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You searched for subject:(Suzuki coupling). Showing records 1 – 30 of 107 total matches.

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University of South Africa

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

Degree: 2011, University of South Africa

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Oyeyiola, Felix Adetunji. “Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .” 2011. Masters Thesis, University of South Africa. Accessed October 14, 2019. http://hdl.handle.net/10500/5842.

MLA Handbook (7th Edition):

Oyeyiola, Felix Adetunji. “Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .” 2011. Web. 14 Oct 2019.

Vancouver:

Oyeyiola FA. Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones . [Internet] [Masters thesis]. University of South Africa; 2011. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10500/5842.

Council of Science Editors:

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


Boston College

2. Chang, Weng Kun. Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles.

Degree: MS, Chemistry, 2014, Boston College

 The Suzuki-Miyaura cross-coupling reaction is a common strategy for the formation of a new carbon-carbon bond in organic synthesis. However, intramolecular coupling of allylboron ester… (more)

Subjects/Keywords: allylboron ester; Pt; Suzuki coupling; Synthesis

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APA (6th Edition):

Chang, W. K. (2014). Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104067

Chicago Manual of Style (16th Edition):

Chang, Weng Kun. “Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles.” 2014. Masters Thesis, Boston College. Accessed October 14, 2019. http://dlib.bc.edu/islandora/object/bc-ir:104067.

MLA Handbook (7th Edition):

Chang, Weng Kun. “Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles.” 2014. Web. 14 Oct 2019.

Vancouver:

Chang WK. Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles. [Internet] [Masters thesis]. Boston College; 2014. [cited 2019 Oct 14]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104067.

Council of Science Editors:

Chang WK. Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles. [Masters Thesis]. Boston College; 2014. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104067


Université de Neuchâtel

3. Chahen, Ludovic. Complexes plan-carrés de palladium à configuration “trans”: nouveaux ligands, coordination et potentiel catalytique pour le couplage de Suzuki.

Degree: 2007, Université de Neuchâtel

 La réaction de couplage carbone-carbone de Suzuki représente une des meilleures voies de synthèse des composés biaryles. Ces composés constituent des blocs de construction fondamentaux… (more)

Subjects/Keywords: Suzuki cross-coupling

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APA (6th Edition):

Chahen, L. (2007). Complexes plan-carrés de palladium à configuration “trans”: nouveaux ligands, coordination et potentiel catalytique pour le couplage de Suzuki. (Thesis). Université de Neuchâtel. Retrieved from http://doc.rero.ch/record/8131

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):

Chahen, Ludovic. “Complexes plan-carrés de palladium à configuration “trans”: nouveaux ligands, coordination et potentiel catalytique pour le couplage de Suzuki.” 2007. Thesis, Université de Neuchâtel. Accessed October 14, 2019. http://doc.rero.ch/record/8131.

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

MLA Handbook (7th Edition):

Chahen, Ludovic. “Complexes plan-carrés de palladium à configuration “trans”: nouveaux ligands, coordination et potentiel catalytique pour le couplage de Suzuki.” 2007. Web. 14 Oct 2019.

Vancouver:

Chahen L. Complexes plan-carrés de palladium à configuration “trans”: nouveaux ligands, coordination et potentiel catalytique pour le couplage de Suzuki. [Internet] [Thesis]. Université de Neuchâtel; 2007. [cited 2019 Oct 14]. Available from: http://doc.rero.ch/record/8131.

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

Council of Science Editors:

Chahen L. Complexes plan-carrés de palladium à configuration “trans”: nouveaux ligands, coordination et potentiel catalytique pour le couplage de Suzuki. [Thesis]. Université de Neuchâtel; 2007. Available from: http://doc.rero.ch/record/8131

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


Queens University

4. LaBine, Emily. Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters .

Degree: Chemistry, 2013, Queens University

 The stereochemical course of the Pd–catalyzed Suzuki-Miyaura cross-coupling of α-substituted, enantioenriched allylic boronic esters with phenyl iodide has been examined. The secondary boronic esters were… (more)

Subjects/Keywords: Suzuki-Miyaura; Regioselective; Catalysis; Enantiospecific; Cross-Coupling

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APA (6th Edition):

LaBine, E. (2013). Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8463

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):

LaBine, Emily. “Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters .” 2013. Thesis, Queens University. Accessed October 14, 2019. http://hdl.handle.net/1974/8463.

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

MLA Handbook (7th Edition):

LaBine, Emily. “Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters .” 2013. Web. 14 Oct 2019.

Vancouver:

LaBine E. Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters . [Internet] [Thesis]. Queens University; 2013. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/1974/8463.

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

Council of Science Editors:

LaBine E. Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/8463

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


Queens University

5. Ziebenhaus, Christopher. Iterative, Chemoselective, Enantiospecific, Protecting Group Free Cross-Coupling of Polyboronates .

Degree: Chemistry, 2016, Queens University

 The Suzuki-Miyaura cross-coupling reaction is broadly defined as a palladium or nickel catalyzed C-C bond forming reaction occurring between a halide or pseudo-halide electrophile and… (more)

Subjects/Keywords: cross-coupling; chemoselective; enantiospecific; Suzuki-Miyaura

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APA (6th Edition):

Ziebenhaus, C. (2016). Iterative, Chemoselective, Enantiospecific, Protecting Group Free Cross-Coupling of Polyboronates . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/14023

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):

Ziebenhaus, Christopher. “Iterative, Chemoselective, Enantiospecific, Protecting Group Free Cross-Coupling of Polyboronates .” 2016. Thesis, Queens University. Accessed October 14, 2019. http://hdl.handle.net/1974/14023.

