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You searched for +publisher:"Youngstown State University" +contributor:("Norris, Peter"). Showing records 1 – 30 of 31 total matches.

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Youngstown State University

1. Adesoye, Olumuyiwa Gbenga. Studies towards the Synthesis of Analogs of Bacillithiol.

Degree: MSin Chemistry, Department of Chemistry, 2012, Youngstown State University

 Low molecular weight thiols relieve oxidative stress by forming disulfide bonds and reduce alkylating agents such as xenobiotics to less harmful adducts by the action… (more)

Subjects/Keywords: Chemistry; Low molecular weight thiols; bacillithiol; fosfomycin; glycosylation

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APA (6th Edition):

Adesoye, O. G. (2012). Studies towards the Synthesis of Analogs of Bacillithiol. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1338764980

Chicago Manual of Style (16th Edition):

Adesoye, Olumuyiwa Gbenga. “Studies towards the Synthesis of Analogs of Bacillithiol.” 2012. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1338764980.

MLA Handbook (7th Edition):

Adesoye, Olumuyiwa Gbenga. “Studies towards the Synthesis of Analogs of Bacillithiol.” 2012. Web. 17 Aug 2019.

Vancouver:

Adesoye OG. Studies towards the Synthesis of Analogs of Bacillithiol. [Internet] [Masters thesis]. Youngstown State University; 2012. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1338764980.

Council of Science Editors:

Adesoye OG. Studies towards the Synthesis of Analogs of Bacillithiol. [Masters Thesis]. Youngstown State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1338764980


Youngstown State University

2. Evans, Michael Ryan. Labeled Mimics of N-Acetyl-D-Fucosamine.

Degree: MSin Chemistry, Department of Chemistry, 2008, Youngstown State University

  The synthesis of N-acetyl-D-fucosamine and derivatives will be attempted from inexpensive commercially available starting materials. The final products contain medicinally important markers such as… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; N-acetyl-D-glucosamine; N-acetyl-D-fucosamine; carbohydrates; carbohydrate chemistry; organic chemistry; Staphylococcus aureus

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APA (6th Edition):

Evans, M. R. (2008). Labeled Mimics of N-Acetyl-D-Fucosamine. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1210527108

Chicago Manual of Style (16th Edition):

Evans, Michael Ryan. “Labeled Mimics of N-Acetyl-D-Fucosamine.” 2008. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1210527108.

MLA Handbook (7th Edition):

Evans, Michael Ryan. “Labeled Mimics of N-Acetyl-D-Fucosamine.” 2008. Web. 17 Aug 2019.

Vancouver:

Evans MR. Labeled Mimics of N-Acetyl-D-Fucosamine. [Internet] [Masters thesis]. Youngstown State University; 2008. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1210527108.

Council of Science Editors:

Evans MR. Labeled Mimics of N-Acetyl-D-Fucosamine. [Masters Thesis]. Youngstown State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1210527108


Youngstown State University

3. Cox, Glen Adam. Towards the Synthesis of N-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives.

Degree: MSin Chemistry, Department of Chemistry, 2007, Youngstown State University

  The following details attempts at a stereoselective synthesis of deoxygenated D-mannose uronic acid derivatives from D-glucurono-6,3-lactone. These derivatives will be tested as potential inhibitors… (more)

Subjects/Keywords: Chemistry; carbohydrate; S. aureus; glycobiology; capsular polysaccharide

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APA (6th Edition):

Cox, G. A. (2007). Towards the Synthesis of N-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1217344144

Chicago Manual of Style (16th Edition):

Cox, Glen Adam. “Towards the Synthesis of N-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives.” 2007. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1217344144.

MLA Handbook (7th Edition):

Cox, Glen Adam. “Towards the Synthesis of N-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives.” 2007. Web. 17 Aug 2019.

Vancouver:

Cox GA. Towards the Synthesis of N-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives. [Internet] [Masters thesis]. Youngstown State University; 2007. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1217344144.

Council of Science Editors:

Cox GA. Towards the Synthesis of N-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives. [Masters Thesis]. Youngstown State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1217344144


Youngstown State University

4. Dobosh, Brian Joseph. The Synthesis of Azides from Alcohols using Sulfonyl Azides.

Degree: MSin Chemistry, Department of Chemistry, 2008, Youngstown State University

 The following thesis deals with the synthesis of azide products from their alcohol starting materials, utilizing sulfonyl azides as the azide nucleophile source. The reactions… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; azide synthesis; alcohols; sulfonyl azides

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APA (6th Edition):

Dobosh, B. J. (2008). The Synthesis of Azides from Alcohols using Sulfonyl Azides. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219459733

Chicago Manual of Style (16th Edition):

Dobosh, Brian Joseph. “The Synthesis of Azides from Alcohols using Sulfonyl Azides.” 2008. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219459733.

MLA Handbook (7th Edition):

Dobosh, Brian Joseph. “The Synthesis of Azides from Alcohols using Sulfonyl Azides.” 2008. Web. 17 Aug 2019.

Vancouver:

Dobosh BJ. The Synthesis of Azides from Alcohols using Sulfonyl Azides. [Internet] [Masters thesis]. Youngstown State University; 2008. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219459733.

Council of Science Editors:

Dobosh BJ. The Synthesis of Azides from Alcohols using Sulfonyl Azides. [Masters Thesis]. Youngstown State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219459733


Youngstown State University

5. Patton, Jennie L. Carbenoid Insertion Chemistry on Furanose Platforms as a Route to Natural Product Frameworks.

Degree: MSin Chemistry, Department of Chemistry, 2008, Youngstown State University

 The following describes a successful synthetic pathway to create an analog of the natural product (+)-dihydrocanadensolide from the inexpensive and readily available D-xylose. The pathway… (more)

Subjects/Keywords: Biomedical Research; Chemistry; Experiments; Organic Chemistry; Pharmaceuticals; carbohydrate; natural products; lactone; rhodium(II) acetate; carbenoid; xylose; diazo

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APA (6th Edition):

Patton, J. L. (2008). Carbenoid Insertion Chemistry on Furanose Platforms as a Route to Natural Product Frameworks. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219534151

Chicago Manual of Style (16th Edition):

Patton, Jennie L. “Carbenoid Insertion Chemistry on Furanose Platforms as a Route to Natural Product Frameworks.” 2008. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219534151.

