien auf semisynthetische Enzyme.” 2005. Web. 08 May 2021.

Vancouver:

Maywald M. Methodenentwicklung zur Anwendung genetischer Optimierungsstrategien auf semisynthetische Enzyme. [Internet] [Thesis]. Ruhr Universität Bochum; 2005. [cited 2021 May 08]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-14107.

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

Council of Science Editors:

Maywald M. Methodenentwicklung zur Anwendung genetischer Optimierungsstrategien auf semisynthetische Enzyme. [Thesis]. Ruhr Universität Bochum; 2005. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-14107

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


Johannes Gutenberg Universität Mainz

21. Rieger, Ralph. Extended donor and acceptor molecules for organic electronics.

Degree: 2009, Johannes Gutenberg Universität Mainz

 Die Untersuchung von halbleitenden Materialien auf der Basis von organischen Molekülen stellt ein Gebiet der angewandten Forschung an der Schwelle zur industriellen Nutzung dar. Geringes… (more)

Subjects/Keywords: organische Elektronik, PAK, Polythiophen, Donor-Akzeptor, Synthese; organic electronics, PAH, polythiophene, donor acceptor, synthesis; Chemistry and allied sciences

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APA (6th Edition):

Rieger, R. (2009). Extended donor and acceptor molecules for organic electronics. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2010/2237/

Chicago Manual of Style (16th Edition):

Rieger, Ralph. “Extended donor and acceptor molecules for organic electronics.” 2009. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed May 08, 2021. http://ubm.opus.hbz-nrw.de/volltexte/2010/2237/.

MLA Handbook (7th Edition):

Rieger, Ralph. “Extended donor and acceptor molecules for organic electronics.” 2009. Web. 08 May 2021.

Vancouver:

Rieger R. Extended donor and acceptor molecules for organic electronics. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2009. [cited 2021 May 08]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2010/2237/.

Council of Science Editors:

Rieger R. Extended donor and acceptor molecules for organic electronics. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2009. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2010/2237/

22. Jensen, Jon Tangaa. Studies towards the total synthesis of latrunculin A and latrunculin B.

Degree: 2005, Universität Dortmund

Subjects/Keywords: latrunculin A; latrunculin B; Organische Synthese; 540

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APA (6th Edition):

Jensen, J. T. (2005). Studies towards the total synthesis of latrunculin A and latrunculin B. (Thesis). Universität Dortmund. Retrieved from http://hdl.handle.net/2003/20359

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):

Jensen, Jon Tangaa. “Studies towards the total synthesis of latrunculin A and latrunculin B.” 2005. Thesis, Universität Dortmund. Accessed May 08, 2021. http://hdl.handle.net/2003/20359.

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

MLA Handbook (7th Edition):

Jensen, Jon Tangaa. “Studies towards the total synthesis of latrunculin A and latrunculin B.” 2005. Web. 08 May 2021.

Vancouver:

Jensen JT. Studies towards the total synthesis of latrunculin A and latrunculin B. [Internet] [Thesis]. Universität Dortmund; 2005. [cited 2021 May 08]. Available from: http://hdl.handle.net/2003/20359.

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

Council of Science Editors:

Jensen JT. Studies towards the total synthesis of latrunculin A and latrunculin B. [Thesis]. Universität Dortmund; 2005. Available from: http://hdl.handle.net/2003/20359

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

23. Bell, R.P.L. Total synthesis of lactarane and marasmane sesquiterpenes.

Degree: 2000, Agricultural University

  Lactarane and marasmane sesquiterpenes are mostly found in nature as metabolites from mushrooms of the genera Lactarius and Russula . Because a considerable number… (more)

Subjects/Keywords: synthese; sesquiterpenen; Organische chemie; synthesis; sesquiterpenes; Organic Chemistry

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APA (6th Edition):

Bell, R. P. L. (2000). Total synthesis of lactarane and marasmane sesquiterpenes. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/63947 ; urn:nbn:nl:ui:32-63947 ; urn:nbn:nl:ui:32-63947 ; http://library.wur.nl/WebQuery/wurpubs/63947

Chicago Manual of Style (16th Edition):

Bell, R P L. “Total synthesis of lactarane and marasmane sesquiterpenes.” 2000. Doctoral Dissertation, Agricultural University. Accessed May 08, 2021. http://library.wur.nl/WebQuery/wurpubs/63947 ; urn:nbn:nl:ui:32-63947 ; urn:nbn:nl:ui:32-63947 ; http://library.wur.nl/WebQuery/wurpubs/63947.

