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NSYSU
1. Chiang, Meng-fan. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.
Degree: Master, Chemistry, 2015, NSYSU
URL: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952
Subjects/Keywords: palladium; C-C coupling; C-H activation; catalyzed reaction; ortho-aroylation
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Chiang, M. (2015). Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952
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):
Chiang, Meng-fan. “Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.” 2015. Thesis, NSYSU. Accessed January 26, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Chiang, Meng-fan. “Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.” 2015. Web. 26 Jan 2021.
Vancouver:
Chiang M. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. [Internet] [Thesis]. NSYSU; 2015. [cited 2021 Jan 26]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Chiang M. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. [Thesis]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
NSYSU
2. Chen, Jiun-hong. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.
Degree: Master, Chemistry, 2016, NSYSU
URL: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826
Subjects/Keywords: palladium; ortho-aroylation; C-C coupling; catalyzed reaction; C-H activation
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Chen, J. (2016). Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826
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):
Chen, Jiun-hong. “Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.” 2016. Thesis, NSYSU. Accessed January 26, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Chen, Jiun-hong. “Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.” 2016. Web. 26 Jan 2021.
Vancouver:
Chen J. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. [Internet] [Thesis]. NSYSU; 2016. [cited 2021 Jan 26]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Chen J. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
University of Illinois – Urbana-Champaign
3. Bailey, Aaron D. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.
Degree: MS, 0335, 2011, University of Illinois – Urbana-Champaign
URL: http://hdl.handle.net/2142/24450
Subjects/Keywords: Palladium-catalyzed cross-coupling reactions; allylic silanes; vinylsilanes
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Bailey, A. D. (2011). Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24450
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):
Bailey, Aaron D. “Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.” 2011. Thesis, University of Illinois – Urbana-Champaign. Accessed January 26, 2021. http://hdl.handle.net/2142/24450.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Bailey, Aaron D. “Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.” 2011. Web. 26 Jan 2021.
Vancouver:
Bailey AD. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2011. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/2142/24450.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Bailey AD. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. [Thesis]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24450
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Université Paris-Sud – Paris XI
4. Roche, Maxime. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.
Degree: Docteur es, Chimie thérapeutique, 2014, Université Paris-Sud – Paris XI
URL: http://www.theses.fr/2014PA114843
Subjects/Keywords: Combrétastatine; Antivasculaire; N-tosylhydrazone; Couplage pallado-catalysé; Réaction tandem; Couplage oxydatif; Combretastatin; Antivascular; N-tosylhydrazone; Palladium catalyzed cross-coupling; Tandem reaction; Oxidative coupling
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Roche, M. (2014). Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA114843
Chicago Manual of Style (16th Edition):
Roche, Maxime. “Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 26, 2021. http://www.theses.fr/2014PA114843.
MLA Handbook (7th Edition):
Roche, Maxime. “Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.” 2014. Web. 26 Jan 2021.
Vancouver:
Roche M. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2014PA114843.
Council of Science Editors:
Roche M. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA114843
5. Geogheghan, Katherine Jayne. Boronic acid speciation in Suzuki-Miyaura cross-coupling.
Degree: PhD, 2018, University of Edinburgh
URL: http://hdl.handle.net/1842/33092
Subjects/Keywords: 660; cross-coupling; Suzuki-Miyaura reaction; palladium catalysed coupling; boronic esters
Record Details
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
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 January 26, 2021. http://hdl.handle.net/1842/33092.
MLA Handbook (7th Edition):
Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Web. 26 Jan 2021.
Vancouver:
Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2021 Jan 26]. 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 Washington
6. Lesniak, Valerie Ann. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.
Degree: 2016, University of Washington
URL: http://hdl.handle.net/1773/37060
Subjects/Keywords: alkenylboronic acid; aziridine; boronic acid; cross-coupling; homoallylic amine; Palladium-catalyzed; Chemistry; Organic chemistry; chemistry
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Lesniak, V. A. (2016). Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/37060
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):
Lesniak, Valerie Ann. “Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.” 2016. Thesis, University of Washington. Accessed January 26, 2021. http://hdl.handle.net/1773/37060.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Lesniak, Valerie Ann. “Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.” 2016. Web. 26 Jan 2021.