MLA Handbook (7th Edition):

Patton, Jennie L. “Carbenoid Insertion Chemistry on Furanose Platforms as a Route to Natural Product Frameworks.” 2008. Web. 17 Aug 2019.

Vancouver:

Patton JL. Carbenoid Insertion Chemistry on Furanose Platforms as a Route to Natural Product Frameworks. [Internet] [Masters thesis]. Youngstown State University; 2008. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219534151.

Council of Science Editors:

Patton JL. Carbenoid Insertion Chemistry on Furanose Platforms as a Route to Natural Product Frameworks. [Masters Thesis]. Youngstown State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219534151


Youngstown State University

6. McCutcheon, David Clark. Towards mimics of UDP-N-acetyl-L-fucosamine (UDP-L-FucNAc) as potential inhibitors of Staphylococcus aureus capsular polysaccharide biosynthesis.

Degree: MSin Chemistry, Department of Chemistry, 2008, Youngstown State University

The following is an account of attempted syntheses toward novel mimics of UDP-<i>N</i>-acetyl-L-fucosamine (UDP-L-FucNAc) to serve as inhibitors of or substrates forbacterial glycosyltransferases responsible for the biosynthesis of the capsularpolysaccharide of <i>Staphylococcus aureus</i>. Advisors/Committee Members: Norris, Peter (Advisor).

Subjects/Keywords: Chemistry; carbohydrates; glycosides; L-fucosamine

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APA (6th Edition):

McCutcheon, D. C. (2008). Towards mimics of UDP-N-acetyl-L-fucosamine (UDP-L-FucNAc) as potential inhibitors of Staphylococcus aureus capsular polysaccharide biosynthesis. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1222137662

Chicago Manual of Style (16th Edition):

McCutcheon, David Clark. “Towards mimics of UDP-N-acetyl-L-fucosamine (UDP-L-FucNAc) as potential inhibitors of Staphylococcus aureus capsular polysaccharide biosynthesis.” 2008. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1222137662.

MLA Handbook (7th Edition):

McCutcheon, David Clark. “Towards mimics of UDP-N-acetyl-L-fucosamine (UDP-L-FucNAc) as potential inhibitors of Staphylococcus aureus capsular polysaccharide biosynthesis.” 2008. Web. 17 Aug 2019.

Vancouver:

McCutcheon DC. Towards mimics of UDP-N-acetyl-L-fucosamine (UDP-L-FucNAc) as potential inhibitors of Staphylococcus aureus capsular polysaccharide biosynthesis. [Internet] [Masters thesis]. Youngstown State University; 2008. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1222137662.

Council of Science Editors:

McCutcheon DC. Towards mimics of UDP-N-acetyl-L-fucosamine (UDP-L-FucNAc) as potential inhibitors of Staphylococcus aureus capsular polysaccharide biosynthesis. [Masters Thesis]. Youngstown State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1222137662


Youngstown State University

7. Malich, Ashley M. Decomposition of Novel Diazosugars: Effects on Regioselectivity.

Degree: MSin Chemistry, Department of Chemistry, 2008, Youngstown State University

 The following work describes the construction and decomposition of azidodeoxy sugars with diazoesters attached. The fate of the projected carbeniod intermediate formed in the presence… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; diazosugars; decomposition chemistry; rhodium catalyst; xylose

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APA (6th Edition):

Malich, A. M. (2008). Decomposition of Novel Diazosugars: Effects on Regioselectivity. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1222195006

Chicago Manual of Style (16th Edition):

Malich, Ashley M. “Decomposition of Novel Diazosugars: Effects on Regioselectivity.” 2008. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1222195006.

MLA Handbook (7th Edition):

Malich, Ashley M. “Decomposition of Novel Diazosugars: Effects on Regioselectivity.” 2008. Web. 17 Aug 2019.

Vancouver:

Malich AM. Decomposition of Novel Diazosugars: Effects on Regioselectivity. [Internet] [Masters thesis]. Youngstown State University; 2008. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1222195006.

Council of Science Editors:

Malich AM. Decomposition of Novel Diazosugars: Effects on Regioselectivity. [Masters Thesis]. Youngstown State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1222195006


Youngstown State University

8. Hartranft, Charles Alan. “One-Pot” Synthesis of Organic Azides from Alcohols and Protected Sugars.

Degree: MSin Chemistry, Department of Chemistry, 2008, Youngstown State University

 This thesis deals with a novel “one-pot” synthesis of organic azides from simple alcohols as well as protected sugars. Experimentation led to the successful azidation… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Pharmaceuticals; one-pot azide synthesis; one-pot azide; organic azides; organic azide synthesis; azidation of protected carbohydrates; azidation of simple alcohols; azides; azide transfer reagent; p-ABSA; p-NBSA

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APA (6th Edition):

Hartranft, C. A. (2008). “One-Pot” Synthesis of Organic Azides from Alcohols and Protected Sugars. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229370336

Chicago Manual of Style (16th Edition):

Hartranft, Charles Alan. ““One-Pot” Synthesis of Organic Azides from Alcohols and Protected Sugars.” 2008. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229370336.

MLA Handbook (7th Edition):

Hartranft, Charles Alan. ““One-Pot” Synthesis of Organic Azides from Alcohols and Protected Sugars.” 2008. Web. 17 Aug 2019.

Vancouver:

Hartranft CA. “One-Pot” Synthesis of Organic Azides from Alcohols and Protected Sugars. [Internet] [Masters thesis]. Youngstown State University; 2008. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229370336.