MLA Handbook (7th Edition):

Bell, R P L. “Total synthesis of lactarane and marasmane sesquiterpenes.” 2000. Web. 08 May 2021.

Vancouver:

Bell RPL. Total synthesis of lactarane and marasmane sesquiterpenes. [Internet] [Doctoral dissertation]. Agricultural University; 2000. [cited 2021 May 08]. Available from: http://library.wur.nl/WebQuery/wurpubs/63947 ; urn:nbn:nl:ui:32-63947 ; urn:nbn:nl:ui:32-63947 ; http://library.wur.nl/WebQuery/wurpubs/63947.

Council of Science Editors:

Bell RPL. Total synthesis of lactarane and marasmane sesquiterpenes. [Doctoral Dissertation]. Agricultural University; 2000. Available from: http://library.wur.nl/WebQuery/wurpubs/63947 ; urn:nbn:nl:ui:32-63947 ; urn:nbn:nl:ui:32-63947 ; http://library.wur.nl/WebQuery/wurpubs/63947


University of Groningen

24. van Oeveren, Arjan. 5-Alkoxy-2(5H)-furanones in asymmetric synthesis.

Degree: PhD, 1996, University of Groningen

 Je kunt je afvragen waarom je stoffen na zou maken, die in de natuur voorkomen. Het is soms eenvoudiger om een boom om te hakken… (more)

Subjects/Keywords: Proefschriften (vorm); Synthese (chemie); Enantiomeren; 35.52 organische synthesen

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APA (6th Edition):

van Oeveren, A. (1996). 5-Alkoxy-2(5H)-furanones in asymmetric synthesis. (Doctoral Dissertation). University of Groningen. Retrieved from http://hdl.handle.net/11370/866a9a82-ed57-4b31-b257-f5e9f9922b25

Chicago Manual of Style (16th Edition):

van Oeveren, Arjan. “5-Alkoxy-2(5H)-furanones in asymmetric synthesis.” 1996. Doctoral Dissertation, University of Groningen. Accessed May 08, 2021. http://hdl.handle.net/11370/866a9a82-ed57-4b31-b257-f5e9f9922b25.

MLA Handbook (7th Edition):

van Oeveren, Arjan. “5-Alkoxy-2(5H)-furanones in asymmetric synthesis.” 1996. Web. 08 May 2021.

Vancouver:

van Oeveren A. 5-Alkoxy-2(5H)-furanones in asymmetric synthesis. [Internet] [Doctoral dissertation]. University of Groningen; 1996. [cited 2021 May 08]. Available from: http://hdl.handle.net/11370/866a9a82-ed57-4b31-b257-f5e9f9922b25.

Council of Science Editors:

van Oeveren A. 5-Alkoxy-2(5H)-furanones in asymmetric synthesis. [Doctoral Dissertation]. University of Groningen; 1996. Available from: http://hdl.handle.net/11370/866a9a82-ed57-4b31-b257-f5e9f9922b25

25. Jensen, Jon Tangaa. Studies towards the total synthesis of latrunculin A and latrunculin B.

Degree: 2005, Technische Universität Dortmund

Subjects/Keywords: Organische Synthese; latrunculin A; latrunculin B; 540

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

APA (6th Edition):

Jensen, J. T. (2005). Studies towards the total synthesis of latrunculin A and latrunculin B. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-7831

Chicago Manual of Style (16th Edition):

Jensen, Jon Tangaa. “Studies towards the total synthesis of latrunculin A and latrunculin B.” 2005. Doctoral Dissertation, Technische Universität Dortmund. Accessed May 08, 2021. http://dx.doi.org/10.17877/DE290R-7831.

MLA Handbook (7th Edition):

Jensen, Jon Tangaa. “Studies towards the total synthesis of latrunculin A and latrunculin B.” 2005. Web. 08 May 2021.

Vancouver:

Jensen JT. Studies towards the total synthesis of latrunculin A and latrunculin B. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2005. [cited 2021 May 08]. Available from: http://dx.doi.org/10.17877/DE290R-7831.

