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You searched for +publisher:"The Ohio State University" +contributor:("Mattson, Anita"). Showing records 1 – 8 of 8 total matches.

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The Ohio State University

1. Dunham, Veronica Vin-yi. Metal-Free Approaches to Sterically-Hindered Bonds.

Degree: PhD, Chemistry, 2016, The Ohio State University

 Developing methods to perform cross coupling reactions by means of catalysis is highly desirable in chemistry. Many industries in today’s society, such as the petroleum,… (more)

Subjects/Keywords: Chemistry; nitrimine; organocatalysis; urea catalysis; silanediol; chromanone; heterocycles; metal-free reactions

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APA (6th Edition):

Dunham, V. V. (2016). Metal-Free Approaches to Sterically-Hindered Bonds. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1467360601

Chicago Manual of Style (16th Edition):

Dunham, Veronica Vin-yi. “Metal-Free Approaches to Sterically-Hindered Bonds.” 2016. Doctoral Dissertation, The Ohio State University. Accessed September 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1467360601.

MLA Handbook (7th Edition):

Dunham, Veronica Vin-yi. “Metal-Free Approaches to Sterically-Hindered Bonds.” 2016. Web. 23 Sep 2020.

Vancouver:

Dunham VV. Metal-Free Approaches to Sterically-Hindered Bonds. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2020 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1467360601.

Council of Science Editors:

Dunham VV. Metal-Free Approaches to Sterically-Hindered Bonds. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1467360601

2. Auvil, Tyler Jay. Unique Reactivity Patterns Catalyzed by Internal Lewis Acid Assisted Hydrogen Bond Donors.

Degree: PhD, Chemistry, 2014, The Ohio State University

 The advancement of hydrogen bond donor (HBD) organocatalysis has been inhibited by a number of challenges. Conventional HBDs suffer from high catalyst loadings and operate… (more)

Subjects/Keywords: Chemistry; Boronate Urea; Hydrogen Bond Donor Catalyst; Organocatalyst; Internal Lewis Acid; Insertion; Nitrocyclopropane Carboxylate; Diazo Compound

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APA (6th Edition):

Auvil, T. J. (2014). Unique Reactivity Patterns Catalyzed by Internal Lewis Acid Assisted Hydrogen Bond Donors. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1395759920

Chicago Manual of Style (16th Edition):

Auvil, Tyler Jay. “Unique Reactivity Patterns Catalyzed by Internal Lewis Acid Assisted Hydrogen Bond Donors.” 2014. Doctoral Dissertation, The Ohio State University. Accessed September 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1395759920.

MLA Handbook (7th Edition):

Auvil, Tyler Jay. “Unique Reactivity Patterns Catalyzed by Internal Lewis Acid Assisted Hydrogen Bond Donors.” 2014. Web. 23 Sep 2020.

Vancouver:

Auvil TJ. Unique Reactivity Patterns Catalyzed by Internal Lewis Acid Assisted Hydrogen Bond Donors. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1395759920.

Council of Science Editors:

Auvil TJ. Unique Reactivity Patterns Catalyzed by Internal Lewis Acid Assisted Hydrogen Bond Donors. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1395759920


The Ohio State University

3. So, Sonia. Boronate Urea Activation of Nitro Compounds.

Degree: PhD, Chemistry, 2014, The Ohio State University

 Boronate ureas have been discovered as enhanced hydrogen bond donor (HBD) catalysts for the activation of various compounds containing nitro functional groups. The enhanced ability… (more)

Subjects/Keywords: Chemistry; hydrogen bond donor; urea catalysis; organocataysis; diazo compound; N-H insertion

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APA (6th Edition):

So, S. (2014). Boronate Urea Activation of Nitro Compounds. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1395764122

Chicago Manual of Style (16th Edition):

So, Sonia. “Boronate Urea Activation of Nitro Compounds.” 2014. Doctoral Dissertation, The Ohio State University. Accessed September 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1395764122.