Council of Science Editors:

Hartranft CA. “One-Pot” Synthesis of Organic Azides from Alcohols and Protected Sugars. [Masters Thesis]. Youngstown State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229370336


Youngstown State University

9. Knapp, Steven E. Synthesis and Structural Analysis of Novel Bis(triazole) UDP Analogs as Potential Glycosyl Transferase Inhibitors.

Degree: MSin Chemistry, Department of Chemistry, 2008, Youngstown State University

 The following details the synthesis of a novel bis(1,2,3-triazole), which is a potential glycosyltransferase inhibitor. A glycosyltransferase is an enzyme that is involved in the… (more)

Subjects/Keywords: Organic Chemistry; Organic chemistry; chemistry; triazole; glycosyltransferase; S. aureus; Staphylococcus aureus; bis(triazole); bis(1,2,3-triazole); aldehyde to alkyne; click chemistry

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APA (6th Edition):

Knapp, S. E. (2008). Synthesis and Structural Analysis of Novel Bis(triazole) UDP Analogs as Potential Glycosyl Transferase Inhibitors. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229371574

Chicago Manual of Style (16th Edition):

Knapp, Steven E. “Synthesis and Structural Analysis of Novel Bis(triazole) UDP Analogs as Potential Glycosyl Transferase Inhibitors.” 2008. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229371574.

MLA Handbook (7th Edition):

Knapp, Steven E. “Synthesis and Structural Analysis of Novel Bis(triazole) UDP Analogs as Potential Glycosyl Transferase Inhibitors.” 2008. Web. 17 Aug 2019.

Vancouver:

Knapp SE. Synthesis and Structural Analysis of Novel Bis(triazole) UDP Analogs as Potential Glycosyl Transferase Inhibitors. [Internet] [Masters thesis]. Youngstown State University; 2008. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229371574.

Council of Science Editors:

Knapp SE. Synthesis and Structural Analysis of Novel Bis(triazole) UDP Analogs as Potential Glycosyl Transferase Inhibitors. [Masters Thesis]. Youngstown State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229371574


Youngstown State University

10. Clymer, Traci M. Preliminary Studies on the Effects of Glycosyl Triazoles on C2C12 stem cells.

Degree: MSin Chemistry, Department of Chemistry, 2010, Youngstown State University

 The C2C12 line of cells differentiates rapidly to form contractile myotubes which give rise to contractile skeletal muscle. The muscle fibers formed from these cells… (more)

Subjects/Keywords: Cellular Biology; Chemistry; Medicine; Molecular Biology; Molecular Chemistry; Molecules; Organic Chemistry; glycosyl triazoles; C2C12 Stem cells; organic chemistry; cell culture

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APA (6th Edition):

Clymer, T. M. (2010). Preliminary Studies on the Effects of Glycosyl Triazoles on C2C12 stem cells. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290536995

Chicago Manual of Style (16th Edition):

Clymer, Traci M. “Preliminary Studies on the Effects of Glycosyl Triazoles on C2C12 stem cells.” 2010. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290536995.

MLA Handbook (7th Edition):

Clymer, Traci M. “Preliminary Studies on the Effects of Glycosyl Triazoles on C2C12 stem cells.” 2010. Web. 17 Aug 2019.

Vancouver:

Clymer TM. Preliminary Studies on the Effects of Glycosyl Triazoles on C2C12 stem cells. [Internet] [Masters thesis]. Youngstown State University; 2010. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290536995.

Council of Science Editors:

Clymer TM. Preliminary Studies on the Effects of Glycosyl Triazoles on C2C12 stem cells. [Masters Thesis]. Youngstown State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290536995


Youngstown State University

11. Okumu, Antony A. Development of a Safe and Efficient Alkyl Azide Synthesis using Arylsulfonyl Azide.

Degree: MSin Chemistry, Department of Chemistry, 2010, Youngstown State University

 Sodium azide has traditionally been used as the source of azide anion for the synthesis of alkyl azides. Besides difficulties with solubility, sodium azide is… (more)

Subjects/Keywords: Chemistry; Experiments; Occupational Safety; Organic Chemistry; <; i>; p<; /i>; -ABSA DBU organic soluble salt; alkyl azide synthesis; 1,2,3-triazole attempted synthesis; suitable solvent

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APA (6th Edition):

Okumu, A. A. (2010). Development of a Safe and Efficient Alkyl Azide Synthesis using Arylsulfonyl Azide. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290962115

Chicago Manual of Style (16th Edition):

Okumu, Antony A. “Development of a Safe and Efficient Alkyl Azide Synthesis using Arylsulfonyl Azide.” 2010. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290962115.

MLA Handbook (7th Edition):

Okumu, Antony A. “Development of a Safe and Efficient Alkyl Azide Synthesis using Arylsulfonyl Azide.” 2010. Web. 17 Aug 2019.

Vancouver:

Okumu AA. Development of a Safe and Efficient Alkyl Azide Synthesis using Arylsulfonyl Azide. [Internet] [Masters thesis]. Youngstown State University; 2010. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290962115.

Council of Science Editors:

Okumu AA. Development of a Safe and Efficient Alkyl Azide Synthesis using Arylsulfonyl Azide. [Masters Thesis]. Youngstown State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290962115


Youngstown State University

12. Kyei-Baffour, Kwaku. "One-pot" Synthesis of Carbamates <i>via</i> Curtius Rearrangement.

Degree: MSin Chemistry, Department of Chemistry, 2014, Youngstown State University

 In this thesis, acyl chlorides were successfully converted to their corresponding carbamates via Curtius rearrangement in a novel "one-pot" synthesis procedure that uses <i>p</i>-nitrobenzenesulfonylazide as… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Organic chemistry; Organic synthesis; Acyl azides; Carbamates; Curtius rearrangement

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APA (6th Edition):

Kyei-Baffour, K. (2014). "One-pot" Synthesis of Carbamates <i>via</i> Curtius Rearrangement. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409143879

Chicago Manual of Style (16th Edition):

Kyei-Baffour, Kwaku. “"One-pot" Synthesis of Carbamates <i>via</i> Curtius Rearrangement.” 2014. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409143879.

