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You searched for +publisher:"Colorado State University" +contributor:("Rovis, Tomislav"). Showing records 1 – 30 of 33 total matches.

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Colorado State University

1. Rhorer, Timothy Benjamin. Development of N-heterocyclic carbenes for application in the intermolecular stetter reaction, The.

Degree: MS(M.S.), Chemistry, 2012, Colorado State University

 An N-heterocyclic carbene scaffold has been developed containing a protected oxygen moiety in the backbone. The oxygen provides a similar electronic effect known to fluorinated… (more)

Subjects/Keywords: carbene

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APA (6th Edition):

Rhorer, T. B. (2012). Development of N-heterocyclic carbenes for application in the intermolecular stetter reaction, The. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/67900

Chicago Manual of Style (16th Edition):

Rhorer, Timothy Benjamin. “Development of N-heterocyclic carbenes for application in the intermolecular stetter reaction, The.” 2012. Masters Thesis, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/67900.

MLA Handbook (7th Edition):

Rhorer, Timothy Benjamin. “Development of N-heterocyclic carbenes for application in the intermolecular stetter reaction, The.” 2012. Web. 07 May 2021.

Vancouver:

Rhorer TB. Development of N-heterocyclic carbenes for application in the intermolecular stetter reaction, The. [Internet] [Masters thesis]. Colorado State University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/67900.

Council of Science Editors:

Rhorer TB. Development of N-heterocyclic carbenes for application in the intermolecular stetter reaction, The. [Masters Thesis]. Colorado State University; 2012. Available from: http://hdl.handle.net/10217/67900


Colorado State University

2. Stache, Erin Elizabeth. Development of ligands for C-H functionalization utilizing amino acid derived directing groups, The.

Degree: MS(M.S.), Chemistry, 2011, Colorado State University

 The functionalization of unreactive bonds has become a focus of new reaction methodology. The foremost difficulty lies within achieving high levels of chemo-, regio-, and… (more)

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APA (6th Edition):

Stache, E. E. (2011). Development of ligands for C-H functionalization utilizing amino acid derived directing groups, The. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/70829

Chicago Manual of Style (16th Edition):

Stache, Erin Elizabeth. “Development of ligands for C-H functionalization utilizing amino acid derived directing groups, The.” 2011. Masters Thesis, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/70829.

MLA Handbook (7th Edition):

Stache, Erin Elizabeth. “Development of ligands for C-H functionalization utilizing amino acid derived directing groups, The.” 2011. Web. 07 May 2021.

Vancouver:

Stache EE. Development of ligands for C-H functionalization utilizing amino acid derived directing groups, The. [Internet] [Masters thesis]. Colorado State University; 2011. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/70829.

Council of Science Editors:

Stache EE. Development of ligands for C-H functionalization utilizing amino acid derived directing groups, The. [Masters Thesis]. Colorado State University; 2011. Available from: http://hdl.handle.net/10217/70829

3. Flanigan, Darrin Miles. Development of asymmetric N-heterocyclic carbene-catalyzed reactions.

Degree: PhD, Chemistry, 2017, Colorado State University

 N-Heterocyclic carbenes (NHCs) are ubiquitous organocatalysts in a variety of asymmetric transformations. The benzoin and Stetter reactions, which couple aldehydes to other aldehydes or Michael… (more)

Subjects/Keywords: organic chemistry; n-heterocyclic carbenes; organocatalysis

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APA (6th Edition):

Flanigan, D. M. (2017). Development of asymmetric N-heterocyclic carbene-catalyzed reactions. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/183966

Chicago Manual of Style (16th Edition):

Flanigan, Darrin Miles. “Development of asymmetric N-heterocyclic carbene-catalyzed reactions.” 2017. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/183966.

MLA Handbook (7th Edition):

Flanigan, Darrin Miles. “Development of asymmetric N-heterocyclic carbene-catalyzed reactions.” 2017. Web. 07 May 2021.

Vancouver:

Flanigan DM. Development of asymmetric N-heterocyclic carbene-catalyzed reactions. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/183966.

Council of Science Editors:

Flanigan DM. Development of asymmetric N-heterocyclic carbene-catalyzed reactions. [Doctoral Dissertation]. Colorado State University; 2017. Available from: http://hdl.handle.net/10217/183966


Colorado State University

4. Glover, Garrett S. Development of an asymmetric intermolecular stetter reaction and organocatalyst design.

Degree: MS(M.S.), Chemistry, 2012, Colorado State University

 The intermolecular Stetter represents a powerful carbon-carbon bond forming reaction that involves addition of an acyl anion equivalent to an untethered Michael acceptor. Despite the… (more)

Subjects/Keywords: asymmetric catalysis; Stetter reaction; organocatalysis; NHC; intermolecular

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APA (6th Edition):

Glover, G. S. (2012). Development of an asymmetric intermolecular stetter reaction and organocatalyst design. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/88358

Chicago Manual of Style (16th Edition):

Glover, Garrett S. “Development of an asymmetric intermolecular stetter reaction and organocatalyst design.” 2012. Masters Thesis, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/88358.

MLA Handbook (7th Edition):

Glover, Garrett S. “Development of an asymmetric intermolecular stetter reaction and organocatalyst design.” 2012. Web. 07 May 2021.