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

MLA Handbook (7th Edition):

Ziebenhaus, Christopher. “Iterative, Chemoselective, Enantiospecific, Protecting Group Free Cross-Coupling of Polyboronates .” 2016. Web. 14 Oct 2019.

Vancouver:

Ziebenhaus C. Iterative, Chemoselective, Enantiospecific, Protecting Group Free Cross-Coupling of Polyboronates . [Internet] [Thesis]. Queens University; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/1974/14023.

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

Council of Science Editors:

Ziebenhaus C. Iterative, Chemoselective, Enantiospecific, Protecting Group Free Cross-Coupling of Polyboronates . [Thesis]. Queens University; 2016. Available from: http://hdl.handle.net/1974/14023

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


University of Illinois – Urbana-Champaign

6. Schmidt, Michael Joseph. Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings.

Degree: MS, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Small molecules have had a tremendous positive impact on human health and society in general. Despite this, small molecule synthesis is still a time and… (more)

Subjects/Keywords: Suzuki; coupling; cross coupling; MIDA boronate; iteration; automation

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APA (6th Edition):

Schmidt, M. J. (2016). Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95599

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):

Schmidt, Michael Joseph. “Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed October 14, 2019. http://hdl.handle.net/2142/95599.

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

MLA Handbook (7th Edition):

Schmidt, Michael Joseph. “Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings.” 2016. Web. 14 Oct 2019.

Vancouver:

Schmidt MJ. Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2142/95599.

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

Council of Science Editors:

Schmidt MJ. Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95599

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


University of Edinburgh

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

Degree: PhD, 2018, University of Edinburgh

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed October 14, 2019. http://hdl.handle.net/1842/33092.

MLA Handbook (7th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Web. 14 Oct 2019.

Vancouver:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2019 Oct 14]. 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

8. Martin, Thibaut. Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores.

Degree: Docteur es, Chimie, 2010, Rouen, INSA

Face à l’apparition alarmante et continue de résistance massive des bactéries à l’arsenal actuel d’antibiotiques, la recherche de nouveaux agents antibactériens est actuellement un enjeu… (more)

Subjects/Keywords: Thiazole; Hétérocycles; Thiopeptides antibiotiques; Arylation directe; Borylation; Couplage de Suzuki; Heterocycles; Thiopeptide family; Suzuki coupling

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APA (6th Edition):

Martin, T. (2010). Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores. (Doctoral Dissertation). Rouen, INSA. Retrieved from http://www.theses.fr/2010ISAM0004

Chicago Manual of Style (16th Edition):

Martin, Thibaut. “Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores.” 2010. Doctoral Dissertation, Rouen, INSA. Accessed October 14, 2019. http://www.theses.fr/2010ISAM0004.

MLA Handbook (7th Edition):

Martin, Thibaut. “Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores.” 2010. Web. 14 Oct 2019.

Vancouver:

Martin T. Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores. [Internet] [Doctoral dissertation]. Rouen, INSA; 2010. [cited 2019 Oct 14]. Available from: http://www.theses.fr/2010ISAM0004.

Council of Science Editors:

Martin T. Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d : Development of new-pallado-catalyzed direct arylation methodologies in the thiazole serie : application to the synthesis of serie d thiopeptide antibiotics cores. [Doctoral Dissertation]. Rouen, INSA; 2010. Available from: http://www.theses.fr/2010ISAM0004


University of Oxford

9. Schäfer, Philipp. Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles.

Degree: PhD, 2017, University of Oxford

 This thesis describes the combination of non-stabilized nucleophiles and prochiral/racemic electrophiles in transition metal catalyzed asymmetric transformations. These enantioselective reactions have tremendous potential for the… (more)

Subjects/Keywords: Enantioselective catalysis; Electrochemistry; Hiyama coupling; Organocatalysis; Boronic Acid; Suzuki-Miyaura coupling; Siloxane

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APA (6th Edition):

Schäfer, P. (2017). Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles. (Doctoral Dissertation). University of Oxford. Retrieved from https://ora.ox.ac.uk/objects/uuid:d69d1861-5368-495a-932d-7e1aa6bc5dfb ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736121

Chicago Manual of Style (16th Edition):

Schäfer, Philipp. “Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles.” 2017. Doctoral Dissertation, University of Oxford. Accessed October 14, 2019. https://ora.ox.ac.uk/objects/uuid:d69d1861-5368-495a-932d-7e1aa6bc5dfb ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736121.

MLA Handbook (7th Edition):

Schäfer, Philipp. “Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles.” 2017. Web. 14 Oct 2019.

Vancouver:

Schäfer P. Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2019 Oct 14]. Available from: https://ora.ox.ac.uk/objects/uuid:d69d1861-5368-495a-932d-7e1aa6bc5dfb ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736121.

