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You searched for +publisher:"Colorado State University" +contributor:("Rovis, Tomislav"). Showing records 1 – 30 of 32 total matches.

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Colorado State University

1. 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 21, 2018. http://hdl.handle.net/10217/183966.

MLA Handbook (7th Edition):

Flanigan, Darrin Miles. “Development of asymmetric N-heterocyclic carbene-catalyzed reactions.” 2017. Web. 21 May 2018.

Vancouver:

Flanigan DM. Development of asymmetric N-heterocyclic carbene-catalyzed reactions. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2018 May 21]. 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

2. 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 21, 2018. http://hdl.handle.net/10217/176635.

MLA Handbook (7th Edition):

Chapman, Alex Michael. “Protein resurfacing to identify macromolecular assemblies.” 2016. Web. 21 May 2018.

Vancouver:

Chapman AM. Protein resurfacing to identify macromolecular assemblies. [Internet] [Doctoral dissertation]. Colorado State University; 2016. [cited 2018 May 21]. 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

3. 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 21, 2018. 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. 21 May 2018.

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 2018 May 21]. 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

4. 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 21, 2018. 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. 21 May 2018.

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 2018 May 21]. 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

5. 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 21, 2018. 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. 21 May 2018.

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 2018 May 21]. 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


Colorado State University

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

Degree: PhD, Chemistry, 2016, 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. (2016). 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.” 2016. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/170358.

MLA Handbook (7th Edition):

White, Nicholas Andrew. “Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis.” 2016. Web. 21 May 2018.

Vancouver:

White NA. Enantioselective β-functionalization of enals via N-heterocyclic carbene catalysis. [Internet] [Doctoral dissertation]. Colorado State University; 2016. [cited 2018 May 21]. 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; 2016. Available from: http://hdl.handle.net/10217/170358

7. 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 21, 2018. 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. 21 May 2018.

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 2018 May 21]. 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

8. Ruhl, Kyle E. The development and applications of light-gated cobalt catalysis.

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). The development and applications of light-gated cobalt catalysis. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/181308

Chicago Manual of Style (16th Edition):

Ruhl, Kyle E. “The development and applications of light-gated cobalt catalysis.” 2017. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/181308.

MLA Handbook (7th Edition):

Ruhl, Kyle E. “The development and applications of light-gated cobalt catalysis.” 2017. Web. 21 May 2018.

Vancouver:

Ruhl KE. The development and applications of light-gated cobalt catalysis. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2018 May 21]. Available from: http://hdl.handle.net/10217/181308.

Council of Science Editors:

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


Colorado State University

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

Degree: MS(M.S.), Chemistry, 2007, 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. (2007). 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.” 2007. Masters Thesis, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/88358.

MLA Handbook (7th Edition):

Glover, Garrett S. “Development of an asymmetric intermolecular stetter reaction and organocatalyst design.” 2007. Web. 21 May 2018.

Vancouver:

Glover GS. Development of an asymmetric intermolecular stetter reaction and organocatalyst design. [Internet] [Masters thesis]. Colorado State University; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/88358


Colorado State University

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

Degree: MS(M.S.), Chemistry, 2007, 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. (2007). The development of N-heterocyclic carbenes for application in the intermolecular stetter reaction. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/67900

Chicago Manual of Style (16th Edition):

Rhorer, Timothy Benjamin. “The development of N-heterocyclic carbenes for application in the intermolecular stetter reaction.” 2007. Masters Thesis, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/67900.

MLA Handbook (7th Edition):

Rhorer, Timothy Benjamin. “The development of N-heterocyclic carbenes for application in the intermolecular stetter reaction.” 2007. Web. 21 May 2018.

Vancouver:

Rhorer TB. The development of N-heterocyclic carbenes for application in the intermolecular stetter reaction. [Internet] [Masters thesis]. Colorado State University; 2007. [cited 2018 May 21]. Available from: http://hdl.handle.net/10217/67900.

