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You searched for subject:(PEPPSI). Showing records 1 – 5 of 5 total matches.

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1. Cassirame, Bénédicte. Couplages C-C utilisant des triarylbismuthines catalysés par le PEPPSI : Cross-Coupling Reactions PEPPSI catalysed starting from triarylbismuthines.

Degree: Docteur es, Chimie, 2012, Université Paris-Est

Les réactions de couplage métallocatalysées mises en avant par l'attribution du Prix Nobel de Chimie 2010 permettent la création de liaison C-C impossible par les… (more)

Subjects/Keywords: Catalyse; Triarylbismuthines; Carbène N-hétérocyclique; PEPPSI; Catalysis; Triarylbismuthines; N-heterocyclic carbene; PEPPSI

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

APA (6th Edition):

Cassirame, B. (2012). Couplages C-C utilisant des triarylbismuthines catalysés par le PEPPSI : Cross-Coupling Reactions PEPPSI catalysed starting from triarylbismuthines. (Doctoral Dissertation). Université Paris-Est. Retrieved from http://www.theses.fr/2012PEST1116

Chicago Manual of Style (16th Edition):

Cassirame, Bénédicte. “Couplages C-C utilisant des triarylbismuthines catalysés par le PEPPSI : Cross-Coupling Reactions PEPPSI catalysed starting from triarylbismuthines.” 2012. Doctoral Dissertation, Université Paris-Est. Accessed October 14, 2019. http://www.theses.fr/2012PEST1116.

MLA Handbook (7th Edition):

Cassirame, Bénédicte. “Couplages C-C utilisant des triarylbismuthines catalysés par le PEPPSI : Cross-Coupling Reactions PEPPSI catalysed starting from triarylbismuthines.” 2012. Web. 14 Oct 2019.

Vancouver:

Cassirame B. Couplages C-C utilisant des triarylbismuthines catalysés par le PEPPSI : Cross-Coupling Reactions PEPPSI catalysed starting from triarylbismuthines. [Internet] [Doctoral dissertation]. Université Paris-Est; 2012. [cited 2019 Oct 14]. Available from: http://www.theses.fr/2012PEST1116.

Council of Science Editors:

Cassirame B. Couplages C-C utilisant des triarylbismuthines catalysés par le PEPPSI : Cross-Coupling Reactions PEPPSI catalysed starting from triarylbismuthines. [Doctoral Dissertation]. Université Paris-Est; 2012. Available from: http://www.theses.fr/2012PEST1116


Uniwersytet im. Adama Mickiewicza w Poznaniu

2. Ostrowska, Sylwia. Nowe N-heterocykliczne karbenowe kompleksy palladu – synteza, struktura, reaktywność i aktywność katalityczna .

Degree: 2018, Uniwersytet im. Adama Mickiewicza w Poznaniu

 Celem niniejszej pracy doktorskiej była synteza nowych kompleksów palladu z N-heterocyklicznymi ligandami karbenowymi. Skupiono się na syntezie kompleksów zawierających ligandy anionowe inne niż powszechnie stosowany… (more)

Subjects/Keywords: NHC kompleksy palladu; kompleksy PEPPSI; reakcje sprzęgania; chemia metaloorganiczna; NHC complexes palladium; PEPPSI catalysts; coupling reactions; organometallic chemistry

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APA (6th Edition):

Ostrowska, S. (2018). Nowe N-heterocykliczne karbenowe kompleksy palladu – synteza, struktura, reaktywność i aktywność katalityczna . (Doctoral Dissertation). Uniwersytet im. Adama Mickiewicza w Poznaniu. Retrieved from http://hdl.handle.net/10593/23449

Chicago Manual of Style (16th Edition):

Ostrowska, Sylwia. “Nowe N-heterocykliczne karbenowe kompleksy palladu – synteza, struktura, reaktywność i aktywność katalityczna .” 2018. Doctoral Dissertation, Uniwersytet im. Adama Mickiewicza w Poznaniu. Accessed October 14, 2019. http://hdl.handle.net/10593/23449.

