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University: The Ohio State University

You searched for subject:(Organic Chemistry). Showing records 1 – 30 of 131 total matches.

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The Ohio State University

1. Duvvuri, Krishnaja. Transition Metal Catalyzed Enantioselective Hydroboration and Hydrovinylation of Alkenes.

Degree: PhD, Chemistry, 2018, The Ohio State University

 Economic methods to stitch feedstocks onto molecules using chemical synthesis can greatly impact the design and manufacture of molecules, from medicine to materials. For example,… (more)

Subjects/Keywords: Chemistry; Organic Chemistry

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APA (6th Edition):

Duvvuri, K. (2018). Transition Metal Catalyzed Enantioselective Hydroboration and Hydrovinylation of Alkenes. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1524049349604356

Chicago Manual of Style (16th Edition):

Duvvuri, Krishnaja. “Transition Metal Catalyzed Enantioselective Hydroboration and Hydrovinylation of Alkenes.” 2018. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1524049349604356.

MLA Handbook (7th Edition):

Duvvuri, Krishnaja. “Transition Metal Catalyzed Enantioselective Hydroboration and Hydrovinylation of Alkenes.” 2018. Web. 24 Jul 2019.

Vancouver:

Duvvuri K. Transition Metal Catalyzed Enantioselective Hydroboration and Hydrovinylation of Alkenes. [Internet] [Doctoral dissertation]. The Ohio State University; 2018. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1524049349604356.

Council of Science Editors:

Duvvuri K. Transition Metal Catalyzed Enantioselective Hydroboration and Hydrovinylation of Alkenes. [Doctoral Dissertation]. The Ohio State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1524049349604356


The Ohio State University

2. Wappes, Ethan Albert. Radical sp3 C-H Functionalization of Amines and Alcohols.

Degree: PhD, Chemistry, 2019, The Ohio State University

 As our world continues to connect and develop, the need for new medicines and treatments for emerging diseases steadily grows. In recent years, global epidemics… (more)

Subjects/Keywords: Chemistry; Organic Chemistry

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APA (6th Edition):

Wappes, E. A. (2019). Radical sp3 C-H Functionalization of Amines and Alcohols. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1555519030868564

Chicago Manual of Style (16th Edition):

Wappes, Ethan Albert. “Radical sp3 C-H Functionalization of Amines and Alcohols.” 2019. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1555519030868564.

MLA Handbook (7th Edition):

Wappes, Ethan Albert. “Radical sp3 C-H Functionalization of Amines and Alcohols.” 2019. Web. 24 Jul 2019.

Vancouver:

Wappes EA. Radical sp3 C-H Functionalization of Amines and Alcohols. [Internet] [Doctoral dissertation]. The Ohio State University; 2019. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1555519030868564.

Council of Science Editors:

Wappes EA. Radical sp3 C-H Functionalization of Amines and Alcohols. [Doctoral Dissertation]. The Ohio State University; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1555519030868564


The Ohio State University

3. Van Ness, Brandon Garrett. Towards the Synthesis of Aplysqualenol A and B.

Degree: PhD, Chemistry, 2012, The Ohio State University

  Aplysqualenol A, a triterpenoid marine natural product, has shown a wide variety of biological activity, including anti-viral activity against the Herpes Simplex viruses and… (more)

Subjects/Keywords: Organic Chemistry

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APA (6th Edition):

Van Ness, B. G. (2012). Towards the Synthesis of Aplysqualenol A and B. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1343741321

Chicago Manual of Style (16th Edition):

Van Ness, Brandon Garrett. “Towards the Synthesis of Aplysqualenol A and B.” 2012. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1343741321.

MLA Handbook (7th Edition):

Van Ness, Brandon Garrett. “Towards the Synthesis of Aplysqualenol A and B.” 2012. Web. 24 Jul 2019.

Vancouver:

Van Ness BG. Towards the Synthesis of Aplysqualenol A and B. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1343741321.

Council of Science Editors:

Van Ness BG. Towards the Synthesis of Aplysqualenol A and B. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1343741321


The Ohio State University

4. Mitra, Soumya. Total synthesis of gomisin O; asymmetric total syntheses of eupomatilones 1, 2 and 5; and studies towards total synthesis of mayolide A.

Degree: PhD, Chemistry, 2007, The Ohio State University

 Gomisins are oriental medicinal plant lignans characterized by a highly electron-rich dibenzocyclooctadiene core structure with a stereogenic axis about the biaryl bond, exhibiting atropisomerism. The… (more)

Subjects/Keywords: Chemistry; Organic

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APA (6th Edition):

Mitra, S. (2007). Total synthesis of gomisin O; asymmetric total syntheses of eupomatilones 1, 2 and 5; and studies towards total synthesis of mayolide A. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1189449580

Chicago Manual of Style (16th Edition):

Mitra, Soumya. “Total synthesis of gomisin O; asymmetric total syntheses of eupomatilones 1, 2 and 5; and studies towards total synthesis of mayolide A.” 2007. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1189449580.

MLA Handbook (7th Edition):

Mitra, Soumya. “Total synthesis of gomisin O; asymmetric total syntheses of eupomatilones 1, 2 and 5; and studies towards total synthesis of mayolide A.” 2007. Web. 24 Jul 2019.

Vancouver:

Mitra S. Total synthesis of gomisin O; asymmetric total syntheses of eupomatilones 1, 2 and 5; and studies towards total synthesis of mayolide A. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1189449580.