Council of Science Editors:

Jensen JT. Studies towards the total synthesis of latrunculin A and latrunculin B. [Doctoral Dissertation]. Technische Universität Dortmund; 2005. Available from: http://dx.doi.org/10.17877/DE290R-7831

26. Kesselmans, R.P.W. Total synthesis of all stereoisomers of eudesm-II-en-4-ol.

Degree: 1992, Agricultural University

  In this thesis the total synthesis of all stereoisomers of eudesm-11-en-4-ol e.g. selin-11-en-4α-ol I , intermedeol II , neointermedeol III , paradisiol IV ,… (more)

Subjects/Keywords: terpenen; synthese; Organische chemie; terpenoids; synthesis; Organic Chemistry

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APA (6th Edition):

Kesselmans, R. P. W. (1992). Total synthesis of all stereoisomers of eudesm-II-en-4-ol. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/17226 ; urn:nbn:nl:ui:32-17226 ; urn:nbn:nl:ui:32-17226 ; http://library.wur.nl/WebQuery/wurpubs/17226

Chicago Manual of Style (16th Edition):

Kesselmans, R P W. “Total synthesis of all stereoisomers of eudesm-II-en-4-ol.” 1992. Doctoral Dissertation, Agricultural University. Accessed May 08, 2021. http://library.wur.nl/WebQuery/wurpubs/17226 ; urn:nbn:nl:ui:32-17226 ; urn:nbn:nl:ui:32-17226 ; http://library.wur.nl/WebQuery/wurpubs/17226.

MLA Handbook (7th Edition):

Kesselmans, R P W. “Total synthesis of all stereoisomers of eudesm-II-en-4-ol.” 1992. Web. 08 May 2021.

Vancouver:

Kesselmans RPW. Total synthesis of all stereoisomers of eudesm-II-en-4-ol. [Internet] [Doctoral dissertation]. Agricultural University; 1992. [cited 2021 May 08]. Available from: http://library.wur.nl/WebQuery/wurpubs/17226 ; urn:nbn:nl:ui:32-17226 ; urn:nbn:nl:ui:32-17226 ; http://library.wur.nl/WebQuery/wurpubs/17226.

Council of Science Editors:

Kesselmans RPW. Total synthesis of all stereoisomers of eudesm-II-en-4-ol. [Doctoral Dissertation]. Agricultural University; 1992. Available from: http://library.wur.nl/WebQuery/wurpubs/17226 ; urn:nbn:nl:ui:32-17226 ; urn:nbn:nl:ui:32-17226 ; http://library.wur.nl/WebQuery/wurpubs/17226

27. Reuvers, J.T.A. The total synthesis of 3Beta-hydroxynagilactone F.

Degree: 1985, Landbouwhogeschool Wageningen

 <p/>The investigations described in this thesis deal with the total synthesis of physiologically active nor- and bisnorditerpenoid dilactones (fig.1).<p/><img src="/wda/abstracts/i1033_1.gif"/><p/>The goal was to design a… (more)

Subjects/Keywords: diterpenoïden; synthese; Organische chemie; diterpenoids; synthesis; Organic Chemistry

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APA (6th Edition):

Reuvers, J. T. A. (1985). The total synthesis of 3Beta-hydroxynagilactone F. (Doctoral Dissertation). Landbouwhogeschool Wageningen. Retrieved from http://library.wur.nl/WebQuery/wurpubs/80971 ; urn:nbn:nl:ui:32-80971 ; urn:nbn:nl:ui:32-80971 ; http://library.wur.nl/WebQuery/wurpubs/80971

Chicago Manual of Style (16th Edition):

Reuvers, J T A. “The total synthesis of 3Beta-hydroxynagilactone F.” 1985. Doctoral Dissertation, Landbouwhogeschool Wageningen. Accessed May 08, 2021. http://library.wur.nl/WebQuery/wurpubs/80971 ; urn:nbn:nl:ui:32-80971 ; urn:nbn:nl:ui:32-80971 ; http://library.wur.nl/WebQuery/wurpubs/80971.

MLA Handbook (7th Edition):

Reuvers, J T A. “The total synthesis of 3Beta-hydroxynagilactone F.” 1985. Web. 08 May 2021.

Vancouver:

Reuvers JTA. The total synthesis of 3Beta-hydroxynagilactone F. [Internet] [Doctoral dissertation]. Landbouwhogeschool Wageningen; 1985. [cited 2021 May 08]. Available from: http://library.wur.nl/WebQuery/wurpubs/80971 ; urn:nbn:nl:ui:32-80971 ; urn:nbn:nl:ui:32-80971 ; http://library.wur.nl/WebQuery/wurpubs/80971.