Council of Science Editors:

Schäfer P. Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles. [Doctoral Dissertation]. University of Oxford; 2017. Available from: https://ora.ox.ac.uk/objects/uuid:d69d1861-5368-495a-932d-7e1aa6bc5dfb ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736121


University of South Africa

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

Degree: 2010, University of South Africa

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Makelane, Hlamulo Reply. “Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .” 2010. Masters Thesis, University of South Africa. Accessed October 14, 2019. http://hdl.handle.net/10500/3838.

MLA Handbook (7th Edition):

Makelane, Hlamulo Reply. “Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes .” 2010. Web. 14 Oct 2019.

Vancouver:

Makelane HR. Regioselectivity of palladium-catalyzed sonogashira cross-coupling of 2-aryl-4-chloro-3-iodoquinoline- derivatives with terminal alkynes . [Internet] [Masters thesis]. University of South Africa; 2010. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10500/3838.

Council of Science Editors:

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


University of Ottawa

11. Ben Halima, Taoufik. Engaging Esters as Cross-Coupling Electrophiles .

Degree: 2019, University of Ottawa

 Cross-coupling reactions, where a transition metal catalyst facilitates the formation of a new carbon-carbon or carbon-heteroatom bond between two coupling partners, has become one of… (more)

Subjects/Keywords: Esters; Electrophiles; cross-coupling reactions; Suzuki-Miyaura coupling; Amide bond formation; High-throughput screening

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APA (6th Edition):

Ben Halima, T. (2019). Engaging Esters as Cross-Coupling Electrophiles . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/39493

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):

Ben Halima, Taoufik. “Engaging Esters as Cross-Coupling Electrophiles .” 2019. Thesis, University of Ottawa. Accessed October 14, 2019. http://hdl.handle.net/10393/39493.

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

MLA Handbook (7th Edition):

Ben Halima, Taoufik. “Engaging Esters as Cross-Coupling Electrophiles .” 2019. Web. 14 Oct 2019.

Vancouver:

Ben Halima T. Engaging Esters as Cross-Coupling Electrophiles . [Internet] [Thesis]. University of Ottawa; 2019. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10393/39493.

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

Council of Science Editors:

Ben Halima T. Engaging Esters as Cross-Coupling Electrophiles . [Thesis]. University of Ottawa; 2019. Available from: http://hdl.handle.net/10393/39493

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


Case Western Reserve University

12. Check, Casey. Design, Synthesis and Characterization of Two-Dimensional Polyelectrolytes.

Degree: PhD, Macromolecular Science and Engineering, 2010, Case Western Reserve University

  A novel two-dimensional poly(1,3,5-phenylene-4,4’-biphenylene-2,2’-disulfonic acid) (CPPSA) was synthesized using palladium-catalyzed Suzuki coupling in water. The postulated architecture is comprised of hexagonal, macrocyclic, 2-dimensional polymer… (more)

Subjects/Keywords: Polymer Chemistry; poly(phenylenesulfonic acid); polyelectrolytes; macrocycle; Suzuki coupling kinetics

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APA (6th Edition):

Check, C. (2010). Design, Synthesis and Characterization of Two-Dimensional Polyelectrolytes. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1291397084

Chicago Manual of Style (16th Edition):

Check, Casey. “Design, Synthesis and Characterization of Two-Dimensional Polyelectrolytes.” 2010. Doctoral Dissertation, Case Western Reserve University. Accessed October 14, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1291397084.

MLA Handbook (7th Edition):

Check, Casey. “Design, Synthesis and Characterization of Two-Dimensional Polyelectrolytes.” 2010. Web. 14 Oct 2019.

Vancouver:

Check C. Design, Synthesis and Characterization of Two-Dimensional Polyelectrolytes. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2010. [cited 2019 Oct 14]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1291397084.

Council of Science Editors:

Check C. Design, Synthesis and Characterization of Two-Dimensional Polyelectrolytes. [Doctoral Dissertation]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1291397084


McMaster University

13. Keskar, Kunal. ADVANCES IN LATE TRANSITION METAL CATALYSIS, OLEFINATION REACTIONS AND APPLICATIONS.

Degree: PhD, 2015, McMaster University

Two series of stable palladium and silver complexes ligated to hemilabile ligands were prepared. The stability and applicability of these well-defined complexes in promoting various… (more)

Subjects/Keywords: Homogeneous catalysis; Nostodione; Indole carboxylates; Suzuki-Miyaura coupling; phosphines; phosphonium salts

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APA (6th Edition):

Keskar, K. (2015). ADVANCES IN LATE TRANSITION METAL CATALYSIS, OLEFINATION REACTIONS AND APPLICATIONS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/16600

Chicago Manual of Style (16th Edition):

Keskar, Kunal. “ADVANCES IN LATE TRANSITION METAL CATALYSIS, OLEFINATION REACTIONS AND APPLICATIONS.” 2015. Doctoral Dissertation, McMaster University. Accessed October 14, 2019. http://hdl.handle.net/11375/16600.

MLA Handbook (7th Edition):

Keskar, Kunal. “ADVANCES IN LATE TRANSITION METAL CATALYSIS, OLEFINATION REACTIONS AND APPLICATIONS.” 2015. Web. 14 Oct 2019.

