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You searched for subject:( Sonogashira cross coupling reaction). Showing records 1 – 30 of 18029 total matches.

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University of South Africa

1. Makelane, Hlamulo Reply. Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .

Degree: 2010, University of South Africa

Sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline derivatives with stoichiometric amount of terminal alkynes in the presence of bis(triphenylphosphine)palladium(II)chloride and copper iodide in triethylamine afforded the 3-(alkynyl)-2-aryl-4-chloroquinoline, exclusively.… (more)

Subjects/Keywords: 2-aryl-4-chloro-3-iodoquinoline; Sonogashira cross-coupling reaction; Suzuki cross-coupling reaction

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APA (6th Edition):

Makelane, H. R. (2010). Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/3838

Chicago Manual of Style (16th Edition):

Makelane, Hlamulo Reply. “Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .” 2010. Masters Thesis, University of South Africa. Accessed October 20, 2019. http://hdl.handle.net/10500/3838.

MLA Handbook (7th Edition):

Makelane, Hlamulo Reply. “Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .” 2010. Web. 20 Oct 2019.

Vancouver:

Makelane HR. Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes . [Internet] [Masters thesis]. University of South Africa; 2010. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10500/3838.

Council of Science Editors:

Makelane HR. Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes . [Masters Thesis]. University of South Africa; 2010. Available from: http://hdl.handle.net/10500/3838


King Abdullah University of Science and Technology

2. Walter, Philipp E. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol.

Degree: 2012, King Abdullah University of Science and Technology

Cross coupling reactions are a well-established tool in modern organic synthesis and play a crucial role in the synthesis of a high number of organic… (more)

Subjects/Keywords: sonogashira; cross-coupling; water; palladium; green

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APA (6th Edition):

Walter, P. E. (2012). Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. (Thesis). King Abdullah University of Science and Technology. Retrieved from http://hdl.handle.net/10754/262732

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):

Walter, Philipp E. “Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol.” 2012. Thesis, King Abdullah University of Science and Technology. Accessed October 20, 2019. http://hdl.handle.net/10754/262732.

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

MLA Handbook (7th Edition):

Walter, Philipp E. “Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol.” 2012. Web. 20 Oct 2019.

Vancouver:

Walter PE. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. [Internet] [Thesis]. King Abdullah University of Science and Technology; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10754/262732.

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

Council of Science Editors:

Walter PE. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. [Thesis]. King Abdullah University of Science and Technology; 2012. Available from: http://hdl.handle.net/10754/262732

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


University of South Africa

3. Lesenyeho, Lehlogonolo Godfrey. Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines .

Degree: 2010, University of South Africa

 The previously described 2-aryl-4-chloro-3-iodoquinolines were prepared following literature procedure and in turn converted to the corresponding hitherto unknown 2-aryl-3-iodo-4-(phenylamino)quinoline derivatives using aniline in refluxing ethanol.… (more)

Subjects/Keywords: 2-Aryl-3-iodo-4-(phenylamino)quinoline; Sonogashira cross-coupling reaction; Intramolecular Heck reaction; 2-Aryl-3-iodo-4-(phenylamino)quinoline; 4-(N,N-allylphenylamino)-2-aryl-3-iodoquinolines; Sonogashira cross-coupling reaction; intramolecular Heck reaction; 1H-pyrrolo[3,2-c]quinolines

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APA (6th Edition):

Lesenyeho, L. G. (2010). Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/3970

Chicago Manual of Style (16th Edition):

Lesenyeho, Lehlogonolo Godfrey. “Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines .” 2010. Masters Thesis, University of South Africa. Accessed October 20, 2019. http://hdl.handle.net/10500/3970.

MLA Handbook (7th Edition):

Lesenyeho, Lehlogonolo Godfrey. “Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines .” 2010. Web. 20 Oct 2019.

Vancouver:

Lesenyeho LG. Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines . [Internet] [Masters thesis]. University of South Africa; 2010. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10500/3970.

Council of Science Editors:

Lesenyeho LG. Palladium-catalyzed heteroannulation of 2-ARYL- 3-IODO-4-(Phenylamino)quinolines and 4-(N,N-allylphenylamino)-2-ARYL-3-iodoquinolines . [Masters Thesis]. University of South Africa; 2010. Available from: http://hdl.handle.net/10500/3970

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

D'Attoma, Joseph. “Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.” 2013. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed October 20, 2019. http://www.theses.fr/2013LYO10243.

MLA Handbook (7th Edition):

D'Attoma, Joseph. “Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.” 2013. Web. 20 Oct 2019.

Vancouver:

D'Attoma J. Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2013. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2013LYO10243.

Council of Science Editors:

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


University of Alberta

5. Way, Jenilee D. 4-[18F]Fluoroiodobenzene and its applications in palladium-mediated Sonogashira cross coupling reactions.

Degree: MS, Department of Oncology, 2014, University of Alberta

 Way, Jenilee1; Wang, Monica1; Wuest, Melinda1; Bergmann, Cody1; Hamann, Ingrit1; Wuest, Frank1* 1 University of Alberta, Department of Oncology, Edmonton, Alberta, Canada The ongoing demand… (more)

Subjects/Keywords: PET Imaging; [18F]Fluoride; Sonogashira cross coupling; Radiotracer

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APA (6th Edition):

Way, J. D. (2014). 4-[18F]Fluoroiodobenzene and its applications in palladium-mediated Sonogashira cross coupling reactions. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/c79407x25d

Chicago Manual of Style (16th Edition):

Way, Jenilee D. “4-[18F]Fluoroiodobenzene and its applications in palladium-mediated Sonogashira cross coupling reactions.” 2014. Masters Thesis, University of Alberta. Accessed October 20, 2019. https://era.library.ualberta.ca/files/c79407x25d.

