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You searched for subject:(Organische chemie). Showing records 1 – 30 of 1111 total matches.

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Ruhr Universität Bochum

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

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 September 15, 2019. 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. 15 Sep 2019.

Vancouver:

Bischof C. Building blocks for multinuclear near-IR luminescent lanthanide complexes. [Internet] [Thesis]. Ruhr Universität Bochum; 2013. [cited 2019 Sep 15]. 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


University of Vienna

2. Malova, Petra. Chiral methylmetals.

Degree: 2010, University of Vienna

Die chemische Stabilität von Fluormethyllithium und die konfigurative Stabilität von verschiedenen Methylpalladiumkomplexen wurden untersucht. Chirale (R)- und (S)-Hydroxy-[D1]methylphosphonsäure, mit ee > 99%, und (R)- und (S)-Amino-[D1]methylphosphonsäure, mit ee > 94%, wurden synthetisiert.

Subjects/Keywords: 35.50 Organische Chemie: Allgemeines; 35.60 Metallorganische Verbindungen; 35.51 Organische Reaktionen, Stereochemie; 35.52 Präparative Organische Chemie; chirale Methylmetalle / Methylpalladiumkomplexe / Phosphonsäuren / Aminomethylphosphonsäuren

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APA (6th Edition):

Malova, P. (2010). Chiral methylmetals. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/10625/

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):

Malova, Petra. “Chiral methylmetals.” 2010. Thesis, University of Vienna. Accessed September 15, 2019. http://othes.univie.ac.at/10625/.

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

MLA Handbook (7th Edition):

Malova, Petra. “Chiral methylmetals.” 2010. Web. 15 Sep 2019.

Vancouver:

Malova P. Chiral methylmetals. [Internet] [Thesis]. University of Vienna; 2010. [cited 2019 Sep 15]. Available from: http://othes.univie.ac.at/10625/.

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

Council of Science Editors:

Malova P. Chiral methylmetals. [Thesis]. University of Vienna; 2010. Available from: http://othes.univie.ac.at/10625/

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


Johannes Gutenberg Universität Mainz

3. Koch, Stefan. Synthesen von C-glycosylierten Aminosäuren und Peptiden unter Einsatz speziell konstruierter Mikroreaktoren.

Degree: 2012, Johannes Gutenberg Universität Mainz

Die chemische Synthese definierter Glycopeptidstrukturen bildet die Basis einiger vielversprechender Ansätze zur Therapie verschiedener Krankheiten. Die Entwicklung hochaffiner Selektininhibitoren könnte der Behandlung chronischer Entzündungen und… (more)

Subjects/Keywords: Glycopeptide, Mikroreaktoren, Organische Chemie; Glycopeptides, Microreactors, Organic Chemistry; Chemistry and allied sciences

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APA (6th Edition):

Koch, S. (2012). Synthesen von C-glycosylierten Aminosäuren und Peptiden unter Einsatz speziell konstruierter Mikroreaktoren. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2014/3772/

Chicago Manual of Style (16th Edition):

Koch, Stefan. “Synthesen von C-glycosylierten Aminosäuren und Peptiden unter Einsatz speziell konstruierter Mikroreaktoren.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 15, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2014/3772/.

MLA Handbook (7th Edition):

Koch, Stefan. “Synthesen von C-glycosylierten Aminosäuren und Peptiden unter Einsatz speziell konstruierter Mikroreaktoren.” 2012. Web. 15 Sep 2019.

Vancouver:

Koch S. Synthesen von C-glycosylierten Aminosäuren und Peptiden unter Einsatz speziell konstruierter Mikroreaktoren. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2019 Sep 15]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3772/.

Council of Science Editors:

Koch S. Synthesen von C-glycosylierten Aminosäuren und Peptiden unter Einsatz speziell konstruierter Mikroreaktoren. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3772/


University of Vienna

4. Lemmerer, Miran. Chemoselective nucleophilic α-amination of amides.

Degree: 2018, University of Vienna

Carbonsäureamide sind in lebenden Organismen omnipräsent. Die Amidbindung spielt eine zentrale Rolle in Proteinenstrukturen, um nur ein Beispiel zu nennen. Wegen ihrer geringen Reaktivität ist… (more)

Subjects/Keywords: 35.52 Präparative Organische Chemie; 35.51 Organische Reaktionen, Stereochemie; Chemoselektive Umpolung / Amide; chemoselective Umpolung / amides

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APA (6th Edition):

Lemmerer, M. (2018). Chemoselective nucleophilic α-amination of amides. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/52890/

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):

Lemmerer, Miran. “Chemoselective nucleophilic α-amination of amides.” 2018. Thesis, University of Vienna. Accessed September 15, 2019. http://othes.univie.ac.at/52890/.

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

MLA Handbook (7th Edition):

Lemmerer, Miran. “Chemoselective nucleophilic α-amination of amides.” 2018. Web. 15 Sep 2019.

Vancouver:

Lemmerer M. Chemoselective nucleophilic α-amination of amides. [Internet] [Thesis]. University of Vienna; 2018. [cited 2019 Sep 15]. Available from: http://othes.univie.ac.at/52890/.

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

Council of Science Editors:

Lemmerer M. Chemoselective nucleophilic α-amination of amides. [Thesis]. University of Vienna; 2018. Available from: http://othes.univie.ac.at/52890/

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


University of Vienna

5. 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 September 15, 2019. 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. 15 Sep 2019.

