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Knisley Thesis .pdf (4.1 MB)
ETD Abstract Container
Abstract Header
Libraries from Libraries Approach to the Synthesis of Arylidene Oxindoles
Author Info
Knisley, Kyle James
Permalink:
http://rave.ohiolink.edu/etdc/view?acc_num=wright1388766101
Abstract Details
Year and Degree
2013, Master of Science (MS), Wright State University, Chemistry.
Abstract
A libraries from libraries combinatorial chemistry approach was employed to synthesize fluorinated derivatives of both oxindoles and isatins as potential pharmaceuticals or targeting agents for imaging purposes related to cancer or Alzheimer's disease. Synthesis for these fluorinated derivatives are described by routes involving, either: a) N-alkylation of 5-substituted isatins followed by Wolff-Kishner reduction to the corresponding oxindoles and final Knoevenagel condensation with aryl aldehydes, or; b) Wolff-Kishner reduction of the isatins followed by condensation and finishing with the N-alkylation of the aldol products. In specific cases, a click reaction followed the N-alkylation of the aldol products to form the isatin 1,2,3-triazole which could be utilized to perform radiochemistry with a [18F]-radiolabel for the imaging of cancer. The strategy for the synthesis of such potential inhibitors was guided by SAR studies of peptide based inhibitors, as well as small-molecule inhibitors based upon the isatins scaffold. Previously, it was shown increasing functionality by adding 3 points of variability with the incorporation of an electron-withdrawing group such as a chlorine atom at the C-5 position allowed for increased potency of the oxindole derived inhibitors. Herein, a library of arylidene oxindoles was synthesized utilizing 3 points of variability with the incorporation of the electron-withdrawing group fluorine. Furthermore, a novel alternative synthesis was established for the creation of arylidene oxindoles which allowed for increased functionality through the incorporation of N-propargyl inhibitors. Finally, the ability to create N-propargyl compounds lead to the synthesis of isatin 1,2,3-triazoles was also explored for the possibility as potential imaging agents for cancer.
Committee
Daniel Ketcha, Ph.D. (Advisor)
Eric Fossum, Ph.D. (Committee Member)
Kenneth Turnbull, Ph.D. (Committee Member)
Pages
222 p.
Subject Headings
Chemistry
Keywords
chemistry
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Citations
Knisley, K. J. (2013).
Libraries from Libraries Approach to the Synthesis of Arylidene Oxindoles
[Master's thesis, Wright State University]. OhioLINK Electronic Theses and Dissertations Center. http://rave.ohiolink.edu/etdc/view?acc_num=wright1388766101
APA Style (7th edition)
Knisley, Kyle.
Libraries from Libraries Approach to the Synthesis of Arylidene Oxindoles.
2013. Wright State University, Master's thesis.
OhioLINK Electronic Theses and Dissertations Center
, http://rave.ohiolink.edu/etdc/view?acc_num=wright1388766101.
MLA Style (8th edition)
Knisley, Kyle. "Libraries from Libraries Approach to the Synthesis of Arylidene Oxindoles." Master's thesis, Wright State University, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=wright1388766101
Chicago Manual of Style (17th edition)
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Document number:
wright1388766101
Download Count:
1,503
Copyright Info
© 2013, all rights reserved.
This open access ETD is published by Wright State University and OhioLINK.