MLA Handbook (7th Edition):

Kyei-Baffour, Kwaku. “"One-pot" Synthesis of Carbamates <i>via</i> Curtius Rearrangement.” 2014. Web. 17 Aug 2019.

Vancouver:

Kyei-Baffour K. "One-pot" Synthesis of Carbamates <i>via</i> Curtius Rearrangement. [Internet] [Masters thesis]. Youngstown State University; 2014. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409143879.

Council of Science Editors:

Kyei-Baffour K. "One-pot" Synthesis of Carbamates <i>via</i> Curtius Rearrangement. [Masters Thesis]. Youngstown State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409143879


Youngstown State University

13. Tatebe, Caleb J. Synthesis of Sugar-Derived Esters and Carbamate Compounds.

Degree: MSin Chemistry, Department of Chemistry, 2014, Youngstown State University

 This thesis deals with the synthesis of sugar-derived esters and carbamate compounds. The attempted decomposition of diazo ester sugars is also a topic of this… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Synthetic chemistry; Carbamate; Ester; Organic chemistry

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APA (6th Edition):

Tatebe, C. J. (2014). Synthesis of Sugar-Derived Esters and Carbamate Compounds. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409833972

Chicago Manual of Style (16th Edition):

Tatebe, Caleb J. “Synthesis of Sugar-Derived Esters and Carbamate Compounds.” 2014. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409833972.

MLA Handbook (7th Edition):

Tatebe, Caleb J. “Synthesis of Sugar-Derived Esters and Carbamate Compounds.” 2014. Web. 17 Aug 2019.

Vancouver:

Tatebe CJ. Synthesis of Sugar-Derived Esters and Carbamate Compounds. [Internet] [Masters thesis]. Youngstown State University; 2014. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409833972.

Council of Science Editors:

Tatebe CJ. Synthesis of Sugar-Derived Esters and Carbamate Compounds. [Masters Thesis]. Youngstown State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409833972


Youngstown State University

14. Buabeng, Emmnauel Ramsey. Towards the Synthesis of Novel Glycomimetics of <i>N</i>-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives.

Degree: MSin Chemistry, Department of Chemistry, 2016, Youngstown State University

 An efficient synthetic scheme has been employed for the synthesis of glycomimetics of <i>N</i>-acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (DManNAcA) and derivatives from easily available D-glucuronolactone in 33-100%… (more)

Subjects/Keywords: Chemistry; Biosynthesis, glycomimetics, Capsular Polysaccharides, Oximes

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APA (6th Edition):

Buabeng, E. R. (2016). Towards the Synthesis of Novel Glycomimetics of <i>N</i>-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1471478050

Chicago Manual of Style (16th Edition):

Buabeng, Emmnauel Ramsey. “Towards the Synthesis of Novel Glycomimetics of <i>N</i>-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives.” 2016. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1471478050.

MLA Handbook (7th Edition):

Buabeng, Emmnauel Ramsey. “Towards the Synthesis of Novel Glycomimetics of <i>N</i>-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives.” 2016. Web. 17 Aug 2019.

Vancouver:

Buabeng ER. Towards the Synthesis of Novel Glycomimetics of <i>N</i>-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives. [Internet] [Masters thesis]. Youngstown State University; 2016. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1471478050.

Council of Science Editors:

Buabeng ER. Towards the Synthesis of Novel Glycomimetics of <i>N</i>-Acetyl-2-amino-2-deoxy-D-mannopyranose uronic acid (D-ManNAcA) and Derivatives. [Masters Thesis]. Youngstown State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1471478050


Youngstown State University

15. Copeland, Christopher N., II. Modified Conditions for Acyl Azide and Carbamate Synthesis.

Degree: MSin Chemistry, Department of Chemistry, 2016, Youngstown State University

 Carbamate chemistry has a wide variety of applications both in synthetic chemistry as well as in biology. This carbon-nitrogen containing functional group is used as… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Azides; Carbamates; Curtius rearrangement

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APA (6th Edition):

Copeland, Christopher N., I. (2016). Modified Conditions for Acyl Azide and Carbamate Synthesis. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1473765784542178

Chicago Manual of Style (16th Edition):

Copeland, Christopher N., II. “Modified Conditions for Acyl Azide and Carbamate Synthesis.” 2016. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1473765784542178.

MLA Handbook (7th Edition):

Copeland, Christopher N., II. “Modified Conditions for Acyl Azide and Carbamate Synthesis.” 2016. Web. 17 Aug 2019.

Vancouver:

Copeland, Christopher N. I. Modified Conditions for Acyl Azide and Carbamate Synthesis. [Internet] [Masters thesis]. Youngstown State University; 2016. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1473765784542178.

Council of Science Editors:

Copeland, Christopher N. I. Modified Conditions for Acyl Azide and Carbamate Synthesis. [Masters Thesis]. Youngstown State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1473765784542178


Youngstown State University

16. Afeke, Cephas Ofoe. Chemistry of Acyl Nitrenes in the Synthesis of Carbamates and Complex Heterocycles.

Degree: MSin Chemistry, Department of Chemistry, 2015, Youngstown State University

 The synthesis of carbamates via Curtius rearrangement utilizing aryl acyl azides together with a wide range of alcohol-containing complex organic molecules was explored through the… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Decomposition of azidoformates; Acyl nitrenes; Azidoformates, nitrene insertion

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APA (6th Edition):

Afeke, C. O. (2015). Chemistry of Acyl Nitrenes in the Synthesis of Carbamates and Complex Heterocycles. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1442410888

Chicago Manual of Style (16th Edition):

Afeke, Cephas Ofoe. “Chemistry of Acyl Nitrenes in the Synthesis of Carbamates and Complex Heterocycles.” 2015. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1442410888.