Vancouver:
Lesniak VA. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. [Internet] [Thesis]. University of Washington; 2016. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1773/37060.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Lesniak VA. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. [Thesis]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/37060
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
University of Pennsylvania
7. McGrew, Genette I. Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes.
Degree: 2011, University of Pennsylvania
URL: https://repository.upenn.edu/edissertations/964
Subjects/Keywords: tricarbonylchromium; palladium-catalyzed; cross-coupling; asymmetric; organolithium; polyarylmethanes; Inorganic Chemistry; Organic Chemistry
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APA (6th Edition):
McGrew, G. I. (2011). Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/964
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):
McGrew, Genette I. “Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes.” 2011. Thesis, University of Pennsylvania. Accessed January 26, 2021. https://repository.upenn.edu/edissertations/964.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
McGrew, Genette I. “Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes.” 2011. Web. 26 Jan 2021.
Vancouver:
McGrew GI. Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes. [Internet] [Thesis]. University of Pennsylvania; 2011. [cited 2021 Jan 26]. Available from: https://repository.upenn.edu/edissertations/964.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
McGrew GI. Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes. [Thesis]. University of Pennsylvania; 2011. Available from: https://repository.upenn.edu/edissertations/964
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
University of Illinois – Chicago
8. Mamidipalli, Phani Raja P. Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes.
Degree: 2015, University of Illinois – Chicago
URL: http://hdl.handle.net/10027/19456
Subjects/Keywords: Copper catalyzed coupling; HDDA reaction
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APA (6th Edition):
Mamidipalli, P. R. P. (2015). Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19456
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):
Mamidipalli, Phani Raja P. “Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes.” 2015. Thesis, University of Illinois – Chicago. Accessed January 26, 2021. http://hdl.handle.net/10027/19456.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Mamidipalli, Phani Raja P. “Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes.” 2015. Web. 26 Jan 2021.
Vancouver:
Mamidipalli PRP. Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/10027/19456.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Mamidipalli PRP. Mechanism of Copper Catalyzed Diazo Coupling and its Applications & Reactions of Multiynes. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19456
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
9. 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
URL: http://www.theses.fr/2010PEST1094
Subjects/Keywords: Pyridazine; Couplage; Electrosynthèse; Organozinciques; Triarylbismuths; Palladium; Pyridazine; Cross-coupling reaction; Electrosynthesis; Organozinc compounds; Triarylbismuths; Palladium
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
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 January 26, 2021. 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. 26 Jan 2021.
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 2021 Jan 26]. 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
University of Alberta
10. 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
URL: https://era.library.ualberta.ca/files/qn59q550n
Subjects/Keywords: Gold-catalyzed cycloisomerization; Suzuki-Miyaura cross-coupling; Chiral alkyl boronates; Heck reaction; Enantioselective conjugate addition
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
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 January 26, 2021. 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. 26 Jan 2021.
Vancouver:
Lee JCH. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2021 Jan 26]. 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
McMaster University
11. Todorovic, Nikola. DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES.
Degree: PhD, 2012, McMaster University
URL: http://hdl.handle.net/11375/12471
Subjects/Keywords: Compound libraries; Isoquinolines; Pyrazolopyrimidines; Toxoflavin; Palladium-catalyzed cross-coupling; Microwave-assisted heating; Organic Chemistry; Organic Chemistry
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Todorovic, N. (2012). DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12471
Chicago Manual of Style (16th Edition):
Todorovic, Nikola. “DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES.” 2012. Doctoral Dissertation, McMaster University. Accessed January 26, 2021. http://hdl.handle.net/11375/12471.
MLA Handbook (7th Edition):
Todorovic, Nikola. “DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES.” 2012. Web. 26 Jan 2021.
Vancouver:
Todorovic N. DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/11375/12471.
