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You searched for +publisher:"University of Illinois – Urbana-Champaign" +contributor:("Denmark, Scott E"). Showing records 1 – 30 of 46 total matches.

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University of Illinois – Urbana-Champaign

1. Seymour, Craig Houghton. Formation and capture of thiiranium ion intermediates using Lewis acids.

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

 The aprotic formation of thiiranium ions and subsequent nucleophilic capture was investigated. It was discovered that β-methoxy and β-acetoxy sulfides could form thiiranium ions in… (more)

Subjects/Keywords: thiiranium ion; organoaluminum

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APA (6th Edition):

Seymour, C. H. (2015). Formation and capture of thiiranium ion intermediates using Lewis acids. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/88173

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):

Seymour, Craig Houghton. “Formation and capture of thiiranium ion intermediates using Lewis acids.” 2015. Thesis, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/88173.

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

MLA Handbook (7th Edition):

Seymour, Craig Houghton. “Formation and capture of thiiranium ion intermediates using Lewis acids.” 2015. Web. 18 Sep 2019.

Vancouver:

Seymour CH. Formation and capture of thiiranium ion intermediates using Lewis acids. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/88173.

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

Council of Science Editors:

Seymour CH. Formation and capture of thiiranium ion intermediates using Lewis acids. [Thesis]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/88173

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


University of Illinois – Urbana-Champaign

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

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

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

Subjects/Keywords: silanolate; cross-coupling

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Yousaf, Zain. “Development of organosilicon cross-coupling reaction.” 2015. Thesis, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/89275.

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

MLA Handbook (7th Edition):

Yousaf, Zain. “Development of organosilicon cross-coupling reaction.” 2015. Web. 18 Sep 2019.

Vancouver:

Yousaf Z. Development of organosilicon cross-coupling reaction. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/89275.

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

Council of Science Editors:

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

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


University of Illinois – Urbana-Champaign

3. Bailey, Aaron D. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.

Degree: MS, 0335, 2011, University of Illinois – Urbana-Champaign

 Palladium-catalyzed cross-coupling of ??-substituted allylic silanolates with aryl bromides was investigated. It was discovered that ??-selectivity is heavily influenced by the substituents at silicon. It… (more)

Subjects/Keywords: Palladium-catalyzed cross-coupling reactions; allylic silanes; vinylsilanes

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APA (6th Edition):

Bailey, A. D. (2011). Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24450

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

Chicago Manual of Style (16th Edition):

Bailey, Aaron D. “Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.” 2011. Thesis, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/24450.

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

MLA Handbook (7th Edition):

Bailey, Aaron D. “Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.” 2011. Web. 18 Sep 2019.

Vancouver:

Bailey AD. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/24450.

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

Council of Science Editors:

Bailey AD. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. [Thesis]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24450

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


University of Illinois – Urbana-Champaign

4. Ambrosi, Andrea. I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis.

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

 The first half of the present dissertation describes the mechanistic investigation of the palladium-catalyzed cross-coupling reaction of alkenyl- and arylsilanolates. The combination of reaction kinetics… (more)

Subjects/Keywords: Cross-coupling; Silanolates; Carbon monoxide; Organic synthesis

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APA (6th Edition):

Ambrosi, A. (2016). I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95551

Chicago Manual of Style (16th Edition):

Ambrosi, Andrea. “I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/95551.

MLA Handbook (7th Edition):

Ambrosi, Andrea. “I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis.” 2016. Web. 18 Sep 2019.

Vancouver:

Ambrosi A. I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/95551.

Council of Science Editors:

Ambrosi A. I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95551


University of Illinois – Urbana-Champaign

5. Thomas, Andy Alexander. Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link.

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

 The Suzuki-Miyaura reaction is currently the most practiced cross-coupling reaction due to its broad applicability, low toxicity of the metal (B), and the wide variety… (more)

Subjects/Keywords: Transmetalation

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APA (6th Edition):

Thomas, A. A. (2017). Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/97541

Chicago Manual of Style (16th Edition):

Thomas, Andy Alexander. “Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/97541.

MLA Handbook (7th Edition):

Thomas, Andy Alexander. “Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link.” 2017. Web. 18 Sep 2019.

Vancouver:

Thomas AA. Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/97541.

Council of Science Editors:

Thomas AA. Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/97541


University of Illinois – Urbana-Champaign

6. Kornfilt, David Jean Pierre. Lewis base catalyzed enantioselective oxysulfenylation of alkenes.

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

 The Lewis base activation of Lewis acids has been harnessed in the development of an enantioselective oxysulfenylation reaction for unactivated alkenes. The weak Lewis acid… (more)

Subjects/Keywords: Catalysis; Lewis Bases; Enantioselecive; Organocatalysis

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APA (6th Edition):

Kornfilt, D. J. P. (2016). Lewis base catalyzed enantioselective oxysulfenylation of alkenes. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95493

Chicago Manual of Style (16th Edition):

Kornfilt, David Jean Pierre. “Lewis base catalyzed enantioselective oxysulfenylation of alkenes.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/95493.

