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You searched for subject:( KIE). Showing records 1 – 13 of 13 total matches.

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Université Paris-Sud – Paris XI

1. Huang, Min. Elucidation des Mécanismes de O- et C-glycosylation par des Moyens Chimiques et Spectroscopiques : Elucidating Mechanisms of O- and C-glycosylation by Chemical and Spectroscopic Means.

Degree: Docteur es, Chimie organique, 2012, Université Paris-Sud – Paris XI

L’effet isotopique cinétique (KIE) est un outil puissant pour obtenir un aperçu sur le mécanisme d'une grande variété réactions. Nous avons observé différentes mesures de… (more)

Subjects/Keywords: Glycosylation; KIE (Effet isotopique cinétique); Ion oxocarbénium; Cinétique relative; Glycosylation; KIE (Kinetic isotope effect); Oxocarbenium ion; Relative kinetics

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APA (6th Edition):

Huang, M. (2012). Elucidation des Mécanismes de O- et C-glycosylation par des Moyens Chimiques et Spectroscopiques : Elucidating Mechanisms of O- and C-glycosylation by Chemical and Spectroscopic Means. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA112272

Chicago Manual of Style (16th Edition):

Huang, Min. “Elucidation des Mécanismes de O- et C-glycosylation par des Moyens Chimiques et Spectroscopiques : Elucidating Mechanisms of O- and C-glycosylation by Chemical and Spectroscopic Means.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed May 10, 2021. http://www.theses.fr/2012PA112272.

MLA Handbook (7th Edition):

Huang, Min. “Elucidation des Mécanismes de O- et C-glycosylation par des Moyens Chimiques et Spectroscopiques : Elucidating Mechanisms of O- and C-glycosylation by Chemical and Spectroscopic Means.” 2012. Web. 10 May 2021.

Vancouver:

Huang M. Elucidation des Mécanismes de O- et C-glycosylation par des Moyens Chimiques et Spectroscopiques : Elucidating Mechanisms of O- and C-glycosylation by Chemical and Spectroscopic Means. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2021 May 10]. Available from: http://www.theses.fr/2012PA112272.

Council of Science Editors:

Huang M. Elucidation des Mécanismes de O- et C-glycosylation par des Moyens Chimiques et Spectroscopiques : Elucidating Mechanisms of O- and C-glycosylation by Chemical and Spectroscopic Means. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA112272


Virginia Tech

2. Mercedes-Camacho, Ana Yokayra. Pin1: WW domain ligands, catalytic inhibitors, and the mechanism.

Degree: PhD, Biochemistry, 2011, Virginia Tech

 The peptidyl prolyl cis/trans isomerase, PPIase, has been the focus of numerous studies in the field of cell cycle regulation since proline-directed phosphorylation is an… (more)

Subjects/Keywords: PPIases; Pin1 inhibitors; WW domain ligands; and KIE; c-Myc; ELEBA

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APA (6th Edition):

Mercedes-Camacho, A. Y. (2011). Pin1: WW domain ligands, catalytic inhibitors, and the mechanism. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77093

Chicago Manual of Style (16th Edition):

Mercedes-Camacho, Ana Yokayra. “Pin1: WW domain ligands, catalytic inhibitors, and the mechanism.” 2011. Doctoral Dissertation, Virginia Tech. Accessed May 10, 2021. http://hdl.handle.net/10919/77093.

MLA Handbook (7th Edition):

Mercedes-Camacho, Ana Yokayra. “Pin1: WW domain ligands, catalytic inhibitors, and the mechanism.” 2011. Web. 10 May 2021.

Vancouver:

Mercedes-Camacho AY. Pin1: WW domain ligands, catalytic inhibitors, and the mechanism. [Internet] [Doctoral dissertation]. Virginia Tech; 2011. [cited 2021 May 10]. Available from: http://hdl.handle.net/10919/77093.