Vancouver:

Keskar K. ADVANCES IN LATE TRANSITION METAL CATALYSIS, OLEFINATION REACTIONS AND APPLICATIONS. [Internet] [Doctoral dissertation]. McMaster University; 2015. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/11375/16600.

Council of Science Editors:

Keskar K. ADVANCES IN LATE TRANSITION METAL CATALYSIS, OLEFINATION REACTIONS AND APPLICATIONS. [Doctoral Dissertation]. McMaster University; 2015. Available from: http://hdl.handle.net/11375/16600


University of Cambridge

14. Todd, Matthew H. Novel encoding strategies for combinatorial chemistry.

Degree: PhD, 1998, University of Cambridge

Subjects/Keywords: 547; Suzuki coupling; Molecule synthesis

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APA (6th Edition):

Todd, M. H. (1998). Novel encoding strategies for combinatorial chemistry. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/272807 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340770

Chicago Manual of Style (16th Edition):

Todd, Matthew H. “Novel encoding strategies for combinatorial chemistry.” 1998. Doctoral Dissertation, University of Cambridge. Accessed October 14, 2019. https://www.repository.cam.ac.uk/handle/1810/272807 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340770.

MLA Handbook (7th Edition):

Todd, Matthew H. “Novel encoding strategies for combinatorial chemistry.” 1998. Web. 14 Oct 2019.

Vancouver:

Todd MH. Novel encoding strategies for combinatorial chemistry. [Internet] [Doctoral dissertation]. University of Cambridge; 1998. [cited 2019 Oct 14]. Available from: https://www.repository.cam.ac.uk/handle/1810/272807 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340770.

Council of Science Editors:

Todd MH. Novel encoding strategies for combinatorial chemistry. [Doctoral Dissertation]. University of Cambridge; 1998. Available from: https://www.repository.cam.ac.uk/handle/1810/272807 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340770


Boston College

15. Mlynarski, Scott Nathan. Utilizing Terminal Alkenes in Asymmetric Synthesis: Development and Application of Efficient Diboration/Cross-Coupling Cascades.

Degree: PhD, Chemistry, 2014, Boston College

 The first highly enantioselective diboration of unfunctionalized terminal alkenes has been developed using a platinum-phosphonite complex. This transformation produces versatile 1,2-bis(boronate)esters that can manipulated chemoselectively… (more)

Subjects/Keywords: Asymmetric Catalysis; Diboration; Suzuki Cross-coupling; Terminal Alkenes

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APA (6th Edition):

Mlynarski, S. N. (2014). Utilizing Terminal Alkenes in Asymmetric Synthesis: Development and Application of Efficient Diboration/Cross-Coupling Cascades. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:103555

Chicago Manual of Style (16th Edition):

Mlynarski, Scott Nathan. “Utilizing Terminal Alkenes in Asymmetric Synthesis: Development and Application of Efficient Diboration/Cross-Coupling Cascades.” 2014. Doctoral Dissertation, Boston College. Accessed October 14, 2019. http://dlib.bc.edu/islandora/object/bc-ir:103555.

MLA Handbook (7th Edition):

Mlynarski, Scott Nathan. “Utilizing Terminal Alkenes in Asymmetric Synthesis: Development and Application of Efficient Diboration/Cross-Coupling Cascades.” 2014. Web. 14 Oct 2019.

Vancouver:

Mlynarski SN. Utilizing Terminal Alkenes in Asymmetric Synthesis: Development and Application of Efficient Diboration/Cross-Coupling Cascades. [Internet] [Doctoral dissertation]. Boston College; 2014. [cited 2019 Oct 14]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:103555.

Council of Science Editors:

Mlynarski SN. Utilizing Terminal Alkenes in Asymmetric Synthesis: Development and Application of Efficient Diboration/Cross-Coupling Cascades. [Doctoral Dissertation]. Boston College; 2014. Available from: http://dlib.bc.edu/islandora/object/bc-ir:103555

16. Anderson, Samantha. CHEMOSELECTIVE SUZUKI-MIYAURA CROSS-COUPLING OF DI AND TRI BORONIC ESTER SUBSTRATES .

Degree: Chemistry, 2015, Queens University

 In industry and academia, the palladium catalyzed Suzuki-Miyaura cross coupling reaction is one of the most often used methods for the synthesis of new C-C… (more)

Subjects/Keywords: Suzuki-Miyaura; Cross Coupling

…List of Schemes Scheme 1-1: Generalized Suzuki-Miyaura Cross Coupling Reaction… …Coupling under Negishi Conditions …..4 Scheme 1-5: Suzuki-Miyaura Cross Coupling of 1… …Coupling of Primary 9BBN Derivative under Suzuki-Miyaura Conditions ...19 Scheme 1-16: Primary… …Sites ...31 Scheme 2-3: Bryce and Coworkers DoM/ 3-Step Suzuki-Miyaura Coupling for… …Three Step Suzuki-Miyaura Cross-Coupling Without the Need for Protecting…... Groups… 

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APA (6th Edition):

Anderson, S. (2015). CHEMOSELECTIVE SUZUKI-MIYAURA CROSS-COUPLING OF DI AND TRI BORONIC ESTER SUBSTRATES . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/12797

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):

Anderson, Samantha. “CHEMOSELECTIVE SUZUKI-MIYAURA CROSS-COUPLING OF DI AND TRI BORONIC ESTER SUBSTRATES .” 2015. Thesis, Queens University. Accessed October 14, 2019. http://hdl.handle.net/1974/12797.