MLA Handbook (7th Edition):

Kornfilt, David Jean Pierre. “Lewis base catalyzed enantioselective oxysulfenylation of alkenes.” 2016. Web. 18 Sep 2019.

Vancouver:

Kornfilt DJP. Lewis base catalyzed enantioselective oxysulfenylation of alkenes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/95493.

Council of Science Editors:

Kornfilt DJP. Lewis base catalyzed enantioselective oxysulfenylation of alkenes. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95493


University of Illinois – Urbana-Champaign

7. Chi, Hyungmin. Lewis base catalyzed enantioselective sulfenoamination of alkenes.

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

 The concept of Lewis base activation of Lewis acid has been successfully applied to the enantioselective sulfenoamination of olefins. The unreactive, achiral Lewis acidic sulfenylating… (more)

Subjects/Keywords: Sulfenoamination; Enantioselective catalysis; Lewis base; Negative catalysis

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APA (6th Edition):

Chi, H. (2016). Lewis base catalyzed enantioselective sulfenoamination of alkenes. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95503

Chicago Manual of Style (16th Edition):

Chi, Hyungmin. “Lewis base catalyzed enantioselective sulfenoamination of alkenes.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/95503.

MLA Handbook (7th Edition):

Chi, Hyungmin. “Lewis base catalyzed enantioselective sulfenoamination of alkenes.” 2016. Web. 18 Sep 2019.

Vancouver:

Chi H. Lewis base catalyzed enantioselective sulfenoamination of alkenes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/95503.

Council of Science Editors:

Chi H. Lewis base catalyzed enantioselective sulfenoamination of alkenes. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95503


University of Illinois – Urbana-Champaign

8. Cullen, Lindsey R. Development of novel methodologies utilizing quaternary ammonium salts as catalysts.

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

 The first half of this thesis (Chapter 2) described the development of a fluoride-promoted conjugate addition of sulfur-stabilized carbanion nucleophiles to α,β-unsaturated ketones and esters.… (more)

Subjects/Keywords: Phase Transfer Catalysis

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APA (6th Edition):

Cullen, L. R. (2015). Development of novel methodologies utilizing quaternary ammonium salts as catalysts. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/88216

Chicago Manual of Style (16th Edition):

Cullen, Lindsey R. “Development of novel methodologies utilizing quaternary ammonium salts as catalysts.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/88216.

MLA Handbook (7th Edition):

Cullen, Lindsey R. “Development of novel methodologies utilizing quaternary ammonium salts as catalysts.” 2015. Web. 18 Sep 2019.

Vancouver:

Cullen LR. Development of novel methodologies utilizing quaternary ammonium salts as catalysts. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/88216.

Council of Science Editors:

Cullen LR. Development of novel methodologies utilizing quaternary ammonium salts as catalysts. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/88216


University of Illinois – Urbana-Champaign

9. Xie, Min. Synthesis of nitrogen-containing heterocycles using nitro compounds as building blocks: Part I: Synthesis of 3-substituted azepanes. Part II: Synthesis of 1-azoniapropellanes as phase transfer catalysts.

Degree: PhD, 0335, 2010, University of Illinois – Urbana-Champaign

 The chemistry of nitroalkenes and nitroalkanes has been explored with regard to synthesis of nitrogen-containing heterocycles, including 3-sustituted azepanes and 1-azoniapropellanes. A general synthesis of… (more)

Subjects/Keywords: synthetic methods; azepanes; azoniapropellane

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APA (6th Edition):

Xie, M. (2010). Synthesis of nitrogen-containing heterocycles using nitro compounds as building blocks: Part I: Synthesis of 3-substituted azepanes. Part II: Synthesis of 1-azoniapropellanes as phase transfer catalysts. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/16534

Chicago Manual of Style (16th Edition):

Xie, Min. “Synthesis of nitrogen-containing heterocycles using nitro compounds as building blocks: Part I: Synthesis of 3-substituted azepanes. Part II: Synthesis of 1-azoniapropellanes as phase transfer catalysts.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/16534.

MLA Handbook (7th Edition):

Xie, Min. “Synthesis of nitrogen-containing heterocycles using nitro compounds as building blocks: Part I: Synthesis of 3-substituted azepanes. Part II: Synthesis of 1-azoniapropellanes as phase transfer catalysts.” 2010. Web. 18 Sep 2019.