Council of Science Editors:

Mercedes-Camacho AY. Pin1: WW domain ligands, catalytic inhibitors, and the mechanism. [Doctoral Dissertation]. Virginia Tech; 2011. Available from: http://hdl.handle.net/10919/77093


University of Wisconsin – Milwaukee

3. Shah, Dhara D. Mechanism of the Hydroxylation Reactions Catalyzed By 4-Hydroxyphenylpyruvate Dioxygenase and Hydroxymandelate Synthase.

Degree: PhD, Chemistry, 2014, University of Wisconsin – Milwaukee

  4-Hydroxyphenylpyruvate dioxygenase (HPPD) and Hydroxymandelate synthase (HMS) carry out highly similar complex dioxygenation reactions using the substrates, 4-hydroxyphenylpyruvate (HPP) and dioxygen. HPPD catalyzes decarboxylation,… (more)

Subjects/Keywords: 4-hydroxyphenylpyruvate Dioxygenase; HMS; HPPD; Hydroxymandelate Synthase; Intermediate Partitioning Kie; Ntbc; Biochemistry

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APA (6th Edition):

Shah, D. D. (2014). Mechanism of the Hydroxylation Reactions Catalyzed By 4-Hydroxyphenylpyruvate Dioxygenase and Hydroxymandelate Synthase. (Doctoral Dissertation). University of Wisconsin – Milwaukee. Retrieved from https://dc.uwm.edu/etd/759

Chicago Manual of Style (16th Edition):

Shah, Dhara D. “Mechanism of the Hydroxylation Reactions Catalyzed By 4-Hydroxyphenylpyruvate Dioxygenase and Hydroxymandelate Synthase.” 2014. Doctoral Dissertation, University of Wisconsin – Milwaukee. Accessed May 10, 2021. https://dc.uwm.edu/etd/759.

MLA Handbook (7th Edition):

Shah, Dhara D. “Mechanism of the Hydroxylation Reactions Catalyzed By 4-Hydroxyphenylpyruvate Dioxygenase and Hydroxymandelate Synthase.” 2014. Web. 10 May 2021.

Vancouver:

Shah DD. Mechanism of the Hydroxylation Reactions Catalyzed By 4-Hydroxyphenylpyruvate Dioxygenase and Hydroxymandelate Synthase. [Internet] [Doctoral dissertation]. University of Wisconsin – Milwaukee; 2014. [cited 2021 May 10]. Available from: https://dc.uwm.edu/etd/759.

Council of Science Editors:

Shah DD. Mechanism of the Hydroxylation Reactions Catalyzed By 4-Hydroxyphenylpyruvate Dioxygenase and Hydroxymandelate Synthase. [Doctoral Dissertation]. University of Wisconsin – Milwaukee; 2014. Available from: https://dc.uwm.edu/etd/759


University of Manchester

4. Hoeven, Robin. Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase.

Degree: PhD, 2015, University of Manchester

 Enzyme dynamics has been established to play a crucial role in catalysis, and it has therefore become an important area of research to better understand… (more)

Subjects/Keywords: 572; protochlorophyllide oxidoreductase; light-activated; KIE pressure dependence; kinetic isotope effect; enzyme dynamics

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APA (6th Edition):

Hoeven, R. (2015). Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-contribution-of-protein-dynamics-to-catalysis-in-protochlorophyllide-oxidoreductase(029dda21-023f-4fdb-a980-26db7eab4833).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.679982

Chicago Manual of Style (16th Edition):

Hoeven, Robin. “Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase.” 2015. Doctoral Dissertation, University of Manchester. Accessed May 10, 2021. https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-contribution-of-protein-dynamics-to-catalysis-in-protochlorophyllide-oxidoreductase(029dda21-023f-4fdb-a980-26db7eab4833).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.679982.

MLA Handbook (7th Edition):

Hoeven, Robin. “Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase.” 2015. Web. 10 May 2021.

Vancouver:

Hoeven R. Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 May 10]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-contribution-of-protein-dynamics-to-catalysis-in-protochlorophyllide-oxidoreductase(029dda21-023f-4fdb-a980-26db7eab4833).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.679982.