Council of Science Editors:

Rhorer TB. The development of N-heterocyclic carbenes for application in the intermolecular stetter reaction. [Masters Thesis]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/67900


Colorado State University

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

Degree: MS(M.S.), Chemistry, 2007, 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. (2007). The development of ligands for C-H functionalization utilizing amino acid derived directing groups. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/70829

Chicago Manual of Style (16th Edition):

Stache, Erin Elizabeth. “The development of ligands for C-H functionalization utilizing amino acid derived directing groups.” 2007. Masters Thesis, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/70829.

MLA Handbook (7th Edition):

Stache, Erin Elizabeth. “The development of ligands for C-H functionalization utilizing amino acid derived directing groups.” 2007. Web. 21 May 2018.

Vancouver:

Stache EE. The development of ligands for C-H functionalization utilizing amino acid derived directing groups. [Internet] [Masters thesis]. Colorado State University; 2007. [cited 2018 May 21]. Available from: http://hdl.handle.net/10217/70829.

Council of Science Editors:

Stache EE. The development of ligands for C-H functionalization utilizing amino acid derived directing groups. [Masters Thesis]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/70829


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. 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.” 2007. Web. 21 May 2018.

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; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/78884


Colorado State University

13. 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, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. 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.” 2007. Web. 21 May 2018.

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; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/71583


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. 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.” 2007. Web. 21 May 2018.

Vancouver:

Vora H. N-heterocyclic carbene catalyzed α-redox reaction : catalytic synthesis of amides and carboxylic acids. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/52114


Colorado State University

15. Oinen, Mark Emil. The enantioseletive rhodium catalyzed [2+2+2] cycloaddition of alkenyl isocyanates with diaryl acetylenes and 1,2-disubstituted alkenyl isocyanates.

Degree: MS(M.S.), Chemistry, 2007, Colorado State University

 Elaborating upon the recent discovery of a [2+2+2] rhodium-catalyzed cycloaddition of alkenyl isocyanates with various alkynes, the scope of this rhodiumcatalyzed cycloaddition with diaryl acetylenes… (more)

Subjects/Keywords: BINOL phosphoramidites; alkenyl isocyanates; diaryl acetylenes; lactam products; cycloadducts; enantioselectivies; [2+2+2] rhodium-catalyzed cycloaddition; Ring formation (Chemistry); Isocyanates; Rhodium catalysts; Lactams

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APA (6th Edition):

Oinen, M. E. (2007). The enantioseletive rhodium catalyzed [2+2+2] cycloaddition of alkenyl isocyanates with diaryl acetylenes and 1,2-disubstituted alkenyl isocyanates. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/37437

Chicago Manual of Style (16th Edition):

Oinen, Mark Emil. “The enantioseletive rhodium catalyzed [2+2+2] cycloaddition of alkenyl isocyanates with diaryl acetylenes and 1,2-disubstituted alkenyl isocyanates.” 2007. Masters Thesis, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/37437.

MLA Handbook (7th Edition):

Oinen, Mark Emil. “The enantioseletive rhodium catalyzed [2+2+2] cycloaddition of alkenyl isocyanates with diaryl acetylenes and 1,2-disubstituted alkenyl isocyanates.” 2007. Web. 21 May 2018.

Vancouver:

Oinen ME. The enantioseletive rhodium catalyzed [2+2+2] cycloaddition of alkenyl isocyanates with diaryl acetylenes and 1,2-disubstituted alkenyl isocyanates. [Internet] [Masters thesis]. Colorado State University; 2007. [cited 2018 May 21]. Available from: http://hdl.handle.net/10217/37437.