MLA Handbook (7th Edition):

Ostrowska, Sylwia. “Nowe N-heterocykliczne karbenowe kompleksy palladu – synteza, struktura, reaktywność i aktywność katalityczna .” 2018. Web. 14 Oct 2019.

Vancouver:

Ostrowska S. Nowe N-heterocykliczne karbenowe kompleksy palladu – synteza, struktura, reaktywność i aktywność katalityczna . [Internet] [Doctoral dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2018. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10593/23449.

Council of Science Editors:

Ostrowska S. Nowe N-heterocykliczne karbenowe kompleksy palladu – synteza, struktura, reaktywność i aktywność katalityczna . [Doctoral Dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2018. Available from: http://hdl.handle.net/10593/23449

3. McCann, Lucas Charles. Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline.

Degree: PhD, Chemistry, 2016, York University

 Part I: An efficient method for alkyl-alkyl Negishi cross-coupling reaction of unactivated primary alkyl halides with higher-order zincate species (synthesized from dialkylzinc and a non-coordinating… (more)

Subjects/Keywords: Inorganic chemistry; Cross-coupling; Palladium; Zincate; Zinc; Chemistry; Organic chemistry; Methodology; Industrial chemistry; Pd-PEPPSI; PEPPSI; PEPPSI catalyst; Synthesis; Organometallic chemistry; Organometallic; Inorganic; Inorganic chemistry; Scale-up; Process chemistry; Optimization; Negishi; Negishi Cross-coupling; Alkyl-alkyl; Bond formation; NHC; N-heterocyclic carbene; Carbene; Mechanistic determination; Reaction mechanism; Aryl-aryl; Pd-PEPPSI-IPent; Pd-PEPPSI-IHept; Pd-PEPPSI-IPr; Pd-PEPPSI-IPentCl; Pd-PEPPSI-IHeptCl; 2; 6-DI(4-HEPTYL)ANILINE; 6-DI(3-PENTYL)ANILINE; Large-scale

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APA (6th Edition):

McCann, L. C. (2016). Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/32194

Chicago Manual of Style (16th Edition):

McCann, Lucas Charles. “Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline.” 2016. Doctoral Dissertation, York University. Accessed October 14, 2019. http://hdl.handle.net/10315/32194.

MLA Handbook (7th Edition):

McCann, Lucas Charles. “Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline.” 2016. Web. 14 Oct 2019.

Vancouver:

McCann LC. Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline. [Internet] [Doctoral dissertation]. York University; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10315/32194.

Council of Science Editors:

McCann LC. Part I: Mechanistic Insight in Alkyl-Alkyl and Aryl-Aryl Negishi Cross-Coupling Part II: Large Scale Synthesis of NHC Precursors: 2,6-DI(3-Pentyl) Aniline and 2,6-DI (4-Heptyl) Aniline. [Doctoral Dissertation]. York University; 2016. Available from: http://hdl.handle.net/10315/32194

4. Farmer, Jennifer Lyn. Part I: Application of Pd-Peppsi Complexes in Regioselective Cross-Coupling and Natural Product Total Synthesis; Part II: Room Temperature, Additive-Free Carbon-Sulfur Coupling Using Novel NHC-Pd Complexes.

Degree: PhD, Chemistry, 2016, York University

 The first part of this research is focused on the development of an efficient method for the regioselective Suzuki-Miyaura cross-coupling of allylboronic acid pinacol ester… (more)

Subjects/Keywords: Organic chemistry; Homogeneous Catalysis; N-Heterocyclic carbenes; PEPPSI; Cross-coupling; Bulky ligands; Suzuki-Miyaura; Sulfination; Palladium

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

APA (6th Edition):

Farmer, J. L. (2016). Part I: Application of Pd-Peppsi Complexes in Regioselective Cross-Coupling and Natural Product Total Synthesis; Part II: Room Temperature, Additive-Free Carbon-Sulfur Coupling Using Novel NHC-Pd Complexes. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/32204

Chicago Manual of Style (16th Edition):

Farmer, Jennifer Lyn. “Part I: Application of Pd-Peppsi Complexes in Regioselective Cross-Coupling and Natural Product Total Synthesis; Part II: Room Temperature, Additive-Free Carbon-Sulfur Coupling Using Novel NHC-Pd Complexes.” 2016. Doctoral Dissertation, York University. Accessed October 14, 2019. http://hdl.handle.net/10315/32204.