Vancouver:

Glover GS. Development of an asymmetric intermolecular stetter reaction and organocatalyst design. [Internet] [Masters thesis]. Colorado State University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/88358.

Council of Science Editors:

Glover GS. Development of an asymmetric intermolecular stetter reaction and organocatalyst design. [Masters Thesis]. Colorado State University; 2012. Available from: http://hdl.handle.net/10217/88358


Colorado State University

5. DiRocco, Daniel A. Development of novel N-heterocyclic carbenes for asymmetric C-C bond forming reactions, The.

Degree: PhD, Chemistry, 2012, Colorado State University

 A variety of novel N-heterocyclic carbenes have been developed as organocatalysts for highly efficient and selective intermolecular C-C bond forming reactions. Problems associated with attaining… (more)

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APA (6th Edition):

DiRocco, D. A. (2012). Development of novel N-heterocyclic carbenes for asymmetric C-C bond forming reactions, The. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/67916

Chicago Manual of Style (16th Edition):

DiRocco, Daniel A. “Development of novel N-heterocyclic carbenes for asymmetric C-C bond forming reactions, The.” 2012. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/67916.

MLA Handbook (7th Edition):

DiRocco, Daniel A. “Development of novel N-heterocyclic carbenes for asymmetric C-C bond forming reactions, The.” 2012. Web. 07 May 2021.

Vancouver:

DiRocco DA. Development of novel N-heterocyclic carbenes for asymmetric C-C bond forming reactions, The. [Internet] [Doctoral dissertation]. Colorado State University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/67916.

Council of Science Editors:

DiRocco DA. Development of novel N-heterocyclic carbenes for asymmetric C-C bond forming reactions, The. [Doctoral Dissertation]. Colorado State University; 2012. Available from: http://hdl.handle.net/10217/67916


Colorado State University

6. Dalton, Derek M. Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions.

Degree: PhD, Chemistry, 2013, Colorado State University

 Described herein are mechanistic studies and ligand development for Rh(I) catalyzed [2+2+2] cycloaddition reactions of alkene tethered isocyanates and exogenous alkynes. A mechanistic hypothesis has… (more)

Subjects/Keywords: cycloaddition; zinc; rhodium; enantioselective; heterocycles; catalysis

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APA (6th Edition):

Dalton, D. M. (2013). Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/80142

Chicago Manual of Style (16th Edition):

Dalton, Derek M. “Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions.” 2013. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/80142.

MLA Handbook (7th Edition):

Dalton, Derek M. “Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions.” 2013. Web. 07 May 2021.

Vancouver:

Dalton DM. Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions. [Internet] [Doctoral dissertation]. Colorado State University; 2013. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/80142.

Council of Science Editors:

Dalton DM. Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions. [Doctoral Dissertation]. Colorado State University; 2013. Available from: http://hdl.handle.net/10217/80142


Colorado State University

7. Rubush, David Michael. Progress toward the total synthesis of stemocurtisine and asymmetric synthesis of endoperoxide anticancer agents via Brønsted acid cascade catalysis.

Degree: PhD, Chemistry, 2012, Colorado State University

 A viable route toward the pyrido-azepine core of stemocurtisine involving an N-heterocyclic carbene catalyzed Stetter reaction has been realized. The key steps involve a formal… (more)

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APA (6th Edition):

Rubush, D. M. (2012). Progress toward the total synthesis of stemocurtisine and asymmetric synthesis of endoperoxide anticancer agents via Brønsted acid cascade catalysis. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/71583

Chicago Manual of Style (16th Edition):

Rubush, David Michael. “Progress toward the total synthesis of stemocurtisine and asymmetric synthesis of endoperoxide anticancer agents via Brønsted acid cascade catalysis.” 2012. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/71583.

MLA Handbook (7th Edition):

Rubush, David Michael. “Progress toward the total synthesis of stemocurtisine and asymmetric synthesis of endoperoxide anticancer agents via Brønsted acid cascade catalysis.” 2012. Web. 07 May 2021.

Vancouver:

Rubush DM. Progress toward the total synthesis of stemocurtisine and asymmetric synthesis of endoperoxide anticancer agents via Brønsted acid cascade catalysis. [Internet] [Doctoral dissertation]. Colorado State University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/71583.

Council of Science Editors:

Rubush DM. Progress toward the total synthesis of stemocurtisine and asymmetric synthesis of endoperoxide anticancer agents via Brønsted acid cascade catalysis. [Doctoral Dissertation]. Colorado State University; 2012. Available from: http://hdl.handle.net/10217/71583


Colorado State University

8. Neely, Jamie M. Reaction development and mechanistic investigation of rhodium-catalyzed pyridine synthesis via C-H activation.

Degree: PhD, Chemistry, 2014, Colorado State University

 Described herein are two complementary rhodium-catalyzed methods for the synthesis of substituted pyridines from unsaturated oxime derivatives and alkenes. In the first, formal [4+2] cycloaddition… (more)

Subjects/Keywords: rhodium; oxime esters; pyridines; alkenes; C-H activation

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APA (6th Edition):

Neely, J. M. (2014). Reaction development and mechanistic investigation of rhodium-catalyzed pyridine synthesis via C-H activation. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/88453

Chicago Manual of Style (16th Edition):

Neely, Jamie M. “Reaction development and mechanistic investigation of rhodium-catalyzed pyridine synthesis via C-H activation.” 2014. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/88453.