Council of Science Editors:

Mitra S. Total synthesis of gomisin O; asymmetric total syntheses of eupomatilones 1, 2 and 5; and studies towards total synthesis of mayolide A. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1189449580


The Ohio State University

5. Detty, Michael Ray. Conjugative and Homoconjugative Interactions of Cyclopropane Rings in Neutral and Cationic Systems.

Degree: PhD, Chemistry, 1977, The Ohio State University

none Advisors/Committee Members: Paquette, Leo A. (Advisor).

Subjects/Keywords: Organic Chemistry

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APA (6th Edition):

Detty, M. R. (1977). Conjugative and Homoconjugative Interactions of Cyclopropane Rings in Neutral and Cationic Systems. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1381857458

Chicago Manual of Style (16th Edition):

Detty, Michael Ray. “Conjugative and Homoconjugative Interactions of Cyclopropane Rings in Neutral and Cationic Systems.” 1977. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1381857458.

MLA Handbook (7th Edition):

Detty, Michael Ray. “Conjugative and Homoconjugative Interactions of Cyclopropane Rings in Neutral and Cationic Systems.” 1977. Web. 24 Jul 2019.

Vancouver:

Detty MR. Conjugative and Homoconjugative Interactions of Cyclopropane Rings in Neutral and Cationic Systems. [Internet] [Doctoral dissertation]. The Ohio State University; 1977. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1381857458.

Council of Science Editors:

Detty MR. Conjugative and Homoconjugative Interactions of Cyclopropane Rings in Neutral and Cationic Systems. [Doctoral Dissertation]. The Ohio State University; 1977. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1381857458


The Ohio State University

6. Barringer, Donald Frederic. Investigations of the synthesis of polycyclic aromatic hydrocarbons containing seven-membered rings.

Degree: PhD, Chemistry, 1960, The Ohio State University

none Advisors/Committee Members: Cava, M. P. (Advisor).

Subjects/Keywords: Organic Chemistry

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APA (6th Edition):

Barringer, D. F. (1960). Investigations of the synthesis of polycyclic aromatic hydrocarbons containing seven-membered rings. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1392109313

Chicago Manual of Style (16th Edition):

Barringer, Donald Frederic. “Investigations of the synthesis of polycyclic aromatic hydrocarbons containing seven-membered rings.” 1960. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1392109313.

MLA Handbook (7th Edition):

Barringer, Donald Frederic. “Investigations of the synthesis of polycyclic aromatic hydrocarbons containing seven-membered rings.” 1960. Web. 24 Jul 2019.

Vancouver:

Barringer DF. Investigations of the synthesis of polycyclic aromatic hydrocarbons containing seven-membered rings. [Internet] [Doctoral dissertation]. The Ohio State University; 1960. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1392109313.

Council of Science Editors:

Barringer DF. Investigations of the synthesis of polycyclic aromatic hydrocarbons containing seven-membered rings. [Doctoral Dissertation]. The Ohio State University; 1960. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1392109313


The Ohio State University

7. Slater, Carl David. The effect of substituents in the rearrangement of allyl m-X-phenyl ethers.

Degree: PhD, Chemistry, 1960, The Ohio State University

none Advisors/Committee Members: White, William N. (Advisor).

Subjects/Keywords: Organic Chemistry

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APA (6th Edition):

Slater, C. D. (1960). The effect of substituents in the rearrangement of allyl m-X-phenyl ethers. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1392912554

Chicago Manual of Style (16th Edition):

Slater, Carl David. “The effect of substituents in the rearrangement of allyl m-X-phenyl ethers.” 1960. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1392912554.

MLA Handbook (7th Edition):

Slater, Carl David. “The effect of substituents in the rearrangement of allyl m-X-phenyl ethers.” 1960. Web. 24 Jul 2019.

Vancouver:

Slater CD. The effect of substituents in the rearrangement of allyl m-X-phenyl ethers. [Internet] [Doctoral dissertation]. The Ohio State University; 1960. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1392912554.

Council of Science Editors:

Slater CD. The effect of substituents in the rearrangement of allyl m-X-phenyl ethers. [Doctoral Dissertation]. The Ohio State University; 1960. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1392912554


The Ohio State University

8. Hartung, Ryan Eugene. I. Synthesis of saturated, DNA, and RNA spirocyclic-4,4-nonane nucleosides. II. Studies toward epoxy carbonate formation and the synthesis of suitable precursors III. Methodological investigations involving the reactions of diazomethane with di-, tri-, an.

Degree: PhD, Chemistry, 2005, The Ohio State University

 Nucleoside analogues, which can be incorporated into oligonucleotide chains, are of considerable current interest in the fight against cancer. When viral reverse transcriptase enzymes encounter… (more)

Subjects/Keywords: Chemistry; Organic

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APA (6th Edition):

Hartung, R. E. (2005). I. Synthesis of saturated, DNA, and RNA spirocyclic-4,4-nonane nucleosides. II. Studies toward epoxy carbonate formation and the synthesis of suitable precursors III. Methodological investigations involving the reactions of diazomethane with di-, tri-, an. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1130940224

Chicago Manual of Style (16th Edition):

Hartung, Ryan Eugene. “I. Synthesis of saturated, DNA, and RNA spirocyclic-4,4-nonane nucleosides. II. Studies toward epoxy carbonate formation and the synthesis of suitable precursors III. Methodological investigations involving the reactions of diazomethane with di-, tri-, an.” 2005. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1130940224.