Council of Science Editors:
Todorovic N. DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12471
Florida International University
12. Pitteloud, Jean-Philippe. New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues.
Degree: Chemistry, 2010, Florida International University
URL: https://digitalcommons.fiu.edu/etd/170
;
10.25148/etd.FI10041621
;
FI10041621
Subjects/Keywords: ORGANOGERMANES; PALLADIUM-CATALYZED; CROSS-COUPLING; TRANSMETALLATION; URIDINE; NUCLEOSIDES
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APA (6th Edition):
Pitteloud, J. (2010). New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues. (Thesis). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621
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):
Pitteloud, Jean-Philippe. “New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues.” 2010. Thesis, Florida International University. Accessed January 26, 2021. https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Pitteloud, Jean-Philippe. “New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues.” 2010. Web. 26 Jan 2021.
Vancouver:
Pitteloud J. New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues. [Internet] [Thesis]. Florida International University; 2010. [cited 2021 Jan 26]. Available from: https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Pitteloud J. New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues. [Thesis]. Florida International University; 2010. Available from: https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Florida International University
13. Liang, Yong. Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides.
Degree: PhD, Chemistry, 2014, Florida International University
URL: https://digitalcommons.fiu.edu/etd/1591
;
10.25148/etd.FI14110716
;
FI14110716
Subjects/Keywords: Nucleoside; Pd-catalyzed Cross-coupling; Palladium; Click Chemistry; Hydrogermylation; C-H activation; Direct Arylation; Organic Chemistry
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APA (6th Edition):
Liang, Y. (2014). Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides. (Doctoral Dissertation). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716
Chicago Manual of Style (16th Edition):
Liang, Yong. “Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides.” 2014. Doctoral Dissertation, Florida International University. Accessed January 26, 2021. https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716.
MLA Handbook (7th Edition):
Liang, Yong. “Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides.” 2014. Web. 26 Jan 2021.
Vancouver:
Liang Y. Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides. [Internet] [Doctoral dissertation]. Florida International University; 2014. [cited 2021 Jan 26]. Available from: https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716.
Council of Science Editors:
Liang Y. Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides. [Doctoral Dissertation]. Florida International University; 2014. Available from: https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716
East Carolina University
14. Harris, Caleb F. Synthesis and Reactions of Novel Heteroarylzirconocene Reagents.
Degree: MS, Chemistry, 2012, East Carolina University
URL: http://hdl.handle.net/10342/4004
Subjects/Keywords: Chemistry; Cross-coupling; Heteroaromatic; Organometallic; Palladium-catalyzed; Zirconocene; Zirconium; Chemical tests and reagents; Organic compounds – Synthesis; Halides
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APA (6th Edition):
Harris, C. F. (2012). Synthesis and Reactions of Novel Heteroarylzirconocene Reagents. (Masters Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4004
Chicago Manual of Style (16th Edition):
Harris, Caleb F. “Synthesis and Reactions of Novel Heteroarylzirconocene Reagents.” 2012. Masters Thesis, East Carolina University. Accessed January 26, 2021. http://hdl.handle.net/10342/4004.
MLA Handbook (7th Edition):
Harris, Caleb F. “Synthesis and Reactions of Novel Heteroarylzirconocene Reagents.” 2012. Web. 26 Jan 2021.
Vancouver:
Harris CF. Synthesis and Reactions of Novel Heteroarylzirconocene Reagents. [Internet] [Masters thesis]. East Carolina University; 2012. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/10342/4004.
Council of Science Editors:
Harris CF. Synthesis and Reactions of Novel Heteroarylzirconocene Reagents. [Masters Thesis]. East Carolina University; 2012. Available from: http://hdl.handle.net/10342/4004
NSYSU
15. 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
URL: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051
Subjects/Keywords: palladium; C-H bond activation; potassium aryltrifluoroborate; Suzuki-Miyaura cross-coupling reaction
Record Details
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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 January 26, 2021. 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. 26 Jan 2021.