Vancouver:

Xie M. Synthesis of nitrogen-containing heterocycles using nitro compounds as building blocks: Part I: Synthesis of 3-substituted azepanes. Part II: Synthesis of 1-azoniapropellanes as phase transfer catalysts. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/16534.

Council of Science Editors:

Xie M. Synthesis of nitrogen-containing heterocycles using nitro compounds as building blocks: Part I: Synthesis of 3-substituted azepanes. Part II: Synthesis of 1-azoniapropellanes as phase transfer catalysts. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/16534


University of Illinois – Urbana-Champaign

10. Smith, Russell C. Preparative and mechanistic aspects of palladium-catalyzed cross-coupling reactions of alkali-metal arylsilanolates.

Degree: PhD, 0335, 2010, University of Illinois – Urbana-Champaign

 The development of alkali-metal arylsilanolates as notable organometallic reagents for the preparation of biaryls has been realized through in depth mechanistic and preparative studies. The… (more)

Subjects/Keywords: arylsilanolates; biaryls; mechanism; palladium

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APA (6th Edition):

Smith, R. C. (2010). Preparative and mechanistic aspects of palladium-catalyzed cross-coupling reactions of alkali-metal arylsilanolates. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/16830

Chicago Manual of Style (16th Edition):

Smith, Russell C. “Preparative and mechanistic aspects of palladium-catalyzed cross-coupling reactions of alkali-metal arylsilanolates.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/16830.

MLA Handbook (7th Edition):

Smith, Russell C. “Preparative and mechanistic aspects of palladium-catalyzed cross-coupling reactions of alkali-metal arylsilanolates.” 2010. Web. 18 Sep 2019.

Vancouver:

Smith RC. Preparative and mechanistic aspects of palladium-catalyzed cross-coupling reactions of alkali-metal arylsilanolates. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/16830.

Council of Science Editors:

Smith RC. Preparative and mechanistic aspects of palladium-catalyzed cross-coupling reactions of alkali-metal arylsilanolates. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/16830


University of Illinois – Urbana-Champaign

11. Burk, Matthew. Asymmetric Lewis base catalysis: I. Lewis base catalyzed halogenation and development of an enantioselective bromocycloetherification reaction; II. enantioselective addition of silyl ketene imines to carbonyl electrophiles.

Degree: PhD, 0335, 2012, University of Illinois – Urbana-Champaign

 The stereochemical stability of bromonium and chloronium ions has been investigated in the context of asymmetric catalysis. Bromonium ions have been found to racemize in… (more)

Subjects/Keywords: enantioselective; Halogenation; chlorination; bromination; iodination; chlorolactonization; chloroetherification; chlorocyloetherification; bromolactonization; bromoetherification; bromocycloetherification; iodolactonization; iodoetherification; iodocycloetherification; halonium; haliranium; bromonium; bromiranium; chloronium; chloriranium; solvolysis; racemization; olefin-to-olefin transfer; Lewis base; chiral; chiral Lewis base; Lewis base catalysis; Silicon tetrachloride; silyl ketene imine; aldol; germanium; crossed aldol; kinetics; chiral Bronsted acid

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APA (6th Edition):

Burk, M. (2012). Asymmetric Lewis base catalysis: I. Lewis base catalyzed halogenation and development of an enantioselective bromocycloetherification reaction; II. enantioselective addition of silyl ketene imines to carbonyl electrophiles. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/34528

Chicago Manual of Style (16th Edition):

Burk, Matthew. “Asymmetric Lewis base catalysis: I. Lewis base catalyzed halogenation and development of an enantioselective bromocycloetherification reaction; II. enantioselective addition of silyl ketene imines to carbonyl electrophiles.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/34528.

MLA Handbook (7th Edition):

Burk, Matthew. “Asymmetric Lewis base catalysis: I. Lewis base catalyzed halogenation and development of an enantioselective bromocycloetherification reaction; II. enantioselective addition of silyl ketene imines to carbonyl electrophiles.” 2012. Web. 18 Sep 2019.

Vancouver:

Burk M. Asymmetric Lewis base catalysis: I. Lewis base catalyzed halogenation and development of an enantioselective bromocycloetherification reaction; II. enantioselective addition of silyl ketene imines to carbonyl electrophiles. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/34528.