MLA Handbook (7th Edition):

Hartung, Ryan Eugene. “I. Synthesis of saturated, DNA, and RNA spirocyclic-4,4-nonane nucleosides. II. Studies toward epoxy carbonate formation and the synthesis of suitable precursors III. Methodological investigations involving the reactions of diazomethane with di-, tri-, an.” 2005. Web. 24 Jul 2019.

Vancouver:

Hartung RE. I. Synthesis of saturated, DNA, and RNA spirocyclic-4,4-nonane nucleosides. II. Studies toward epoxy carbonate formation and the synthesis of suitable precursors III. Methodological investigations involving the reactions of diazomethane with di-, tri-, an. [Internet] [Doctoral dissertation]. The Ohio State University; 2005. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1130940224.

Council of Science Editors:

Hartung RE. I. Synthesis of saturated, DNA, and RNA spirocyclic-4,4-nonane nucleosides. II. Studies toward epoxy carbonate formation and the synthesis of suitable precursors III. Methodological investigations involving the reactions of diazomethane with di-, tri-, an. [Doctoral Dissertation]. The Ohio State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1130940224


The Ohio State University

9. Chang, Shuh-Kuen. Studies toward the total synthesis of amphidinol 3.

Degree: PhD, Chemistry, 2006, The Ohio State University

 Amphidinol 3, one of dinoflagellate derived polyketides, has attracted much attention as a potential therapeutic compound due to its potent membrane-permeabilizing activities in terms of… (more)

Subjects/Keywords: Chemistry; Organic

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APA (6th Edition):

Chang, S. (2006). Studies toward the total synthesis of amphidinol 3. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1150261354

Chicago Manual of Style (16th Edition):

Chang, Shuh-Kuen. “Studies toward the total synthesis of amphidinol 3.” 2006. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1150261354.

MLA Handbook (7th Edition):

Chang, Shuh-Kuen. “Studies toward the total synthesis of amphidinol 3.” 2006. Web. 24 Jul 2019.

Vancouver:

Chang S. Studies toward the total synthesis of amphidinol 3. [Internet] [Doctoral dissertation]. The Ohio State University; 2006. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1150261354.

Council of Science Editors:

Chang S. Studies toward the total synthesis of amphidinol 3. [Doctoral Dissertation]. The Ohio State University; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1150261354


The Ohio State University

10. Peng, Xiaowen. Total synthesis of the phytopathogen (+)-fomannosin.

Degree: PhD, Chemistry, 2006, The Ohio State University

 Fomannosin (1) is a sesquiterpene metabolite isolated in 1967 from the medium of the still culture of the wood-rotting fungus, Fomes annosus (Kr.) Karst. It… (more)

Subjects/Keywords: Chemistry; Organic

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APA (6th Edition):

Peng, X. (2006). Total synthesis of the phytopathogen (+)-fomannosin. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1155158634

Chicago Manual of Style (16th Edition):

Peng, Xiaowen. “Total synthesis of the phytopathogen (+)-fomannosin.” 2006. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1155158634.

MLA Handbook (7th Edition):

Peng, Xiaowen. “Total synthesis of the phytopathogen (+)-fomannosin.” 2006. Web. 24 Jul 2019.

Vancouver:

Peng X. Total synthesis of the phytopathogen (+)-fomannosin. [Internet] [Doctoral dissertation]. The Ohio State University; 2006. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1155158634.

Council of Science Editors:

Peng X. Total synthesis of the phytopathogen (+)-fomannosin. [Doctoral Dissertation]. The Ohio State University; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1155158634


The Ohio State University

11. Rhee, Jong. PartI. Synthesiss of <i>N</i>-heterocyclic furanosides and pyranosides via 5- or 6-Exo-<i>trig</i>-radical cyclization. Part II. (a) Palladium catalyzed silystannylative cyclization of diynes and allenynes (b) Regioselective Diels-Alder reaction of vinyls.

Degree: PhD, Chemistry, 2004, The Ohio State University

  Part One: The Barton-McCombie reaction has been widely acknowledged for the efficient deoxygenation of 2° alcohols through radical process. For the chain process, the… (more)

Subjects/Keywords: Chemistry, Organic; chemistry

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APA (6th Edition):

Rhee, J. (2004). PartI. Synthesiss of <i>N</i>-heterocyclic furanosides and pyranosides via 5- or 6-Exo-<i>trig</i>-radical cyclization. Part II. (a) Palladium catalyzed silystannylative cyclization of diynes and allenynes (b) Regioselective Diels-Alder reaction of vinyls. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1078850581

Chicago Manual of Style (16th Edition):

Rhee, Jong. “PartI. Synthesiss of <i>N</i>-heterocyclic furanosides and pyranosides via 5- or 6-Exo-<i>trig</i>-radical cyclization. Part II. (a) Palladium catalyzed silystannylative cyclization of diynes and allenynes (b) Regioselective Diels-Alder reaction of vinyls.” 2004. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1078850581.

MLA Handbook (7th Edition):

Rhee, Jong. “PartI. Synthesiss of <i>N</i>-heterocyclic furanosides and pyranosides via 5- or 6-Exo-<i>trig</i>-radical cyclization. Part II. (a) Palladium catalyzed silystannylative cyclization of diynes and allenynes (b) Regioselective Diels-Alder reaction of vinyls.” 2004. Web. 24 Jul 2019.

Vancouver:

Rhee J. PartI. Synthesiss of <i>N</i>-heterocyclic furanosides and pyranosides via 5- or 6-Exo-<i>trig</i>-radical cyclization. Part II. (a) Palladium catalyzed silystannylative cyclization of diynes and allenynes (b) Regioselective Diels-Alder reaction of vinyls. [Internet] [Doctoral dissertation]. The Ohio State University; 2004. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1078850581.