MLA Handbook (7th Edition):

Way, Jenilee D. “4-[18F]Fluoroiodobenzene and its applications in palladium-mediated Sonogashira cross coupling reactions.” 2014. Web. 20 Oct 2019.

Vancouver:

Way JD. 4-[18F]Fluoroiodobenzene and its applications in palladium-mediated Sonogashira cross coupling reactions. [Internet] [Masters thesis]. University of Alberta; 2014. [cited 2019 Oct 20]. Available from: https://era.library.ualberta.ca/files/c79407x25d.

Council of Science Editors:

Way JD. 4-[18F]Fluoroiodobenzene and its applications in palladium-mediated Sonogashira cross coupling reactions. [Masters Thesis]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/c79407x25d


University of South Africa

6. Paumo, Hugues Kamdem. 2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties .

Degree: 2014, University of South Africa

 The 2-aryl-6,8-dibromoquinazolin-4(3H)-ones were prepared in a single-pot operation by condensing 6,8-dibromoanthranilamide and aryl aldehydes in the presence of molecular iodine in ethanol. Treatment of the… (more)

Subjects/Keywords: 2-aryl-6,8-dibromoquinazolin-4(3H)-ones; 2-aryl-4-chloro-6; 8-dibromoquinazolines; 2-aryl-6,8-dibromo-4-(phenylethynyl)quinazolines; 2,6,8-triaryl-4-(phenylethynyl)quinazolines; Sonogashira cross-coupling reaction; Suzuki-Miyaura cross-coupling reaction; Absorption and emission properties

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APA (6th Edition):

Paumo, H. K. (2014). 2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/14197

Chicago Manual of Style (16th Edition):

Paumo, Hugues Kamdem. “2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties .” 2014. Masters Thesis, University of South Africa. Accessed October 20, 2019. http://hdl.handle.net/10500/14197.

MLA Handbook (7th Edition):

Paumo, Hugues Kamdem. “2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties .” 2014. Web. 20 Oct 2019.

Vancouver:

Paumo HK. 2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties . [Internet] [Masters thesis]. University of South Africa; 2014. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10500/14197.

Council of Science Editors:

Paumo HK. 2-Aryl-6,8-Dibromo-4-Chloroquinazoline as scaffold for the synthesis of Novel 2,6,8-Triaryl-4-(Phenylethynyl)Quinazolines with potential photophysical properties . [Masters Thesis]. University of South Africa; 2014. Available from: http://hdl.handle.net/10500/14197

7. Allouch, Fatima. Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes.

Degree: Docteur es, Chimie, 2013, Dijon; Université libanaise

Ce mémoire porte sur l’accès simple et peu coûteux à de nouveaux ligands ferrocéniques aminés et aminophosphinés et leur coordination avec des métaux de transition… (more)

Subjects/Keywords: Métallo-ligands ferrocéniques aminés et aminophosphinés; Palladation; Amination réductrice; Ligands hybrides (N,P); Réaction de couplage carbone-carbone; Suzuki; Sonogashira; Amino and aminophosphine ferrocenyl metallo-ligand; Palladation; Reductive amination; N,P hybrid ligands; C-C cross-coupling reaction; Suzuki; Sonogashira; 541.2; 541.39; 547

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APA (6th Edition):

Allouch, F. (2013). Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes. (Doctoral Dissertation). Dijon; Université libanaise. Retrieved from http://www.theses.fr/2013DIJOS002

Chicago Manual of Style (16th Edition):

Allouch, Fatima. “Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes.” 2013. Doctoral Dissertation, Dijon; Université libanaise. Accessed October 20, 2019. http://www.theses.fr/2013DIJOS002.

MLA Handbook (7th Edition):

Allouch, Fatima. “Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes.” 2013. Web. 20 Oct 2019.

Vancouver:

Allouch F. Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes. [Internet] [Doctoral dissertation]. Dijon; Université libanaise; 2013. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2013DIJOS002.

Council of Science Editors:

Allouch F. Synthèse et applications de nouveaux complexes métallocéniques multidentes : Synthesis and applications of new multidentate metallocenic complexes. [Doctoral Dissertation]. Dijon; Université libanaise; 2013. Available from: http://www.theses.fr/2013DIJOS002


University of South Africa

8. Oyeyiola, Felix Adetunji. Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .

Degree: 2011, University of South Africa

 The 2-aryl-2,3-dihydroquinolin-4(1H)-ones were prepared via acid-catalyzed cyclization of the corresponding 2-aminochalcones, which were in turn, prepared by base-promoted Claisen-Schmidt aldol condensation of 2-aminoacetophenone and benzaldehyde… (more)

Subjects/Keywords: 2-aminochalcones; Cross-coupling reaction; Suzuki-Miyaura

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APA (6th Edition):

Oyeyiola, F. A. (2011). Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/5842

Chicago Manual of Style (16th Edition):

Oyeyiola, Felix Adetunji. “Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .” 2011. Masters Thesis, University of South Africa. Accessed October 20, 2019. http://hdl.handle.net/10500/5842.

MLA Handbook (7th Edition):

Oyeyiola, Felix Adetunji. “Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .” 2011. Web. 20 Oct 2019.

Vancouver:

Oyeyiola FA. Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones . [Internet] [Masters thesis]. University of South Africa; 2011. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10500/5842.