Council of Science Editors:

Reuvers JTA. The total synthesis of 3Beta-hydroxynagilactone F. [Doctoral Dissertation]. Landbouwhogeschool Wageningen; 1985. Available from: http://library.wur.nl/WebQuery/wurpubs/80971 ; urn:nbn:nl:ui:32-80971 ; urn:nbn:nl:ui:32-80971 ; http://library.wur.nl/WebQuery/wurpubs/80971


University of Groningen

28. Xianming, Hu. Chiral nonracemic 1-Aryl-2,2-dimethyl-1,3-propanediols: reactions and applications in asymmetric synthesis.

Degree: Faculty of Science and Engineering, 1995, University of Groningen

Dit proefschrift beschrijft de studie naar reacties en toepassingen van chirale 1-aryl-2,2-dimethyl-1,3-propaandiolenin de asymmetrische synthese. Chirale 1-aryl-2,2-dimethyl-1,3-propaandiolen kunnen worden gebruikt als chirale synthons in asymmetrische synthese. Cyclische fosforderivaten daarvan waren al bekend vanwege hun uitstekende resolutie eigenschappen.

Subjects/Keywords: Proefschriften (vorm); Aryldimethylpropaandiolen; Chiraliteit, Synthese (chemie); fysische organische chemie

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APA (6th Edition):

Xianming, H. (1995). Chiral nonracemic 1-Aryl-2,2-dimethyl-1,3-propanediols: reactions and applications in asymmetric synthesis. (Doctoral Dissertation). University of Groningen. Retrieved from https://www.rug.nl/research/portal/en/publications/chiral-nonracemic-1aryl22dimethyl13propanediols(954339a8-b631-48fb-a487-15a1cc0df446).html ; urn:nbn:nl:ui:11-dbi/456ebf402f737 ; 954339a8-b631-48fb-a487-15a1cc0df446 ; 11370/954339a8-b631-48fb-a487-15a1cc0df446 ; urn:nbn:nl:ui:11-dbi/456ebf402f737 ; https://www.rug.nl/research/portal/en/publications/chiral-nonracemic-1aryl22dimethyl13propanediols(954339a8-b631-48fb-a487-15a1cc0df446).html

Chicago Manual of Style (16th Edition):

Xianming, Hu. “Chiral nonracemic 1-Aryl-2,2-dimethyl-1,3-propanediols: reactions and applications in asymmetric synthesis.” 1995. Doctoral Dissertation, University of Groningen. Accessed May 08, 2021. https://www.rug.nl/research/portal/en/publications/chiral-nonracemic-1aryl22dimethyl13propanediols(954339a8-b631-48fb-a487-15a1cc0df446).html ; urn:nbn:nl:ui:11-dbi/456ebf402f737 ; 954339a8-b631-48fb-a487-15a1cc0df446 ; 11370/954339a8-b631-48fb-a487-15a1cc0df446 ; urn:nbn:nl:ui:11-dbi/456ebf402f737 ; https://www.rug.nl/research/portal/en/publications/chiral-nonracemic-1aryl22dimethyl13propanediols(954339a8-b631-48fb-a487-15a1cc0df446).html.

MLA Handbook (7th Edition):

Xianming, Hu. “Chiral nonracemic 1-Aryl-2,2-dimethyl-1,3-propanediols: reactions and applications in asymmetric synthesis.” 1995. Web. 08 May 2021.

Vancouver:

Xianming H. Chiral nonracemic 1-Aryl-2,2-dimethyl-1,3-propanediols: reactions and applications in asymmetric synthesis. [Internet] [Doctoral dissertation]. University of Groningen; 1995. [cited 2021 May 08]. Available from: https://www.rug.nl/research/portal/en/publications/chiral-nonracemic-1aryl22dimethyl13propanediols(954339a8-b631-48fb-a487-15a1cc0df446).html ; urn:nbn:nl:ui:11-dbi/456ebf402f737 ; 954339a8-b631-48fb-a487-15a1cc0df446 ; 11370/954339a8-b631-48fb-a487-15a1cc0df446 ; urn:nbn:nl:ui:11-dbi/456ebf402f737 ; https://www.rug.nl/research/portal/en/publications/chiral-nonracemic-1aryl22dimethyl13propanediols(954339a8-b631-48fb-a487-15a1cc0df446).html.

