Awesome
Doctor Carrick is easily my favorite professor I've ever had at Tennessee Tech University. He's the first professor that really made me adapt my study habits to prepare for quizzes and exams and to focus. He catches a lot of heat. It's only because he wants to push you to actually learn something about Organic Chemistry. He's very respected and not for the type of students that were unfocused.
Tennessee Tech University - Chemistry
Assistant Professor of Chemistry at TN Tech University
Research
Jesse
Carrick
Greater Nashville Area, TN
Specialties: Process Development, Total Synthesis, Asymmetric Synthesis, Catalysis, Methodology, Chemical Education
Graduate Research Assistant
Enhanced research skills related to the total synthesis of marine natural products during the completion of the formal synthesis of (-)-clavosolide A. Streamlined communication skills by serving as the laboratory instructor of organic chemistry for six semesters.
Assistant Professor of Chemistry
o Teaching: CHEM 3010/3020 (Organic Chemistry I/II Lecture and Lab),
CHEM 6210 (Advanced Organic Chemistry)
o Research: natural product total synthesis, synthesis of novel bis-1,2,4-triazines for minor actinide extraction, and catalytic C-H activation of alkenes.
o Service: Committees: student research grant (chair), new science building, NMR user, and organic chemistry tenure-track search. Faculty seminar coordinator
Senior Research Scientist, Chemical Development
Supplemented academic experience by performing applied pharmaceutical research on the process development and kilogram synthesis of APIs selected for scale up utilizing a variety of modern process analytical technologies including: HPLC, NMR, GC, LC/MS, and IR.
Graduate Research Assistant
Gained extensive experience in the total synthesis of natural products while completing the C18-C26 fragment of the marine natural product amphidinolide C. Continued this experience while working on the C10-C17 fragment of amphidinolide C. Expanded leadership capabilities by overseeing the discussion section for organic chemistry lectures and the accompanying laboratory course for four semesters.
Visiting Assistant Professor of Chemistry
Served as the instructor of record for Organic Chemistry I lecture/lab and General Chemistry I lab while engaged in natural product synthesis research with undergraduate students from diverse backgrounds.
Ph.D.
Organic Chemistry
Advisor: Prof. Michael P. Jennings, Dissertation title: The Formal Synthesis of (−)-Clavosolide A.
Graduate Research Assistant
Enhanced research skills related to the total synthesis of marine natural products during the completion of the formal synthesis of (-)-clavosolide A. Streamlined communication skills by serving as the laboratory instructor of organic chemistry for six semesters.
B.S
ACS-Certified Chemistry
Advisor: Prof. Norma K. Dunlap, Senior thesis: Progress Towards the Synthesis of Two Linear Peptidomimetics of D-Ala-D-Ala.
M.S
Organic Chemistry
Advisor: Prof. David R. Williams, Thesis title: Progress Towards the Total Synthesis of the Potent Antitumor Antibiotic Amphidinolide C.
Graduate Research Assistant
Gained extensive experience in the total synthesis of natural products while completing the C18-C26 fragment of the marine natural product amphidinolide C. Continued this experience while working on the C10-C17 fragment of amphidinolide C. Expanded leadership capabilities by overseeing the discussion section for organic chemistry lectures and the accompanying laboratory course for four semesters.
Tetrahedron Letters
Oxidative cleavage of a series of glycols using NaIO4 on silica gel in the presence of a series of stabilized ylides provides access to a number of synthetically useful alkenes. The ease and general utility of this reaction is demonstrated here using several carbohydrates and amino acid derived glycols.
Tetrahedron Letters
Oxidative cleavage of a series of glycols using NaIO4 on silica gel in the presence of a series of stabilized ylides provides access to a number of synthetically useful alkenes. The ease and general utility of this reaction is demonstrated here using several carbohydrates and amino acid derived glycols.
Organic Letters
The enantioselective formal synthesis of the polyketide marine natural product (−)-clavosolide A is presented. The construction of the β-C-glycoside subunit is highlighted by a one-pot oxocarbenium cation formation/reduction sequence. Yamaguchi dimerization afforded the diolide aglycon in 18 steps (longest linear sequence).