MLA Handbook (7th Edition):

Neely, Jamie M. “Reaction development and mechanistic investigation of rhodium-catalyzed pyridine synthesis via C-H activation.” 2014. Web. 07 May 2021.

Vancouver:

Neely JM. Reaction development and mechanistic investigation of rhodium-catalyzed pyridine synthesis via C-H activation. [Internet] [Doctoral dissertation]. Colorado State University; 2014. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/88453.

Council of Science Editors:

Neely JM. Reaction development and mechanistic investigation of rhodium-catalyzed pyridine synthesis via C-H activation. [Doctoral Dissertation]. Colorado State University; 2014. Available from: http://hdl.handle.net/10217/88453


Colorado State University

9. Pan, Guojun. Total syntheses of (±)-fawcettimine, (±)-fawcettidine, (±)-lycoflexine, and (±)-lycoposerramine B.

Degree: PhD, Chemistry, 2012, Colorado State University

 The total syntheses of (±)-fawcettimine, (±)-lycoflexine, (±)-fawcettidine, and (±)-lycoposerramine B have been accomplished through an efficient, unified, and stereocontrolled strategy that required sixteen, sixteen, seventeen,… (more)

Subjects/Keywords: fawcettimine; total synthesis; lycoposerramine B; lycoflexine; lycopodium; fawcettidine

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APA (6th Edition):

Pan, G. (2012). Total syntheses of (±)-fawcettimine, (±)-fawcettidine, (±)-lycoflexine, and (±)-lycoposerramine B. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/67622

Chicago Manual of Style (16th Edition):

Pan, Guojun. “Total syntheses of (±)-fawcettimine, (±)-fawcettidine, (±)-lycoflexine, and (±)-lycoposerramine B.” 2012. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/67622.

MLA Handbook (7th Edition):

Pan, Guojun. “Total syntheses of (±)-fawcettimine, (±)-fawcettidine, (±)-lycoflexine, and (±)-lycoposerramine B.” 2012. Web. 07 May 2021.

Vancouver:

Pan G. Total syntheses of (±)-fawcettimine, (±)-fawcettidine, (±)-lycoflexine, and (±)-lycoposerramine B. [Internet] [Doctoral dissertation]. Colorado State University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/67622.

Council of Science Editors:

Pan G. Total syntheses of (±)-fawcettimine, (±)-fawcettidine, (±)-lycoflexine, and (±)-lycoposerramine B. [Doctoral Dissertation]. Colorado State University; 2012. Available from: http://hdl.handle.net/10217/67622


Colorado State University

10. Dong, Ping. Synthetic approach towards cephalezomine A and phomoidride D.

Degree: PhD, Chemistry, 2011, Colorado State University

 Two synthetic approaches towards cephalezomine A and phomoidride D are described separately. The first approach towards cephalezomine A invented a new method for the synthesis… (more)

Subjects/Keywords: Eschenmoser coupling; synthetic approach; samarium diiodide mediated radical cascade cyclization; phenolic oxidation and Diels-Alder reaction; phomoidride D; cephalezomine A

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APA (6th Edition):

Dong, P. (2011). Synthetic approach towards cephalezomine A and phomoidride D. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/47380

Chicago Manual of Style (16th Edition):

Dong, Ping. “Synthetic approach towards cephalezomine A and phomoidride D.” 2011. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/47380.

MLA Handbook (7th Edition):

Dong, Ping. “Synthetic approach towards cephalezomine A and phomoidride D.” 2011. Web. 07 May 2021.

Vancouver:

Dong P. Synthetic approach towards cephalezomine A and phomoidride D. [Internet] [Doctoral dissertation]. Colorado State University; 2011. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/47380.

Council of Science Editors:

Dong P. Synthetic approach towards cephalezomine A and phomoidride D. [Doctoral Dissertation]. Colorado State University; 2011. Available from: http://hdl.handle.net/10217/47380


Colorado State University

11. Wheeler, Philip Andrew Merris. Catalytically generated acyl triazoliums as versatile acylating reagents and progress toward the total synthesis of okilactomycin.

Degree: PhD, Chemistry, 2013, Colorado State University

 The first chapter of this dissertation describes the development of reactions involving the NHC-catalyzed acylation of carbon and nitrogen nucleophiles. The overall goal of this… (more)

Subjects/Keywords: NHC; polyketide

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APA (6th Edition):

Wheeler, P. A. M. (2013). Catalytically generated acyl triazoliums as versatile acylating reagents and progress toward the total synthesis of okilactomycin. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/78884

Chicago Manual of Style (16th Edition):

Wheeler, Philip Andrew Merris. “Catalytically generated acyl triazoliums as versatile acylating reagents and progress toward the total synthesis of okilactomycin.” 2013. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/78884.

MLA Handbook (7th Edition):

Wheeler, Philip Andrew Merris. “Catalytically generated acyl triazoliums as versatile acylating reagents and progress toward the total synthesis of okilactomycin.” 2013. Web. 07 May 2021.

Vancouver:

Wheeler PAM. Catalytically generated acyl triazoliums as versatile acylating reagents and progress toward the total synthesis of okilactomycin. [Internet] [Doctoral dissertation]. Colorado State University; 2013. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/78884.