Council of Science Editors:

Xianming H. Chiral nonracemic 1-Aryl-2,2-dimethyl-1,3-propanediols: reactions and applications in asymmetric synthesis. [Doctoral Dissertation]. University of Groningen; 1995. Available from: https://www.rug.nl/research/portal/en/publications/chiral-nonracemic-1aryl22dimethyl13propanediols(954339a8-b631-48fb-a487-15a1cc0df446).html ; urn:nbn:nl:ui:11-dbi/456ebf402f737 ; 954339a8-b631-48fb-a487-15a1cc0df446 ; 11370/954339a8-b631-48fb-a487-15a1cc0df446 ; urn:nbn:nl:ui:11-dbi/456ebf402f737 ; https://www.rug.nl/research/portal/en/publications/chiral-nonracemic-1aryl22dimethyl13propanediols(954339a8-b631-48fb-a487-15a1cc0df446).html


University of Groningen

29. Jansen, Johan Franz Gradus Antonius. Stereoselective 1,4-additions.

Degree: Faculty of Science and Engineering, 1991, University of Groningen

 De synthese van enantiomeer zuivere verbindingen speelt een steeds grotere rol in de chemie. Met name voor geneesmiddelen is het belangrijk om specifiek één enantiomeer… (more)

Subjects/Keywords: Proefschriften (vorm); Additiereacties; Synthese (chemie); Enantiomeren; 35.52 organische synthesen

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

APA (6th Edition):

Jansen, J. F. G. A. (1991). Stereoselective 1,4-additions. (Doctoral Dissertation). University of Groningen. Retrieved from https://www.rug.nl/research/portal/en/publications/stereoselective-14additions(7d11c5ec-1240-4845-9f47-0630e71486d2).html ; urn:nbn:nl:ui:11-dbi/487f0eadd03a9 ; 7d11c5ec-1240-4845-9f47-0630e71486d2 ; 11370/7d11c5ec-1240-4845-9f47-0630e71486d2 ; urn:nbn:nl:ui:11-dbi/487f0eadd03a9 ; https://www.rug.nl/research/portal/en/publications/stereoselective-14additions(7d11c5ec-1240-4845-9f47-0630e71486d2).html

Chicago Manual of Style (16th Edition):

Jansen, Johan Franz Gradus Antonius. “Stereoselective 1,4-additions.” 1991. Doctoral Dissertation, University of Groningen. Accessed May 08, 2021. https://www.rug.nl/research/portal/en/publications/stereoselective-14additions(7d11c5ec-1240-4845-9f47-0630e71486d2).html ; urn:nbn:nl:ui:11-dbi/487f0eadd03a9 ; 7d11c5ec-1240-4845-9f47-0630e71486d2 ; 11370/7d11c5ec-1240-4845-9f47-0630e71486d2 ; urn:nbn:nl:ui:11-dbi/487f0eadd03a9 ; https://www.rug.nl/research/portal/en/publications/stereoselective-14additions(7d11c5ec-1240-4845-9f47-0630e71486d2).html.

MLA Handbook (7th Edition):

Jansen, Johan Franz Gradus Antonius. “Stereoselective 1,4-additions.” 1991. Web. 08 May 2021.

Vancouver:

Jansen JFGA. Stereoselective 1,4-additions. [Internet] [Doctoral dissertation]. University of Groningen; 1991. [cited 2021 May 08]. Available from: https://www.rug.nl/research/portal/en/publications/stereoselective-14additions(7d11c5ec-1240-4845-9f47-0630e71486d2).html ; urn:nbn:nl:ui:11-dbi/487f0eadd03a9 ; 7d11c5ec-1240-4845-9f47-0630e71486d2 ; 11370/7d11c5ec-1240-4845-9f47-0630e71486d2 ; urn:nbn:nl:ui:11-dbi/487f0eadd03a9 ; https://www.rug.nl/research/portal/en/publications/stereoselective-14additions(7d11c5ec-1240-4845-9f47-0630e71486d2).html.