MLA Handbook (7th Edition):

Afeke, Cephas Ofoe. “Chemistry of Acyl Nitrenes in the Synthesis of Carbamates and Complex Heterocycles.” 2015. Web. 17 Aug 2019.

Vancouver:

Afeke CO. Chemistry of Acyl Nitrenes in the Synthesis of Carbamates and Complex Heterocycles. [Internet] [Masters thesis]. Youngstown State University; 2015. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1442410888.

Council of Science Editors:

Afeke CO. Chemistry of Acyl Nitrenes in the Synthesis of Carbamates and Complex Heterocycles. [Masters Thesis]. Youngstown State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1442410888


Youngstown State University

17. Delost, Michael D. Synthesis of Amine Derivatives from a “One-Pot” Synthesis of Biphenyl-4-methylazide.

Degree: MSin Chemistry, Department of Chemistry, 2015, Youngstown State University

 This thesis explores the synthesis of amine derivatives such as amides and imines from biphenyl-4-methylazide using Staudinger chemistry. A robust one-pot synthesis of biphenyl-4-methylazide was… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Pharmaceuticals; one-pot synthesis of alkyl with arylsulfonyl azides; Staudinger reduction with DPPE; aza Wittig and Staudinger ligation chemistry; bioorthogonal and chemoselective chemistry

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APA (6th Edition):

Delost, M. D. (2015). Synthesis of Amine Derivatives from a “One-Pot” Synthesis of Biphenyl-4-methylazide. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1442407733

Chicago Manual of Style (16th Edition):

Delost, Michael D. “Synthesis of Amine Derivatives from a “One-Pot” Synthesis of Biphenyl-4-methylazide.” 2015. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1442407733.

MLA Handbook (7th Edition):

Delost, Michael D. “Synthesis of Amine Derivatives from a “One-Pot” Synthesis of Biphenyl-4-methylazide.” 2015. Web. 17 Aug 2019.

Vancouver:

Delost MD. Synthesis of Amine Derivatives from a “One-Pot” Synthesis of Biphenyl-4-methylazide. [Internet] [Masters thesis]. Youngstown State University; 2015. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1442407733.

Council of Science Editors:

Delost MD. Synthesis of Amine Derivatives from a “One-Pot” Synthesis of Biphenyl-4-methylazide. [Masters Thesis]. Youngstown State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1442407733


Youngstown State University

18. Kiptoo, Daniel. Synthesis of Novel N-Glycoside Analogs of D-Galactose.

Degree: MSin Chemistry, Department of Chemistry, 2018, Youngstown State University

 Galactosyl triazoles have shown potential as drug candidates and, as a consequence, the synthesis of these carbohydrate-based mimitics by the use of a modified form… (more)

Subjects/Keywords: Chemistry; Click chemistry; Triazoles; Stereospecific

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APA (6th Edition):

Kiptoo, D. (2018). Synthesis of Novel N-Glycoside Analogs of D-Galactose. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1547483536049585

Chicago Manual of Style (16th Edition):

Kiptoo, Daniel. “Synthesis of Novel N-Glycoside Analogs of D-Galactose.” 2018. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1547483536049585.

MLA Handbook (7th Edition):

Kiptoo, Daniel. “Synthesis of Novel N-Glycoside Analogs of D-Galactose.” 2018. Web. 17 Aug 2019.

Vancouver:

Kiptoo D. Synthesis of Novel N-Glycoside Analogs of D-Galactose. [Internet] [Masters thesis]. Youngstown State University; 2018. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1547483536049585.

Council of Science Editors:

Kiptoo D. Synthesis of Novel N-Glycoside Analogs of D-Galactose. [Masters Thesis]. Youngstown State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1547483536049585


Youngstown State University

19. LaLama, Matthew. Rhodium-Catalyzed Decomposition of Carbohydrate Diazo Esters.

Degree: MSin Chemistry, Department of Chemistry, 2018, Youngstown State University

 This thesis herein reports the synthesis of two diazo ester sugars and their decomposition in the presence of catalytic rhodium acetate dimer. Reactions were designed… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Rhodium; Catalysis; Azide; Natural product synthesis; Carbohydrate; Diazo

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APA (6th Edition):

LaLama, M. (2018). Rhodium-Catalyzed Decomposition of Carbohydrate Diazo Esters. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1532881612843223

Chicago Manual of Style (16th Edition):

LaLama, Matthew. “Rhodium-Catalyzed Decomposition of Carbohydrate Diazo Esters.” 2018. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1532881612843223.

MLA Handbook (7th Edition):

LaLama, Matthew. “Rhodium-Catalyzed Decomposition of Carbohydrate Diazo Esters.” 2018. Web. 17 Aug 2019.

Vancouver:

LaLama M. Rhodium-Catalyzed Decomposition of Carbohydrate Diazo Esters. [Internet] [Masters thesis]. Youngstown State University; 2018. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1532881612843223.

Council of Science Editors:

LaLama M. Rhodium-Catalyzed Decomposition of Carbohydrate Diazo Esters. [Masters Thesis]. Youngstown State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1532881612843223


Youngstown State University

20. Beagle, Lucas Kyle. Synthesis and Characterization of Carbohydrate Mimics.

Degree: MSin Chemistry, Department of Chemistry, 2008, Youngstown State University

  The synthesis of <i>N</i>-acetyl-D-fucosamine and <i>N</i>-((2R,3R,4R)-2,4-dihydroxy-6-methylene-5-oxo-tetrahydro-2H-pyran-3-yl)acetamide will be pursued from theinexpensive starting material <i>N</i>-acetyl-D-glucosamine. These carbohydrates are mimicsof intermediates used by <i>Staphylococcus aureus</i> in… (more)

Subjects/Keywords: Analytical Chemistry; Chemistry; Organic Chemistry; carbohyrate; organic; NMR; Nuclear Magnetic Resonance Spectroscopy

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APA (6th Edition):

Beagle, L. K. (2008). Synthesis and Characterization of Carbohydrate Mimics. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219687360

Chicago Manual of Style (16th Edition):

Beagle, Lucas Kyle. “Synthesis and Characterization of Carbohydrate Mimics.” 2008. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219687360.