Council of Science Editors:

Hoeven R. Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-contribution-of-protein-dynamics-to-catalysis-in-protochlorophyllide-oxidoreductase(029dda21-023f-4fdb-a980-26db7eab4833).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.679982


University of Illinois – Urbana-Champaign

5. Hyatt, Michael George. Controlling the end groups and rates of catalytic polymerization.

Degree: PhD, Chemistry, 2020, University of Illinois – Urbana-Champaign

 Functionalizing polymer end groups, telechelic polymers, can be synthesized through multiple methods including chain transfer polymerization. Chain transfer polymerization involves a catalyst that is capable… (more)

Subjects/Keywords: ROMP; Grubbs; norbornene; KIE; RDS; chelation; polyethylene; palladium; cobalt; diimine; chain transfer

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APA (6th Edition):

Hyatt, M. G. (2020). Controlling the end groups and rates of catalytic polymerization. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/108440

Chicago Manual of Style (16th Edition):

Hyatt, Michael George. “Controlling the end groups and rates of catalytic polymerization.” 2020. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed May 10, 2021. http://hdl.handle.net/2142/108440.

MLA Handbook (7th Edition):

Hyatt, Michael George. “Controlling the end groups and rates of catalytic polymerization.” 2020. Web. 10 May 2021.

Vancouver:

Hyatt MG. Controlling the end groups and rates of catalytic polymerization. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2020. [cited 2021 May 10]. Available from: http://hdl.handle.net/2142/108440.

Council of Science Editors:

Hyatt MG. Controlling the end groups and rates of catalytic polymerization. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2020. Available from: http://hdl.handle.net/2142/108440


University of Manchester

6. Hoeven, Robin. Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase.

Degree: 2015, University of Manchester

 Enzyme dynamics has been established to play a crucial role in catalysis, and it has therefore become an important area of research to better understand… (more)

Subjects/Keywords: protochlorophyllide oxidoreductase; light-activated; KIE pressure dependence; kinetic isotope effect; enzyme dynamics

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

APA (6th Edition):

Hoeven, R. (2015). Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:292889

Chicago Manual of Style (16th Edition):

Hoeven, Robin. “Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase.” 2015. Doctoral Dissertation, University of Manchester. Accessed May 10, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:292889.

MLA Handbook (7th Edition):

Hoeven, Robin. “Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase.” 2015. Web. 10 May 2021.

Vancouver:

Hoeven R. Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 May 10]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:292889.

Council of Science Editors:

Hoeven R. Investigating the contribution of protein dynamics to catalysis in protochlorophyllide oxidoreductase. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:292889


University of California – Merced

7. Xiang, Shuhuai. Mechanistic Origins of Activity and Selectivity in Transition Metal Catalyzed Organic Reactions.

Degree: Chemistry and Chemical Biology, 2016, University of California – Merced

 Transition states are the gate keepers of chemical reactions. The free energies associated with transition states determine everything of interest in a chemical reaction, namely… (more)

Subjects/Keywords: Chemistry; 2+2 cycloaddition; Alder-ene reaction; C-H functionaization; Kinetic Isotope Effect; Product specific KIE; Rhodium

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APA (6th Edition):

Xiang, S. (2016). Mechanistic Origins of Activity and Selectivity in Transition Metal Catalyzed Organic Reactions. (Thesis). University of California – Merced. Retrieved from http://www.escholarship.org/uc/item/2sj60690

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):

Xiang, Shuhuai. “Mechanistic Origins of Activity and Selectivity in Transition Metal Catalyzed Organic Reactions.” 2016. Thesis, University of California – Merced. Accessed May 10, 2021. http://www.escholarship.org/uc/item/2sj60690.

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

MLA Handbook (7th Edition):

Xiang, Shuhuai. “Mechanistic Origins of Activity and Selectivity in Transition Metal Catalyzed Organic Reactions.” 2016. Web. 10 May 2021.