Council of Science Editors:

Rhee J. PartI. Synthesiss of <i>N</i>-heterocyclic furanosides and pyranosides via 5- or 6-Exo-<i>trig</i>-radical cyclization. Part II. (a) Palladium catalyzed silystannylative cyclization of diynes and allenynes (b) Regioselective Diels-Alder reaction of vinyls. [Doctoral Dissertation]. The Ohio State University; 2004. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1078850581


The Ohio State University

12. Campbell, Erica L. Total Synthesis of Lucilactaene and Efforts Towards the Total Synthesis of Ceratamines A and B.

Degree: PhD, Chemistry, 2008, The Ohio State University

  Lucilactaene, a cytotoxic natural product isolated from the fungi of the genus Fusarium in 2001 by Osada and co-workers, was found to arrest cell… (more)

Subjects/Keywords: Organic Chemistry; organic; chemistry; lucilactaene; ceratamine; synthesis; natural product

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APA (6th Edition):

Campbell, E. L. (2008). Total Synthesis of Lucilactaene and Efforts Towards the Total Synthesis of Ceratamines A and B. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1218650229

Chicago Manual of Style (16th Edition):

Campbell, Erica L. “Total Synthesis of Lucilactaene and Efforts Towards the Total Synthesis of Ceratamines A and B.” 2008. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1218650229.

MLA Handbook (7th Edition):

Campbell, Erica L. “Total Synthesis of Lucilactaene and Efforts Towards the Total Synthesis of Ceratamines A and B.” 2008. Web. 24 Jul 2019.

Vancouver:

Campbell EL. Total Synthesis of Lucilactaene and Efforts Towards the Total Synthesis of Ceratamines A and B. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218650229.

Council of Science Editors:

Campbell EL. Total Synthesis of Lucilactaene and Efforts Towards the Total Synthesis of Ceratamines A and B. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218650229


The Ohio State University

13. Baddeley, Christopher Peter. Structure-Function Studies of Modular Aromatics That Form Molecular Organogels.

Degree: MS, Chemistry, 2009, The Ohio State University

 Three urea-based aromatics 1-3, each with distinct steric and electronic characteristics,have been synthesized and their ability to undergo hierarchical assembly and gel organicsolvents investigated. We… (more)

Subjects/Keywords: Chemistry; Gels; Gelation; Physical Organic; ChemistryGels; Gelation; Physical Organic; Chemistry

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APA (6th Edition):

Baddeley, C. P. (2009). Structure-Function Studies of Modular Aromatics That Form Molecular Organogels. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1243445872

Chicago Manual of Style (16th Edition):

Baddeley, Christopher Peter. “Structure-Function Studies of Modular Aromatics That Form Molecular Organogels.” 2009. Masters Thesis, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1243445872.

MLA Handbook (7th Edition):

Baddeley, Christopher Peter. “Structure-Function Studies of Modular Aromatics That Form Molecular Organogels.” 2009. Web. 24 Jul 2019.

Vancouver:

Baddeley CP. Structure-Function Studies of Modular Aromatics That Form Molecular Organogels. [Internet] [Masters thesis]. The Ohio State University; 2009. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1243445872.

Council of Science Editors:

Baddeley CP. Structure-Function Studies of Modular Aromatics That Form Molecular Organogels. [Masters Thesis]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1243445872


The Ohio State University

14. Dewese, Kendra R. Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes.

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

 The catalysis of organic reactions by metal complexes is an effective way to improve atom economy and environmental friendliness for many synthetic transformations. Particularly, the… (more)

Subjects/Keywords: Organic Chemistry; Cobalt-Catalyzed Hydrofunctionalization; 1,3-Dienes; organic chemistry; synthetic transformations

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APA (6th Edition):

Dewese, K. R. (2016). Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1471783775

Chicago Manual of Style (16th Edition):

Dewese, Kendra R. “Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes.” 2016. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1471783775.

MLA Handbook (7th Edition):

Dewese, Kendra R. “Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes.” 2016. Web. 24 Jul 2019.

Vancouver:

Dewese KR. Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1471783775.

Council of Science Editors:

Dewese KR. Cobalt-Catalyzed Hydrofunctionalization of 1,3-Dienes. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1471783775


The Ohio State University

15. Kenton, Nathaniel T. Total Synthesis of Azaspiracid-3, C20-epi-Azaspiracid-3, and Structural Definition of the Azaspiracids.

Degree: PhD, Chemistry, 2018, The Ohio State University

 The azaspiracids are structurally complex marine toxins that have been linked to seafood-borne illness since their discovery in 1995 and structural elucidation in 1998. The… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; organic synthesis; natural products; marine toxins; azaspiracid

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APA (6th Edition):

Kenton, N. T. (2018). Total Synthesis of Azaspiracid-3, C20-epi-Azaspiracid-3, and Structural Definition of the Azaspiracids. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1523545452232749

Chicago Manual of Style (16th Edition):

Kenton, Nathaniel T. “Total Synthesis of Azaspiracid-3, C20-epi-Azaspiracid-3, and Structural Definition of the Azaspiracids.” 2018. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1523545452232749.

MLA Handbook (7th Edition):

Kenton, Nathaniel T. “Total Synthesis of Azaspiracid-3, C20-epi-Azaspiracid-3, and Structural Definition of the Azaspiracids.” 2018. Web. 24 Jul 2019.