Vancouver:

Dank C. Synthesis of novel antimalarials. [Internet] [Thesis]. University of Vienna; 2015. [cited 2019 Sep 15]. 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


ETH Zürich

6. Buser, Hans-Peter. Zur Chemie der α-Aminonitrile:: γ,{delta}-Dehydroleucin-Nitril.

Degree: 1985, ETH Zürich

Subjects/Keywords: AMINONITRILE (ORGANISCHE CHEMIE); TERPENE (ORGANISCHE CHEMIE); AMINONITRILES (ORGANIC CHEMISTRY); TERPENES (ORGANIC CHEMISTRY)

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APA (6th Edition):

Buser, H. (1985). Zur Chemie der α-Aminonitrile:: γ,{delta}-Dehydroleucin-Nitril. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/138594

Chicago Manual of Style (16th Edition):

Buser, Hans-Peter. “Zur Chemie der α-Aminonitrile:: γ,{delta}-Dehydroleucin-Nitril.” 1985. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/138594.

MLA Handbook (7th Edition):

Buser, Hans-Peter. “Zur Chemie der α-Aminonitrile:: γ,{delta}-Dehydroleucin-Nitril.” 1985. Web. 15 Sep 2019.

Vancouver:

Buser H. Zur Chemie der α-Aminonitrile:: γ,{delta}-Dehydroleucin-Nitril. [Internet] [Doctoral dissertation]. ETH Zürich; 1985. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/138594.

Council of Science Editors:

Buser H. Zur Chemie der α-Aminonitrile:: γ,{delta}-Dehydroleucin-Nitril. [Doctoral Dissertation]. ETH Zürich; 1985. Available from: http://hdl.handle.net/20.500.11850/138594


ETH Zürich

7. Bold, Guido Hermann. Zur Chemie des 2-Amino-propennitrils.

Degree: 1984, ETH Zürich

Subjects/Keywords: AMINONITRILE (ORGANISCHE CHEMIE); AMINONITRILES (ORGANIC CHEMISTRY)

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APA (6th Edition):

Bold, G. H. (1984). Zur Chemie des 2-Amino-propennitrils. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/138389

Chicago Manual of Style (16th Edition):

Bold, Guido Hermann. “Zur Chemie des 2-Amino-propennitrils.” 1984. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/138389.

MLA Handbook (7th Edition):

Bold, Guido Hermann. “Zur Chemie des 2-Amino-propennitrils.” 1984. Web. 15 Sep 2019.

Vancouver:

Bold GH. Zur Chemie des 2-Amino-propennitrils. [Internet] [Doctoral dissertation]. ETH Zürich; 1984. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/138389.

Council of Science Editors:

Bold GH. Zur Chemie des 2-Amino-propennitrils. [Doctoral Dissertation]. ETH Zürich; 1984. Available from: http://hdl.handle.net/20.500.11850/138389


ETH Zürich

8. Schreiber, Jakob. Zur Totalsynthese von Steroiden.

Degree: 1953, ETH Zürich

Subjects/Keywords: STEROIDE (ORGANISCHE CHEMIE); STEROIDS (ORGANIC CHEMISTRY)

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APA (6th Edition):

Schreiber, J. (1953). Zur Totalsynthese von Steroiden. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/137806

Chicago Manual of Style (16th Edition):

Schreiber, Jakob. “Zur Totalsynthese von Steroiden.” 1953. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/137806.

MLA Handbook (7th Edition):

Schreiber, Jakob. “Zur Totalsynthese von Steroiden.” 1953. Web. 15 Sep 2019.

Vancouver:

Schreiber J. Zur Totalsynthese von Steroiden. [Internet] [Doctoral dissertation]. ETH Zürich; 1953. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/137806.

Council of Science Editors:

Schreiber J. Zur Totalsynthese von Steroiden. [Doctoral Dissertation]. ETH Zürich; 1953. Available from: http://hdl.handle.net/20.500.11850/137806


ETH Zürich

9. Elsinger, Fritz. Umwandlungen an D-Homo-18-nor-Steroiden.

Degree: 1960, ETH Zürich

Subjects/Keywords: STEROIDE (ORGANISCHE CHEMIE); STEROIDS (ORGANIC CHEMISTRY)

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APA (6th Edition):

Elsinger, F. (1960). Umwandlungen an D-Homo-18-nor-Steroiden. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/134165

Chicago Manual of Style (16th Edition):

Elsinger, Fritz. “Umwandlungen an D-Homo-18-nor-Steroiden.” 1960. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/134165.

MLA Handbook (7th Edition):

Elsinger, Fritz. “Umwandlungen an D-Homo-18-nor-Steroiden.” 1960. Web. 15 Sep 2019.

Vancouver:

Elsinger F. Umwandlungen an D-Homo-18-nor-Steroiden. [Internet] [Doctoral dissertation]. ETH Zürich; 1960. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/134165.

Council of Science Editors:

Elsinger F. Umwandlungen an D-Homo-18-nor-Steroiden. [Doctoral Dissertation]. ETH Zürich; 1960. Available from: http://hdl.handle.net/20.500.11850/134165


University of Vienna

10. 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 September 15, 2019. 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. 15 Sep 2019.