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

MLA Handbook (7th Edition):

Anderson, Samantha. “CHEMOSELECTIVE SUZUKI-MIYAURA CROSS-COUPLING OF DI AND TRI BORONIC ESTER SUBSTRATES .” 2015. Web. 14 Oct 2019.

Vancouver:

Anderson S. CHEMOSELECTIVE SUZUKI-MIYAURA CROSS-COUPLING OF DI AND TRI BORONIC ESTER SUBSTRATES . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/1974/12797.

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

Council of Science Editors:

Anderson S. CHEMOSELECTIVE SUZUKI-MIYAURA CROSS-COUPLING OF DI AND TRI BORONIC ESTER SUBSTRATES . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/12797

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


University of South Carolina

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Key, Ryan J. “Development of Nickel Catalyzed Cross-Coupling Methodologies.” 2019. Doctoral Dissertation, University of South Carolina. Accessed October 14, 2019. https://scholarcommons.sc.edu/etd/5324.

MLA Handbook (7th Edition):

Key, Ryan J. “Development of Nickel Catalyzed Cross-Coupling Methodologies.” 2019. Web. 14 Oct 2019.

Vancouver:

Key RJ. Development of Nickel Catalyzed Cross-Coupling Methodologies. [Internet] [Doctoral dissertation]. University of South Carolina; 2019. [cited 2019 Oct 14]. Available from: https://scholarcommons.sc.edu/etd/5324.

Council of Science Editors:

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


University of Illinois – Urbana-Champaign

18. Gillis, Eric P. Iterative cross-coupling with MIDA boronates.

Degree: PhD, Chemistry, 2010, University of Illinois – Urbana-Champaign

 Many small molecules targeted for synthesis in the laboratory are inherently modular in their construction. Harnessing this modularity towards a unified strategy for the synthesis… (more)

Subjects/Keywords: MIDA; N-methyliminodiacetic acid; iterative cross-coupling; slow-release; MIDA boronate; boronate; cross-coupling; Suzuki cross-coupling

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APA (6th Edition):

Gillis, E. P. (2010). Iterative cross-coupling with MIDA boronates. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/91591

Chicago Manual of Style (16th Edition):

Gillis, Eric P. “Iterative cross-coupling with MIDA boronates.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 14, 2019. http://hdl.handle.net/2142/91591.

MLA Handbook (7th Edition):

Gillis, Eric P. “Iterative cross-coupling with MIDA boronates.” 2010. Web. 14 Oct 2019.

Vancouver:

Gillis EP. Iterative cross-coupling with MIDA boronates. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2142/91591.

Council of Science Editors:

Gillis EP. Iterative cross-coupling with MIDA boronates. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/91591


Universidade Federal de Viçosa

19. Guilherme Carvalho Geraldo. Síntese e avaliação da atividade fitotóxica de análogos ao alternariol.

Degree: 2008, Universidade Federal de Viçosa

O alternariol é uma lactona aromática produzida por espécies fúngicas fitopatogênicas dos gêneros Nimbya e Alternaria. Estas espécies são conhecidas por causarem necroses foliares ocasionando… (more)

Subjects/Keywords: Alternariol; Herbicidas; Fungos fitopatogênicos; Acoplamento de Suzuki; QUIMICA ORGANICA; Alternariol; Herbicides; Plant pathogenic fungi; Suzuki coupling reaction

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APA (6th Edition):

Geraldo, G. C. (2008). Síntese e avaliação da atividade fitotóxica de análogos ao alternariol. (Thesis). Universidade Federal de Viçosa. Retrieved from http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=1891

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):

Geraldo, Guilherme Carvalho. “Síntese e avaliação da atividade fitotóxica de análogos ao alternariol.” 2008. Thesis, Universidade Federal de Viçosa. Accessed October 14, 2019. http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=1891.

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

MLA Handbook (7th Edition):

Geraldo, Guilherme Carvalho. “Síntese e avaliação da atividade fitotóxica de análogos ao alternariol.” 2008. Web. 14 Oct 2019.

Vancouver:

Geraldo GC. Síntese e avaliação da atividade fitotóxica de análogos ao alternariol. [Internet] [Thesis]. Universidade Federal de Viçosa; 2008. [cited 2019 Oct 14]. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=1891.

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

Council of Science Editors:

Geraldo GC. Síntese e avaliação da atividade fitotóxica de análogos ao alternariol. [Thesis]. Universidade Federal de Viçosa; 2008. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=1891

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

20. Bochicchio, Antonella. Towards the atropo-stereoselective total synthesis of myricanol : Vers la synthèse totale atropo-stéréosélective du myricanol.