Council of Science Editors:

Jansen JFGA. Stereoselective 1,4-additions. [Doctoral Dissertation]. University of Groningen; 1991. Available from: https://www.rug.nl/research/portal/en/publications/stereoselective-14additions(7d11c5ec-1240-4845-9f47-0630e71486d2).html ; urn:nbn:nl:ui:11-dbi/487f0eadd03a9 ; 7d11c5ec-1240-4845-9f47-0630e71486d2 ; 11370/7d11c5ec-1240-4845-9f47-0630e71486d2 ; urn:nbn:nl:ui:11-dbi/487f0eadd03a9 ; https://www.rug.nl/research/portal/en/publications/stereoselective-14additions(7d11c5ec-1240-4845-9f47-0630e71486d2).html


University of Groningen

30. van der Deen, Johanna. Enantiopure furanones and pyranones: New approaches and applications.

Degree: 2001, University of Groningen

Subjects/Keywords: Proefschriften (vorm); Stereoselectiviteit, Synthese (chemie),; Furfural; fysische organische chemie

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

APA (6th Edition):

van der Deen, J. (2001). Enantiopure furanones and pyranones: New approaches and applications. (Doctoral Dissertation). University of Groningen. Retrieved from https://www.rug.nl/research/portal/en/publications/enantiopure-furanones-and-pyranones(d6b996a5-41c9-4f35-a111-d9c40fde121a).html ; urn:nbn:nl:ui:11-dbi/4a9260a6f0769 ; d6b996a5-41c9-4f35-a111-d9c40fde121a ; 11370/d6b996a5-41c9-4f35-a111-d9c40fde121a ; urn:isbn:9036714265 ; urn:nbn:nl:ui:11-dbi/4a9260a6f0769 ; https://www.rug.nl/research/portal/en/publications/enantiopure-furanones-and-pyranones(d6b996a5-41c9-4f35-a111-d9c40fde121a).html

Chicago Manual of Style (16th Edition):

van der Deen, Johanna. “Enantiopure furanones and pyranones: New approaches and applications.” 2001. Doctoral Dissertation, University of Groningen. Accessed May 08, 2021. https://www.rug.nl/research/portal/en/publications/enantiopure-furanones-and-pyranones(d6b996a5-41c9-4f35-a111-d9c40fde121a).html ; urn:nbn:nl:ui:11-dbi/4a9260a6f0769 ; d6b996a5-41c9-4f35-a111-d9c40fde121a ; 11370/d6b996a5-41c9-4f35-a111-d9c40fde121a ; urn:isbn:9036714265 ; urn:nbn:nl:ui:11-dbi/4a9260a6f0769 ; https://www.rug.nl/research/portal/en/publications/enantiopure-furanones-and-pyranones(d6b996a5-41c9-4f35-a111-d9c40fde121a).html.

MLA Handbook (7th Edition):

van der Deen, Johanna. “Enantiopure furanones and pyranones: New approaches and applications.” 2001. Web. 08 May 2021.

Vancouver:

van der Deen J. Enantiopure furanones and pyranones: New approaches and applications. [Internet] [Doctoral dissertation]. University of Groningen; 2001. [cited 2021 May 08]. Available from: https://www.rug.nl/research/portal/en/publications/enantiopure-furanones-and-pyranones(d6b996a5-41c9-4f35-a111-d9c40fde121a).html ; urn:nbn:nl:ui:11-dbi/4a9260a6f0769 ; d6b996a5-41c9-4f35-a111-d9c40fde121a ; 11370/d6b996a5-41c9-4f35-a111-d9c40fde121a ; urn:isbn:9036714265 ; urn:nbn:nl:ui:11-dbi/4a9260a6f0769 ; https://www.rug.nl/research/portal/en/publications/enantiopure-furanones-and-pyranones(d6b996a5-41c9-4f35-a111-d9c40fde121a).html.

Council of Science Editors:

van der Deen J. Enantiopure furanones and pyranones: New approaches and applications. [Doctoral Dissertation]. University of Groningen; 2001. Available from: https://www.rug.nl/research/portal/en/publications/enantiopure-furanones-and-pyranones(d6b996a5-41c9-4f35-a111-d9c40fde121a).html ; urn:nbn:nl:ui:11-dbi/4a9260a6f0769 ; d6b996a5-41c9-4f35-a111-d9c40fde121a ; 11370/d6b996a5-41c9-4f35-a111-d9c40fde121a ; urn:isbn:9036714265 ; urn:nbn:nl:ui:11-dbi/4a9260a6f0769 ; https://www.rug.nl/research/portal/en/publications/enantiopure-furanones-and-pyranones(d6b996a5-41c9-4f35-a111-d9c40fde121a).html

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