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 2021 Jan 26]. 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
16. Souffrin, Agathe. Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase.
Degree: Docteur es, Sciences de la vie et de la santé, spécialité Chimie organique, 2012, Université François-Rabelais de Tours
URL: http://www.theses.fr/2012TOUR3801
Subjects/Keywords: SIDA; VIH; Intégrase; Enzyme à DDE; Transposase; Inhibiteur; Maléimide; Pharmacomodulation; Synthèse multi-étape; Chimie hétérocyclique; Réaction de couplage pallado-catalysée; Modélisation moléculaire; Complexation; Évaluation pharmacologique; Photoactivation; AIDS; HIV; Integrase; DDE enzyme; Transposase; Inhibitor; Maleimide; Pharmacomodulation; Multi-step synthesis; Heterocyclic chemistry; Palladium-catalyzed cross-coupling reaction; Molecular modeling; Complexation; Pharmacological evaluation; Photoaffinity labeling
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APA (6th Edition):
Souffrin, A. (2012). Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2012TOUR3801
Chicago Manual of Style (16th Edition):
Souffrin, Agathe. “Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase.” 2012. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed January 26, 2021. http://www.theses.fr/2012TOUR3801.
MLA Handbook (7th Edition):
Souffrin, Agathe. “Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase.” 2012. Web. 26 Jan 2021.
Vancouver:
Souffrin A. Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2012. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2012TOUR3801.
Council of Science Editors:
Souffrin A. Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1 : Design, synthesis and pharmacological evaluation of maleimides, potential inhibitors of HIV-1 integrase. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2012. Available from: http://www.theses.fr/2012TOUR3801
17. Naas, Mohammed. Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential.
Degree: Docteur es, Chimie organique. Pharmacochimie, 2016, Orléans; Université Mohamed V
URL: http://www.theses.fr/2016ORLE2009
Subjects/Keywords: Indazoles; Suzuki-Miyaura; (hétéro)arylation directe; Alcénylation directe; One-pot; Réactions pallado-catallysées; Indazoles; Suzuki-Miyaura cross-coupling; Direct (hetero)arylation; Direct alkenylation; One-pot; Palladium-catalyzed reactions; 547.59
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APA (6th Edition):
Naas, M. (2016). Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential. (Doctoral Dissertation). Orléans; Université Mohamed V. Retrieved from http://www.theses.fr/2016ORLE2009
Chicago Manual of Style (16th Edition):
Naas, Mohammed. “Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential.” 2016. Doctoral Dissertation, Orléans; Université Mohamed V. Accessed January 26, 2021. http://www.theses.fr/2016ORLE2009.
MLA Handbook (7th Edition):
Naas, Mohammed. “Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential.” 2016. Web. 26 Jan 2021.
Vancouver:
Naas M. Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential. [Internet] [Doctoral dissertation]. Orléans; Université Mohamed V; 2016. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2016ORLE2009.
Council of Science Editors:
Naas M. Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential. [Doctoral Dissertation]. Orléans; Université Mohamed V; 2016. Available from: http://www.theses.fr/2016ORLE2009
18. LeBlond, Carl. Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction.
Degree: PhD, Chemistry, 2011, Seton Hall University
URL: https://scholarship.shu.edu/dissertations/1242
Subjects/Keywords: Cross coupling; palladium catalyzed; pallium on carbon; Chemistry; Organic Chemistry
…of the Suzuki Cross-Coupling Reaction… …PdIC Catalyzed Suzuki Cross-Coupling with Aryl Bromides… …69 PdIC Catalyzed Suzuki Cross-Coupling with Aryl Chlorides… …62 Figure 10. Hammett plot for the heterogeneous Suzuki cross-coupling reaction using Pd/C… …45 Table 3 . Pd/C catalyzed Suzuki cross-coupling results reported by Buchecker et a1…
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
LeBlond, C. (2011). Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction. (Doctoral Dissertation). Seton Hall University. Retrieved from https://scholarship.shu.edu/dissertations/1242
Chicago Manual of Style (16th Edition):
LeBlond, Carl. “Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction.” 2011. Doctoral Dissertation, Seton Hall University. Accessed January 26, 2021. https://scholarship.shu.edu/dissertations/1242.
MLA Handbook (7th Edition):
LeBlond, Carl. “Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction.” 2011. Web. 26 Jan 2021.
Vancouver:
LeBlond C. Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction. [Internet] [Doctoral dissertation]. Seton Hall University; 2011. [cited 2021 Jan 26]. Available from: https://scholarship.shu.edu/dissertations/1242.