Degree: Docteur es, Chimie organique, 2016, Strasbourg; Università degli studi della Basilicata

Le myricanol est un [7,0]-métacyclophane naturel qui appartient à la famille des diarylheptanoïdes cycliques et qui possède des propriétés structurales et biologiques intéressantes (activité anti-Alzheimer… (more)

Subjects/Keywords: Myricanol; Diarylheptanoïdes; Métathèse croisée; Couplage de Suzuki-Miyaura domino; Myricanol; Diarylheptanoids; Cross-metathesis; Domino Suzuki-Miyaura cross-coupling; 547.2

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APA (6th Edition):

Bochicchio, A. (2016). Towards the atropo-stereoselective total synthesis of myricanol : Vers la synthèse totale atropo-stéréosélective du myricanol. (Doctoral Dissertation). Strasbourg; Università degli studi della Basilicata. Retrieved from http://www.theses.fr/2016STRAF004

Chicago Manual of Style (16th Edition):

Bochicchio, Antonella. “Towards the atropo-stereoselective total synthesis of myricanol : Vers la synthèse totale atropo-stéréosélective du myricanol.” 2016. Doctoral Dissertation, Strasbourg; Università degli studi della Basilicata. Accessed October 14, 2019. http://www.theses.fr/2016STRAF004.

MLA Handbook (7th Edition):

Bochicchio, Antonella. “Towards the atropo-stereoselective total synthesis of myricanol : Vers la synthèse totale atropo-stéréosélective du myricanol.” 2016. Web. 14 Oct 2019.

Vancouver:

Bochicchio A. Towards the atropo-stereoselective total synthesis of myricanol : Vers la synthèse totale atropo-stéréosélective du myricanol. [Internet] [Doctoral dissertation]. Strasbourg; Università degli studi della Basilicata; 2016. [cited 2019 Oct 14]. Available from: http://www.theses.fr/2016STRAF004.

Council of Science Editors:

Bochicchio A. Towards the atropo-stereoselective total synthesis of myricanol : Vers la synthèse totale atropo-stéréosélective du myricanol. [Doctoral Dissertation]. Strasbourg; Università degli studi della Basilicata; 2016. Available from: http://www.theses.fr/2016STRAF004

21. Nagaradja, Elisabeth. Bases bimétalliques fer-lithium et zinc-lithium pour la fonctionnalisation (hétéro)aromatique : étude comparative et applications en série azolique : Iron-Lithium and Zinc-Lithium bimetallic bases for the funtionalization of (hetero)aromatic compounds : comparative study and applications to the azole series.

Degree: Docteur es, Chimie, 2013, Rennes 1; Université européenne de Bretagne

Le but principal de ce travail a été de mettre en évidence le potentiel synthétique de nouvelles bases mixtes fer-lithium dans des réactions de déprotométallation… (more)

Subjects/Keywords: Déprotométallation; Bases bimétalliques; Fer; Zinc; Lithium; Triazoles; Couplage de Suzuki; Resvératrol; Deprotometallation; Bimetallic bases; Iron; Zinc; Lithium; Triazoles; Suzuki coupling; Resveratrol

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APA (6th Edition):

Nagaradja, E. (2013). Bases bimétalliques fer-lithium et zinc-lithium pour la fonctionnalisation (hétéro)aromatique : étude comparative et applications en série azolique : Iron-Lithium and Zinc-Lithium bimetallic bases for the funtionalization of (hetero)aromatic compounds : comparative study and applications to the azole series. (Doctoral Dissertation). Rennes 1; Université européenne de Bretagne. Retrieved from http://www.theses.fr/2013REN1S177

Chicago Manual of Style (16th Edition):

Nagaradja, Elisabeth. “Bases bimétalliques fer-lithium et zinc-lithium pour la fonctionnalisation (hétéro)aromatique : étude comparative et applications en série azolique : Iron-Lithium and Zinc-Lithium bimetallic bases for the funtionalization of (hetero)aromatic compounds : comparative study and applications to the azole series.” 2013. Doctoral Dissertation, Rennes 1; Université européenne de Bretagne. Accessed October 14, 2019. http://www.theses.fr/2013REN1S177.

MLA Handbook (7th Edition):

Nagaradja, Elisabeth. “Bases bimétalliques fer-lithium et zinc-lithium pour la fonctionnalisation (hétéro)aromatique : étude comparative et applications en série azolique : Iron-Lithium and Zinc-Lithium bimetallic bases for the funtionalization of (hetero)aromatic compounds : comparative study and applications to the azole series.” 2013. Web. 14 Oct 2019.

Vancouver:

Nagaradja E. Bases bimétalliques fer-lithium et zinc-lithium pour la fonctionnalisation (hétéro)aromatique : étude comparative et applications en série azolique : Iron-Lithium and Zinc-Lithium bimetallic bases for the funtionalization of (hetero)aromatic compounds : comparative study and applications to the azole series. [Internet] [Doctoral dissertation]. Rennes 1; Université européenne de Bretagne; 2013. [cited 2019 Oct 14]. Available from: http://www.theses.fr/2013REN1S177.

Council of Science Editors:

Nagaradja E. Bases bimétalliques fer-lithium et zinc-lithium pour la fonctionnalisation (hétéro)aromatique : étude comparative et applications en série azolique : Iron-Lithium and Zinc-Lithium bimetallic bases for the funtionalization of (hetero)aromatic compounds : comparative study and applications to the azole series. [Doctoral Dissertation]. Rennes 1; Université européenne de Bretagne; 2013. Available from: http://www.theses.fr/2013REN1S177

22. Wang, Zi. One-Pot Synthesis of meta-Substituted Phenols via Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling and Oxidation.