Council of Science Editors:

Oyeyiola FA. Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones . [Masters Thesis]. University of South Africa; 2011. Available from: http://hdl.handle.net/10500/5842


Brigham Young University

9. Ma, Bing. Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C.

Degree: PhD, 2009, Brigham Young University

  Project I. Cinchona alkaloid-derived quaternary ammonium salts have been successfully used as phase-transfer catalysts, particularly in asymmetric alkylations. Our group applied this type of… (more)

Subjects/Keywords: Cinchona alkaloids; beta-Hydroxy alpha-amino acids; Sonogashira coupling; Heck reaction; Asymmetric aldol reaction; natural products; Celogentin C; oxidative coupling; peptides; radical reaction; total synthesis; Biochemistry; Chemistry

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APA (6th Edition):

Ma, B. (2009). Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3194&context=etd

Chicago Manual of Style (16th Edition):

Ma, Bing. “Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C.” 2009. Doctoral Dissertation, Brigham Young University. Accessed October 20, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3194&context=etd.

MLA Handbook (7th Edition):

Ma, Bing. “Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C.” 2009. Web. 20 Oct 2019.

Vancouver:

Ma B. Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C. [Internet] [Doctoral dissertation]. Brigham Young University; 2009. [cited 2019 Oct 20]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3194&context=etd.

Council of Science Editors:

Ma B. Novel Cinchona Alkoloid Derived Ammonium Salts as Phase-Transfer Catalysts for the Asymmetric Synthesis of Beta-Hydroxy Alpha-Amino Acids Via Aldol Reactions and Total Synthesis of Celogentin C. [Doctoral Dissertation]. Brigham Young University; 2009. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3194&context=etd


University of Edinburgh

10. Geogheghan, Katherine Jayne. Boronic acid speciation in Suzuki-Miyaura cross-coupling.

Degree: PhD, 2018, University of Edinburgh

 Since its discovery in 1979, the Suzuki-Miyaura (SM) reaction has become one of the most widely utilised tools for carbon-carbon bond formation. The palladium catalysed… (more)

Subjects/Keywords: cross-coupling; Suzuki-Miyaura reaction; palladium catalysed coupling; boronic esters

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APA (6th Edition):

Geogheghan, K. J. (2018). Boronic acid speciation in Suzuki-Miyaura cross-coupling. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/33092

Chicago Manual of Style (16th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed October 20, 2019. http://hdl.handle.net/1842/33092.

MLA Handbook (7th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Web. 20 Oct 2019.

Vancouver:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1842/33092.

Council of Science Editors:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/33092


University of Manchester

11. Hussain, Jakir. Approaches toward the synthesis of lactonamycin utilising a new benzannulation reaction.

Degree: PhD, 2013, University of Manchester

 The Bull-Hutchings-Quayle (BHQ) reaction is a novel method for the synthesis of 1-(bromo/chloro)napthalenes from 2-allyphenyl-2’,2’,2’-tri(bromo/chloro)acetates. The reaction is also known as Atom Transfer Radical Cyclisation-Benzannulation… (more)

Subjects/Keywords: 547; ATRC; Benzannulation; Aromatic ring synthesis; Polyacene; BHQ; Chloronaphthalene; Lactonamycin; Cross-coupling; Diels-Alder; Suzuki; Sonogashira

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APA (6th Edition):

Hussain, J. (2013). Approaches toward the synthesis of lactonamycin utilising a new benzannulation reaction. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/approaches-toward-the-synthesis-of-lactonamycin-utilising-a-new-benzannulation-reaction(1157cbe4-21f4-4d9e-a10d-cf20518eb30b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.606964

Chicago Manual of Style (16th Edition):

Hussain, Jakir. “Approaches toward the synthesis of lactonamycin utilising a new benzannulation reaction.” 2013. Doctoral Dissertation, University of Manchester. Accessed October 20, 2019. https://www.research.manchester.ac.uk/portal/en/theses/approaches-toward-the-synthesis-of-lactonamycin-utilising-a-new-benzannulation-reaction(1157cbe4-21f4-4d9e-a10d-cf20518eb30b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.606964.

MLA Handbook (7th Edition):

Hussain, Jakir. “Approaches toward the synthesis of lactonamycin utilising a new benzannulation reaction.” 2013. Web. 20 Oct 2019.

Vancouver:

Hussain J. Approaches toward the synthesis of lactonamycin utilising a new benzannulation reaction. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Oct 20]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/approaches-toward-the-synthesis-of-lactonamycin-utilising-a-new-benzannulation-reaction(1157cbe4-21f4-4d9e-a10d-cf20518eb30b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.606964.

Council of Science Editors:

Hussain J. Approaches toward the synthesis of lactonamycin utilising a new benzannulation reaction. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/approaches-toward-the-synthesis-of-lactonamycin-utilising-a-new-benzannulation-reaction(1157cbe4-21f4-4d9e-a10d-cf20518eb30b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.606964

12. Figueira, João Luis Camacho Baptista. New metallomolecular wires based on carbon-rich bridging systems: a systematic study.

Degree: 2014, Universidade da Madeira

This dissertation presents and discusses the preparation of molecular wires (MW) candidates that would then be probed for electron transfer properties. These wires are bridged… (more)

Subjects/Keywords: Molecular wires; X-ray diffraction; Sonogashira cross-coupling; Palladium; Ruthenium; Química; .; Centro de Ciências Exatas e de Engenharia

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APA (6th Edition):

Figueira, J. L. C. B. (2014). New metallomolecular wires based on carbon-rich bridging systems: a systematic study. (Thesis). Universidade da Madeira. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:digituma.uma.pt:10400.13/569

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):

Figueira, João Luis Camacho Baptista. “New metallomolecular wires based on carbon-rich bridging systems: a systematic study.” 2014. Thesis, Universidade da Madeira. Accessed October 20, 2019. http://www.rcaap.pt/detail.jsp?id=oai:digituma.uma.pt:10400.13/569.