Council of Science Editors:

Oinen ME. The enantioseletive rhodium catalyzed [2+2+2] cycloaddition of alkenyl isocyanates with diaryl acetylenes and 1,2-disubstituted alkenyl isocyanates. [Masters Thesis]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/37437


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). The synthesis of the pentacyclic carbon framework of the PF1270 family of natural products. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/83811

Chicago Manual of Style (16th Edition):

Sanchez, Michelle A. “The synthesis of the pentacyclic carbon framework of the PF1270 family of natural products.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/83811.

MLA Handbook (7th Edition):

Sanchez, Michelle A. “The synthesis of the pentacyclic carbon framework of the PF1270 family of natural products.” 2007. Web. 21 May 2018.

Vancouver:

Sanchez MA. The synthesis of the pentacyclic carbon framework of the PF1270 family of natural products. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. Available from: http://hdl.handle.net/10217/83811.

Council of Science Editors:

Sanchez MA. The synthesis of the pentacyclic carbon framework of the PF1270 family of natural products. [Doctoral Dissertation]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/83811


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). The formation and reactivity of α,β-unsaturated platinum carbenes : new approaches to heterocycle synthesis. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/83710

Chicago Manual of Style (16th Edition):

Allegretti, Paul Andrew. “The formation and reactivity of α,β-unsaturated platinum carbenes : new approaches to heterocycle synthesis.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/83710.

MLA Handbook (7th Edition):

Allegretti, Paul Andrew. “The formation and reactivity of α,β-unsaturated platinum carbenes : new approaches to heterocycle synthesis.” 2007. Web. 21 May 2018.

Vancouver:

Allegretti PA. The formation and reactivity of α,β-unsaturated platinum carbenes : new approaches to heterocycle synthesis. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. Available from: http://hdl.handle.net/10217/83710.

Council of Science Editors:

Allegretti PA. The formation and reactivity of α,β-unsaturated platinum carbenes : new approaches to heterocycle synthesis. [Doctoral Dissertation]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/83710


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/47380.

MLA Handbook (7th Edition):

Dong, Ping. “Synthetic approach towards cephalezomine A and phomoidride D.” 2007. Web. 21 May 2018.

Vancouver:

Dong P. Synthetic approach towards cephalezomine A and phomoidride D. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/47380


Colorado State University

19. Burnett, Cameron Moeller. Studies toward the total synthesis of microsclerodermin G.

Degree: PhD, Chemistry, 2007, Colorado State University

 We report our studies toward the synthesis of microsclerodermin G, a cyclic hexapeptide with antifungal and antitumor activity. The dehydrotryptophan amino acid was synthesized according… (more)

Subjects/Keywords: synthesis; AMPTD; microsclerodermin G; organic; Macrocyclic compounds  – Synthesis; Peptides  – Synthesis; Amino acids  – Synthesis

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APA (6th Edition):

Burnett, C. M. (2007). Studies toward the total synthesis of microsclerodermin G. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/39035

Chicago Manual of Style (16th Edition):

Burnett, Cameron Moeller. “Studies toward the total synthesis of microsclerodermin G.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/39035.

MLA Handbook (7th Edition):

Burnett, Cameron Moeller. “Studies toward the total synthesis of microsclerodermin G.” 2007. Web. 21 May 2018.

Vancouver:

Burnett CM. Studies toward the total synthesis of microsclerodermin G. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. Available from: http://hdl.handle.net/10217/39035.

Council of Science Editors:

Burnett CM. Studies toward the total synthesis of microsclerodermin G. [Doctoral Dissertation]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/39035


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. 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.” 2007. Web. 21 May 2018.

Vancouver:

Oberg KM. Rhodium-catalyzed cycloadditions to construct nitrogen heterocycles and progress towards the synthesis of ionomycin. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/82524


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. 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.” 2007. Web. 21 May 2018.

Vancouver:

Neely JM. Reaction development and mechanistic investigation of rhodium-catalyzed pyridine synthesis via C-H activation. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/88453


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. 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.” 2007. Web. 21 May 2018.

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; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/80154


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. 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.” 2007. Web. 21 May 2018.

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; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/47287


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/48168.