MLA Handbook (7th Edition):

Beagle, Lucas Kyle. “Synthesis and Characterization of Carbohydrate Mimics.” 2008. Web. 17 Aug 2019.

Vancouver:

Beagle LK. Synthesis and Characterization of Carbohydrate Mimics. [Internet] [Masters thesis]. Youngstown State University; 2008. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219687360.

Council of Science Editors:

Beagle LK. Synthesis and Characterization of Carbohydrate Mimics. [Masters Thesis]. Youngstown State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219687360


Youngstown State University

21. Pavlidakey, Katherine Irene. Testing glycomimetic compounds for their ability to disrupt capsular polysaccharide production in type 5 Staphylococcus aureus.

Degree: MSin Chemistry, Department of Chemistry, 2008, Youngstown State University

 The potentially fatal nature of <i>Staphylococcus aureus</i> is exponentially enhanced by its incredible ability to evade medical treatment. At the current time <i>S. aureus</i> has… (more)

Subjects/Keywords: Biology; Chemistry; Health Care; Immunology; Carbohydrate mimetics; capsular polysaccharide; testing glycomimetic compounds; Antibiotic Resistant Staphylococcus aureus

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APA (6th Edition):

Pavlidakey, K. I. (2008). Testing glycomimetic compounds for their ability to disrupt capsular polysaccharide production in type 5 Staphylococcus aureus. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1220366478

Chicago Manual of Style (16th Edition):

Pavlidakey, Katherine Irene. “Testing glycomimetic compounds for their ability to disrupt capsular polysaccharide production in type 5 Staphylococcus aureus.” 2008. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1220366478.

MLA Handbook (7th Edition):

Pavlidakey, Katherine Irene. “Testing glycomimetic compounds for their ability to disrupt capsular polysaccharide production in type 5 Staphylococcus aureus.” 2008. Web. 17 Aug 2019.

Vancouver:

Pavlidakey KI. Testing glycomimetic compounds for their ability to disrupt capsular polysaccharide production in type 5 Staphylococcus aureus. [Internet] [Masters thesis]. Youngstown State University; 2008. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1220366478.

Council of Science Editors:

Pavlidakey KI. Testing glycomimetic compounds for their ability to disrupt capsular polysaccharide production in type 5 Staphylococcus aureus. [Masters Thesis]. Youngstown State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1220366478

22. Ngoje, Philemon O. Synthons of UDP-<i>N</i>-acetyl-L-Fucosamine (UDP-L-FucNAc) as potential inhibitors of <i>Staphylococcus aureus</i> Capsular Polysaccharide Biosynthesis.

Degree: MSin Chemistry, Department of Chemistry, 2015, Youngstown State University

 Non-traceless modified Staudinger reaction was utilized as a safe method in this work to synthesize novel synthons of UDP-<i>N</i>-acetyl-L-fucosamine as potential inhibitors of or substrates… (more)

Subjects/Keywords: Chemistry; Staphylococcus aureus; Capsular polysaccharide biosynthesis; UDP-N-acetyl-L-Fucosamine; UDP-L-FucNAc; Inhibitors

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APA (6th Edition):

Ngoje, P. O. (2015). Synthons of UDP-<i>N</i>-acetyl-L-Fucosamine (UDP-L-FucNAc) as potential inhibitors of <i>Staphylococcus aureus</i> Capsular Polysaccharide Biosynthesis. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1441880943

Chicago Manual of Style (16th Edition):

Ngoje, Philemon O. “Synthons of UDP-<i>N</i>-acetyl-L-Fucosamine (UDP-L-FucNAc) as potential inhibitors of <i>Staphylococcus aureus</i> Capsular Polysaccharide Biosynthesis.” 2015. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1441880943.

MLA Handbook (7th Edition):

Ngoje, Philemon O. “Synthons of UDP-<i>N</i>-acetyl-L-Fucosamine (UDP-L-FucNAc) as potential inhibitors of <i>Staphylococcus aureus</i> Capsular Polysaccharide Biosynthesis.” 2015. Web. 17 Aug 2019.

Vancouver:

Ngoje PO. Synthons of UDP-<i>N</i>-acetyl-L-Fucosamine (UDP-L-FucNAc) as potential inhibitors of <i>Staphylococcus aureus</i> Capsular Polysaccharide Biosynthesis. [Internet] [Masters thesis]. Youngstown State University; 2015. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1441880943.

Council of Science Editors:

Ngoje PO. Synthons of UDP-<i>N</i>-acetyl-L-Fucosamine (UDP-L-FucNAc) as potential inhibitors of <i>Staphylococcus aureus</i> Capsular Polysaccharide Biosynthesis. [Masters Thesis]. Youngstown State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1441880943

23. Kwarkoh, Angela. Conversion of Alcohols to Alkyl Azides Using <i>O</i>-Nitrobenzenesulfonyl Azide.

Degree: MSin Chemistry, Department of Chemistry, 2013, Youngstown State University

 In this thesis, primary alcohols, secondary alcohols as well as sugars were successfully converted to their corresponding alkyl azides using <i>o</i>-nitrobenzesulfonyl azide as the azide… (more)

Subjects/Keywords: Analytical Chemistry; Chemistry; Organic Chemistry; o-nitrobenzesulfonyl azide; alkyl azides; alcholos; n-butyllithium

…of Youngstown State University who synthesized organic azides using pABSA as the azide… 

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APA (6th Edition):

Kwarkoh, A. (2013). Conversion of Alcohols to Alkyl Azides Using <i>O</i>-Nitrobenzenesulfonyl Azide. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1380022166

Chicago Manual of Style (16th Edition):

Kwarkoh, Angela. “Conversion of Alcohols to Alkyl Azides Using <i>O</i>-Nitrobenzenesulfonyl Azide.” 2013. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1380022166.