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

MLA Handbook (7th Edition):

Figueira, João Luis Camacho Baptista. “New metallomolecular wires based on carbon-rich bridging systems: a systematic study.” 2014. Web. 20 Oct 2019.

Vancouver:

Figueira JLCB. New metallomolecular wires based on carbon-rich bridging systems: a systematic study. [Internet] [Thesis]. Universidade da Madeira; 2014. [cited 2019 Oct 20]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:digituma.uma.pt:10400.13/569.

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

Council of Science Editors:

Figueira JLCB. New metallomolecular wires based on carbon-rich bridging systems: a systematic study. [Thesis]. Universidade da Madeira; 2014. Available from: http://www.rcaap.pt/detail.jsp?id=oai:digituma.uma.pt:10400.13/569

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


University of Lund

13. Johansson, Niclas. Synchrotron-based In Situ Electron Spectroscopy Applied to Oxide Formation and Catalysis.

Degree: 2017, University of Lund

 In this thesis, in situ ambient pressure X-ray photoelectron spectroscopy has been used to address chemical reactions on surfaces. The presented work aims at the… (more)

Subjects/Keywords: Naturvetenskap; CO oxidation; Sonogashira cross-coupling; trilayer FeO; vicinal FeO; Mn(III)-salen; APXPS; XAS; Fysicumarkivet A:2017:Johansson

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APA (6th Edition):

Johansson, N. (2017). Synchrotron-based In Situ Electron Spectroscopy Applied to Oxide Formation and Catalysis. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/7f36564e-c221-4225-9b2a-84d1fe11979d ; http://portal.research.lu.se/ws/files/33150356/Thesis_N_Johansson.pdf

Chicago Manual of Style (16th Edition):

Johansson, Niclas. “Synchrotron-based In Situ Electron Spectroscopy Applied to Oxide Formation and Catalysis.” 2017. Doctoral Dissertation, University of Lund. Accessed October 20, 2019. http://lup.lub.lu.se/record/7f36564e-c221-4225-9b2a-84d1fe11979d ; http://portal.research.lu.se/ws/files/33150356/Thesis_N_Johansson.pdf.

MLA Handbook (7th Edition):

Johansson, Niclas. “Synchrotron-based In Situ Electron Spectroscopy Applied to Oxide Formation and Catalysis.” 2017. Web. 20 Oct 2019.

Vancouver:

Johansson N. Synchrotron-based In Situ Electron Spectroscopy Applied to Oxide Formation and Catalysis. [Internet] [Doctoral dissertation]. University of Lund; 2017. [cited 2019 Oct 20]. Available from: http://lup.lub.lu.se/record/7f36564e-c221-4225-9b2a-84d1fe11979d ; http://portal.research.lu.se/ws/files/33150356/Thesis_N_Johansson.pdf.

Council of Science Editors:

Johansson N. Synchrotron-based In Situ Electron Spectroscopy Applied to Oxide Formation and Catalysis. [Doctoral Dissertation]. University of Lund; 2017. Available from: http://lup.lub.lu.se/record/7f36564e-c221-4225-9b2a-84d1fe11979d ; http://portal.research.lu.se/ws/files/33150356/Thesis_N_Johansson.pdf


Brock University

14. Yalagala, Ravi Shekar. A. Discovery of novel reactivity under the Sonogashira reaction conditions B. Synthesis of functionalized BODIPYs and BODIPY-sugar conjugates .

Degree: Department of Chemistry, Brock University

 A. During our attempts to synthesize substituted enediynes, coupling reactions between terminal alkynes and 1,2-cis-dihaloalkenes under the Sonogashira reaction conditions failed to give the corresponding… (more)

Subjects/Keywords: enediyne; Sonogashira coupling reaction; BODIPY; bromovinylboronoate; Azide alkyne Click reaction

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APA (6th Edition):

Yalagala, R. S. (n.d.). A. Discovery of novel reactivity under the Sonogashira reaction conditions B. Synthesis of functionalized BODIPYs and BODIPY-sugar conjugates . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/9496

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

Chicago Manual of Style (16th Edition):

Yalagala, Ravi Shekar. “A. Discovery of novel reactivity under the Sonogashira reaction conditions B. Synthesis of functionalized BODIPYs and BODIPY-sugar conjugates .” Thesis, Brock University. Accessed October 20, 2019. http://hdl.handle.net/10464/9496.

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

MLA Handbook (7th Edition):

Yalagala, Ravi Shekar. “A. Discovery of novel reactivity under the Sonogashira reaction conditions B. Synthesis of functionalized BODIPYs and BODIPY-sugar conjugates .” Web. 20 Oct 2019.

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

Vancouver:

Yalagala RS. A. Discovery of novel reactivity under the Sonogashira reaction conditions B. Synthesis of functionalized BODIPYs and BODIPY-sugar conjugates . [Internet] [Thesis]. Brock University; [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10464/9496.

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

Council of Science Editors:

Yalagala RS. A. Discovery of novel reactivity under the Sonogashira reaction conditions B. Synthesis of functionalized BODIPYs and BODIPY-sugar conjugates . [Thesis]. Brock University; Available from: http://hdl.handle.net/10464/9496

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


Missouri University of Science and Technology

15. Wang, Xiaojiang. Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials.

Degree: M.S. in Chemistry, Chemistry, Missouri University of Science and Technology

 "Immobilization of catalysts is a promising approach to combine the advantages of heterogeneous and homogeneous catalysts. Pd(PPh₃)₂Cl₂ known as an extremely active homogeneous catalyst for… (more)

Subjects/Keywords: Sonogashira coupling; Chemistry

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APA (6th Edition):

Wang, X. (n.d.). Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials. (Masters Thesis). Missouri University of Science and Technology. Retrieved from http://scholarsmine.mst.edu/masters_theses/5905

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

Chicago Manual of Style (16th Edition):

Wang, Xiaojiang. “Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials.” Masters Thesis, Missouri University of Science and Technology. Accessed October 20, 2019. http://scholarsmine.mst.edu/masters_theses/5905.