Vancouver:

Riedl B. Contributions toward the synthesis of bioactive compounds. [Internet] [Thesis]. University of Vienna; 2018. [cited 2019 Sep 15]. 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

11. Kooyman, R.P.H. Complexes and aggregates of chlorophylls.

Degree: 1980, Landbouwhogeschool Wageningen

 Chlorophyll (Chl) molecules can form complexes in two important ways: by ligation at the magnesium atom and/or by hydrogen bonding at the keto- carbonyl group.… (more)

Subjects/Keywords: chlorofyl; Organische chemie; chlorophyll; Organic Chemistry

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APA (6th Edition):

Kooyman, R. P. H. (1980). Complexes and aggregates of chlorophylls. (Doctoral Dissertation). Landbouwhogeschool Wageningen. Retrieved from http://library.wur.nl/WebQuery/wurpubs/73330 ; urn:nbn:nl:ui:32-73330 ; urn:nbn:nl:ui:32-73330 ; http://library.wur.nl/WebQuery/wurpubs/73330

Chicago Manual of Style (16th Edition):

Kooyman, R P H. “Complexes and aggregates of chlorophylls.” 1980. Doctoral Dissertation, Landbouwhogeschool Wageningen. Accessed September 15, 2019. http://library.wur.nl/WebQuery/wurpubs/73330 ; urn:nbn:nl:ui:32-73330 ; urn:nbn:nl:ui:32-73330 ; http://library.wur.nl/WebQuery/wurpubs/73330.

MLA Handbook (7th Edition):

Kooyman, R P H. “Complexes and aggregates of chlorophylls.” 1980. Web. 15 Sep 2019.

Vancouver:

Kooyman RPH. Complexes and aggregates of chlorophylls. [Internet] [Doctoral dissertation]. Landbouwhogeschool Wageningen; 1980. [cited 2019 Sep 15]. Available from: http://library.wur.nl/WebQuery/wurpubs/73330 ; urn:nbn:nl:ui:32-73330 ; urn:nbn:nl:ui:32-73330 ; http://library.wur.nl/WebQuery/wurpubs/73330.

Council of Science Editors:

Kooyman RPH. Complexes and aggregates of chlorophylls. [Doctoral Dissertation]. Landbouwhogeschool Wageningen; 1980. Available from: http://library.wur.nl/WebQuery/wurpubs/73330 ; urn:nbn:nl:ui:32-73330 ; urn:nbn:nl:ui:32-73330 ; http://library.wur.nl/WebQuery/wurpubs/73330

12. Savenije, T.J. Artificial photosynthesis : towards the development of molecular photodiodes.

Degree: 1997, Agricultural University

  Since quite some time similarities have been noted between the photo-generation of charge carriers (electrons and holes) in a molecular semiconductor and the photosynthetic… (more)

Subjects/Keywords: fotosynthese; Organische chemie; photosynthesis; Organic Chemistry

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APA (6th Edition):

Savenije, T. J. (1997). Artificial photosynthesis : towards the development of molecular photodiodes. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/36493 ; urn:nbn:nl:ui:32-36493 ; urn:nbn:nl:ui:32-36493 ; http://library.wur.nl/WebQuery/wurpubs/36493

Chicago Manual of Style (16th Edition):

Savenije, T J. “Artificial photosynthesis : towards the development of molecular photodiodes.” 1997. Doctoral Dissertation, Agricultural University. Accessed September 15, 2019. http://library.wur.nl/WebQuery/wurpubs/36493 ; urn:nbn:nl:ui:32-36493 ; urn:nbn:nl:ui:32-36493 ; http://library.wur.nl/WebQuery/wurpubs/36493.

MLA Handbook (7th Edition):

Savenije, T J. “Artificial photosynthesis : towards the development of molecular photodiodes.” 1997. Web. 15 Sep 2019.

Vancouver:

Savenije TJ. Artificial photosynthesis : towards the development of molecular photodiodes. [Internet] [Doctoral dissertation]. Agricultural University; 1997. [cited 2019 Sep 15]. Available from: http://library.wur.nl/WebQuery/wurpubs/36493 ; urn:nbn:nl:ui:32-36493 ; urn:nbn:nl:ui:32-36493 ; http://library.wur.nl/WebQuery/wurpubs/36493.

Council of Science Editors:

Savenije TJ. Artificial photosynthesis : towards the development of molecular photodiodes. [Doctoral Dissertation]. Agricultural University; 1997. Available from: http://library.wur.nl/WebQuery/wurpubs/36493 ; urn:nbn:nl:ui:32-36493 ; urn:nbn:nl:ui:32-36493 ; http://library.wur.nl/WebQuery/wurpubs/36493

13. 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 September 15, 2019. 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. 15 Sep 2019.

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 2019 Sep 15]. 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

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

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 September 15, 2019. 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. 15 Sep 2019.

Vancouver:

Jahandideh SZ. Synthese von primären (Thio)amiden aus silylierten Iso(thio)cyanaten. [Internet] [Thesis]. University of Vienna; 2017. [cited 2019 Sep 15]. 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

15. Richter, Anja. Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen.

Degree: 2011, Technische Universität Dortmund

 Die phytotoxische Wirkung des Naturstoffs Fusiocccin A, erstmals isoliert von Ballio et al. aus dem Pilz Fusicoccum amygadali, lässt sich auf die Stabilisierung der Interaktion… (more)

Subjects/Keywords: Fusicoccin; Organische Chemie; Protein-Protein-Interaktionen; Totalsynthese; 540; 570

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APA (6th Edition):

Richter, A. (2011). Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/29051

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):

Richter, Anja. “Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen.” 2011. Thesis, Technische Universität Dortmund. Accessed September 15, 2019. http://hdl.handle.net/2003/29051.