Vancouver:

Xiang S. Mechanistic Origins of Activity and Selectivity in Transition Metal Catalyzed Organic Reactions. [Internet] [Thesis]. University of California – Merced; 2016. [cited 2021 May 10]. Available from: http://www.escholarship.org/uc/item/2sj60690.

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

Council of Science Editors:

Xiang S. Mechanistic Origins of Activity and Selectivity in Transition Metal Catalyzed Organic Reactions. [Thesis]. University of California – Merced; 2016. Available from: http://www.escholarship.org/uc/item/2sj60690

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


University of Miami

8. Giebel, Brian M. Advancement and Application of Gas Chromatography Isotope Ratio Mass Spectrometry Techniques for Atmospheric Trace Gas Analysis.

Degree: PhD, Marine and Atmospheric Chemistry (Marine), 2011, University of Miami

 The use of gas chromatography isotope ratio mass spectrometry (GC-IRMS) for compound specific stable isotope analysis is an underutilized technique because of the complexity of… (more)

Subjects/Keywords: OVOCs; Gas Chromatography Isotope Ratio Mass Spectrometry; Atmospheric Trace Gas; Ethanol; Sources and Sinks; Kinetic Isotope Effect (KIE)

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APA (6th Edition):

Giebel, B. M. (2011). Advancement and Application of Gas Chromatography Isotope Ratio Mass Spectrometry Techniques for Atmospheric Trace Gas Analysis. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/610

Chicago Manual of Style (16th Edition):

Giebel, Brian M. “Advancement and Application of Gas Chromatography Isotope Ratio Mass Spectrometry Techniques for Atmospheric Trace Gas Analysis.” 2011. Doctoral Dissertation, University of Miami. Accessed May 10, 2021. https://scholarlyrepository.miami.edu/oa_dissertations/610.

MLA Handbook (7th Edition):

Giebel, Brian M. “Advancement and Application of Gas Chromatography Isotope Ratio Mass Spectrometry Techniques for Atmospheric Trace Gas Analysis.” 2011. Web. 10 May 2021.

Vancouver:

Giebel BM. Advancement and Application of Gas Chromatography Isotope Ratio Mass Spectrometry Techniques for Atmospheric Trace Gas Analysis. [Internet] [Doctoral dissertation]. University of Miami; 2011. [cited 2021 May 10]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/610.

Council of Science Editors:

Giebel BM. Advancement and Application of Gas Chromatography Isotope Ratio Mass Spectrometry Techniques for Atmospheric Trace Gas Analysis. [Doctoral Dissertation]. University of Miami; 2011. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/610


Penn State University

9. Ludlow, Michelle Kathryn. PROTON–COUPLED ELECTRON TRANSFER REACTIONS: THEORETICAL INSIGHT INTO EXPERIMENTAL RESULTS.

Degree: 2010, Penn State University

 A theoretical formulation for vibronically nonadiabatic proton–coupled electron transfer (PCET) reactions is applied to several PCET systems. This theory allows for the calculation of rates… (more)

Subjects/Keywords: PCET; vibronic coupling; KIE; quinol oxidation; phenoxyl/phenol; Tafel plot

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APA (6th Edition):

Ludlow, M. K. (2010). PROTON–COUPLED ELECTRON TRANSFER REACTIONS: THEORETICAL INSIGHT INTO EXPERIMENTAL RESULTS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/10982

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):

Ludlow, Michelle Kathryn. “PROTON–COUPLED ELECTRON TRANSFER REACTIONS: THEORETICAL INSIGHT INTO EXPERIMENTAL RESULTS.” 2010. Thesis, Penn State University. Accessed May 10, 2021. https://submit-etda.libraries.psu.edu/catalog/10982.

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

MLA Handbook (7th Edition):

Ludlow, Michelle Kathryn. “PROTON–COUPLED ELECTRON TRANSFER REACTIONS: THEORETICAL INSIGHT INTO EXPERIMENTAL RESULTS.” 2010. Web. 10 May 2021.