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

MLA Handbook (7th Edition):

Wang, Xiaojiang. “Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials.” Web. 20 Oct 2019.

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

Vancouver:

Wang X. Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials. [Internet] [Masters thesis]. Missouri University of Science and Technology; [cited 2019 Oct 20]. Available from: http://scholarsmine.mst.edu/masters_theses/5905.

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

Council of Science Editors:

Wang X. Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials. [Masters Thesis]. Missouri University of Science and Technology; Available from: http://scholarsmine.mst.edu/masters_theses/5905

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


University of Edinburgh

16. Corrie, Thomas James Alexander. Intramolecular direct arylation.

Degree: PhD, 2017, University of Edinburgh

 The research conducted for this thesis has led to the development of an intramolecular gold-catalysed direct arylation protocol whereby tethered arenes and aryltrimethylsilanes are coupled… (more)

Subjects/Keywords: gold-catalysis; cross-coupling; intermolecular reaction; tethered arenes; aryltrimethylsilanes

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APA (6th Edition):

Corrie, T. J. A. (2017). Intramolecular direct arylation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28820

Chicago Manual of Style (16th Edition):

Corrie, Thomas James Alexander. “Intramolecular direct arylation.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed October 20, 2019. http://hdl.handle.net/1842/28820.

MLA Handbook (7th Edition):

Corrie, Thomas James Alexander. “Intramolecular direct arylation.” 2017. Web. 20 Oct 2019.

Vancouver:

Corrie TJA. Intramolecular direct arylation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1842/28820.

Council of Science Editors:

Corrie TJA. Intramolecular direct arylation. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28820


University of Arizona

17. Bell, Christan Elizabeth. Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds .

Degree: 2012, University of Arizona

 This research focused on the synthesis of novel ogranoboron reagents in efforts to perform a variety of synthetic transformations, and additionally, the development of new… (more)

Subjects/Keywords: multicomponent reaction; Chemistry; cross-coupling; Frustrated Lewis pairs

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APA (6th Edition):

Bell, C. E. (2012). Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/265557

Chicago Manual of Style (16th Edition):

Bell, Christan Elizabeth. “Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds .” 2012. Doctoral Dissertation, University of Arizona. Accessed October 20, 2019. http://hdl.handle.net/10150/265557.

MLA Handbook (7th Edition):

Bell, Christan Elizabeth. “Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds .” 2012. Web. 20 Oct 2019.

Vancouver:

Bell CE. Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10150/265557.

Council of Science Editors:

Bell CE. Synthesis and Reactivity of New Organoboron Reagents and Development of New Methodologies for the Generation of Novel Drug-Like Scaffolds . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/265557


University of South Carolina

18. Key, Ryan J. Development of Nickel Catalyzed Cross-Coupling Methodologies.

Degree: PhD, Chemistry and Biochemistry, 2019, University of South Carolina

  In this work, we have addressed some of the issues surrounding catalytic crosscoupling reactions by using a nickel terpyridine catalyst, [Ni(tpy)(py)(CH3CN)2](PF6)2 in the Buchwald-Hartwig… (more)

Subjects/Keywords: Chemistry; nickel; cross-coupling; Atomic Layer Deposition; Suzuki reaction

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APA (6th Edition):

Key, R. J. (2019). Development of Nickel Catalyzed Cross-Coupling Methodologies. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/5324

Chicago Manual of Style (16th Edition):

Key, Ryan J. “Development of Nickel Catalyzed Cross-Coupling Methodologies.” 2019. Doctoral Dissertation, University of South Carolina. Accessed October 20, 2019. https://scholarcommons.sc.edu/etd/5324.

MLA Handbook (7th Edition):

Key, Ryan J. “Development of Nickel Catalyzed Cross-Coupling Methodologies.” 2019. Web. 20 Oct 2019.

Vancouver:

Key RJ. Development of Nickel Catalyzed Cross-Coupling Methodologies. [Internet] [Doctoral dissertation]. University of South Carolina; 2019. [cited 2019 Oct 20]. Available from: https://scholarcommons.sc.edu/etd/5324.

Council of Science Editors:

Key RJ. Development of Nickel Catalyzed Cross-Coupling Methodologies. [Doctoral Dissertation]. University of South Carolina; 2019. Available from: https://scholarcommons.sc.edu/etd/5324


Indian Institute of Science

19. Dhineshkumar, J. Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.

Degree: 2016, Indian Institute of Science

 Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions” is divided into two sections. Section-A, contains two chapters, describes the catalytic ability of iodine… (more)

Subjects/Keywords: Carbon-heteroatom Bond; Cross Dehydrogenative Coupling; Tetrabutylammonium Iodide; Cross-Hetero-Dehydrogenative Coupling Reaction; Phosphites; Quaternary Azides; Organic Chemistry

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APA (6th Edition):

Dhineshkumar, J. (2016). Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/3020

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):

Dhineshkumar, J. “Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.” 2016. Thesis, Indian Institute of Science. Accessed October 20, 2019. http://hdl.handle.net/2005/3020.

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

MLA Handbook (7th Edition):

Dhineshkumar, J. “Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions.” 2016. Web. 20 Oct 2019.

Vancouver:

Dhineshkumar J. Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions. [Internet] [Thesis]. Indian Institute of Science; 2016. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2005/3020.