Degree: MSc -MS, Chemistry, 2018, York University

 We have developed a two-step synthesis of meta-substituted phenols in one pot, in good to excellent yield. A Pd2+ source is the catalyst for both… (more)

Subjects/Keywords: Chemistry; Chemistry; Organic chemistry; Synthetic chemistry; Synthesis; Phenols; Phenol synthesis; Cross-coupling; Oxidation; Suzuki; Suzuki-Miyaura; Aerobic oxidation; Boronic acid

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APA (6th Edition):

Wang, Z. (2018). One-Pot Synthesis of meta-Substituted Phenols via Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling and Oxidation. (Masters Thesis). York University. Retrieved from http://hdl.handle.net/10315/34276

Chicago Manual of Style (16th Edition):

Wang, Zi. “One-Pot Synthesis of meta-Substituted Phenols via Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling and Oxidation.” 2018. Masters Thesis, York University. Accessed October 14, 2019. http://hdl.handle.net/10315/34276.

MLA Handbook (7th Edition):

Wang, Zi. “One-Pot Synthesis of meta-Substituted Phenols via Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling and Oxidation.” 2018. Web. 14 Oct 2019.

Vancouver:

Wang Z. One-Pot Synthesis of meta-Substituted Phenols via Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling and Oxidation. [Internet] [Masters thesis]. York University; 2018. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10315/34276.

Council of Science Editors:

Wang Z. One-Pot Synthesis of meta-Substituted Phenols via Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling and Oxidation. [Masters Thesis]. York University; 2018. Available from: http://hdl.handle.net/10315/34276

23. François, Benjamin. Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds.

Degree: Docteur es, Chimie moléculaire et macromoléculaire, 2018, Rennes 1

Les composés organoborés constituent des outils remarquables en synthèse organique de par leur chimie très diversifiée. Les travaux présentés dans ce mémoire abordent de nouveaux… (more)

Subjects/Keywords: Synthèse; Cascade; Organoboranes; Couplage de Suzuki; Réaction ène; Pyrrole; Synthesis; Cascade; Organoboranes; Suzuki coupling; Ene reaction; Pyrrole

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APA (6th Edition):

François, B. (2018). Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2018REN1S114

Chicago Manual of Style (16th Edition):

François, Benjamin. “Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds.” 2018. Doctoral Dissertation, Rennes 1. Accessed October 14, 2019. http://www.theses.fr/2018REN1S114.

MLA Handbook (7th Edition):

François, Benjamin. “Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds.” 2018. Web. 14 Oct 2019.

Vancouver:

François B. Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds. [Internet] [Doctoral dissertation]. Rennes 1; 2018. [cited 2019 Oct 14]. Available from: http://www.theses.fr/2018REN1S114.

Council of Science Editors:

François B. Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds. [Doctoral Dissertation]. Rennes 1; 2018. Available from: http://www.theses.fr/2018REN1S114


University of Alberta

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Lee, Jack C H. “Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.” 2013. Doctoral Dissertation, University of Alberta. Accessed October 14, 2019. https://era.library.ualberta.ca/files/qn59q550n.

MLA Handbook (7th Edition):

Lee, Jack C H. “Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.” 2013. Web. 14 Oct 2019.

Vancouver:

Lee JCH. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2019 Oct 14]. Available from: https://era.library.ualberta.ca/files/qn59q550n.

Council of Science Editors:

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


NSYSU

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

Degree: Master, Chemistry, 2013, NSYSU

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Huang, Hao-ping. “Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.” 2013. Thesis, NSYSU. Accessed October 14, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051.

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

MLA Handbook (7th Edition):

Huang, Hao-ping. “Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.” 2013. Web. 14 Oct 2019.

Vancouver:

Huang H. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. [Internet] [Thesis]. NSYSU; 2013. [cited 2019 Oct 14]. 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


Université de Montréal

26. Constantineau-Forget, Lea. Études vers la synthèse totale du cylindrocyclophane F et Synthèse d’hétérocycles azotés fluorescents .

Degree: 2015, Université de Montréal

 Dans ce mémoire, deux principaux sujets seront présentés. Nos efforts se sont d’abord tournés vers la synthèse du cylindrocyclophane F, un [7,7]-paracyclophane naturel, puis vers… (more)

Subjects/Keywords: Macrocyclisation; Indolizines; Catalytic; Palladium; Catalyse; Couplage; Suzuki; Coupling; Cyclopropénation; Cyclopropanation; Enantioselective; énantiosélective; Cyclopropenation

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

APA (6th Edition):

Constantineau-Forget, L. (2015). Études vers la synthèse totale du cylindrocyclophane F et Synthèse d’hétérocycles azotés fluorescents . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/11967

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):

Constantineau-Forget, Lea. “Études vers la synthèse totale du cylindrocyclophane F et Synthèse d’hétérocycles azotés fluorescents .” 2015. Thesis, Université de Montréal. Accessed October 14, 2019. http://hdl.handle.net/1866/11967.

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

MLA Handbook (7th Edition):

Constantineau-Forget, Lea. “Études vers la synthèse totale du cylindrocyclophane F et Synthèse d’hétérocycles azotés fluorescents .” 2015. Web. 14 Oct 2019.