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

MLA Handbook (7th Edition):

Richter, Anja. “Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen.” 2011. Web. 15 Sep 2019.

Vancouver:

Richter A. Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen. [Internet] [Thesis]. Technische Universität Dortmund; 2011. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/2003/29051.

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

Council of Science Editors:

Richter A. Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen. [Thesis]. Technische Universität Dortmund; 2011. Available from: http://hdl.handle.net/2003/29051

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


Radboud University Nijmegen

16. Raaijmakers, Henricus Wilhelmus Carolina. Some aspects of the synthesis and properties of carbohydrate-based amphiphiles.

Degree: 2007, Radboud University Nijmegen

Subjects/Keywords: Surfactantia; Koolhydraten; koolhydraten (organische chemie)

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APA (6th Edition):

Raaijmakers, H. W. C. (2007). Some aspects of the synthesis and properties of carbohydrate-based amphiphiles. (Doctoral Dissertation). Radboud University Nijmegen. Retrieved from http://hdl.handle.net/2066/30076

Chicago Manual of Style (16th Edition):

Raaijmakers, Henricus Wilhelmus Carolina. “Some aspects of the synthesis and properties of carbohydrate-based amphiphiles.” 2007. Doctoral Dissertation, Radboud University Nijmegen. Accessed September 15, 2019. http://hdl.handle.net/2066/30076.

MLA Handbook (7th Edition):

Raaijmakers, Henricus Wilhelmus Carolina. “Some aspects of the synthesis and properties of carbohydrate-based amphiphiles.” 2007. Web. 15 Sep 2019.

Vancouver:

Raaijmakers HWC. Some aspects of the synthesis and properties of carbohydrate-based amphiphiles. [Internet] [Doctoral dissertation]. Radboud University Nijmegen; 2007. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/2066/30076.

Council of Science Editors:

Raaijmakers HWC. Some aspects of the synthesis and properties of carbohydrate-based amphiphiles. [Doctoral Dissertation]. Radboud University Nijmegen; 2007. Available from: http://hdl.handle.net/2066/30076


University of Vienna

17. Preinfalk, Alexander. Part I: A Gold(I)-Catalysed Domino Coupling of Alcohols with Allenes Enables the Synthesis of Highly Substituted Indenes Part II: Synthetic Studies on the Asymmetric Synthesis of Allenes.

Degree: 2016, University of Vienna

 Diese Arbeit gliedert sich in zwei Teile: Im ersten Teil beschreiben wir eine Gold(I)-katalysierte Kaskadenzyklisierung von Aryl-substituierten Allenen mit Alkoholen, welche hochsubstituierte Indene liefert. Um… (more)

Subjects/Keywords: 35.07 Chemisches Labor, chemische Methoden; 35.17 Katalyse; 35.52 Präparative Organische Chemie; 35.60 Metallorganische Verbindungen; 35.69 Organische Chemie: Sonstiges; 35.51 Organische Reaktionen, Stereochemie; Gold-Katalyse / Indene / Asymmetrische Katalyse / Palladium-Katalyse / Allene

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APA (6th Edition):

Preinfalk, A. (2016). Part I: A Gold(I)-Catalysed Domino Coupling of Alcohols with Allenes Enables the Synthesis of Highly Substituted Indenes Part II: Synthetic Studies on the Asymmetric Synthesis of Allenes. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/43244/

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):

Preinfalk, Alexander. “Part I: A Gold(I)-Catalysed Domino Coupling of Alcohols with Allenes Enables the Synthesis of Highly Substituted Indenes Part II: Synthetic Studies on the Asymmetric Synthesis of Allenes.” 2016. Thesis, University of Vienna. Accessed September 15, 2019. http://othes.univie.ac.at/43244/.

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

MLA Handbook (7th Edition):

Preinfalk, Alexander. “Part I: A Gold(I)-Catalysed Domino Coupling of Alcohols with Allenes Enables the Synthesis of Highly Substituted Indenes Part II: Synthetic Studies on the Asymmetric Synthesis of Allenes.” 2016. Web. 15 Sep 2019.

Vancouver:

Preinfalk A. Part I: A Gold(I)-Catalysed Domino Coupling of Alcohols with Allenes Enables the Synthesis of Highly Substituted Indenes Part II: Synthetic Studies on the Asymmetric Synthesis of Allenes. [Internet] [Thesis]. University of Vienna; 2016. [cited 2019 Sep 15]. Available from: http://othes.univie.ac.at/43244/.

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

Council of Science Editors:

Preinfalk A. Part I: A Gold(I)-Catalysed Domino Coupling of Alcohols with Allenes Enables the Synthesis of Highly Substituted Indenes Part II: Synthetic Studies on the Asymmetric Synthesis of Allenes. [Thesis]. University of Vienna; 2016. Available from: http://othes.univie.ac.at/43244/

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


ETH Zürich

18. Neumann, Helmut. Versuche um Carben-Metall-Komplexe.

Degree: 1968, ETH Zürich

Subjects/Keywords: KOMPLEXCHEMIE; CARBENE (ORGANISCHE CHEMIE); COMPLEX CHEMISTRY; CARBENES (ORGANIC CHEMISTRY)

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APA (6th Edition):

Neumann, H. (1968). Versuche um Carben-Metall-Komplexe. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/136418

Chicago Manual of Style (16th Edition):

Neumann, Helmut. “Versuche um Carben-Metall-Komplexe.” 1968. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/136418.