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

Council of Science Editors:

Dhineshkumar J. Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions. [Thesis]. Indian Institute of Science; 2016. Available from: http://hdl.handle.net/2005/3020

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

20. Matarazzo, Augusto. Design, Synthesis and Study of Novel Nucleobase Analogs.

Degree: 2015, University of Western Ontario

 This thesis focused on nucleobase modified peptide nucleic acid (PNA) and DNA to expand the repertoire of available nucleobase analogs used in the study of… (more)

Subjects/Keywords: Peptide nucleic acid; PNA; DNA; 5-aminouracil; 9-aminoacridine; acridone; fluorescence; environmentally sensitive fluorescence; solvatochromicity; 7-deazaadenine; Sonogashira cross-coupling; intrinsic nucleobase quencher; Stern-Volmer plots

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APA (6th Edition):

Matarazzo, A. (2015). Design, Synthesis and Study of Novel Nucleobase Analogs. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3128

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):

Matarazzo, Augusto. “Design, Synthesis and Study of Novel Nucleobase Analogs.” 2015. Thesis, University of Western Ontario. Accessed October 20, 2019. https://ir.lib.uwo.ca/etd/3128.

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

MLA Handbook (7th Edition):

Matarazzo, Augusto. “Design, Synthesis and Study of Novel Nucleobase Analogs.” 2015. Web. 20 Oct 2019.

Vancouver:

Matarazzo A. Design, Synthesis and Study of Novel Nucleobase Analogs. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2019 Oct 20]. Available from: https://ir.lib.uwo.ca/etd/3128.

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

Council of Science Editors:

Matarazzo A. Design, Synthesis and Study of Novel Nucleobase Analogs. [Thesis]. University of Western Ontario; 2015. Available from: https://ir.lib.uwo.ca/etd/3128

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


University of South Africa

21. Oyeyiola, Felix Adetunji. 2-ARYL-6,8-Dibromoquinolinones as synthons for the synthesis of Polysubstituted 4-ARYL-6-Oxopyrrolo [3,2,1-ij] Quinolines.

Degree: 2015, University of South Africa

 The known 2-aryl-6,8-dibromo-2,3-dihydroquinolin-4(1H)-ones 122 were dehydrogenated using thallium(III) p-tolylsulfonate in dimethoxyethane under reflux to afford the 2-aryl-6,8-dibromoquinolin-4(1H)-ones 136. Palladium-catalyzed Sonogashira cross-coupling of the 2-aryl-6,8-dibromo-2,3-dihydroquinolin-4(1H)-ones with… (more)

Subjects/Keywords: 2-aryl-2,3-dihydroquinolin-4(1H)-ones; 2-aryl-6,8-dibromo-2,3-dihydroquinolin-4(1H)-ones; Sonogashira cross-coupling reaction; 8-alkynyl-2-aryl-6-bromo-2,3-dihydroquinolin-4(1H)-ones; 6,8-dialkynyl-2-aryl-2,3-dihydroquinolin-4(1H)-ones; 4-aryl-8-bromo-2-phenyl-6H-pyrrolo[3,2,1-ij]quinolin-6-ones; 2-aryl-6-bromo-8-(4-hydroxybutanoyl)-2,3-dihydroquinolin-4(1H)-ones; 2-substituted 4-aryl-8-bromo-6-oxopyrrolo[3,2,1-ij]quinolines; 2-substituted 8-alkynyl 4-aryl-6-oxopyrrolo[3,2,1-ij]quinolines; Suzuki-Miyaura cross-coupling reaction; 8-substituted 2-phenyl-6H-pyrrolo[3,2,1-ij]quinolin-6-ones; 2,8-disubstituted 4-aryl-6-oxopyrrolo[3,2,1-ij]quinolines

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APA (6th Edition):

Oyeyiola, F. A. (2015). 2-ARYL-6,8-Dibromoquinolinones as synthons for the synthesis of Polysubstituted 4-ARYL-6-Oxopyrrolo [3,2,1-ij] Quinolines. (Doctoral Dissertation). University of South Africa. Retrieved from http://hdl.handle.net/10500/21206

Chicago Manual of Style (16th Edition):

Oyeyiola, Felix Adetunji. “2-ARYL-6,8-Dibromoquinolinones as synthons for the synthesis of Polysubstituted 4-ARYL-6-Oxopyrrolo [3,2,1-ij] Quinolines.” 2015. Doctoral Dissertation, University of South Africa. Accessed October 20, 2019. http://hdl.handle.net/10500/21206.

MLA Handbook (7th Edition):

Oyeyiola, Felix Adetunji. “2-ARYL-6,8-Dibromoquinolinones as synthons for the synthesis of Polysubstituted 4-ARYL-6-Oxopyrrolo [3,2,1-ij] Quinolines.” 2015. Web. 20 Oct 2019.

Vancouver:

Oyeyiola FA. 2-ARYL-6,8-Dibromoquinolinones as synthons for the synthesis of Polysubstituted 4-ARYL-6-Oxopyrrolo [3,2,1-ij] Quinolines. [Internet] [Doctoral dissertation]. University of South Africa; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10500/21206.

Council of Science Editors:

Oyeyiola FA. 2-ARYL-6,8-Dibromoquinolinones as synthons for the synthesis of Polysubstituted 4-ARYL-6-Oxopyrrolo [3,2,1-ij] Quinolines. [Doctoral Dissertation]. University of South Africa; 2015. Available from: http://hdl.handle.net/10500/21206


Freie Universität Berlin

22. Vogel, Michael. neue Synthese, Eliminierungsreaktionen und systematische Studien von Heck- und Sonogashirakreuzkupplungen.