Vancouver:

Ludlow MK. PROTON–COUPLED ELECTRON TRANSFER REACTIONS: THEORETICAL INSIGHT INTO EXPERIMENTAL RESULTS. [Internet] [Thesis]. Penn State University; 2010. [cited 2021 May 10]. Available from: https://submit-etda.libraries.psu.edu/catalog/10982.

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

Council of Science Editors:

Ludlow MK. PROTON–COUPLED ELECTRON TRANSFER REACTIONS: THEORETICAL INSIGHT INTO EXPERIMENTAL RESULTS. [Thesis]. Penn State University; 2010. Available from: https://submit-etda.libraries.psu.edu/catalog/10982

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

10. James, Ollie. Recrossing and Heavy-atom Tunneling in Common Organic Reactions.

Degree: PhD, Chemistry, 2012, Texas A&M University

 Non-statistical recrossing in ketene cycloadditions with alkenes, heavy-atom tunneling and the mechanism of the decarboxylation of Mandelylthiamin is investigated in this dissertation. A combination of… (more)

Subjects/Keywords: kinetic isotope effects; KIE; dynamics, non-statistical recrossing; mechanism; tunneling

…1.2 Experimental KIE Measurements .............................................. 1.3… …Dichloroketene and Cis-2-butene ................. 2.3 KIE and Dynamic Effects in the Cycloaddition of… …Cyclohexene and Dichloroketene............................................. 2.4 KIE and Dynamic… …dichloroketene with cis-2-butene ................... 25 Figure 2.5 Extrapolation of the KIE for the… …Dynamic trajectory results for the 28C, 44C, 76C, or 140C isotopes and the resulting KIE… 

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APA (6th Edition):

James, O. (2012). Recrossing and Heavy-atom Tunneling in Common Organic Reactions. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10307

Chicago Manual of Style (16th Edition):

James, Ollie. “Recrossing and Heavy-atom Tunneling in Common Organic Reactions.” 2012. Doctoral Dissertation, Texas A&M University. Accessed May 10, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10307.

MLA Handbook (7th Edition):

James, Ollie. “Recrossing and Heavy-atom Tunneling in Common Organic Reactions.” 2012. Web. 10 May 2021.

Vancouver:

James O. Recrossing and Heavy-atom Tunneling in Common Organic Reactions. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2021 May 10]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10307.

Council of Science Editors:

James O. Recrossing and Heavy-atom Tunneling in Common Organic Reactions. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10307


Monash University

11. Ryan, Sarah Jean. N-Heterocyclic carbenes as catalysts for substrates in the ester oxidation state.

Degree: Science, 2017, Monash University

 N-Heterocyclic carbenes (NHCs) are renowned for their ability to invert the polarity of an aldehyde, and for many years their application was centralized around the… (more)

Subjects/Keywords: Uncategorized; Acyl fluoride; ethesis-20121129-111733; NHC; thesis(doctorate); Restricted access; 1959.1/732965; monash:89862; Carbene; Enol ether; Claisen rearrangement; Cycloaddition; KIE; 2012

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APA (6th Edition):

Ryan, S. J. (2017). N-Heterocyclic carbenes as catalysts for substrates in the ester oxidation state. (Thesis). Monash University. Retrieved from https://doi.org/10.4225/03/58a26eefb7bd8

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):

Ryan, Sarah Jean. “N-Heterocyclic carbenes as catalysts for substrates in the ester oxidation state.” 2017. Thesis, Monash University. Accessed May 10, 2021. https://doi.org/10.4225/03/58a26eefb7bd8.

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

MLA Handbook (7th Edition):

Ryan, Sarah Jean. “N-Heterocyclic carbenes as catalysts for substrates in the ester oxidation state.” 2017. Web. 10 May 2021.