Council of Science Editors:
LeBlond C. Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction. [Doctoral Dissertation]. Seton Hall University; 2011. Available from: https://scholarship.shu.edu/dissertations/1242
19. Charpenay, Mélanie. Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction.
Degree: Docteur es, Chimie, 2012, Université de Strasbourg
URL: http://www.theses.fr/2012STRAF040
Subjects/Keywords: Fenestrane; Cyclooctatriene; Réaction en cascade; Catalyse au palladium; Fenestradienes; Cyclooctatrienes; Cascade reaction; Palladium-catalyzed; 541.39
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APA (6th Edition):
Charpenay, M. (2012). Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAF040
Chicago Manual of Style (16th Edition):
Charpenay, Mélanie. “Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed January 26, 2021. http://www.theses.fr/2012STRAF040.
MLA Handbook (7th Edition):
Charpenay, Mélanie. “Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction.” 2012. Web. 26 Jan 2021.
Vancouver:
Charpenay M. Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2012STRAF040.
Council of Science Editors:
Charpenay M. Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée : Fenestradienes and cyclooctatrienes : direct synthesis using a palladium-catalyzed cascade reaction. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAF040
King Abdullah University of Science and Technology
20. Walter, Philipp E. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol.
Degree: 2012, King Abdullah University of Science and Technology
URL: http://hdl.handle.net/10754/262732
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 January 26, 2021. 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. 26 Jan 2021.
Vancouver:
Walter PE. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. [Internet] [Thesis]. King Abdullah University of Science and Technology; 2012. [cited 2021 Jan 26]. 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
Boston College
21. Le, Hai. Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls.
Degree: PhD, Chemistry, 2014, Boston College
URL: http://dlib.bc.edu/islandora/object/bc-ir:104389
Subjects/Keywords: allyl; asymmetric; cross-coupling; organometallic; palladium; synthesis
Record Details
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Le, H. (2014). Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104389
Chicago Manual of Style (16th Edition):
Le, Hai. “Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls.” 2014. Doctoral Dissertation, Boston College. Accessed January 26, 2021. http://dlib.bc.edu/islandora/object/bc-ir:104389.
MLA Handbook (7th Edition):
Le, Hai. “Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls.” 2014. Web. 26 Jan 2021.
Vancouver:
Le H. Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls. [Internet] [Doctoral dissertation]. Boston College; 2014. [cited 2021 Jan 26]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104389.
Council of Science Editors:
Le H. Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls. [Doctoral Dissertation]. Boston College; 2014. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104389
Boston College
22. Edelstein, Emma Kate. Enantioselective synthesis and stereospecific transformations of organoboronic esters.
Degree: PhD, Chemistry, 2018, Boston College
URL: http://dlib.bc.edu/islandora/object/bc-ir:108038
Subjects/Keywords: Boron; Catalysis; Cross-Coupling; Enantioselective; Palladium; Stereospecific
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APA (6th Edition):
Edelstein, E. K. (2018). Enantioselective synthesis and stereospecific transformations of organoboronic esters. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:108038
Chicago Manual of Style (16th Edition):
Edelstein, Emma Kate. “Enantioselective synthesis and stereospecific transformations of organoboronic esters.” 2018. Doctoral Dissertation, Boston College. Accessed January 26, 2021. http://dlib.bc.edu/islandora/object/bc-ir:108038.
MLA Handbook (7th Edition):
Edelstein, Emma Kate. “Enantioselective synthesis and stereospecific transformations of organoboronic esters.” 2018. Web. 26 Jan 2021.
Vancouver:
Edelstein EK. Enantioselective synthesis and stereospecific transformations of organoboronic esters. [Internet] [Doctoral dissertation]. Boston College; 2018. [cited 2021 Jan 26]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:108038.
Council of Science Editors:
Edelstein EK. Enantioselective synthesis and stereospecific transformations of organoboronic esters. [Doctoral Dissertation]. Boston College; 2018. Available from: http://dlib.bc.edu/islandora/object/bc-ir:108038
Queens University
23. Fraser, Andrew. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .
Degree: Chemistry, 2013, Queens University
URL: http://hdl.handle.net/1974/8094
Subjects/Keywords: Catalysis ; Palladium ; Cross-Coupling ; Organometallic Chemistry
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APA (6th Edition):
Fraser, A. (2013). Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8094
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):
Fraser, Andrew. “Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .” 2013. Thesis, Queens University. Accessed January 26, 2021. http://hdl.handle.net/1974/8094.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Fraser, Andrew. “Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .” 2013. Web. 26 Jan 2021.