Council of Science Editors:

Burk M. Asymmetric Lewis base catalysis: I. Lewis base catalyzed halogenation and development of an enantioselective bromocycloetherification reaction; II. enantioselective addition of silyl ketene imines to carbonyl electrophiles. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/34528


University of Illinois – Urbana-Champaign

12. Ibrahim, Malek Y. S. Carbon monoxide-driven reductive organic transformations and precious metals recycling.

Degree: PhD, Chemical Engineering, 2018, University of Illinois – Urbana-Champaign

 Herein we present the efforts made toward employing the homogeneously-catalyzed Water-Gas Shift Reaction (WGSR) to drive essential reductive chemical transformations, and selectively extract rhodium from… (more)

Subjects/Keywords: Water-Gas Shift; rhodium carbonyl hydride; reductive carbonylation; alkylation; amination; rhodium recycling.

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APA (6th Edition):

Ibrahim, M. Y. S. (2018). Carbon monoxide-driven reductive organic transformations and precious metals recycling. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/102409

Chicago Manual of Style (16th Edition):

Ibrahim, Malek Y S. “Carbon monoxide-driven reductive organic transformations and precious metals recycling.” 2018. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/102409.

MLA Handbook (7th Edition):

Ibrahim, Malek Y S. “Carbon monoxide-driven reductive organic transformations and precious metals recycling.” 2018. Web. 18 Sep 2019.

Vancouver:

Ibrahim MYS. Carbon monoxide-driven reductive organic transformations and precious metals recycling. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2018. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/102409.

Council of Science Editors:

Ibrahim MYS. Carbon monoxide-driven reductive organic transformations and precious metals recycling. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2018. Available from: http://hdl.handle.net/2142/102409


University of Illinois – Urbana-Champaign

13. Macor, Joseph Alexander. On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds.

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

 The work described herein details the synthesis of a variety of pentavalent organophosphorus compounds and their applications as ligands to address important problems in coordination… (more)

Subjects/Keywords: Asymmetric Synthesis; Minor Actinide Separations; Heterogeneous Asymmetric Catalysis

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APA (6th Edition):

Macor, J. A. (2015). On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78615

Chicago Manual of Style (16th Edition):

Macor, Joseph Alexander. “On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/78615.

MLA Handbook (7th Edition):

Macor, Joseph Alexander. “On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds.” 2015. Web. 18 Sep 2019.

Vancouver:

Macor JA. On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/78615.

Council of Science Editors:

Macor JA. On the coordination chemistry of pentavalent (σ⁴, λ⁵) phosphorus compounds. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78615


University of Illinois – Urbana-Champaign

14. Wilson, Tyler. Synthesis, study and application of silyl ketene imines in Lewis base catalyzed carbonyl addition.

Degree: PhD, 0335, 2012, University of Illinois – Urbana-Champaign

 The activation of Lewis acids by chiral Lewis bases has allowed for the development of a robust and highly selective catalyst system for the addition… (more)

Subjects/Keywords: Silyl Ketene Imines; Lewis Base Catalysis; Enantioselective Synthesis

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APA (6th Edition):

Wilson, T. (2012). Synthesis, study and application of silyl ketene imines in Lewis base catalyzed carbonyl addition. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29486

Chicago Manual of Style (16th Edition):

Wilson, Tyler. “Synthesis, study and application of silyl ketene imines in Lewis base catalyzed carbonyl addition.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/29486.

MLA Handbook (7th Edition):

Wilson, Tyler. “Synthesis, study and application of silyl ketene imines in Lewis base catalyzed carbonyl addition.” 2012. Web. 18 Sep 2019.

Vancouver:

Wilson T. Synthesis, study and application of silyl ketene imines in Lewis base catalyzed carbonyl addition. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/29486.

Council of Science Editors:

Wilson T. Synthesis, study and application of silyl ketene imines in Lewis base catalyzed carbonyl addition. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29486


University of Illinois – Urbana-Champaign

15. Bemis, Christopher Yngwie. Synthesis of sesquiterpene-tropolones.

Degree: PhD, Chemistry, 2019, University of Illinois – Urbana-Champaign

 A modular synthetic platform for the synthesis of the multi-bioactive sesquiterpene-tropolone natural products has been developed in an effort to provide general synthetic access to… (more)

Subjects/Keywords: total synthesis; organic synthesis; sesquiterpene-tropolones; meroterpenoids; tropolone; pycnidione; epolone A; epolone B; eupenifeldin

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APA (6th Edition):

Bemis, C. Y. (2019). Synthesis of sesquiterpene-tropolones. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/104826

Chicago Manual of Style (16th Edition):

Bemis, Christopher Yngwie. “Synthesis of sesquiterpene-tropolones.” 2019. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/104826.

MLA Handbook (7th Edition):

Bemis, Christopher Yngwie. “Synthesis of sesquiterpene-tropolones.” 2019. Web. 18 Sep 2019.

Vancouver:

Bemis CY. Synthesis of sesquiterpene-tropolones. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2019. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/104826.