Vancouver:

Kenton NT. Total Synthesis of Azaspiracid-3, C20-epi-Azaspiracid-3, and Structural Definition of the Azaspiracids. [Internet] [Doctoral dissertation]. The Ohio State University; 2018. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1523545452232749.

Council of Science Editors:

Kenton NT. Total Synthesis of Azaspiracid-3, C20-epi-Azaspiracid-3, and Structural Definition of the Azaspiracids. [Doctoral Dissertation]. The Ohio State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1523545452232749


The Ohio State University

16. Schwindeman, James A. Studies on the total synthesis of natural products.

Degree: PhD, Graduate School, 1981, The Ohio State University

Subjects/Keywords: Chemistry; Organic compounds

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APA (6th Edition):

Schwindeman, J. A. (1981). Studies on the total synthesis of natural products. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487157953418896

Chicago Manual of Style (16th Edition):

Schwindeman, James A. “Studies on the total synthesis of natural products.” 1981. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487157953418896.

MLA Handbook (7th Edition):

Schwindeman, James A. “Studies on the total synthesis of natural products.” 1981. Web. 24 Jul 2019.

Vancouver:

Schwindeman JA. Studies on the total synthesis of natural products. [Internet] [Doctoral dissertation]. The Ohio State University; 1981. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487157953418896.

Council of Science Editors:

Schwindeman JA. Studies on the total synthesis of natural products. [Doctoral Dissertation]. The Ohio State University; 1981. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487157953418896


The Ohio State University

17. Forties, Christina E. Synthesis and Characterization of a Ru Coordinated Azobenzene Metallofoldamer.

Degree: MS, Chemistry, 2008, The Ohio State University

 Inspired by naturally occurring molecules that fold, twist and interact, the formation and conformation of molecular structure is a wide area of research in synthetic… (more)

Subjects/Keywords: Chemistry; Metallofoldamer: metallated organic compounds; azobenzene oligomers

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APA (6th Edition):

Forties, C. E. (2008). Synthesis and Characterization of a Ru Coordinated Azobenzene Metallofoldamer. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1218630365

Chicago Manual of Style (16th Edition):

Forties, Christina E. “Synthesis and Characterization of a Ru Coordinated Azobenzene Metallofoldamer.” 2008. Masters Thesis, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1218630365.

MLA Handbook (7th Edition):

Forties, Christina E. “Synthesis and Characterization of a Ru Coordinated Azobenzene Metallofoldamer.” 2008. Web. 24 Jul 2019.

Vancouver:

Forties CE. Synthesis and Characterization of a Ru Coordinated Azobenzene Metallofoldamer. [Internet] [Masters thesis]. The Ohio State University; 2008. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218630365.

Council of Science Editors:

Forties CE. Synthesis and Characterization of a Ru Coordinated Azobenzene Metallofoldamer. [Masters Thesis]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218630365


The Ohio State University

18. Woodward, Robert L., Jr. Applications of Chemical Biology in Drug Discovery and Systems Biology: Fragment-based Design of Histone Deacetylase Inhibitors & A Chemical Approach to Understanding Polysaccharide Biosynthesis and Protein Glycosylation.

Degree: PhD, Chemistry, 2010, The Ohio State University

  The development of the field of chemical biology has highlighted the utility of chemically synthesized small molecules for the targeting and study of various… (more)

Subjects/Keywords: Organic Chemistry; histone deacetylase; polysaccharide; oligosaccharide; glycosylation

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APA (6th Edition):

Woodward, Robert L., J. (2010). Applications of Chemical Biology in Drug Discovery and Systems Biology: Fragment-based Design of Histone Deacetylase Inhibitors & A Chemical Approach to Understanding Polysaccharide Biosynthesis and Protein Glycosylation. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1275136100

Chicago Manual of Style (16th Edition):

Woodward, Robert L., Jr. “Applications of Chemical Biology in Drug Discovery and Systems Biology: Fragment-based Design of Histone Deacetylase Inhibitors & A Chemical Approach to Understanding Polysaccharide Biosynthesis and Protein Glycosylation.” 2010. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1275136100.

MLA Handbook (7th Edition):

Woodward, Robert L., Jr. “Applications of Chemical Biology in Drug Discovery and Systems Biology: Fragment-based Design of Histone Deacetylase Inhibitors & A Chemical Approach to Understanding Polysaccharide Biosynthesis and Protein Glycosylation.” 2010. Web. 24 Jul 2019.

Vancouver:

Woodward, Robert L. J. Applications of Chemical Biology in Drug Discovery and Systems Biology: Fragment-based Design of Histone Deacetylase Inhibitors & A Chemical Approach to Understanding Polysaccharide Biosynthesis and Protein Glycosylation. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1275136100.

Council of Science Editors:

Woodward, Robert L. J. Applications of Chemical Biology in Drug Discovery and Systems Biology: Fragment-based Design of Histone Deacetylase Inhibitors & A Chemical Approach to Understanding Polysaccharide Biosynthesis and Protein Glycosylation. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1275136100


The Ohio State University

19. Mier, Lynetta M. Electron Transfer Dynamics between 9-anthracenecarboxylic acid and TiO2 Nanoparticles with Applications for Novel Photovoltaic Devices.