Vancouver:
Fraser A. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . [Internet] [Thesis]. Queens University; 2013. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1974/8094.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Fraser A. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/8094
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
24. Peramo, Arnaud. Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction.
Degree: Docteur es, Pharmacotechnie et biopharmacie, 2019, Université Paris-Saclay (ComUE)
URL: http://www.theses.fr/2019SACLS600
Subjects/Keywords: Palladium nanoparticules; Réaction de Suzuki-Myaura; Chimie in vivo; Thyroglobuline; Protémoque; Palladium nanoparticles; Suzuki-Myaura cross-Coupling reaction; In vivo chemistry; Thyroglobulin; Proteomic
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Peramo, A. (2019). Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS600
Chicago Manual of Style (16th Edition):
Peramo, Arnaud. “Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed January 26, 2021. http://www.theses.fr/2019SACLS600.
MLA Handbook (7th Edition):
Peramo, Arnaud. “Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction.” 2019. Web. 26 Jan 2021.
Vancouver:
Peramo A. Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2019SACLS600.
Council of Science Editors:
Peramo A. Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS600
25. Da Costa, Laurène. Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections.
Degree: Docteur es, Sciences Chimiques, 2017, Aix Marseille Université
URL: http://www.theses.fr/2017AIXM0350
Subjects/Keywords: Rhinovirus; Capsid-Binder; Réaction par transfert monoélectronique; Tdae; Couplages pallado-Catalysés; Méthode de Mosher; Rhinovirus; Capsid-Binder; Single electron transfer (SET) reaction; Tdae; Pallado-Catalyzed cross-Coupling reactions; Mosher’s method
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APA (6th Edition):
Da Costa, L. (2017). Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0350
Chicago Manual of Style (16th Edition):
Da Costa, Laurène. “Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed January 26, 2021. http://www.theses.fr/2017AIXM0350.
MLA Handbook (7th Edition):
Da Costa, Laurène. “Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections.” 2017. Web. 26 Jan 2021.
Vancouver:
Da Costa L. Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2017AIXM0350.
Council of Science Editors:
Da Costa L. Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0350
Université de Bordeaux I
26. Pradhan, Anirban. Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés.
Degree: Docteur es, Chimie, 2013, Université de Bordeaux I
URL: http://www.theses.fr/2013BOR14849
Subjects/Keywords: Composés aromatiques polycycliques; Nanorubans de carbone; Hélicènes; Réaction de Scholl; Réactions catalysées de couplages croisés; Polycyclic aromatic compounds (PAC); Carbon nanoribbons; Helicenes; Scholl reaction; Catalyzed cross-coupling reactions
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Pradhan, A. (2013). Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés. (Doctoral Dissertation). Université de Bordeaux I. Retrieved from http://www.theses.fr/2013BOR14849
Chicago Manual of Style (16th Edition):
Pradhan, Anirban. “Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés.” 2013. Doctoral Dissertation, Université de Bordeaux I. Accessed January 26, 2021. http://www.theses.fr/2013BOR14849.
MLA Handbook (7th Edition):
Pradhan, Anirban. “Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés.” 2013. Web. 26 Jan 2021.
Vancouver:
Pradhan A. Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés. [Internet] [Doctoral dissertation]. Université de Bordeaux I; 2013. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2013BOR14849.
Council of Science Editors:
Pradhan A. Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés. [Doctoral Dissertation]. Université de Bordeaux I; 2013. Available from: http://www.theses.fr/2013BOR14849
University of Gothenburg / Göteborgs Universitet
27. Kleimark, Jonatan. MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS.
Degree: 2011, University of Gothenburg / Göteborgs Universitet
URL: http://hdl.handle.net/2077/27967
Subjects/Keywords: alkene insertion; allylic alkylation; catalysis; cross coupling; density funtional theory; free energy surface; iron; kinetic investigation; Mizoroki-Heck reaction; nickel; palladium; reaction mechanism; sulfinylation; transition metal
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Kleimark, J. (2011). MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/27967
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):
Kleimark, Jonatan. “MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS.” 2011. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed January 26, 2021. http://hdl.handle.net/2077/27967.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Kleimark, Jonatan. “MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS.” 2011. Web. 26 Jan 2021.