Council of Science Editors:

Bemis CY. Synthesis of sesquiterpene-tropolones. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2019. Available from: http://hdl.handle.net/2142/104826


University of Illinois – Urbana-Champaign

16. Dailey, Ian. Synthesis and function of the conserved motif of mycosamine-containing polyene macrolides.

Degree: PhD, Chemistry, 2012, University of Illinois – Urbana-Champaign

 Mycosamine-containing polyene macrolides represent a large family of natural products with antifungal activity, of which amphotericin B (AmB) is an important member. Several of these… (more)

Subjects/Keywords: amphotericin B; amphotericin; natamycin; polyene; polyene macrolide; ergosterol; sterol binding; mycosamine; lactonization; diastereotopic group selective lactonization; iterative cross-coupling; ICC; Suzuki; isothermal titration calorimetry; ITC

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APA (6th Edition):

Dailey, I. (2012). Synthesis and function of the conserved motif of mycosamine-containing polyene macrolides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95658

Chicago Manual of Style (16th Edition):

Dailey, Ian. “Synthesis and function of the conserved motif of mycosamine-containing polyene macrolides.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/95658.

MLA Handbook (7th Edition):

Dailey, Ian. “Synthesis and function of the conserved motif of mycosamine-containing polyene macrolides.” 2012. Web. 18 Sep 2019.

Vancouver:

Dailey I. Synthesis and function of the conserved motif of mycosamine-containing polyene macrolides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/95658.

Council of Science Editors:

Dailey I. Synthesis and function of the conserved motif of mycosamine-containing polyene macrolides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/95658


University of Illinois – Urbana-Champaign

17. Liu, Wei. Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis.

Degree: PhD, Chemistry, 2018, University of Illinois – Urbana-Champaign

 Asymmetric C–H functionalization could deliver a highly efficient transformation by installing both oxidized functionality and absolute stereochemistry simultaneously. In this context, palladium(II)-catalyzed asymmetric allylic C–H… (more)

Subjects/Keywords: C–H Activation; Asymmetric Catalysis

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APA (6th Edition):

Liu, W. (2018). Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/102431

Chicago Manual of Style (16th Edition):

Liu, Wei. “Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis.” 2018. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/102431.

MLA Handbook (7th Edition):

Liu, Wei. “Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis.” 2018. Web. 18 Sep 2019.

Vancouver:

Liu W. Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2018. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/102431.

Council of Science Editors:

Liu W. Asymmetric allylic C–H functionalization via palladium(II)/sulfoxide-oxazoline catalysis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2018. Available from: http://hdl.handle.net/2142/102431


University of Illinois – Urbana-Champaign

18. Klinkenberg, Jessica. Palladium-catalyzed reactions of ammonia, carbon monoxide, and cyanide.

Degree: PhD, 0335, 2012, University of Illinois – Urbana-Champaign

 The reductive eliminations of primary arylamines from a series of bisphosphine-ligated arylpalladium(II) parent amido complexes countered several established trends. In contrast to arylamido and alkylamido… (more)

Subjects/Keywords: palladium; catalysis; ammonia; carbon monoxide; cyanide; carbonylation; amination; cyanation

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APA (6th Edition):

Klinkenberg, J. (2012). Palladium-catalyzed reactions of ammonia, carbon monoxide, and cyanide. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/32015

Chicago Manual of Style (16th Edition):

Klinkenberg, Jessica. “Palladium-catalyzed reactions of ammonia, carbon monoxide, and cyanide.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/32015.

MLA Handbook (7th Edition):

Klinkenberg, Jessica. “Palladium-catalyzed reactions of ammonia, carbon monoxide, and cyanide.” 2012. Web. 18 Sep 2019.

Vancouver:

Klinkenberg J. Palladium-catalyzed reactions of ammonia, carbon monoxide, and cyanide. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/32015.

Council of Science Editors:

Klinkenberg J. Palladium-catalyzed reactions of ammonia, carbon monoxide, and cyanide. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/32015


University of Illinois – Urbana-Champaign

19. Bair, Joseph. The development of deoxynyboquinone as a personalized anticancer compound.

Degree: PhD, 0335, 2012, University of Illinois – Urbana-Champaign

 The major challenge in cancer therapy is to selectively destroy cancer cells in the presence of healthy tissue. One viable strategy relies on targeting the… (more)

Subjects/Keywords: Cancer; personalized medicine; quinone; total synthesis; reactive oxygen species; NQO1

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APA (6th Edition):

Bair, J. (2012). The development of deoxynyboquinone as a personalized anticancer compound. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/32020

Chicago Manual of Style (16th Edition):

Bair, Joseph. “The development of deoxynyboquinone as a personalized anticancer compound.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/32020.