Council of Science Editors:

Wheeler PAM. Catalytically generated acyl triazoliums as versatile acylating reagents and progress toward the total synthesis of okilactomycin. [Doctoral Dissertation]. Colorado State University; 2013. Available from: http://hdl.handle.net/10217/78884


Colorado State University

12. Oberg, Kevin Martin. Rhodium-catalyzed cycloadditions to construct nitrogen heterocycles and progress towards the synthesis of ionomycin.

Degree: PhD, Chemistry, 2014, Colorado State University

 The ability to construct molecules in a rapid, atom-economical fashion is a major goal of organic chemistry. This work describes four topics; pyridone synthesis, mechanistic… (more)

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APA (6th Edition):

Oberg, K. M. (2014). Rhodium-catalyzed cycloadditions to construct nitrogen heterocycles and progress towards the synthesis of ionomycin. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/82524

Chicago Manual of Style (16th Edition):

Oberg, Kevin Martin. “Rhodium-catalyzed cycloadditions to construct nitrogen heterocycles and progress towards the synthesis of ionomycin.” 2014. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/82524.

MLA Handbook (7th Edition):

Oberg, Kevin Martin. “Rhodium-catalyzed cycloadditions to construct nitrogen heterocycles and progress towards the synthesis of ionomycin.” 2014. Web. 07 May 2021.

Vancouver:

Oberg KM. Rhodium-catalyzed cycloadditions to construct nitrogen heterocycles and progress towards the synthesis of ionomycin. [Internet] [Doctoral dissertation]. Colorado State University; 2014. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/82524.

Council of Science Editors:

Oberg KM. Rhodium-catalyzed cycloadditions to construct nitrogen heterocycles and progress towards the synthesis of ionomycin. [Doctoral Dissertation]. Colorado State University; 2014. Available from: http://hdl.handle.net/10217/82524


Colorado State University

13. Vora, Harit. N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids.

Degree: PhD, Chemistry, 2011, Colorado State University

 N-heterocyclic carbene catalyzed α-redox reaction has been utilized towards the catalytic synthesis of amides utilizing amines and substoichiometric quantities of an acyl transfer reagent in… (more)

Subjects/Keywords: synthesis; NHC catalysis; organic chemistry; asymmetric; catalysis

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APA (6th Edition):

Vora, H. (2011). N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/52114

Chicago Manual of Style (16th Edition):

Vora, Harit. “N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids.” 2011. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/52114.

MLA Handbook (7th Edition):

Vora, Harit. “N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids.” 2011. Web. 07 May 2021.

Vancouver:

Vora H. N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids. [Internet] [Doctoral dissertation]. Colorado State University; 2011. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/52114.

Council of Science Editors:

Vora H. N-heterocyclic carbene catalyzed α-redox reaction: catalytic synthesis of amides and carboxylic acids. [Doctoral Dissertation]. Colorado State University; 2011. Available from: http://hdl.handle.net/10217/52114


Colorado State University

14. Chapman, Alex Michael. Protein resurfacing to identify macromolecular assemblies.

Degree: PhD, Chemistry, 2016, Colorado State University

 Protein engineering is an emerging discipline that dovetails modern molecular biology techniques with high-throughput screening, laboratory evolution technologies, and computational approaches to modify sequence, structure,… (more)

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APA (6th Edition):

Chapman, A. M. (2016). Protein resurfacing to identify macromolecular assemblies. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/176635

Chicago Manual of Style (16th Edition):

Chapman, Alex Michael. “Protein resurfacing to identify macromolecular assemblies.” 2016. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/176635.

MLA Handbook (7th Edition):

Chapman, Alex Michael. “Protein resurfacing to identify macromolecular assemblies.” 2016. Web. 07 May 2021.

Vancouver:

Chapman AM. Protein resurfacing to identify macromolecular assemblies. [Internet] [Doctoral dissertation]. Colorado State University; 2016. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/176635.

Council of Science Editors:

Chapman AM. Protein resurfacing to identify macromolecular assemblies. [Doctoral Dissertation]. Colorado State University; 2016. Available from: http://hdl.handle.net/10217/176635


Colorado State University

15. Welch, Timothy R. Epidithiodioxopiperazines: synthetic studies of (+)-chetomin and (-)-sporidesmin A.

Degree: PhD, Chemistry, 2012, Colorado State University

 This dissertation documents efforts toward the asymmetric total syntheses of the natural products (+)-chetomin and (-)-sporidesmin A. Synthetic methods have been developed to efficiently construct… (more)

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APA (6th Edition):

Welch, T. R. (2012). Epidithiodioxopiperazines: synthetic studies of (+)-chetomin and (-)-sporidesmin A. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/71601

Chicago Manual of Style (16th Edition):

Welch, Timothy R. “Epidithiodioxopiperazines: synthetic studies of (+)-chetomin and (-)-sporidesmin A.” 2012. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/71601.

MLA Handbook (7th Edition):

Welch, Timothy R. “Epidithiodioxopiperazines: synthetic studies of (+)-chetomin and (-)-sporidesmin A.” 2012. Web. 07 May 2021.

Vancouver:

Welch TR. Epidithiodioxopiperazines: synthetic studies of (+)-chetomin and (-)-sporidesmin A. [Internet] [Doctoral dissertation]. Colorado State University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/71601.