MLA Handbook (7th Edition):

Farmer, Jennifer Lyn. “Part I: Application of Pd-Peppsi Complexes in Regioselective Cross-Coupling and Natural Product Total Synthesis; Part II: Room Temperature, Additive-Free Carbon-Sulfur Coupling Using Novel NHC-Pd Complexes.” 2016. Web. 14 Oct 2019.

Vancouver:

Farmer JL. Part I: Application of Pd-Peppsi Complexes in Regioselective Cross-Coupling and Natural Product Total Synthesis; Part II: Room Temperature, Additive-Free Carbon-Sulfur Coupling Using Novel NHC-Pd Complexes. [Internet] [Doctoral dissertation]. York University; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10315/32204.

Council of Science Editors:

Farmer JL. Part I: Application of Pd-Peppsi Complexes in Regioselective Cross-Coupling and Natural Product Total Synthesis; Part II: Room Temperature, Additive-Free Carbon-Sulfur Coupling Using Novel NHC-Pd Complexes. [Doctoral Dissertation]. York University; 2016. Available from: http://hdl.handle.net/10315/32204

5. Khadra, Abir. Part I: Palladium PEPPSI-IPENT CI, A Useful Catalyst for Challenging Amination Reactions Part II: Generation Of Benzynes in Flow Reactors followed by Subsequent Diels-Alder Reactions.

Degree: PhD, Chemistry, 2018, York University

 The first part of this research focuses on developing efficient methods to address challenging Buchwald Hartwig amination reactions using Pd-NHC pre-catalysts. Specifically, we focused on:… (more)

Subjects/Keywords: Chemistry; Flow; Benzyne; Diels-Alder; Reactive; Intermediate; Catalysis; Amination; 2-aminopyridine; PEPPSI-PentCl; Cross-coupling; Na-BHT; Palladium.

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APA (6th Edition):

Khadra, A. (2018). Part I: Palladium PEPPSI-IPENT CI, A Useful Catalyst for Challenging Amination Reactions Part II: Generation Of Benzynes in Flow Reactors followed by Subsequent Diels-Alder Reactions. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/35032

Chicago Manual of Style (16th Edition):

Khadra, Abir. “Part I: Palladium PEPPSI-IPENT CI, A Useful Catalyst for Challenging Amination Reactions Part II: Generation Of Benzynes in Flow Reactors followed by Subsequent Diels-Alder Reactions.” 2018. Doctoral Dissertation, York University. Accessed October 14, 2019. http://hdl.handle.net/10315/35032.

MLA Handbook (7th Edition):

Khadra, Abir. “Part I: Palladium PEPPSI-IPENT CI, A Useful Catalyst for Challenging Amination Reactions Part II: Generation Of Benzynes in Flow Reactors followed by Subsequent Diels-Alder Reactions.” 2018. Web. 14 Oct 2019.

Vancouver:

Khadra A. Part I: Palladium PEPPSI-IPENT CI, A Useful Catalyst for Challenging Amination Reactions Part II: Generation Of Benzynes in Flow Reactors followed by Subsequent Diels-Alder Reactions. [Internet] [Doctoral dissertation]. York University; 2018. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10315/35032.

Council of Science Editors:

Khadra A. Part I: Palladium PEPPSI-IPENT CI, A Useful Catalyst for Challenging Amination Reactions Part II: Generation Of Benzynes in Flow Reactors followed by Subsequent Diels-Alder Reactions. [Doctoral Dissertation]. York University; 2018. Available from: http://hdl.handle.net/10315/35032

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