MLA Handbook (7th Edition):

Bair, Joseph. “The development of deoxynyboquinone as a personalized anticancer compound.” 2012. Web. 18 Sep 2019.

Vancouver:

Bair J. The development of deoxynyboquinone as a personalized anticancer compound. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/32020.

Council of Science Editors:

Bair J. The development of deoxynyboquinone as a personalized anticancer compound. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/32020


University of Illinois – Urbana-Champaign

20. Osberger, Thomas Joseph. Catalytic C-H oxidation reactions for the synthesis and diversification of hydroxyamino acid motifs.

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

 Hydroxyamino acid motifs are well-represented structures in natural products and pharmaceuticals, and are widely employed as synthetic building blocks in organic synthesis. In nature, such… (more)

Subjects/Keywords: C-H Functionalization; C-H Oxidation; Catalysis

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APA (6th Edition):

Osberger, T. J. (2016). Catalytic C-H oxidation reactions for the synthesis and diversification of hydroxyamino acid motifs. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/92900

Chicago Manual of Style (16th Edition):

Osberger, Thomas Joseph. “Catalytic C-H oxidation reactions for the synthesis and diversification of hydroxyamino acid motifs.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/92900.

MLA Handbook (7th Edition):

Osberger, Thomas Joseph. “Catalytic C-H oxidation reactions for the synthesis and diversification of hydroxyamino acid motifs.” 2016. Web. 18 Sep 2019.

Vancouver:

Osberger TJ. Catalytic C-H oxidation reactions for the synthesis and diversification of hydroxyamino acid motifs. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/92900.

Council of Science Editors:

Osberger TJ. Catalytic C-H oxidation reactions for the synthesis and diversification of hydroxyamino acid motifs. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/92900


University of Illinois – Urbana-Champaign

21. Kortman, Gregory Dean. Zirconium-mediated alkyene-aldehyde coupling, rhodium-catalyzed alkene hydrothiolation, and copper-catalyzed alkyne hydroarylation: Reaction development and mechanistic investigations.

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

 In the last 150 years, we have seen a boon in the development of new methodologies for the synthesis of organic compounds, which has led… (more)

Subjects/Keywords: Alkene; Alkyne; Hydrothiolation; Hydroarylation; Rhodium; Copper; Zirconium; Mechanism; Methodology

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APA (6th Edition):

Kortman, G. D. (2017). Zirconium-mediated alkyene-aldehyde coupling, rhodium-catalyzed alkene hydrothiolation, and copper-catalyzed alkyne hydroarylation: Reaction development and mechanistic investigations. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/99327

Chicago Manual of Style (16th Edition):

Kortman, Gregory Dean. “Zirconium-mediated alkyene-aldehyde coupling, rhodium-catalyzed alkene hydrothiolation, and copper-catalyzed alkyne hydroarylation: Reaction development and mechanistic investigations.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/99327.

MLA Handbook (7th Edition):

Kortman, Gregory Dean. “Zirconium-mediated alkyene-aldehyde coupling, rhodium-catalyzed alkene hydrothiolation, and copper-catalyzed alkyne hydroarylation: Reaction development and mechanistic investigations.” 2017. Web. 18 Sep 2019.

Vancouver:

Kortman GD. Zirconium-mediated alkyene-aldehyde coupling, rhodium-catalyzed alkene hydrothiolation, and copper-catalyzed alkyne hydroarylation: Reaction development and mechanistic investigations. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/99327.

Council of Science Editors:

Kortman GD. Zirconium-mediated alkyene-aldehyde coupling, rhodium-catalyzed alkene hydrothiolation, and copper-catalyzed alkyne hydroarylation: Reaction development and mechanistic investigations. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/99327


University of Illinois – Urbana-Champaign

22. Bultman, Michael Scott. Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine.

Degree: PhD, 0335, 2010, University of Illinois – Urbana-Champaign

 Our developments toward the total synthesis of the original and revised structures of palau’amine are presented in this study. This includes the construction of the… (more)

Subjects/Keywords: palau'amine; alkaloid; natural product; synthetic studies

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APA (6th Edition):

Bultman, M. S. (2010). Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/14694

Chicago Manual of Style (16th Edition):

Bultman, Michael Scott. “Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/14694.

MLA Handbook (7th Edition):

Bultman, Michael Scott. “Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine.” 2010. Web. 18 Sep 2019.

Vancouver:

Bultman MS. Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/14694.

Council of Science Editors:

Bultman MS. Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/14694


University of Illinois – Urbana-Champaign

23. Rice, Grant. Development of palladium catalyzed intramolecular allylic C―H amination and oxidation towards pharmacological motifs.