Vancouver:

Constantineau-Forget L. Études vers la synthèse totale du cylindrocyclophane F et Synthèse d’hétérocycles azotés fluorescents . [Internet] [Thesis]. Université de Montréal; 2015. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/1866/11967.

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

Council of Science Editors:

Constantineau-Forget L. Études vers la synthèse totale du cylindrocyclophane F et Synthèse d’hétérocycles azotés fluorescents . [Thesis]. Université de Montréal; 2015. Available from: http://hdl.handle.net/1866/11967

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


NSYSU

27. Wu, Chung-chiu. Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation.

Degree: Master, Chemistry, 2012, NSYSU

 A one-pot synthesis of ortho-arylated 9-(pyridin-2-yl)-9H-carbazoles via C-H bond activation, in which palladium(II)-catalyzed cross-coupling of 9-(pyridin-2-yl)-9H-carbazoles with potassium aryltrifluoroborates is presented. Silver nitrate and tert-butanol… (more)

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

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

APA (6th Edition):

Wu, C. (2012). Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941

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):

Wu, Chung-chiu. “Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation.” 2012. Thesis, NSYSU. Accessed October 14, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941.

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

MLA Handbook (7th Edition):

Wu, Chung-chiu. “Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation.” 2012. Web. 14 Oct 2019.

Vancouver:

Wu C. Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation. [Internet] [Thesis]. NSYSU; 2012. [cited 2019 Oct 14]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941.

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

Council of Science Editors:

Wu C. Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941

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


University of Manchester

28. Ayuso Carrillo, Josue Israel. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.

Degree: 2016, University of Manchester

 As key components of flexible organic electronics, the synthesis ofpolythiophenes via less toxic and more cost-effective routes is demanded. Anefficient synthetic route for the production… (more)

Subjects/Keywords: conjugated polymers; Suzuki-Miyaura cross-coupling; Electrophilic borylation; MIDA boronates; slow release; thiophenes; organic electronics

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

APA (6th Edition):

Ayuso Carrillo, J. I. (2016). Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874

Chicago Manual of Style (16th Edition):

Ayuso Carrillo, Josue Israel. “Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 14, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874.

MLA Handbook (7th Edition):

Ayuso Carrillo, Josue Israel. “Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.” 2016. Web. 14 Oct 2019.

Vancouver:

Ayuso Carrillo JI. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 14]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874.

Council of Science Editors:

Ayuso Carrillo JI. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874


Virginia Commonwealth University

29. Broderick, Meghann. Characterization of Stabilized Palladium Nanocatalysts.

Degree: MS, Chemistry, 2010, Virginia Commonwealth University

 Metal nanoparticles have received much interest for their application in catalysis due to high surface-to-volume ratios resulting in more available active sites. Ideally these catalysts… (more)

Subjects/Keywords: Palladium; Nanocatalyst; XPS; Synthesis; Carbon-Carbon Coupling; Suzuki; Nanoparticle; Stablized; Chemistry; Physical Sciences and Mathematics

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

APA (6th Edition):

Broderick, M. (2010). Characterization of Stabilized Palladium Nanocatalysts. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2201

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):

Broderick, Meghann. “Characterization of Stabilized Palladium Nanocatalysts.” 2010. Thesis, Virginia Commonwealth University. Accessed October 14, 2019. https://scholarscompass.vcu.edu/etd/2201.

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

MLA Handbook (7th Edition):

Broderick, Meghann. “Characterization of Stabilized Palladium Nanocatalysts.” 2010. Web. 14 Oct 2019.

Vancouver:

Broderick M. Characterization of Stabilized Palladium Nanocatalysts. [Internet] [Thesis]. Virginia Commonwealth University; 2010. [cited 2019 Oct 14]. Available from: https://scholarscompass.vcu.edu/etd/2201.

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

Council of Science Editors:

Broderick M. Characterization of Stabilized Palladium Nanocatalysts. [Thesis]. Virginia Commonwealth University; 2010. Available from: https://scholarscompass.vcu.edu/etd/2201

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

30. Zhang, Na. Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles.

Degree: 2015, University of Pennsylvania

 The Suzuki-Miyaura cross-coupling is widely used in the synthesis of pharmaceuticals, agrochemicals, and organic light-emitting materials. Utilization of phenol derivatives in Suzuki-Miyaura coupling is economically,… (more)

Subjects/Keywords: Borylation; C-O Electrophile; Cross-Coupling; Nickel; Suzuki-Miyaura; Chemistry; Inorganic Chemistry; Organic Chemistry

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

APA (6th Edition):

Zhang, N. (2015). Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1170

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):

Zhang, Na. “Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles.” 2015. Thesis, University of Pennsylvania. Accessed October 14, 2019. https://repository.upenn.edu/edissertations/1170.

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

MLA Handbook (7th Edition):

Zhang, Na. “Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles.” 2015. Web. 14 Oct 2019.

Vancouver:

Zhang N. Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2019 Oct 14]. Available from: https://repository.upenn.edu/edissertations/1170.

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

Council of Science Editors:

Zhang N. Nickel Catalyzed Borylation and Cross-Coupling of Representative C-O Based Electrophiles. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/1170

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

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