Council of Science Editors:

Welch TR. Epidithiodioxopiperazines: synthetic studies of (+)-chetomin and (-)-sporidesmin A. [Doctoral Dissertation]. Colorado State University; 2012. Available from: http://hdl.handle.net/10217/71601


Colorado State University

16. Sanchez, Michelle A. Synthesis of the pentacyclic carbon framework of the PF1270 family of natural products, The.

Degree: PhD, Chemistry, 2014, Colorado State University

 The PF1270 family of natural products contains novel indole alkaloids that display interesting biological activity; the synthesis of these natural products and their analogs could… (more)

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APA (6th Edition):

Sanchez, M. A. (2014). Synthesis of the pentacyclic carbon framework of the PF1270 family of natural products, The. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/83811

Chicago Manual of Style (16th Edition):

Sanchez, Michelle A. “Synthesis of the pentacyclic carbon framework of the PF1270 family of natural products, The.” 2014. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/83811.

MLA Handbook (7th Edition):

Sanchez, Michelle A. “Synthesis of the pentacyclic carbon framework of the PF1270 family of natural products, The.” 2014. Web. 07 May 2021.

Vancouver:

Sanchez MA. Synthesis of the pentacyclic carbon framework of the PF1270 family of natural products, The. [Internet] [Doctoral dissertation]. Colorado State University; 2014. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/83811.

Council of Science Editors:

Sanchez MA. Synthesis of the pentacyclic carbon framework of the PF1270 family of natural products, The. [Doctoral Dissertation]. Colorado State University; 2014. Available from: http://hdl.handle.net/10217/83811


Colorado State University

17. Williams, Catherine Marie. Application of metallacycles for the synthesis of small molecules.

Degree: PhD, Chemistry, 2011, Colorado State University

 A method for the nickel-catalyzed hydrocarboxylation of styrene derivatives has been developed that affords exclusively the branched carboxylic acids in moderate to excellent yields. The… (more)

Subjects/Keywords: anhydride desymmetrization; organometallic; metallacycles

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APA (6th Edition):

Williams, C. M. (2011). Application of metallacycles for the synthesis of small molecules. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/48168

Chicago Manual of Style (16th Edition):

Williams, Catherine Marie. “Application of metallacycles for the synthesis of small molecules.” 2011. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/48168.

MLA Handbook (7th Edition):

Williams, Catherine Marie. “Application of metallacycles for the synthesis of small molecules.” 2011. Web. 07 May 2021.

Vancouver:

Williams CM. Application of metallacycles for the synthesis of small molecules. [Internet] [Doctoral dissertation]. Colorado State University; 2011. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/48168.

Council of Science Editors:

Williams CM. Application of metallacycles for the synthesis of small molecules. [Doctoral Dissertation]. Colorado State University; 2011. Available from: http://hdl.handle.net/10217/48168

18. Stache, Erin Elizabeth. Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis.

Degree: PhD, Chemistry, 2018, Colorado State University

 Described herein is the application of photoredox catalysis in the development of new synthetic methods. A dual nickel- and photoredox catalyzed desymmetrization of meso succinic… (more)

Subjects/Keywords: nickel catalysis; photochemistry; organic synthesis; asymmetric catalysis

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APA (6th Edition):

Stache, E. E. (2018). Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/191328

Chicago Manual of Style (16th Edition):

Stache, Erin Elizabeth. “Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis.” 2018. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/191328.

MLA Handbook (7th Edition):

Stache, Erin Elizabeth. “Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis.” 2018. Web. 07 May 2021.

Vancouver:

Stache EE. Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis. [Internet] [Doctoral dissertation]. Colorado State University; 2018. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/191328.

Council of Science Editors:

Stache EE. Dual nickel- and photoredox-catalyzed enantioselective desymmetrization of meso anhydrides and C-O bond activation via phosphines and photoredox catalysis. [Doctoral Dissertation]. Colorado State University; 2018. Available from: http://hdl.handle.net/10217/191328


Colorado State University

19. Allegretti, Paul Andrew. Formation and reactivity of α,β-unsaturated platinum carbenes: new approaches to heterocycle synthesis, The.

Degree: PhD, Chemistry, 2014, Colorado State University

 The use of transition metal carbenes in organic synthesis has enabled chemists to promote an incredible variety of bond-forming reactions. These intermediates are traditionally accessed… (more)

Subjects/Keywords: heterocycles; alkyne activation; carbene

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APA (6th Edition):

Allegretti, P. A. (2014). Formation and reactivity of α,β-unsaturated platinum carbenes: new approaches to heterocycle synthesis, The. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/83710

Chicago Manual of Style (16th Edition):

Allegretti, Paul Andrew. “Formation and reactivity of α,β-unsaturated platinum carbenes: new approaches to heterocycle synthesis, The.” 2014. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/83710.

MLA Handbook (7th Edition):

Allegretti, Paul Andrew. “Formation and reactivity of α,β-unsaturated platinum carbenes: new approaches to heterocycle synthesis, The.” 2014. Web. 07 May 2021.

Vancouver:

Allegretti PA. Formation and reactivity of α,β-unsaturated platinum carbenes: new approaches to heterocycle synthesis, The. [Internet] [Doctoral dissertation]. Colorado State University; 2014. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/83710.

Council of Science Editors:

Allegretti PA. Formation and reactivity of α,β-unsaturated platinum carbenes: new approaches to heterocycle synthesis, The. [Doctoral Dissertation]. Colorado State University; 2014. Available from: http://hdl.handle.net/10217/83710


Colorado State University

20. Levine, Samantha Roslyn. Part I: The total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids and Part II: The use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof: Total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids, The: Use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof, The.