Degree: PhD, 0335, 2013, University of Illinois – Urbana-Champaign

 It is often said that with enough time, money and resources organic chemists can synthesize any complex organic small molecule. While those sentiments are rooted… (more)

Subjects/Keywords: C-H Activation; Palladium; Bis-Sulfoxide; Allylic Amination; Allylic Oxidation

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APA (6th Edition):

Rice, G. (2013). Development of palladium catalyzed intramolecular allylic C―H amination and oxidation towards pharmacological motifs. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42435

Chicago Manual of Style (16th Edition):

Rice, Grant. “Development of palladium catalyzed intramolecular allylic C―H amination and oxidation towards pharmacological motifs.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/42435.

MLA Handbook (7th Edition):

Rice, Grant. “Development of palladium catalyzed intramolecular allylic C―H amination and oxidation towards pharmacological motifs.” 2013. Web. 18 Sep 2019.

Vancouver:

Rice G. Development of palladium catalyzed intramolecular allylic C―H amination and oxidation towards pharmacological motifs. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/42435.

Council of Science Editors:

Rice G. Development of palladium catalyzed intramolecular allylic C―H amination and oxidation towards pharmacological motifs. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42435


University of Illinois – Urbana-Champaign

24. Chu, Wan-Yi. Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights.

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

 The utility of transition metal catalysts has greatly expanded the scope of organic reactions. Historically, homogenous catalysis is dominated by platinum group metals (PGMs) due… (more)

Subjects/Keywords: organometallic compounds; hydrosilylation; catalysis; non-innocent ligands

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APA (6th Edition):

Chu, W. (2016). Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90874

Chicago Manual of Style (16th Edition):

Chu, Wan-Yi. “Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/90874.

MLA Handbook (7th Edition):

Chu, Wan-Yi. “Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights.” 2016. Web. 18 Sep 2019.

Vancouver:

Chu W. Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/90874.

Council of Science Editors:

Chu W. Metal-ligand cooperativity in first row transition metals: hydrosilylation catalysis and mechanistic insights. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90874


University of Illinois – Urbana-Champaign

25. 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 September 18, 2019. http://hdl.handle.net/2142/91591.

MLA Handbook (7th Edition):

Gillis, Eric P. “Iterative cross-coupling with MIDA boronates.” 2010. Web. 18 Sep 2019.

Vancouver:

Gillis EP. Iterative cross-coupling with MIDA boronates. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 18]. 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


University of Illinois – Urbana-Champaign

26. Vo, Giang D. Development and mechanistic investigation of the palladium-catalyzed α-arylation of aldehydes and N-arylation of ammonia.

Degree: PhD, 0335, 2011, University of Illinois – Urbana-Champaign

 A general method for the palladium-catalyzed α-arylation of aldehydes was developed to couple linear and branched aldehydes with electron-poor and electron-rich bromo- and chloroarenes in… (more)

Subjects/Keywords: cross-coupling; palladium; homogeneous catalysis; ammonia; aldehydes; arylation; amination

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APA (6th Edition):

Vo, G. D. (2011). Development and mechanistic investigation of the palladium-catalyzed α-arylation of aldehydes and N-arylation of ammonia. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18494

Chicago Manual of Style (16th Edition):

Vo, Giang D. “Development and mechanistic investigation of the palladium-catalyzed α-arylation of aldehydes and N-arylation of ammonia.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/18494.

MLA Handbook (7th Edition):

Vo, Giang D. “Development and mechanistic investigation of the palladium-catalyzed α-arylation of aldehydes and N-arylation of ammonia.” 2011. Web. 18 Sep 2019.

Vancouver:

Vo GD. Development and mechanistic investigation of the palladium-catalyzed α-arylation of aldehydes and N-arylation of ammonia. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/18494.

Council of Science Editors:

Vo GD. Development and mechanistic investigation of the palladium-catalyzed α-arylation of aldehydes and N-arylation of ammonia. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18494


University of Illinois – Urbana-Champaign

27. Delcamp, Jared H. Oxidative Heck Reactions with Terminal Olefins.

Degree: PhD, 0335, 2011, University of Illinois – Urbana-Champaign

 Sequential transformations in a single reaction have the potential to dramatically increase efficiency with respect to resources, time, and number of steps to access key… (more)

Subjects/Keywords: Heck reaction; oxidative; Palladium; arylation; vinylation; transition metal catalysis

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APA (6th Edition):

Delcamp, J. H. (2011). Oxidative Heck Reactions with Terminal Olefins. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18626

Chicago Manual of Style (16th Edition):

Delcamp, Jared H. “Oxidative Heck Reactions with Terminal Olefins.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/18626.