MLA Handbook (7th Edition):

Kwarkoh, Angela. “Conversion of Alcohols to Alkyl Azides Using <i>O</i>-Nitrobenzenesulfonyl Azide.” 2013. Web. 17 Aug 2019.

Vancouver:

Kwarkoh A. Conversion of Alcohols to Alkyl Azides Using <i>O</i>-Nitrobenzenesulfonyl Azide. [Internet] [Masters thesis]. Youngstown State University; 2013. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1380022166.

Council of Science Editors:

Kwarkoh A. Conversion of Alcohols to Alkyl Azides Using <i>O</i>-Nitrobenzenesulfonyl Azide. [Masters Thesis]. Youngstown State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1380022166

24. Adero, Philip O. Heterocycle Synthesis via Rhodium (II)-Catalyzed Azido Carbenoid Cyclization.

Degree: MSin Chemistry, Department of Chemistry, 2012, Youngstown State University

 Rhodium (II)-catalyzed reactions of diazocarbonyl compounds have been a very fertile field for the development of new synthetic methods. The resulting metal-carbenoid intermediates are capable… (more)

Subjects/Keywords: Chemistry; Inorganic Chemistry; Organic Chemistry; Pharmaceuticals; Azido carbenoid; cyclization; heterocycle; rhodium(II)-catalyzed

…of Masters of Science in the Chemistry Program YOUNGSTOWN STATE UNIVERSITY August, 2012… …Youngstown State University and the School of Graduate Studies for giving me the opportunity to… 

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APA (6th Edition):

Adero, P. O. (2012). Heterocycle Synthesis via Rhodium (II)-Catalyzed Azido Carbenoid Cyclization. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1348595887

Chicago Manual of Style (16th Edition):

Adero, Philip O. “Heterocycle Synthesis via Rhodium (II)-Catalyzed Azido Carbenoid Cyclization.” 2012. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1348595887.

MLA Handbook (7th Edition):

Adero, Philip O. “Heterocycle Synthesis via Rhodium (II)-Catalyzed Azido Carbenoid Cyclization.” 2012. Web. 17 Aug 2019.

Vancouver:

Adero PO. Heterocycle Synthesis via Rhodium (II)-Catalyzed Azido Carbenoid Cyclization. [Internet] [Masters thesis]. Youngstown State University; 2012. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1348595887.

Council of Science Editors:

Adero PO. Heterocycle Synthesis via Rhodium (II)-Catalyzed Azido Carbenoid Cyclization. [Masters Thesis]. Youngstown State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1348595887

25. Mills, Isaac N. Click Chemistry Synthesis of Neoglycooligomers and Neoglycopolymers.

Degree: MSin Chemistry, Department of Chemistry, 2012, Youngstown State University

 This thesis deals with the click chemistry synthesis of neoglycooligomers and the attempted click chemistry synthesis of a neoglycopolymer. Experimentation led to successful synthesis of… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; neoglycooligomer; neoglycopolymer; carbohydrate; click chemistry

…at Youngstown State University.[19] In this method, an acetylated carbohydrate… 

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APA (6th Edition):

Mills, I. N. (2012). Click Chemistry Synthesis of Neoglycooligomers and Neoglycopolymers. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1348850012

Chicago Manual of Style (16th Edition):

Mills, Isaac N. “Click Chemistry Synthesis of Neoglycooligomers and Neoglycopolymers.” 2012. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1348850012.

MLA Handbook (7th Edition):

Mills, Isaac N. “Click Chemistry Synthesis of Neoglycooligomers and Neoglycopolymers.” 2012. Web. 17 Aug 2019.

Vancouver:

Mills IN. Click Chemistry Synthesis of Neoglycooligomers and Neoglycopolymers. [Internet] [Masters thesis]. Youngstown State University; 2012. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1348850012.

Council of Science Editors:

Mills IN. Click Chemistry Synthesis of Neoglycooligomers and Neoglycopolymers. [Masters Thesis]. Youngstown State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1348850012

26. Curry, Omadee S. Reaction of o-Nitrobenzenesulfonyl Azide/n-Butyl Lithium with Hindered Alcohols.

Degree: MSin Chemistry, Department of Chemistry, 2013, Youngstown State University

 This thesis utilizes the method of "One Pot" synthesis to synthesize a series of alkyl functional groups. These group include...an alkyl azide, alkyl esters, and… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Bimolecular nucleophilic substitution with Hindered Alcohols

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APA (6th Edition):

Curry, O. S. (2013). Reaction of o-Nitrobenzenesulfonyl Azide/n-Butyl Lithium with Hindered Alcohols. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1379945812

Chicago Manual of Style (16th Edition):

Curry, Omadee S. “Reaction of o-Nitrobenzenesulfonyl Azide/n-Butyl Lithium with Hindered Alcohols.” 2013. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1379945812.

MLA Handbook (7th Edition):

Curry, Omadee S. “Reaction of o-Nitrobenzenesulfonyl Azide/n-Butyl Lithium with Hindered Alcohols.” 2013. Web. 17 Aug 2019.

Vancouver:

Curry OS. Reaction of o-Nitrobenzenesulfonyl Azide/n-Butyl Lithium with Hindered Alcohols. [Internet] [Masters thesis]. Youngstown State University; 2013. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1379945812.

Council of Science Editors:

Curry OS. Reaction of o-Nitrobenzenesulfonyl Azide/n-Butyl Lithium with Hindered Alcohols. [Masters Thesis]. Youngstown State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1379945812


Youngstown State University

27. Wei, Li. Studies towards the synthesis of new carbohydrate-derived heterocycles.

Degree: MSin Chemistry, Department of Chemistry, 1998, Youngstown State University

The purpose of this research is to study the synthesis of novel carbohydrate-derived heterocycles by using 1,3-dipole (nitrile oxide), the synthesis of new C-glycosides by using sulfonium-ylide and Wittig reagent, and the preparation of carbohydrate-derived azides. Advisors/Committee Members: Norris, Peter (Advisor).