Degree: MS, Chemistry, 2010, The Ohio State University

 We present work on the fundamental photophysics of electron transfer between 9-anthracenecarboxylic acid (9-AC) and TiO2 as a first step in understanding the photophysical properties… (more)

Subjects/Keywords: Chemistry; ultrafast spectroscopy; organic photovoltaics; electron transfer

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APA (6th Edition):

Mier, L. M. (2010). Electron Transfer Dynamics between 9-anthracenecarboxylic acid and TiO2 Nanoparticles with Applications for Novel Photovoltaic Devices. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1265921233

Chicago Manual of Style (16th Edition):

Mier, Lynetta M. “Electron Transfer Dynamics between 9-anthracenecarboxylic acid and TiO2 Nanoparticles with Applications for Novel Photovoltaic Devices.” 2010. Masters Thesis, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1265921233.

MLA Handbook (7th Edition):

Mier, Lynetta M. “Electron Transfer Dynamics between 9-anthracenecarboxylic acid and TiO2 Nanoparticles with Applications for Novel Photovoltaic Devices.” 2010. Web. 24 Jul 2019.

Vancouver:

Mier LM. Electron Transfer Dynamics between 9-anthracenecarboxylic acid and TiO2 Nanoparticles with Applications for Novel Photovoltaic Devices. [Internet] [Masters thesis]. The Ohio State University; 2010. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1265921233.

Council of Science Editors:

Mier LM. Electron Transfer Dynamics between 9-anthracenecarboxylic acid and TiO2 Nanoparticles with Applications for Novel Photovoltaic Devices. [Masters Thesis]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1265921233


The Ohio State University

20. Raya, Balaram. Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene.

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

Organic reactions catalyzed by metal complexes are an effective way to improve atom economy and environmental friendliness for many synthetic transformations. Among the various synthetic… (more)

Subjects/Keywords: Organic Chemistry; Cyclization, Hydrosilylation, Hydrogenation and Hydrovinylation

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APA (6th Edition):

Raya, B. (2016). Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1480602126518218

Chicago Manual of Style (16th Edition):

Raya, Balaram. “Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene.” 2016. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1480602126518218.

MLA Handbook (7th Edition):

Raya, Balaram. “Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene.” 2016. Web. 24 Jul 2019.

Vancouver:

Raya B. Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1480602126518218.

Council of Science Editors:

Raya B. Nickel and Cobalt-Catalyzed Hydrofunctionalization Reaction of Alkene. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1480602126518218


The Ohio State University

21. Butler, Sean Colin. Construction of the Carbon Skeleton of Salvinorin A.

Degree: PhD, Chemistry, 2011, The Ohio State University

  The Mexican sage, <i>Salvia divinorum</i>, has been used for many years by the Mazatec Indians of Oaxaca, Mexico for medicinal purposes and in religious… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Salvia divinorum; Salvia; Salvinorin; Organic synthesis; Diels&8211; Alder; Tsuji allylation

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APA (6th Edition):

Butler, S. C. (2011). Construction of the Carbon Skeleton of Salvinorin A. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1306524854

Chicago Manual of Style (16th Edition):

Butler, Sean Colin. “Construction of the Carbon Skeleton of Salvinorin A.” 2011. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1306524854.

MLA Handbook (7th Edition):

Butler, Sean Colin. “Construction of the Carbon Skeleton of Salvinorin A.” 2011. Web. 24 Jul 2019.

Vancouver:

Butler SC. Construction of the Carbon Skeleton of Salvinorin A. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1306524854.

Council of Science Editors:

Butler SC. Construction of the Carbon Skeleton of Salvinorin A. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1306524854


The Ohio State University

22. Varshneya, Pooja. Studies toward the total synthesis of hyperaspine.

Degree: PhD, Chemistry, 2007, The Ohio State University

  Ladybird beetles, commonly referred to as ladybugs, are part of the Coccinellidae family, which comprises approximately 5,200 species worldwide. Folk wisdom attributes good fortune… (more)

Subjects/Keywords: Chemistry, Organic; Natural Product Chemistry; N-Acyliminium Ion Cyclization

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APA (6th Edition):

Varshneya, P. (2007). Studies toward the total synthesis of hyperaspine. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1187044430

Chicago Manual of Style (16th Edition):

Varshneya, Pooja. “Studies toward the total synthesis of hyperaspine.” 2007. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1187044430.

MLA Handbook (7th Edition):

Varshneya, Pooja. “Studies toward the total synthesis of hyperaspine.” 2007. Web. 24 Jul 2019.

Vancouver:

Varshneya P. Studies toward the total synthesis of hyperaspine. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1187044430.

Council of Science Editors:

Varshneya P. Studies toward the total synthesis of hyperaspine. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1187044430


The Ohio State University

23. McDaniel, Christopher George. The Dendritic Effect on Enantioselectivity of Organocatalytic Reactions and the Effect of Local Compaction on a Titanium Mediated Allylation of Aldehydes.

Degree: PhD, Chemistry, 2010, The Ohio State University

 The synthesis, study and catalytic properties of chiral terminated dendrons based on an intramolecularly folded pyridine-2,6-dicarboxamide branch unit is reported. Two differently terminated chiral dendrons… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Dendrimers; dendrons; organocatalysis; kinetic resolution; allylation

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APA (6th Edition):

McDaniel, C. G. (2010). The Dendritic Effect on Enantioselectivity of Organocatalytic Reactions and the Effect of Local Compaction on a Titanium Mediated Allylation of Aldehydes. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1281293828

Chicago Manual of Style (16th Edition):

McDaniel, Christopher George. “The Dendritic Effect on Enantioselectivity of Organocatalytic Reactions and the Effect of Local Compaction on a Titanium Mediated Allylation of Aldehydes.” 2010. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1281293828.