MLA Handbook (7th Edition):

Neumann, Helmut. “Versuche um Carben-Metall-Komplexe.” 1968. Web. 15 Sep 2019.

Vancouver:

Neumann H. Versuche um Carben-Metall-Komplexe. [Internet] [Doctoral dissertation]. ETH Zürich; 1968. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/136418.

Council of Science Editors:

Neumann H. Versuche um Carben-Metall-Komplexe. [Doctoral Dissertation]. ETH Zürich; 1968. Available from: http://hdl.handle.net/20.500.11850/136418


Johannes Gutenberg Universität Mainz

19. Misuk, Viktor. Tropfenbasierte Multiphasen – Mikroreaktionstechnologie in organisch-chemischer Synthese.

Degree: 2014, Johannes Gutenberg Universität Mainz

In der vorliegenden Doktorarbeit werden neue, mikrofluidische Verfahren, zur Durchführung chemischer Reaktionen in mehrphasigen Systemen präsentiert. rnDas Einschließen von Reaktionspartnern in einzelne Segmente, deren Volumina… (more)

Subjects/Keywords: Mikroreaktor; segmentierter Fluss; Organische Chemie; Mikroprozesstechnik; Microreactor; segmented flow; organic chemistry; micro-process-engineering; Chemistry and allied sciences

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APA (6th Edition):

Misuk, V. (2014). Tropfenbasierte Multiphasen – Mikroreaktionstechnologie in organisch-chemischer Synthese. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2015/4028/

Chicago Manual of Style (16th Edition):

Misuk, Viktor. “Tropfenbasierte Multiphasen – Mikroreaktionstechnologie in organisch-chemischer Synthese.” 2014. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 15, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2015/4028/.

MLA Handbook (7th Edition):

Misuk, Viktor. “Tropfenbasierte Multiphasen – Mikroreaktionstechnologie in organisch-chemischer Synthese.” 2014. Web. 15 Sep 2019.

Vancouver:

Misuk V. Tropfenbasierte Multiphasen – Mikroreaktionstechnologie in organisch-chemischer Synthese. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2014. [cited 2019 Sep 15]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4028/.

Council of Science Editors:

Misuk V. Tropfenbasierte Multiphasen – Mikroreaktionstechnologie in organisch-chemischer Synthese. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2014. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4028/


Johannes Gutenberg Universität Mainz

20. Zöphel, Lukas Julian. Chemical transformations of the pyrene K-region for functional materials.

Degree: 2012, Johannes Gutenberg Universität Mainz

In dieser Arbeit wurde eine neue Methode zur asymmetrischen Substitution der K-Regionen von Pyren entwickelt, auf welcher das Design und die Synthese von neuartigen, Pyren-basierten… (more)

Subjects/Keywords: Organische Synthese; organische Elektronik; Pyren-Chemie; Suzuki Kupplung; Nichtplanar; organic synthesis; organic electronics; pyrene chemistry; Suzuki coupling; non-planar; Chemistry and allied sciences

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APA (6th Edition):

Zöphel, L. J. (2012). Chemical transformations of the pyrene K-region for functional materials. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2012/3228/

Chicago Manual of Style (16th Edition):

Zöphel, Lukas Julian. “Chemical transformations of the pyrene K-region for functional materials.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 15, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2012/3228/.

MLA Handbook (7th Edition):

Zöphel, Lukas Julian. “Chemical transformations of the pyrene K-region for functional materials.” 2012. Web. 15 Sep 2019.

Vancouver:

Zöphel LJ. Chemical transformations of the pyrene K-region for functional materials. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2019 Sep 15]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3228/.

Council of Science Editors:

Zöphel LJ. Chemical transformations of the pyrene K-region for functional materials. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3228/


ETH Zürich

21. Sturzenegger, August. Ueber einige aliphatische Sulfochloramide.

Degree: 1949, ETH Zürich

Subjects/Keywords: CHLORAMINE + CHLORAMIDE (ORGANISCHE CHEMIE); SULFONAMIDE (ORGANISCHE CHEMIE); ORGANISCHE SYNTHESE (CHEMIE); CHLORAMINES + CHLORAMIDES (ORGANIC CHEMISTRY); SULFONAMIDES (ORGANIC CHEMISTRY); ORGANIC SYNTHESIS (CHEMISTRY); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Sturzenegger, A. (1949). Ueber einige aliphatische Sulfochloramide. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/133538

Chicago Manual of Style (16th Edition):

Sturzenegger, August. “Ueber einige aliphatische Sulfochloramide.” 1949. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/133538.

MLA Handbook (7th Edition):

Sturzenegger, August. “Ueber einige aliphatische Sulfochloramide.” 1949. Web. 15 Sep 2019.

Vancouver:

Sturzenegger A. Ueber einige aliphatische Sulfochloramide. [Internet] [Doctoral dissertation]. ETH Zürich; 1949. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/133538.