MLA Handbook (7th Edition):

So, Sonia. “Boronate Urea Activation of Nitro Compounds.” 2014. Web. 23 Sep 2020.

Vancouver:

So S. Boronate Urea Activation of Nitro Compounds. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1395764122.

Council of Science Editors:

So S. Boronate Urea Activation of Nitro Compounds. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1395764122


The Ohio State University

4. Schafer, Andrew Gerard. Silanediols As Hydrogen Bond Donor Catalysts.

Degree: PhD, Chemistry, 2014, The Ohio State University

 The design of new catalysts for complex molecule synthesis is a critical endeavor for enabling facile access to medicines and materials. One relatively new direction… (more)

Subjects/Keywords: Chemistry; organocatalysis; silanediol; anion-binding; hydrogen bond donor

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APA (6th Edition):

Schafer, A. G. (2014). Silanediols As Hydrogen Bond Donor Catalysts. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1396442513

Chicago Manual of Style (16th Edition):

Schafer, Andrew Gerard. “Silanediols As Hydrogen Bond Donor Catalysts.” 2014. Doctoral Dissertation, The Ohio State University. Accessed September 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1396442513.

MLA Handbook (7th Edition):

Schafer, Andrew Gerard. “Silanediols As Hydrogen Bond Donor Catalysts.” 2014. Web. 23 Sep 2020.

Vancouver:

Schafer AG. Silanediols As Hydrogen Bond Donor Catalysts. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1396442513.

Council of Science Editors:

Schafer AG. Silanediols As Hydrogen Bond Donor Catalysts. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1396442513

5. Baldwin, Andrea Michelle. Synthesis and Functionalization of Heterocycles via Non-Covalent Catalysis.

Degree: PhD, Chemistry, 2016, The Ohio State University

 Hydrogen-bond donor (HBD) catalysis has emerged as a remarkable platform for the activation of reactants through non-covalent interactions. This class of organocatalysts provides a sustainable… (more)

Subjects/Keywords: Organic Chemistry; organocatalysis; hydrogen bond donor catalysis; silanediols; boronate ureas; oxazinanes; carbonates; chromanones; asymmetric catalysis

…Graduate Program of Chemistry and Biochemistry, The Ohio State University Publications… 

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APA (6th Edition):

Baldwin, A. M. (2016). Synthesis and Functionalization of Heterocycles via Non-Covalent Catalysis. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1467277822

Chicago Manual of Style (16th Edition):

Baldwin, Andrea Michelle. “Synthesis and Functionalization of Heterocycles via Non-Covalent Catalysis.” 2016. Doctoral Dissertation, The Ohio State University. Accessed September 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1467277822.

MLA Handbook (7th Edition):

Baldwin, Andrea Michelle. “Synthesis and Functionalization of Heterocycles via Non-Covalent Catalysis.” 2016. Web. 23 Sep 2020.

Vancouver:

Baldwin AM. Synthesis and Functionalization of Heterocycles via Non-Covalent Catalysis. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2020 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1467277822.

Council of Science Editors:

Baldwin AM. Synthesis and Functionalization of Heterocycles via Non-Covalent Catalysis. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1467277822

6. Wieting, Joshua Merlin. Silanediol-Catalyzed Stereoselective Functionalization of Heterocycles.

Degree: PhD, Chemistry, 2015, The Ohio State University

 Small molecules that participate in molecular recognition via hydrogen bonding interactions provide a powerful platform for a host of applications. It has been established that… (more)

Subjects/Keywords: Chemistry; Silanediols; Silanediol; Organocatalysis; Hydrogen Bond Donor Catalysis; Asymmetric Catalysis; Silicon Chemistry

…Research Associate, Department of Chemistry and Biochemistry, The Ohio State University… …hydrogen bonding molecular recognition came from the laboratory of Jack Hine at The Ohio State… …University.38 Hine and coworkers discovered that 1,8-biphenylenediol (II-1) possessed… 

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APA (6th Edition):

Wieting, J. M. (2015). Silanediol-Catalyzed Stereoselective Functionalization of Heterocycles. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1448891366

Chicago Manual of Style (16th Edition):

Wieting, Joshua Merlin. “Silanediol-Catalyzed Stereoselective Functionalization of Heterocycles.” 2015. Doctoral Dissertation, The Ohio State University. Accessed September 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1448891366.