Degree: 2009, Freie Universität Berlin

 Im Rahmen dieser Arbeit wird eine effiziente Umsetzung von leicht zugänglichen Carbonylverbindungen zu Alkenylnonaflaten oder Alkinen beschrieben. Der große Vorteil dieses Protokolls liegt in der… (more)

Subjects/Keywords: alkenyl nonaflates; elimination reactions; Heck cross-coupling; Sonogashira cross-coupling; homogeneous catalysis; one-pot; 500 Naturwissenschaften und Mathematik::540 Chemie

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APA (6th Edition):

Vogel, M. (2009). neue Synthese, Eliminierungsreaktionen und systematische Studien von Heck- und Sonogashirakreuzkupplungen. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-9060

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):

Vogel, Michael. “neue Synthese, Eliminierungsreaktionen und systematische Studien von Heck- und Sonogashirakreuzkupplungen.” 2009. Thesis, Freie Universität Berlin. Accessed October 20, 2019. http://dx.doi.org/10.17169/refubium-9060.

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

MLA Handbook (7th Edition):

Vogel, Michael. “neue Synthese, Eliminierungsreaktionen und systematische Studien von Heck- und Sonogashirakreuzkupplungen.” 2009. Web. 20 Oct 2019.

Vancouver:

Vogel M. neue Synthese, Eliminierungsreaktionen und systematische Studien von Heck- und Sonogashirakreuzkupplungen. [Internet] [Thesis]. Freie Universität Berlin; 2009. [cited 2019 Oct 20]. Available from: http://dx.doi.org/10.17169/refubium-9060.

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

Council of Science Editors:

Vogel M. neue Synthese, Eliminierungsreaktionen und systematische Studien von Heck- und Sonogashirakreuzkupplungen. [Thesis]. Freie Universität Berlin; 2009. Available from: http://dx.doi.org/10.17169/refubium-9060

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


University of Alberta

23. Lee, Jack C. H. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.

Degree: PhD, Department of Chemistry, 2013, University of Alberta

 As Organic Chemistry evolves into the 21st Century, the goal of this discipline has altered dramatically from merely accessing target molecules to efficiently synthesizing these… (more)

Subjects/Keywords: Gold-catalyzed cycloisomerization; Suzuki-Miyaura cross-coupling; Chiral alkyl boronates; Heck reaction; Enantioselective conjugate addition

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APA (6th Edition):

Lee, J. C. H. (2013). Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/qn59q550n

Chicago Manual of Style (16th Edition):

Lee, Jack C H. “Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.” 2013. Doctoral Dissertation, University of Alberta. Accessed October 20, 2019. https://era.library.ualberta.ca/files/qn59q550n.

MLA Handbook (7th Edition):

Lee, Jack C H. “Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.” 2013. Web. 20 Oct 2019.

Vancouver:

Lee JCH. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2019 Oct 20]. Available from: https://era.library.ualberta.ca/files/qn59q550n.

Council of Science Editors:

Lee JCH. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/qn59q550n


NSYSU

24. Huang, Hao-ping. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.

Degree: Master, Chemistry, 2013, NSYSU

 The direct ortho arylation of 4-methyl-N-phenylpyridin-2-amines via palladium(II)-catalyzed C-H activation is described. Treatment of 4-methyl-N-phenylpyridin-2-amine with potassium aryltrifluoroborate using ten mol % of Pd(OAc)2 as… (more)

Subjects/Keywords: palladium; C-H bond activation; potassium aryltrifluoroborate; Suzuki-Miyaura cross-coupling reaction

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APA (6th Edition):

Huang, H. (2013). Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051

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):

Huang, Hao-ping. “Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.” 2013. Thesis, NSYSU. Accessed October 20, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051.

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

MLA Handbook (7th Edition):

Huang, Hao-ping. “Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.” 2013. Web. 20 Oct 2019.

Vancouver:

Huang H. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. [Internet] [Thesis]. NSYSU; 2013. [cited 2019 Oct 20]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051.

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

Council of Science Editors:

Huang H. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051

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

25. Urgin, Karene. Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2010, Université Paris-Est

Les hétérocycles aromatiques sont des motifs structuraux rencontrés dans un grand nombre de substances d'intérêts biologiques ou pharmacologiques. Plus particulièrement, les pyridazines substituées font l'objet… (more)

Subjects/Keywords: Pyridazine; Couplage; Electrosynthèse; Organozinciques; Triarylbismuths; Palladium; Pyridazine; Cross-coupling reaction; Electrosynthesis; Organozinc compounds; Triarylbismuths; Palladium

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APA (6th Edition):

Urgin, K. (2010). Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic. (Doctoral Dissertation). Université Paris-Est. Retrieved from http://www.theses.fr/2010PEST1094

Chicago Manual of Style (16th Edition):

Urgin, Karene. “Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic.” 2010. Doctoral Dissertation, Université Paris-Est. Accessed October 20, 2019. http://www.theses.fr/2010PEST1094.

MLA Handbook (7th Edition):

Urgin, Karene. “Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic.” 2010. Web. 20 Oct 2019.

Vancouver:

Urgin K. Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic. [Internet] [Doctoral dissertation]. Université Paris-Est; 2010. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2010PEST1094.

Council of Science Editors:

Urgin K. Préparation de dérivés aryl- et hétéroaryl- pyridazine(s) par voies organométalliques chimiques ou électrochimiques : Preparation of heteroaryl and aryl pyridazine derivatives by organometallic. [Doctoral Dissertation]. Université Paris-Est; 2010. Available from: http://www.theses.fr/2010PEST1094


Boston College

26. Zhang, Liang. Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions.

Degree: PhD, Chemistry, 2017, Boston College

 This dissertation will present four main projects focused on stereoselective construction of borylated compounds as well as their applications in asymmetric syntheses. The first two… (more)

Subjects/Keywords: boron-Wittig reaction; catalytic conjunctive cross-coupling; catalytic diboration; enantioselective synthesis; organoboronates

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

APA (6th Edition):

Zhang, L. (2017). Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107561

Chicago Manual of Style (16th Edition):

Zhang, Liang. “Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions.” 2017. Doctoral Dissertation, Boston College. Accessed October 20, 2019. http://dlib.bc.edu/islandora/object/bc-ir:107561.