Degree: PhD, Chemistry, 2014, Colorado State University

 In part I, the total syntheses of (±)-securinine ((±)-1.001) and (±)-allosecurinine ((±)-1.003) are described. The syntheses feature the use of a Rh-initiated O—H insertion/Claisen rearrangement/1,2-allyl… (more)

Subjects/Keywords: securinine; allosecurinine; indolocarbazole; (+)-K252a

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APA (6th Edition):

Levine, S. R. (2014). Part I: The total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids and Part II: The use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof: Total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids, The: Use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof, The. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/82561

Chicago Manual of Style (16th Edition):

Levine, Samantha Roslyn. “Part I: The total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids and Part II: The use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof: Total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids, The: Use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof, The.” 2014. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/82561.

MLA Handbook (7th Edition):

Levine, Samantha Roslyn. “Part I: The total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids and Part II: The use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof: Total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids, The: Use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof, The.” 2014. Web. 07 May 2021.

Vancouver:

Levine SR. Part I: The total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids and Part II: The use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof: Total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids, The: Use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof, The. [Internet] [Doctoral dissertation]. Colorado State University; 2014. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/82561.

Council of Science Editors:

Levine SR. Part I: The total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids and Part II: The use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof: Total synthesis of (±)-securinine and (±)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids, The: Use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and novel analogs thereof, The. [Doctoral Dissertation]. Colorado State University; 2014. Available from: http://hdl.handle.net/10217/82561


Colorado State University

21. Filloux, Claire M. Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity.

Degree: PhD, Chemistry, 2015, Colorado State University

 The chapters that follow describe two independent investigations. Both relay the development of experimental methods for the catalytic, asymmetric addition of carbon-hydrogen bonds to alkenes.… (more)

Subjects/Keywords: catalysis; organic; asymmetric; rhodium; N-heterocyclic carbene

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APA (6th Edition):

Filloux, C. M. (2015). Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/166906

Chicago Manual of Style (16th Edition):

Filloux, Claire M. “Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity.” 2015. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/166906.

MLA Handbook (7th Edition):

Filloux, Claire M. “Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity.” 2015. Web. 07 May 2021.

Vancouver:

Filloux CM. Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity. [Internet] [Doctoral dissertation]. Colorado State University; 2015. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/166906.

Council of Science Editors:

Filloux CM. Organocatalytic, Michael-Stetter reaction and rhodium(I)-catalyzed hydroheteroarylation of acrylates with benzoxazoles: reaction development and investigations into origins of enantioselectivity. [Doctoral Dissertation]. Colorado State University; 2015. Available from: http://hdl.handle.net/10217/166906


Colorado State University

22. Ozboya, Kerem. Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals.

Degree: PhD, Chemistry, 2015, Colorado State University

 A cascade reaction is developed to form complex cyclopentanones using an asymmetric Michael/Benzoin sequence. This reaction employs simple aliphatic aldehydes and ketoesters in conjunction with… (more)

Subjects/Keywords: NHC; organocatalysis; organic synthesis; asymmetric catalysis

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APA (6th Edition):

Ozboya, K. (2015). Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/166865

Chicago Manual of Style (16th Edition):

Ozboya, Kerem. “Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals.” 2015. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/166865.

MLA Handbook (7th Edition):

Ozboya, Kerem. “Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals.” 2015. Web. 07 May 2021.

Vancouver:

Ozboya K. Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals. [Internet] [Doctoral dissertation]. Colorado State University; 2015. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/166865.

Council of Science Editors:

Ozboya K. Development of an asymmetric NHC-catalyzed cascade reaction and studies towards the asymmetric aminomethylation of enals. [Doctoral Dissertation]. Colorado State University; 2015. Available from: http://hdl.handle.net/10217/166865


Colorado State University

23. Sameenoi, Yupaporn. Development of methods for assessing oxidative stress caused by atmospheric aerosols.

Degree: PhD, Chemistry, 2012, Colorado State University

 Extensive epidemiological studies show strong associations between the exposure to atmospheric aerosol particulate matter (PM) in the size range of 0.1- 10 µm and health… (more)

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APA (6th Edition):

Sameenoi, Y. (2012). Development of methods for assessing oxidative stress caused by atmospheric aerosols. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/71584

Chicago Manual of Style (16th Edition):

Sameenoi, Yupaporn. “Development of methods for assessing oxidative stress caused by atmospheric aerosols.” 2012. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/71584.

MLA Handbook (7th Edition):

Sameenoi, Yupaporn. “Development of methods for assessing oxidative stress caused by atmospheric aerosols.” 2012. Web. 07 May 2021.

Vancouver:

Sameenoi Y. Development of methods for assessing oxidative stress caused by atmospheric aerosols. [Internet] [Doctoral dissertation]. Colorado State University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/71584.

Council of Science Editors:

Sameenoi Y. Development of methods for assessing oxidative stress caused by atmospheric aerosols. [Doctoral Dissertation]. Colorado State University; 2012. Available from: http://hdl.handle.net/10217/71584


Colorado State University

24. Hyster, Todd K. Ligand and reaction development in the Rhodium(III)-catalyzed C-H activation-mediated synthesis of n-heterocycles.