Council of Science Editors:

Sturzenegger A. Ueber einige aliphatische Sulfochloramide. [Doctoral Dissertation]. ETH Zürich; 1949. Available from: http://hdl.handle.net/20.500.11850/133538


ETH Zürich

22. El Heweihi, Zaki. Mercaptale und Xanthogenate der Kohlenhydrate und Derivate der 6-Thioglucose.

Degree: 1950, ETH Zürich

Subjects/Keywords: KOHLENHYDRATE (ORGANISCHE CHEMIE); THIOACETALE + THIOHEMIACETALE (ORGANISCHE CHEMIE); ORGANISCHE SYNTHESE (CHEMIE); CARBOHYDRATES (ORGANIC CHEMISTRY); THIOACETALES + THIOHEMIACATALES (ORGANIC CHEMISTRY); ORGANIC SYNTHESIS (CHEMISTRY); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

El Heweihi, Z. (1950). Mercaptale und Xanthogenate der Kohlenhydrate und Derivate der 6-Thioglucose. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/135041

Chicago Manual of Style (16th Edition):

El Heweihi, Zaki. “Mercaptale und Xanthogenate der Kohlenhydrate und Derivate der 6-Thioglucose.” 1950. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/135041.

MLA Handbook (7th Edition):

El Heweihi, Zaki. “Mercaptale und Xanthogenate der Kohlenhydrate und Derivate der 6-Thioglucose.” 1950. Web. 15 Sep 2019.

Vancouver:

El Heweihi Z. Mercaptale und Xanthogenate der Kohlenhydrate und Derivate der 6-Thioglucose. [Internet] [Doctoral dissertation]. ETH Zürich; 1950. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/135041.

Council of Science Editors:

El Heweihi Z. Mercaptale und Xanthogenate der Kohlenhydrate und Derivate der 6-Thioglucose. [Doctoral Dissertation]. ETH Zürich; 1950. Available from: http://hdl.handle.net/20.500.11850/135041


ETH Zürich

23. Bourquin, Jean-Pierre. Synthese einiger neuartiger Alkohole in der aliphatischen Monoterpenreihe.

Degree: 1942, ETH Zürich

Subjects/Keywords: TERPENE (ORGANISCHE CHEMIE); ALKOHOLE (ORGANISCHE CHEMIE); ORGANISCHE SYNTHESE (CHEMIE); TERPENES (ORGANIC CHEMISTRY); ALCOHOLS (ORGANIC CHEMISTRY); ORGANIC SYNTHESIS (CHEMISTRY); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Bourquin, J. (1942). Synthese einiger neuartiger Alkohole in der aliphatischen Monoterpenreihe. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/132049

Chicago Manual of Style (16th Edition):

Bourquin, Jean-Pierre. “Synthese einiger neuartiger Alkohole in der aliphatischen Monoterpenreihe.” 1942. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/132049.

MLA Handbook (7th Edition):

Bourquin, Jean-Pierre. “Synthese einiger neuartiger Alkohole in der aliphatischen Monoterpenreihe.” 1942. Web. 15 Sep 2019.

Vancouver:

Bourquin J. Synthese einiger neuartiger Alkohole in der aliphatischen Monoterpenreihe. [Internet] [Doctoral dissertation]. ETH Zürich; 1942. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/132049.

Council of Science Editors:

Bourquin J. Synthese einiger neuartiger Alkohole in der aliphatischen Monoterpenreihe. [Doctoral Dissertation]. ETH Zürich; 1942. Available from: http://hdl.handle.net/20.500.11850/132049


ETH Zürich

24. Le Chapelain, Camille. Towards the Enantioselective Total Synthesis of Schiglautone A: Synthesis and Biological Evaluation of Chlorinated Analogs of Leukotoxin Diol.

Degree: 2015, ETH Zürich

Subjects/Keywords: ORGANISCHE SYNTHESE (CHEMIE); NATURSTOFFE (ORGANISCHE CHEMIE); TRITERPENE (ORGANISCHE CHEMIE); ORGANIC SYNTHESIS (CHEMISTRY); NATURAL SUBSTANCES (ORGANIC CHEMISTRY); TRITERPENES (ORGANIC CHEMISTRY); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Le Chapelain, C. (2015). Towards the Enantioselective Total Synthesis of Schiglautone A: Synthesis and Biological Evaluation of Chlorinated Analogs of Leukotoxin Diol. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/155227

Chicago Manual of Style (16th Edition):

Le Chapelain, Camille. “Towards the Enantioselective Total Synthesis of Schiglautone A: Synthesis and Biological Evaluation of Chlorinated Analogs of Leukotoxin Diol.” 2015. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/155227.

MLA Handbook (7th Edition):

Le Chapelain, Camille. “Towards the Enantioselective Total Synthesis of Schiglautone A: Synthesis and Biological Evaluation of Chlorinated Analogs of Leukotoxin Diol.” 2015. Web. 15 Sep 2019.

Vancouver:

Le Chapelain C. Towards the Enantioselective Total Synthesis of Schiglautone A: Synthesis and Biological Evaluation of Chlorinated Analogs of Leukotoxin Diol. [Internet] [Doctoral dissertation]. ETH Zürich; 2015. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/155227.