MLA Handbook (7th Edition):

Zhang, Liang. “Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions.” 2017. Web. 20 Oct 2019.

Vancouver:

Zhang L. Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions. [Internet] [Doctoral dissertation]. Boston College; 2017. [cited 2019 Oct 20]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107561.

Council of Science Editors:

Zhang L. Catalytic Conjunctive Cross-Coupling and Catalytic Diboration Reactions. [Doctoral Dissertation]. Boston College; 2017. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107561


University of Illinois – Urbana-Champaign

27. Yousaf, Zain. Development of organosilicon cross-coupling reaction.

Degree: MS, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Use of palladium catalyzed cross-couplings have found widespread use in the pharmaceutical industry and there is a significant ongoing effort to either improve or devise… (more)

Subjects/Keywords: silanolate; cross-coupling

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APA (6th Edition):

Yousaf, Z. (2015). Development of organosilicon cross-coupling reaction. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89275

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):

Yousaf, Zain. “Development of organosilicon cross-coupling reaction.” 2015. Thesis, University of Illinois – Urbana-Champaign. Accessed October 20, 2019. http://hdl.handle.net/2142/89275.

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

MLA Handbook (7th Edition):

Yousaf, Zain. “Development of organosilicon cross-coupling reaction.” 2015. Web. 20 Oct 2019.

Vancouver:

Yousaf Z. Development of organosilicon cross-coupling reaction. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2142/89275.

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

Council of Science Editors:

Yousaf Z. Development of organosilicon cross-coupling reaction. [Thesis]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89275

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


University of Ottawa

28. Masson-Makdissi, Jeanne. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .

Degree: 2018, University of Ottawa

 First popularized in the 1970s, transition metal-catalyzed cross-couplings now constitute staple reactions for the formation of carbon-carbon and carbon-heteroatom bonds. Recent endeavours in the field… (more)

Subjects/Keywords: cross-coupling; esters

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APA (6th Edition):

Masson-Makdissi, J. (2018). Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/38398

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):

Masson-Makdissi, Jeanne. “Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .” 2018. Thesis, University of Ottawa. Accessed October 20, 2019. http://hdl.handle.net/10393/38398.

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

MLA Handbook (7th Edition):

Masson-Makdissi, Jeanne. “Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .” 2018. Web. 20 Oct 2019.

Vancouver:

Masson-Makdissi J. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10393/38398.

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

Council of Science Editors:

Masson-Makdissi J. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/38398

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


Queens University

29. Holland, Amy Marie. INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS .

Degree: Chemistry, 2010, Queens University

 Until recently, secondary organoboronic esters were not viable substrates in the Suzuki-Miyaura cross-coupling reaction; however under recently reported conditions from the Crudden group1, which includes… (more)

Subjects/Keywords: Organometallics; Cross-Coupling

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APA (6th Edition):

Holland, A. M. (2010). INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6071

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):

Holland, Amy Marie. “INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS .” 2010. Thesis, Queens University. Accessed October 20, 2019. http://hdl.handle.net/1974/6071.

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

MLA Handbook (7th Edition):

Holland, Amy Marie. “INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS .” 2010. Web. 20 Oct 2019.

Vancouver:

Holland AM. INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS . [Internet] [Thesis]. Queens University; 2010. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1974/6071.

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

Council of Science Editors:

Holland AM. INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS . [Thesis]. Queens University; 2010. Available from: http://hdl.handle.net/1974/6071

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


Freie Universität Berlin

30. Henze, Oliver. Shape-persistent Macrocycles with 2,2´-Bipyridines: Synthesis, Selforganisation, and Complexation.

Degree: 2000, Freie Universität Berlin

 Summary The report describes the syntheses of pyridines, 2,2ý-bipyridines and benzene derivatives and the connection of these units using the chemo- and regioselectivity in Pd°… (more)

Subjects/Keywords: 2; 2´-Bipyridine; macrocycles; Hagihara/Sonogashira cross-coupling; Stille cross-coupling; supramolecular chemistry; ruthenium complexes; 500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften

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APA (6th Edition):

Henze, O. (2000). Shape-persistent Macrocycles with 2,2´-Bipyridines: Synthesis, Selforganisation, and Complexation. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-12186

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):

Henze, Oliver. “Shape-persistent Macrocycles with 2,2´-Bipyridines: Synthesis, Selforganisation, and Complexation.” 2000. Thesis, Freie Universität Berlin. Accessed October 20, 2019. http://dx.doi.org/10.17169/refubium-12186.

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

MLA Handbook (7th Edition):

Henze, Oliver. “Shape-persistent Macrocycles with 2,2´-Bipyridines: Synthesis, Selforganisation, and Complexation.” 2000. Web. 20 Oct 2019.

Vancouver:

Henze O. Shape-persistent Macrocycles with 2,2´-Bipyridines: Synthesis, Selforganisation, and Complexation. [Internet] [Thesis]. Freie Universität Berlin; 2000. [cited 2019 Oct 20]. Available from: http://dx.doi.org/10.17169/refubium-12186.

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

Council of Science Editors:

Henze O. Shape-persistent Macrocycles with 2,2´-Bipyridines: Synthesis, Selforganisation, and Complexation. [Thesis]. Freie Universität Berlin; 2000. Available from: http://dx.doi.org/10.17169/refubium-12186

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

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