Degree: PhD, Chemistry, 2013, Colorado State University

 Described herein are the development of new directing groups and new ligands for Rh(III)- catalyzed, multi-component synthesis of nitrogen containing heterocycles. The amide directing group… (more)

Subjects/Keywords: C-H activation; rhodium; metalloenzyme; cyclopentadienyl ligand

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APA (6th Edition):

Hyster, T. K. (2013). Ligand and reaction development in the Rhodium(III)-catalyzed C-H activation-mediated synthesis of n-heterocycles. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/80154

Chicago Manual of Style (16th Edition):

Hyster, Todd K. “Ligand and reaction development in the Rhodium(III)-catalyzed C-H activation-mediated synthesis of n-heterocycles.” 2013. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/80154.

MLA Handbook (7th Edition):

Hyster, Todd K. “Ligand and reaction development in the Rhodium(III)-catalyzed C-H activation-mediated synthesis of n-heterocycles.” 2013. Web. 07 May 2021.

Vancouver:

Hyster TK. Ligand and reaction development in the Rhodium(III)-catalyzed C-H activation-mediated synthesis of n-heterocycles. [Internet] [Doctoral dissertation]. Colorado State University; 2013. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/80154.

Council of Science Editors:

Hyster TK. Ligand and reaction development in the Rhodium(III)-catalyzed C-H activation-mediated synthesis of n-heterocycles. [Doctoral Dissertation]. Colorado State University; 2013. Available from: http://hdl.handle.net/10217/80154


Colorado State University

25. Lathrop, Stephen Paul. N-Heterocyclic carbene catalysis: application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions.

Degree: PhD, Chemistry, 2011, Colorado State University

 Application of the N-Heterocyclic carbene catalyzed Stetter reaction to the total synthesis of 9-epi-cephalimysin A has been realized. The approach centers on the use of… (more)

Subjects/Keywords: carbenes; Stetter reaction; cephalimysin A; cascade reactions; benzoin reaction

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APA (6th Edition):

Lathrop, S. P. (2011). N-Heterocyclic carbene catalysis: application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/47287

Chicago Manual of Style (16th Edition):

Lathrop, Stephen Paul. “N-Heterocyclic carbene catalysis: application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions.” 2011. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/47287.

MLA Handbook (7th Edition):

Lathrop, Stephen Paul. “N-Heterocyclic carbene catalysis: application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions.” 2011. Web. 07 May 2021.

Vancouver:

Lathrop SP. N-Heterocyclic carbene catalysis: application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions. [Internet] [Doctoral dissertation]. Colorado State University; 2011. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/47287.

Council of Science Editors:

Lathrop SP. N-Heterocyclic carbene catalysis: application to the total synthesis of cephalimysin A, and development of multicatalytic cascade reactions. [Doctoral Dissertation]. Colorado State University; 2011. Available from: http://hdl.handle.net/10217/47287


Colorado State University

26. Finefield, Jennifer M. Studies on the biosynthesis of prenylated indole secondary metabolites from Aspergillus versicolor and Aspergillus sp.; and A novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin: Novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin, A.

Degree: PhD, Chemistry, 2011, Colorado State University

 Herein are documented our efforts in two projects, beginning with studies toward elucidating the biosynthesis of prenylated indole alkaloids from two different Aspergillus species. Marine-derived… (more)

Subjects/Keywords: naphthyridine; Aspergillus

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APA (6th Edition):

Finefield, J. M. (2011). Studies on the biosynthesis of prenylated indole secondary metabolites from Aspergillus versicolor and Aspergillus sp.; and A novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin: Novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin, A. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/46212

Chicago Manual of Style (16th Edition):

Finefield, Jennifer M. “Studies on the biosynthesis of prenylated indole secondary metabolites from Aspergillus versicolor and Aspergillus sp.; and A novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin: Novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin, A.” 2011. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/46212.

MLA Handbook (7th Edition):

Finefield, Jennifer M. “Studies on the biosynthesis of prenylated indole secondary metabolites from Aspergillus versicolor and Aspergillus sp.; and A novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin: Novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin, A.” 2011. Web. 07 May 2021.

Vancouver:

Finefield JM. Studies on the biosynthesis of prenylated indole secondary metabolites from Aspergillus versicolor and Aspergillus sp.; and A novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin: Novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin, A. [Internet] [Doctoral dissertation]. Colorado State University; 2011. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/46212.

Council of Science Editors:

Finefield JM. Studies on the biosynthesis of prenylated indole secondary metabolites from Aspergillus versicolor and Aspergillus sp.; and A novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin: Novel approach to tumor specific drug delivery: use of a naphthyridine drug linker with a DNA hairpin, A. [Doctoral Dissertation]. Colorado State University; 2011. Available from: http://hdl.handle.net/10217/46212


Colorado State University

27. White, Nicholas Andrew. Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis.

Degree: PhD, Chemistry, 2015, Colorado State University

 A series of δ-nitroesters were synthesized through the N-heterocyclic carbene catalyzed coupling of enals and nitroalkenes. The asymmetric coupling of these substrates via the homoenolate… (more)

Subjects/Keywords: asymmetric; carbene; catalysis; organic

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APA (6th Edition):

White, N. A. (2015). Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/170358

Chicago Manual of Style (16th Edition):

White, Nicholas Andrew. “Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis.” 2015. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/170358.