MLA Handbook (7th Edition):

Williams, Catherine Marie. “Application of metallacycles for the synthesis of small molecules.” 2007. Web. 21 May 2018.

Vancouver:

Williams CM. Application of metallacycles for the synthesis of small molecules. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/48168


Colorado State University

25. Friedman, Rebecca Ann Keller. Rhodium-catalyzed cycloadditions between alkenyl isocyanates and alkynes : study of scope, mechanism and applications toward total synthesis.

Degree: PhD, Chemistry, 2007, Colorado State University

 Rhodium-catalyzed cycloadditions between alkenyl isocyanates and unsymmetrical, internal alkynes has been studied. A wide variety of alkynes have proven successful components in the [2+2+2] cycloaddition.… (more)

Subjects/Keywords: organometallic; methodology; cycloaddition; Alkynes; Rhodium catalysts; Ring formation (Chemistry); Combinatorial chemistry

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APA (6th Edition):

Friedman, R. A. K. (2007). Rhodium-catalyzed cycloadditions between alkenyl isocyanates and alkynes : study of scope, mechanism and applications toward total synthesis. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/44960

Chicago Manual of Style (16th Edition):

Friedman, Rebecca Ann Keller. “Rhodium-catalyzed cycloadditions between alkenyl isocyanates and alkynes : study of scope, mechanism and applications toward total synthesis.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/44960.

MLA Handbook (7th Edition):

Friedman, Rebecca Ann Keller. “Rhodium-catalyzed cycloadditions between alkenyl isocyanates and alkynes : study of scope, mechanism and applications toward total synthesis.” 2007. Web. 21 May 2018.

Vancouver:

Friedman RAK. Rhodium-catalyzed cycloadditions between alkenyl isocyanates and alkynes : study of scope, mechanism and applications toward total synthesis. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. Available from: http://hdl.handle.net/10217/44960.

Council of Science Editors:

Friedman RAK. Rhodium-catalyzed cycloadditions between alkenyl isocyanates and alkynes : study of scope, mechanism and applications toward total synthesis. [Doctoral Dissertation]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/44960


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. 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.” 2007. Web. 21 May 2018.

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; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/80142


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/67622.

MLA Handbook (7th Edition):

Pan, Guojun. “Total syntheses of (±)-fawcettimine, (±)-fawcettidine, (±)-lycoflexine, and (±)-lycoposerramine B.” 2007. Web. 21 May 2018.

Vancouver:

Pan G. Total syntheses of (±)-fawcettimine, (±)-fawcettidine, (±)-lycoflexine, and (±)-lycoposerramine B. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/67622


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/71584.

MLA Handbook (7th Edition):

Sameenoi, Yupaporn. “Development of methods for assessing oxidative stress caused by atmospheric aerosols.” 2007. Web. 21 May 2018.

Vancouver:

Sameenoi Y. Development of methods for assessing oxidative stress caused by atmospheric aerosols. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/71584


Colorado State University

29. 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: The 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.

Degree: PhD, Chemistry, 2007, 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. (2007). 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: The 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. (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: The 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. 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: The 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.” 2007. Web. 21 May 2018.

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: The 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. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. 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: The 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. [Doctoral Dissertation]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/82561


Colorado State University

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

Degree: PhD, Chemistry, 2007, 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. (2007). 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.” 2007. Doctoral Dissertation, Colorado State University. Accessed May 21, 2018. http://hdl.handle.net/10217/71601.

MLA Handbook (7th Edition):

Welch, Timothy R. “Epidithiodioxopiperazines : synthetic studies of (+)-chetomin and (-)-sporidesmin A.” 2007. Web. 21 May 2018.

Vancouver:

Welch TR. Epidithiodioxopiperazines : synthetic studies of (+)-chetomin and (-)-sporidesmin A. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2018 May 21]. 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; 2007. Available from: http://hdl.handle.net/10217/71601

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