Vancouver:
Kleimark J. MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2011. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/2077/27967.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Kleimark J. MECHANISTIC INVESTIGATIONS OF TRANSITION METAL CATALYZED REACTIONS. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2011. Available from: http://hdl.handle.net/2077/27967
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
University of Rochester
28. Anka-Lufford, Lukiana L. (1988 - ). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles.
Degree: PhD, 2016, University of Rochester
URL: http://hdl.handle.net/1802/30406
Subjects/Keywords: Alkyl electrophiles; Aryl halides; Cross-coupling; Nickel-catalyzed
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Anka-Lufford, L. L. (. -. ). (2016). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30406
Chicago Manual of Style (16th Edition):
Anka-Lufford, Lukiana L (1988 - ). “Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles.” 2016. Doctoral Dissertation, University of Rochester. Accessed January 26, 2021. http://hdl.handle.net/1802/30406.
MLA Handbook (7th Edition):
Anka-Lufford, Lukiana L (1988 - ). “Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles.” 2016. Web. 26 Jan 2021.
Vancouver:
Anka-Lufford LL(-). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles. [Internet] [Doctoral dissertation]. University of Rochester; 2016. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1802/30406.
Council of Science Editors:
Anka-Lufford LL(-). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles. [Doctoral Dissertation]. University of Rochester; 2016. Available from: http://hdl.handle.net/1802/30406
NSYSU
29. Huang, Nan-Yuan. Development of New Synthesis of Sulfur-oxazoline Ligands.
Degree: Master, Chemistry, 2011, NSYSU
URL: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108
Subjects/Keywords: CuI-catalyzed reaction; Iodooxazoline; Pd-catalyzed asymmetric alkylation; Carbon-sulfur coupling reaction; Chiral sulfur-oxazoline ligands
Record Details
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Huang, N. (2011). Development of New Synthesis of Sulfur-oxazoline Ligands. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108
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, Nan-Yuan. “Development of New Synthesis of Sulfur-oxazoline Ligands.” 2011. Thesis, NSYSU. Accessed January 26, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Huang, Nan-Yuan. “Development of New Synthesis of Sulfur-oxazoline Ligands.” 2011. Web. 26 Jan 2021.
Vancouver:
Huang N. Development of New Synthesis of Sulfur-oxazoline Ligands. [Internet] [Thesis]. NSYSU; 2011. [cited 2021 Jan 26]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Huang N. Development of New Synthesis of Sulfur-oxazoline Ligands. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1003111-232108
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
30. Gigant, Nicolas. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.
Degree: Docteur es, Chimie organique, 2012, Université d'Orléans
URL: http://www.theses.fr/2012ORLE2039
Subjects/Keywords: Enamide; Diversité moléculaire; Synthèse orientée vers la diversité; Phosphates vinyliques; Additions d’aza-Michaël; Nitrènes; Réactions de couplage pallado-catalysées; Réactions en cascades; Enamides; Molecular diversity; Diversity-oriented synthesis; Vinylphosphates; Aza-Michael additions; Nitrenes; Palladium-catalyzed cross-coupling reactions; Cascade reactions
Record Details
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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager
APA (6th Edition):
Gigant, N. (2012). Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2012ORLE2039
Chicago Manual of Style (16th Edition):
Gigant, Nicolas. “Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.” 2012. Doctoral Dissertation, Université d'Orléans. Accessed January 26, 2021. http://www.theses.fr/2012ORLE2039.
MLA Handbook (7th Edition):
Gigant, Nicolas. “Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.” 2012. Web. 26 Jan 2021.
Vancouver:
Gigant N. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. [Internet] [Doctoral dissertation]. Université d'Orléans; 2012. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2012ORLE2039.
Council of Science Editors:
Gigant N. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. [Doctoral Dissertation]. Université d'Orléans; 2012. Available from: http://www.theses.fr/2012ORLE2039