MLA Handbook (7th Edition):

McDaniel, Christopher George. “The Dendritic Effect on Enantioselectivity of Organocatalytic Reactions and the Effect of Local Compaction on a Titanium Mediated Allylation of Aldehydes.” 2010. Web. 24 Jul 2019.

Vancouver:

McDaniel CG. The Dendritic Effect on Enantioselectivity of Organocatalytic Reactions and the Effect of Local Compaction on a Titanium Mediated Allylation of Aldehydes. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1281293828.

Council of Science Editors:

McDaniel CG. The Dendritic Effect on Enantioselectivity of Organocatalytic Reactions and the Effect of Local Compaction on a Titanium Mediated Allylation of Aldehydes. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1281293828


The Ohio State University

24. Tie, Chenyang. Conformation and Assembly Research on Dendron Derivatives: Azobenzene Oligomers and Dendritic Peptides.

Degree: PhD, Chemistry, 2010, The Ohio State University

 Chapter one covers latest azobenzene research. There are two parts on this review. First focuses on synthesis, conformation and photo energy transferring of azobenzene derivatives.… (more)

Subjects/Keywords: Chemistry; Materials Science; Organic Chemistry; Azobenzene; Dedron; Peptide; Nanoassembly

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APA (6th Edition):

Tie, C. (2010). Conformation and Assembly Research on Dendron Derivatives: Azobenzene Oligomers and Dendritic Peptides. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1282077432

Chicago Manual of Style (16th Edition):

Tie, Chenyang. “Conformation and Assembly Research on Dendron Derivatives: Azobenzene Oligomers and Dendritic Peptides.” 2010. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1282077432.

MLA Handbook (7th Edition):

Tie, Chenyang. “Conformation and Assembly Research on Dendron Derivatives: Azobenzene Oligomers and Dendritic Peptides.” 2010. Web. 24 Jul 2019.

Vancouver:

Tie C. Conformation and Assembly Research on Dendron Derivatives: Azobenzene Oligomers and Dendritic Peptides. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1282077432.

Council of Science Editors:

Tie C. Conformation and Assembly Research on Dendron Derivatives: Azobenzene Oligomers and Dendritic Peptides. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1282077432


The Ohio State University

25. Chellat, Mathieu François. Studies Toward the Total Synthesis and Structure Determination of Leiodelide A.

Degree: PhD, Chemistry, 2011, The Ohio State University

  Leiodelide A was isolated from the deep-water marine sponge Leiodermatium off the coast of Palau by Fenical and co-workers in 2006. Along with leiodelide… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; leiodelide A; total synthesis; macrolactone; oxazole; halogen dance

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APA (6th Edition):

Chellat, M. F. (2011). Studies Toward the Total Synthesis and Structure Determination of Leiodelide A. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1313173469

Chicago Manual of Style (16th Edition):

Chellat, Mathieu François. “Studies Toward the Total Synthesis and Structure Determination of Leiodelide A.” 2011. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1313173469.

MLA Handbook (7th Edition):

Chellat, Mathieu François. “Studies Toward the Total Synthesis and Structure Determination of Leiodelide A.” 2011. Web. 24 Jul 2019.

Vancouver:

Chellat MF. Studies Toward the Total Synthesis and Structure Determination of Leiodelide A. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1313173469.

Council of Science Editors:

Chellat MF. Studies Toward the Total Synthesis and Structure Determination of Leiodelide A. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1313173469


The Ohio State University

26. Okumu, Antony A. Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34.

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

 Azaspiracids are a class of marine natural products that accumulate in shellfish. Azaspiracid 1 was first reported in 1995 in the Netherlands after a poisoning… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Azaspiracid; Natural Product Synthesis; NHK Coupling

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APA (6th Edition):

Okumu, A. A. (2016). Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1461282755

Chicago Manual of Style (16th Edition):

Okumu, Antony A. “Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34.” 2016. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1461282755.

MLA Handbook (7th Edition):

Okumu, Antony A. “Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34.” 2016. Web. 24 Jul 2019.

Vancouver:

Okumu AA. Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1461282755.

Council of Science Editors:

Okumu AA. Toward Total Synthesis of Azaspiracid-3 and Azaspiracid-34. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1461282755


The Ohio State University

27. Akwaboah, Daniel C. Synthetic Study of Amphidinolides C, C2, C3, and F: Construction of the C1–C9 and the C10–C25 Building Blocks.

Degree: PhD, Chemistry, 2017, The Ohio State University

 Amphidinolides C, C2, C3, and F are cytotoxic secondary metabolites that occur naturally from symbiotic marine dinoflagellates Amphidinium sp. from the Okinawan flatworm. They share… (more)

Subjects/Keywords: Organic Chemistry; Chemistry; Amphidinolide C, total synthesis, marine natural products, anticancer

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APA (6th Edition):

Akwaboah, D. C. (2017). Synthetic Study of Amphidinolides C, C2, C3, and F: Construction of the C1–C9 and the C10–C25 Building Blocks. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1512079123614577

Chicago Manual of Style (16th Edition):

Akwaboah, Daniel C. “Synthetic Study of Amphidinolides C, C2, C3, and F: Construction of the C1–C9 and the C10–C25 Building Blocks.” 2017. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1512079123614577.

MLA Handbook (7th Edition):

Akwaboah, Daniel C. “Synthetic Study of Amphidinolides C, C2, C3, and F: Construction of the C1–C9 and the C10–C25 Building Blocks.” 2017. Web. 24 Jul 2019.