Council of Science Editors:

Le Chapelain C. Towards the Enantioselective Total Synthesis of Schiglautone A: Synthesis and Biological Evaluation of Chlorinated Analogs of Leukotoxin Diol. [Doctoral Dissertation]. ETH Zürich; 2015. Available from: http://hdl.handle.net/20.500.11850/155227


University of Vienna

25. Krizková, Petra. Synthesis and reactions of chiral, nonracemic compounds with general formula XCHDY and [16O,17O,18O]phosphoenolpyruvate.

Degree: 2015, University of Vienna

 Der Palladiumkomplex (R)-[D1]2.19 wurde ausgehend vom entsprechenden enantiomerenreinen Dimethyl(phenyl)silyl-[D1]methylboronat hergestellt. Die mikroskopische konfigurative Stabilität des Komplexes während einer Suzuki-Miyaura Kupplung wurde erfolgreich untersucht und es… (more)

Subjects/Keywords: 35.50 Organische Chemie: Allgemeines; 35.51 Organische Reaktionen, Stereochemie; Fluoromethyllithium / Suzuki-Miyaura Kupplung / deuterierte Diole / Bromchlorfluormethan / [16O,17O,18O]-Phosphoenolpyruvat

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APA (6th Edition):

Krizková, P. (2015). Synthesis and reactions of chiral, nonracemic compounds with general formula XCHDY and [16O,17O,18O]phosphoenolpyruvate. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/37380/

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):

Krizková, Petra. “Synthesis and reactions of chiral, nonracemic compounds with general formula XCHDY and [16O,17O,18O]phosphoenolpyruvate.” 2015. Thesis, University of Vienna. Accessed September 15, 2019. http://othes.univie.ac.at/37380/.

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

MLA Handbook (7th Edition):

Krizková, Petra. “Synthesis and reactions of chiral, nonracemic compounds with general formula XCHDY and [16O,17O,18O]phosphoenolpyruvate.” 2015. Web. 15 Sep 2019.

Vancouver:

Krizková P. Synthesis and reactions of chiral, nonracemic compounds with general formula XCHDY and [16O,17O,18O]phosphoenolpyruvate. [Internet] [Thesis]. University of Vienna; 2015. [cited 2019 Sep 15]. Available from: http://othes.univie.ac.at/37380/.

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

Council of Science Editors:

Krizková P. Synthesis and reactions of chiral, nonracemic compounds with general formula XCHDY and [16O,17O,18O]phosphoenolpyruvate. [Thesis]. University of Vienna; 2015. Available from: http://othes.univie.ac.at/37380/

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


University of Groningen

26. Haest, Albertus Durk van der. Classical resolutions; design of resolving agents and studies of diastereomeric salts.

Degree: Faculty of Science and Engineering, 1992, University of Groningen

Subjects/Keywords: Proefschriften (vorm); Scheidingstechnieken; Organische verbindingen, Enantiomeren ,; fysische organische chemie

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APA (6th Edition):

Haest, A. D. v. d. (1992). Classical resolutions; design of resolving agents and studies of diastereomeric salts. (Doctoral Dissertation). University of Groningen. Retrieved from https://www.rug.nl/research/portal/en/publications/classical-resolutions-design-of-resolving-agents-and-studies-of-diastereomeric-salts(ee52e66c-ba7b-4d6c-a28c-f13150bc579e).html ; urn:nbn:nl:ui:11-dbi/49271cf75ff69 ; ee52e66c-ba7b-4d6c-a28c-f13150bc579e ; 11370/ee52e66c-ba7b-4d6c-a28c-f13150bc579e ; urn:nbn:nl:ui:11-dbi/49271cf75ff69 ; https://www.rug.nl/research/portal/en/publications/classical-resolutions-design-of-resolving-agents-and-studies-of-diastereomeric-salts(ee52e66c-ba7b-4d6c-a28c-f13150bc579e).html

Chicago Manual of Style (16th Edition):

Haest, Albertus Durk van der. “Classical resolutions; design of resolving agents and studies of diastereomeric salts.” 1992. Doctoral Dissertation, University of Groningen. Accessed September 15, 2019. https://www.rug.nl/research/portal/en/publications/classical-resolutions-design-of-resolving-agents-and-studies-of-diastereomeric-salts(ee52e66c-ba7b-4d6c-a28c-f13150bc579e).html ; urn:nbn:nl:ui:11-dbi/49271cf75ff69 ; ee52e66c-ba7b-4d6c-a28c-f13150bc579e ; 11370/ee52e66c-ba7b-4d6c-a28c-f13150bc579e ; urn:nbn:nl:ui:11-dbi/49271cf75ff69 ; https://www.rug.nl/research/portal/en/publications/classical-resolutions-design-of-resolving-agents-and-studies-of-diastereomeric-salts(ee52e66c-ba7b-4d6c-a28c-f13150bc579e).html.

MLA Handbook (7th Edition):

Haest, Albertus Durk van der. “Classical resolutions; design of resolving agents and studies of diastereomeric salts.” 1992. Web. 15 Sep 2019.