MLA Handbook (7th Edition):

Wieting, Joshua Merlin. “Silanediol-Catalyzed Stereoselective Functionalization of Heterocycles.” 2015. Web. 23 Sep 2020.

Vancouver:

Wieting JM. Silanediol-Catalyzed Stereoselective Functionalization of Heterocycles. [Internet] [Doctoral dissertation]. The Ohio State University; 2015. [cited 2020 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1448891366.

Council of Science Editors:

Wieting JM. Silanediol-Catalyzed Stereoselective Functionalization of Heterocycles. [Doctoral Dissertation]. The Ohio State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1448891366

7. Nickerson, David M. Unique Reactivity Patterns of Enhanced Urea Catalysts.

Degree: PhD, Chemistry, 2014, The Ohio State University

 Strategic enhancement of urea organocatalysts using internally coordinated Lewis acids has allowed for the discovery of new and useful reactions. Specifically, the incorporation of transition… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Organocatalysis; Organocatalyst; Urea Catalysis; Thiourea Catalysis; Urea Catalyst; Thiourea Catalyst; Palladacycle; Nitroimine; Nitrimine; Nitroenamine; Nitroamine; Internal Lewis Acid; Alkylidene Malonate; Biaryl Coupling

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APA (6th Edition):

Nickerson, D. M. (2014). Unique Reactivity Patterns of Enhanced Urea Catalysts. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1395859006

Chicago Manual of Style (16th Edition):

Nickerson, David M. “Unique Reactivity Patterns of Enhanced Urea Catalysts.” 2014. Doctoral Dissertation, The Ohio State University. Accessed September 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1395859006.

MLA Handbook (7th Edition):

Nickerson, David M. “Unique Reactivity Patterns of Enhanced Urea Catalysts.” 2014. Web. 23 Sep 2020.

Vancouver:

Nickerson DM. Unique Reactivity Patterns of Enhanced Urea Catalysts. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1395859006.

Council of Science Editors:

Nickerson DM. Unique Reactivity Patterns of Enhanced Urea Catalysts. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1395859006

8. Couch, Erica Dawn. Difluoroboronate Urea-Induced Acid Amplification for Insertion Chemistry.

Degree: MS, Chemistry, 2014, The Ohio State University

 Development of a new enhanced boronate urea that benefits from internal coordination of the urea carbonyl to a strategically placed Lewis acid has enabled a… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; hydrogen bond donor; HBD; catalyst; urea; insertion chemistry; diazo compounds; difluoroboronate urea; organic acid; acid amplification

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

APA (6th Edition):

Couch, E. D. (2014). Difluoroboronate Urea-Induced Acid Amplification for Insertion Chemistry. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1404225572

Chicago Manual of Style (16th Edition):

Couch, Erica Dawn. “Difluoroboronate Urea-Induced Acid Amplification for Insertion Chemistry.” 2014. Masters Thesis, The Ohio State University. Accessed September 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1404225572.

MLA Handbook (7th Edition):

Couch, Erica Dawn. “Difluoroboronate Urea-Induced Acid Amplification for Insertion Chemistry.” 2014. Web. 23 Sep 2020.

Vancouver:

Couch ED. Difluoroboronate Urea-Induced Acid Amplification for Insertion Chemistry. [Internet] [Masters thesis]. The Ohio State University; 2014. [cited 2020 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1404225572.

Council of Science Editors:

Couch ED. Difluoroboronate Urea-Induced Acid Amplification for Insertion Chemistry. [Masters Thesis]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1404225572

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