Subjects/Keywords: heterocycles; 1,3-dipole

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APA (6th Edition):

Wei, L. (1998). Studies towards the synthesis of new carbohydrate-derived heterocycles. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu997108452

Chicago Manual of Style (16th Edition):

Wei, Li. “Studies towards the synthesis of new carbohydrate-derived heterocycles.” 1998. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu997108452.

MLA Handbook (7th Edition):

Wei, Li. “Studies towards the synthesis of new carbohydrate-derived heterocycles.” 1998. Web. 17 Aug 2019.

Vancouver:

Wei L. Studies towards the synthesis of new carbohydrate-derived heterocycles. [Internet] [Masters thesis]. Youngstown State University; 1998. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu997108452.

Council of Science Editors:

Wei L. Studies towards the synthesis of new carbohydrate-derived heterocycles. [Masters Thesis]. Youngstown State University; 1998. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu997108452


Youngstown State University

28. Moore, Martin. New Dipolar Cycloaddition reactions of a Carbohydrate-derived Vinyl Sulfoxide Alkyne Equivalent and a Polymer-supported Alkyne with Azides.

Degree: MSin Chemistry, Department of Chemistry, 1998, Youngstown State University

 This attempted synthesis of a class of carbohydrate analogs known as pseudodisaccharides and the study of soluble polymer supports were the focus of this research.… (more)

Subjects/Keywords: pseudodisaccharides; polymer support; carbohydrates

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APA (6th Edition):

Moore, M. (1998). New Dipolar Cycloaddition reactions of a Carbohydrate-derived Vinyl Sulfoxide Alkyne Equivalent and a Polymer-supported Alkyne with Azides. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu997197481

Chicago Manual of Style (16th Edition):

Moore, Martin. “New Dipolar Cycloaddition reactions of a Carbohydrate-derived Vinyl Sulfoxide Alkyne Equivalent and a Polymer-supported Alkyne with Azides.” 1998. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu997197481.

MLA Handbook (7th Edition):

Moore, Martin. “New Dipolar Cycloaddition reactions of a Carbohydrate-derived Vinyl Sulfoxide Alkyne Equivalent and a Polymer-supported Alkyne with Azides.” 1998. Web. 17 Aug 2019.

Vancouver:

Moore M. New Dipolar Cycloaddition reactions of a Carbohydrate-derived Vinyl Sulfoxide Alkyne Equivalent and a Polymer-supported Alkyne with Azides. [Internet] [Masters thesis]. Youngstown State University; 1998. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu997197481.

Council of Science Editors:

Moore M. New Dipolar Cycloaddition reactions of a Carbohydrate-derived Vinyl Sulfoxide Alkyne Equivalent and a Polymer-supported Alkyne with Azides. [Masters Thesis]. Youngstown State University; 1998. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu997197481


Youngstown State University

29. Cicchillo, Robert Michael. Formation of C-Glyosides via Dithioacetal Chemistry.

Degree: MSin Chemistry, Department of Chemistry, 2000, Youngstown State University

 The following work describes new synthetic routes toward C-glycosides with an emphasis on the total stereoselective formation of C-disaccharides. Several different approaches to C-glycosides have… (more)

Subjects/Keywords: Chemistry, General; Dithioacetal Chemistry

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

APA (6th Edition):

Cicchillo, R. M. (2000). Formation of C-Glyosides via Dithioacetal Chemistry. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1004539703

Chicago Manual of Style (16th Edition):

Cicchillo, Robert Michael. “Formation of C-Glyosides via Dithioacetal Chemistry.” 2000. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1004539703.

MLA Handbook (7th Edition):

Cicchillo, Robert Michael. “Formation of C-Glyosides via Dithioacetal Chemistry.” 2000. Web. 17 Aug 2019.

Vancouver:

Cicchillo RM. Formation of C-Glyosides via Dithioacetal Chemistry. [Internet] [Masters thesis]. Youngstown State University; 2000. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1004539703.

Council of Science Editors:

Cicchillo RM. Formation of C-Glyosides via Dithioacetal Chemistry. [Masters Thesis]. Youngstown State University; 2000. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1004539703


Youngstown State University

30. Fluxe, Andrew James. Studies Toward the Synthesis of Aminosugars Related to Components of the S. aureus Capsular Polysaccharide.

Degree: MSin Chemistry, Department of Chemistry, 2001, Youngstown State University

 The following work describes new synthetic pathways toward one of the monosaccharide units, and analogs thereof, of the Staphylococcus aureus Type 5 and Type 8… (more)

Subjects/Keywords: Chemistry, General; Monosaccharides; Poloysaccharides; Staphylococcus aureus

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

APA (6th Edition):

Fluxe, A. J. (2001). Studies Toward the Synthesis of Aminosugars Related to Components of the S. aureus Capsular Polysaccharide. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1008343078

Chicago Manual of Style (16th Edition):

Fluxe, Andrew James. “Studies Toward the Synthesis of Aminosugars Related to Components of the S. aureus Capsular Polysaccharide.” 2001. Masters Thesis, Youngstown State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1008343078.

MLA Handbook (7th Edition):

Fluxe, Andrew James. “Studies Toward the Synthesis of Aminosugars Related to Components of the S. aureus Capsular Polysaccharide.” 2001. Web. 17 Aug 2019.

Vancouver:

Fluxe AJ. Studies Toward the Synthesis of Aminosugars Related to Components of the S. aureus Capsular Polysaccharide. [Internet] [Masters thesis]. Youngstown State University; 2001. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1008343078.

Council of Science Editors:

Fluxe AJ. Studies Toward the Synthesis of Aminosugars Related to Components of the S. aureus Capsular Polysaccharide. [Masters Thesis]. Youngstown State University; 2001. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1008343078

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