Vancouver:

Haest ADvd. Classical resolutions; design of resolving agents and studies of diastereomeric salts. [Internet] [Doctoral dissertation]. University of Groningen; 1992. [cited 2019 Sep 15]. Available from: https://www.rug.nl/research/portal/en/publications/classical-resolutions-design-of-resolving-agents-and-studies-of-diastereomeric-salts(ee52e66c-ba7b-4d6c-a28c-f13150bc579e).html ; urn:nbn:nl:ui:11-dbi/49271cf75ff69 ; ee52e66c-ba7b-4d6c-a28c-f13150bc579e ; 11370/ee52e66c-ba7b-4d6c-a28c-f13150bc579e ; urn:nbn:nl:ui:11-dbi/49271cf75ff69 ; https://www.rug.nl/research/portal/en/publications/classical-resolutions-design-of-resolving-agents-and-studies-of-diastereomeric-salts(ee52e66c-ba7b-4d6c-a28c-f13150bc579e).html.

Council of Science Editors:

Haest ADvd. Classical resolutions; design of resolving agents and studies of diastereomeric salts. [Doctoral Dissertation]. University of Groningen; 1992. Available from: https://www.rug.nl/research/portal/en/publications/classical-resolutions-design-of-resolving-agents-and-studies-of-diastereomeric-salts(ee52e66c-ba7b-4d6c-a28c-f13150bc579e).html ; urn:nbn:nl:ui:11-dbi/49271cf75ff69 ; ee52e66c-ba7b-4d6c-a28c-f13150bc579e ; 11370/ee52e66c-ba7b-4d6c-a28c-f13150bc579e ; urn:nbn:nl:ui:11-dbi/49271cf75ff69 ; https://www.rug.nl/research/portal/en/publications/classical-resolutions-design-of-resolving-agents-and-studies-of-diastereomeric-salts(ee52e66c-ba7b-4d6c-a28c-f13150bc579e).html


ETH Zürich

27. Büchi, Jakob. Ueber Merkaptole und Disulfone hydroaromatischer und aromatischer Merkaptane.

Degree: 1929, ETH Zürich

Subjects/Keywords: SULFONE (ORGANISCHE CHEMIE); THIOLE (ORGANISCHE CHEMIE); THIOACETALE + THIOHEMIACETALE (ORGANISCHE CHEMIE); ORGANISCHE SYNTHESE (CHEMIE); SULFONES (ORGANIC CHEMISTRY); THIOLS (ORGANIC CHEMISTRY); THIOACETALES + THIOHEMIACATALES (ORGANIC CHEMISTRY); ORGANIC SYNTHESIS (CHEMISTRY); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Büchi, J. (1929). Ueber Merkaptole und Disulfone hydroaromatischer und aromatischer Merkaptane. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/134615

Chicago Manual of Style (16th Edition):

Büchi, Jakob. “Ueber Merkaptole und Disulfone hydroaromatischer und aromatischer Merkaptane.” 1929. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/134615.

MLA Handbook (7th Edition):

Büchi, Jakob. “Ueber Merkaptole und Disulfone hydroaromatischer und aromatischer Merkaptane.” 1929. Web. 15 Sep 2019.

Vancouver:

Büchi J. Ueber Merkaptole und Disulfone hydroaromatischer und aromatischer Merkaptane. [Internet] [Doctoral dissertation]. ETH Zürich; 1929. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/134615.

Council of Science Editors:

Büchi J. Ueber Merkaptole und Disulfone hydroaromatischer und aromatischer Merkaptane. [Doctoral Dissertation]. ETH Zürich; 1929. Available from: http://hdl.handle.net/20.500.11850/134615


ETH Zürich

28. Müller, Robert Karl. Beitrag zur Chemie der N-Amino-aziridine.

Degree: 1972, ETH Zürich

Subjects/Keywords: HETEROCYCLISCHE KOHLENWASSERSTOFFE (ORGANISCHE CHEMIE); HETEROCYCLIC HYDROCARBONS (ORGANIC CHEMISTRY)

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

APA (6th Edition):

Müller, R. K. (1972). Beitrag zur Chemie der N-Amino-aziridine. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/132384

Chicago Manual of Style (16th Edition):

Müller, Robert Karl. “Beitrag zur Chemie der N-Amino-aziridine.” 1972. Doctoral Dissertation, ETH Zürich. Accessed September 15, 2019. http://hdl.handle.net/20.500.11850/132384.

MLA Handbook (7th Edition):

Müller, Robert Karl. “Beitrag zur Chemie der N-Amino-aziridine.” 1972. Web. 15 Sep 2019.

Vancouver:

Müller RK. Beitrag zur Chemie der N-Amino-aziridine. [Internet] [Doctoral dissertation]. ETH Zürich; 1972. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/20.500.11850/132384.

Council of Science Editors:

Müller RK. Beitrag zur Chemie der N-Amino-aziridine. [Doctoral Dissertation]. ETH Zürich; 1972. Available from: http://hdl.handle.net/20.500.11850/132384

29. 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 <strong>I</strong> , intermedeol <strong>II</strong> , neointermedeol <strong>III</strong> , paradisiol <strong>IV</strong> ,… (more)

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

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

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 September 15, 2019. 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. 15 Sep 2019.

Vancouver:

Kesselmans RPW. Total synthesis of all stereoisomers of eudesm-II-en-4-ol. [Internet] [Doctoral dissertation]. Agricultural University; 1992. [cited 2019 Sep 15]. 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

30. 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 September 15, 2019. 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. 15 Sep 2019.

Vancouver:

Reuvers JTA. The total synthesis of 3Beta-hydroxynagilactone F. [Internet] [Doctoral dissertation]. Landbouwhogeschool Wageningen; 1985. [cited 2019 Sep 15]. 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

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