MLA Handbook (7th Edition):

White, Nicholas Andrew. “Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis.” 2015. Web. 07 May 2021.

Vancouver:

White NA. Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis. [Internet] [Doctoral dissertation]. Colorado State University; 2015. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/170358.

Council of Science Editors:

White NA. Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis. [Doctoral Dissertation]. Colorado State University; 2015. Available from: http://hdl.handle.net/10217/170358

28. Chu, John Chun Kit. Synthesis of nitrogen-containing molecules by zinc-catalyzed [4+2] cycloaddition and photoredox-catalyzed C-H functionalization.

Degree: PhD, Chemistry, 2017, Colorado State University

 This work first describes an enantioselective Zn-catalyzed [4+2] cycloaddition of 1-azadienes and nitro-alkenes for the synthesis of medicinally valuable piperidines. The detrimental coordination of 1-azadienes… (more)

Subjects/Keywords: cycloaddition; nitrogen-containing molecules; zinc; hydrogen atom transfer; C-H functionalization; radical

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APA (6th Edition):

Chu, J. C. K. (2017). Synthesis of nitrogen-containing molecules by zinc-catalyzed [4+2] cycloaddition and photoredox-catalyzed C-H functionalization. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/181323

Chicago Manual of Style (16th Edition):

Chu, John Chun Kit. “Synthesis of nitrogen-containing molecules by zinc-catalyzed [4+2] cycloaddition and photoredox-catalyzed C-H functionalization.” 2017. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/181323.

MLA Handbook (7th Edition):

Chu, John Chun Kit. “Synthesis of nitrogen-containing molecules by zinc-catalyzed [4+2] cycloaddition and photoredox-catalyzed C-H functionalization.” 2017. Web. 07 May 2021.

Vancouver:

Chu JCK. Synthesis of nitrogen-containing molecules by zinc-catalyzed [4+2] cycloaddition and photoredox-catalyzed C-H functionalization. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/181323.

Council of Science Editors:

Chu JCK. Synthesis of nitrogen-containing molecules by zinc-catalyzed [4+2] cycloaddition and photoredox-catalyzed C-H functionalization. [Doctoral Dissertation]. Colorado State University; 2017. Available from: http://hdl.handle.net/10217/181323

29. Semakul, Natthawat. Rhodium(III)-catalyzed amide-directed C-H activation and [4+2] cycloaddition for modular assembly of nitrogen heterocycles.

Degree: PhD, Chemistry, 2017, Colorado State University

 This dissertation describes the ligand and reaction developments by amide-directed rhodium(III)-catalyzed C(sp2)-H bond activation followed by amidoannulation with alkenes to form nitrogen-containing heterocycles. Chapter 1… (more)

Subjects/Keywords: amides; heteroannulation; rhodium(III) catalysis; C-H activation; alkenes; N-heterocycles

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APA (6th Edition):

Semakul, N. (2017). Rhodium(III)-catalyzed amide-directed C-H activation and [4+2] cycloaddition for modular assembly of nitrogen heterocycles. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/183892

Chicago Manual of Style (16th Edition):

Semakul, Natthawat. “Rhodium(III)-catalyzed amide-directed C-H activation and [4+2] cycloaddition for modular assembly of nitrogen heterocycles.” 2017. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/183892.

MLA Handbook (7th Edition):

Semakul, Natthawat. “Rhodium(III)-catalyzed amide-directed C-H activation and [4+2] cycloaddition for modular assembly of nitrogen heterocycles.” 2017. Web. 07 May 2021.

Vancouver:

Semakul N. Rhodium(III)-catalyzed amide-directed C-H activation and [4+2] cycloaddition for modular assembly of nitrogen heterocycles. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/183892.

Council of Science Editors:

Semakul N. Rhodium(III)-catalyzed amide-directed C-H activation and [4+2] cycloaddition for modular assembly of nitrogen heterocycles. [Doctoral Dissertation]. Colorado State University; 2017. Available from: http://hdl.handle.net/10217/183892

30. Ruhl, Kyle E. Development and applications of light-gated cobalt catalysis, The.

Degree: PhD, Chemistry, 2017, Colorado State University

 Transition metals are an important natural resource and an essential component of many industrial processes and applications. Examples of these include air-quality control, electronics manufacture,… (more)

Subjects/Keywords: cobalt; light; catalysis; photoredox; gated

…experimentation platform at Colorado State University, the 20 initial experiment included six cobalt… 

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APA (6th Edition):

Ruhl, K. E. (2017). Development and applications of light-gated cobalt catalysis, The. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/181308

Chicago Manual of Style (16th Edition):

Ruhl, Kyle E. “Development and applications of light-gated cobalt catalysis, The.” 2017. Doctoral Dissertation, Colorado State University. Accessed May 07, 2021. http://hdl.handle.net/10217/181308.

MLA Handbook (7th Edition):

Ruhl, Kyle E. “Development and applications of light-gated cobalt catalysis, The.” 2017. Web. 07 May 2021.

Vancouver:

Ruhl KE. Development and applications of light-gated cobalt catalysis, The. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/10217/181308.

Council of Science Editors:

Ruhl KE. Development and applications of light-gated cobalt catalysis, The. [Doctoral Dissertation]. Colorado State University; 2017. Available from: http://hdl.handle.net/10217/181308

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