Vancouver:

Akwaboah DC. Synthetic Study of Amphidinolides C, C2, C3, and F: Construction of the C1–C9 and the C10–C25 Building Blocks. [Internet] [Doctoral dissertation]. The Ohio State University; 2017. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1512079123614577.

Council of Science Editors:

Akwaboah DC. Synthetic Study of Amphidinolides C, C2, C3, and F: Construction of the C1–C9 and the C10–C25 Building Blocks. [Doctoral Dissertation]. The Ohio State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1512079123614577

28. Hermann, Keith R. Novel Architectures in Cavitand Chemistry: Shaping Molecular Inner Space.

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

 As long as chemists have marveled at the specificity of interactions in enzymes, nucleic acids, and other biological motifs that contain an inner cavity, there… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Molecules

…Beilstein Journal of Organic Chemistry, 8, 90–99. Rieth, S., Hermann, K., Wang, B.-Y., & Badjić, J… …Catalyzed Cyclialkylation that Provides Rapid Access to a Twisted Molecular Basket. Chemistry – A… …Chemical Society Reviews, 40(3), 1609–1622. Fields of Study Major Field: Chemistry… …C4CS00140K. Copyrighted by Royal Society of Chemistry, 2014. 1.1 Introduction Since the first… …are capped with an amide functional group,23 and in non-competitive organic solvents form a… 

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APA (6th Edition):

Hermann, K. R. (2014). Novel Architectures in Cavitand Chemistry: Shaping Molecular Inner Space. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1406148569

Chicago Manual of Style (16th Edition):

Hermann, Keith R. “Novel Architectures in Cavitand Chemistry: Shaping Molecular Inner Space.” 2014. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1406148569.

MLA Handbook (7th Edition):

Hermann, Keith R. “Novel Architectures in Cavitand Chemistry: Shaping Molecular Inner Space.” 2014. Web. 24 Jul 2019.

Vancouver:

Hermann KR. Novel Architectures in Cavitand Chemistry: Shaping Molecular Inner Space. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1406148569.

Council of Science Editors:

Hermann KR. Novel Architectures in Cavitand Chemistry: Shaping Molecular Inner Space. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1406148569

29. Andert, William D. Palladium Catalyzed Suzuki-Miyaura Cross-Coupling of Axially Chiral Biaryls.

Degree: MS, Chemistry, 2013, The Ohio State University

 Cross-coupling reactions have been of interest to organic chemists much of the past century. It has only been in the last half century that prominent… (more)

Subjects/Keywords: Chemistry; Organic Chemistry

…transformations of organic chemistry involve the formation of carbon-carbon bonds. The carbon-carbon… …However, some of the most well known reactions used in organic chemistry are not atom economical… …chemistry has proved an invaluable tool in organic synthesis. When used in catalytic amounts… …solve some current questions in organic chemistry. 2 1.2 Axial Chirality in Natural Product… …organic chemistry. 1.3.1 Ullmann Coupling Several coupling reactions are well suited for use in… 

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

APA (6th Edition):

Andert, W. D. (2013). Palladium Catalyzed Suzuki-Miyaura Cross-Coupling of Axially Chiral Biaryls. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1367536419

Chicago Manual of Style (16th Edition):

Andert, William D. “Palladium Catalyzed Suzuki-Miyaura Cross-Coupling of Axially Chiral Biaryls.” 2013. Masters Thesis, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1367536419.

MLA Handbook (7th Edition):

Andert, William D. “Palladium Catalyzed Suzuki-Miyaura Cross-Coupling of Axially Chiral Biaryls.” 2013. Web. 24 Jul 2019.

Vancouver:

Andert WD. Palladium Catalyzed Suzuki-Miyaura Cross-Coupling of Axially Chiral Biaryls. [Internet] [Masters thesis]. The Ohio State University; 2013. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1367536419.

Council of Science Editors:

Andert WD. Palladium Catalyzed Suzuki-Miyaura Cross-Coupling of Axially Chiral Biaryls. [Masters Thesis]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1367536419

30. Line, Nathan. Total Synthesis of Salvinorin A via an IMDA-Tsuji Allylation Strategy.

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

 Salvia divinorum, a Mexican sage, was used for hundreds of years by the MazatecIndians for both medicinal and religious purposes. These hallucinogenic properties havecaused a… (more)

Subjects/Keywords: Organic Chemistry; Chemistry

…May 2011 .......................................................B.A. Chemistry, Wabash… …Research Associate Department of Chemistry and Biochemistry The Ohio State University… …Salvinorin A. J. Am. Chem. Soc. 2016, Submitted. FIELDS OF STUDY Major Field: Chemistry vii… …challenging target for organic chemists. Two separate groups, Ortega and Valdés, accomplished the… 

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

APA (6th Edition):

Line, N. (2016). Total Synthesis of Salvinorin A via an IMDA-Tsuji Allylation Strategy. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1461161309

Chicago Manual of Style (16th Edition):

Line, Nathan. “Total Synthesis of Salvinorin A via an IMDA-Tsuji Allylation Strategy.” 2016. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1461161309.

MLA Handbook (7th Edition):

Line, Nathan. “Total Synthesis of Salvinorin A via an IMDA-Tsuji Allylation Strategy.” 2016. Web. 24 Jul 2019.

Vancouver:

Line N. Total Synthesis of Salvinorin A via an IMDA-Tsuji Allylation Strategy. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1461161309.

Council of Science Editors:

Line N. Total Synthesis of Salvinorin A via an IMDA-Tsuji Allylation Strategy. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1461161309

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