MLA Handbook (7th Edition):

Delcamp, Jared H. “Oxidative Heck Reactions with Terminal Olefins.” 2011. Web. 18 Sep 2019.

Vancouver:

Delcamp JH. Oxidative Heck Reactions with Terminal Olefins. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/18626.

Council of Science Editors:

Delcamp JH. Oxidative Heck Reactions with Terminal Olefins. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18626


University of Illinois – Urbana-Champaign

28. Ibrahim, Abdulrahman D. Catalytic hydrofunctionalization and small molecule reactivity at a low-valent cobalt center supported by a bis(carbene) CCC pincer ligand.

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

 The ubiquity of noble metal catalysts in both industrial and academic settings is a testament to their impressive reactivity, versatility, and modularity. Recent advances in… (more)

Subjects/Keywords: Cobalt; Catalyst; Chemoselective; Alkene; Nitrile; Hydrosilylation; Two-electron; Electron-rich; Low-Valent; Pincer; Selective; Oxidative addition; Hydroboration

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APA (6th Edition):

Ibrahim, A. D. (2017). Catalytic hydrofunctionalization and small molecule reactivity at a low-valent cobalt center supported by a bis(carbene) CCC pincer ligand. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/97705

Chicago Manual of Style (16th Edition):

Ibrahim, Abdulrahman D. “Catalytic hydrofunctionalization and small molecule reactivity at a low-valent cobalt center supported by a bis(carbene) CCC pincer ligand.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/97705.

MLA Handbook (7th Edition):

Ibrahim, Abdulrahman D. “Catalytic hydrofunctionalization and small molecule reactivity at a low-valent cobalt center supported by a bis(carbene) CCC pincer ligand.” 2017. Web. 18 Sep 2019.

Vancouver:

Ibrahim AD. Catalytic hydrofunctionalization and small molecule reactivity at a low-valent cobalt center supported by a bis(carbene) CCC pincer ligand. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/97705.

Council of Science Editors:

Ibrahim AD. Catalytic hydrofunctionalization and small molecule reactivity at a low-valent cobalt center supported by a bis(carbene) CCC pincer ligand. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/97705

29. Carson, Nessa. 1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design.

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

 In Chapter 1, attempts to reproduce eight, putative, enantioselective dibromination and chlorohydroxylation reactions from oft-cited literature studies are described. The reactions were performed with full… (more)

Subjects/Keywords: Chemistry; Siloxaborolates; Silylboranes; Silicon; Boron; Cross-coupling; Hiyama-Denmark; Suzuki; Silanolates; Enantioselective; Dibromination; SnAP; Stannyl amines; Morpholines; Bisoxazolines; Computational; Modeling; Cyclization; Chlorohydroxylation; Chlorohydrins; Olefins; Palladium; Halofunctionalization; Dibromides; Predictive; Catalytic; Copper

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

APA (6th Edition):

Carson, N. (2016). 1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95419

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):

Carson, Nessa. “1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/95419.

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

MLA Handbook (7th Edition):

Carson, Nessa. “1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design.” 2016. Web. 18 Sep 2019.

Vancouver:

Carson N. 1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/95419.

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

Council of Science Editors:

Carson N. 1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95419

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

30. Weintraub, Robert. Phase transfer catalysis: catalyst screening, reaction development, and mechanism analysis.

Degree: MS, 0335, 2012, University of Illinois – Urbana-Champaign

 The asymmetric alkylation of a glycine Schiff base in addition to the development of a [2,3]-Wittig rearrangement under phase transfer catalysis (PTC) reaction conditions was… (more)

Subjects/Keywords: asymmetric phase transfer catalysis; phase transfer catalysis; tetraalkylammonium salts; Cinchona alkaloids; organic synthesis; [2,3]-Wittig Rearrangement

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

APA (6th Edition):

Weintraub, R. (2012). Phase transfer catalysis: catalyst screening, reaction development, and mechanism analysis. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/31186

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):

Weintraub, Robert. “Phase transfer catalysis: catalyst screening, reaction development, and mechanism analysis.” 2012. Thesis, University of Illinois – Urbana-Champaign. Accessed September 18, 2019. http://hdl.handle.net/2142/31186.

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

MLA Handbook (7th Edition):

Weintraub, Robert. “Phase transfer catalysis: catalyst screening, reaction development, and mechanism analysis.” 2012. Web. 18 Sep 2019.

Vancouver:

Weintraub R. Phase transfer catalysis: catalyst screening, reaction development, and mechanism analysis. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/2142/31186.

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

Council of Science Editors:

Weintraub R. Phase transfer catalysis: catalyst screening, reaction development, and mechanism analysis. [Thesis]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/31186

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

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