Vancouver:

Ryan SJ. N-Heterocyclic carbenes as catalysts for substrates in the ester oxidation state. [Internet] [Thesis]. Monash University; 2017. [cited 2021 May 10]. Available from: https://doi.org/10.4225/03/58a26eefb7bd8.

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

Council of Science Editors:

Ryan SJ. N-Heterocyclic carbenes as catalysts for substrates in the ester oxidation state. [Thesis]. Monash University; 2017. Available from: https://doi.org/10.4225/03/58a26eefb7bd8

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

12. Huynh, Mioy T. Proton-coupled electron transfer reactions in bio-inspired catalysis.

Degree: PhD, Chemistry, 2017, University of Illinois – Urbana-Champaign

 Nature often serves as a seminal source of inspiration for the design of catalysts, which is likely due to the efficiency of many biological systems.… (more)

Subjects/Keywords: Proton-coupled electron transfer (PCET); Solar energy conversion; Hydrogenase; Hydrogen evolution; Electrocatalysis; Catalysis; Quinones; Mediators; Computational; Density functional theory (DFT); Rate theory; Kinetic isotope effects (KIE); Proton transfer; Electron transfer; Hydrogenase; FeFe; NiFe; Tyr-His; Benzimidazole phenol; Photosystem II; Artificial photosynthesis; Bio-inspired; Catalyst design; Design principles; Inorganic

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APA (6th Edition):

Huynh, M. T. (2017). Proton-coupled electron transfer reactions in bio-inspired catalysis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/98390

Chicago Manual of Style (16th Edition):

Huynh, Mioy T. “Proton-coupled electron transfer reactions in bio-inspired catalysis.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed May 10, 2021. http://hdl.handle.net/2142/98390.

MLA Handbook (7th Edition):

Huynh, Mioy T. “Proton-coupled electron transfer reactions in bio-inspired catalysis.” 2017. Web. 10 May 2021.

Vancouver:

Huynh MT. Proton-coupled electron transfer reactions in bio-inspired catalysis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2021 May 10]. Available from: http://hdl.handle.net/2142/98390.

Council of Science Editors:

Huynh MT. Proton-coupled electron transfer reactions in bio-inspired catalysis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/98390


Australian National University

13. Lording, William James. A deeper understanding of the Diels–Alder reaction .

Degree: 2010, Australian National University

 The Diels-Alder reaction was discovered in 1928 and has become the most efficient and practical method for the synthesis of six-membered carbocyclic and heterocyclic rings.… (more)

Subjects/Keywords: organic chemistry; physical organic chemistry; chemical synthesis; chemical kinetics; computational chemistry; density functional theory; DFT; nuclear magnetic resonance; NMR; Diels-Alder; Diels-Alder reaction; 4+2 cycloaddition; cycloaddition; 4+2 diene; dienophile; cyclohexene; stereochemistry; stereoselectivity; endo-exo selectivity; endo selective; exo selective; secondary orbital interaction; SOI; electrostatic interaction; butadiene; deuterium; isotopic label; kinetic isotope effect; KIE; natural abundance; transition structure; intramolecular Diels-Alder reaction; rate study; transition state; activation barrier

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APA (6th Edition):

Lording, W. J. (2010). A deeper understanding of the Diels–Alder reaction . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/11776

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):

Lording, William James. “A deeper understanding of the Diels–Alder reaction .” 2010. Thesis, Australian National University. Accessed May 10, 2021. http://hdl.handle.net/1885/11776.

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

MLA Handbook (7th Edition):

Lording, William James. “A deeper understanding of the Diels–Alder reaction .” 2010. Web. 10 May 2021.

Vancouver:

Lording WJ. A deeper understanding of the Diels–Alder reaction . [Internet] [Thesis]. Australian National University; 2010. [cited 2021 May 10]. Available from: http://hdl.handle.net/1885/11776.

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

Council of Science Editors:

Lording WJ. A deeper understanding of the Diels–Alder reaction . [Thesis]. Australian National University; 2010. Available from: http://hdl.handle.net/1885/11776

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

.