Title
Cyclic enaminones: synthons for piperidine containing natural products and natural product analogs.
Abstract
Cyclic Enaminones: Synthons for Piperidine Containing Natural Products and Natural Product Analogs.
Cyclic enaminones are important synthetic intermediates for the preparation of
piperidine containing natural products and target molecules such as drugs, which require
a piperidine moiety for bioactivity. They are valuable synthons because of their unique
reactivity and chemical stability. In this thesis, I developed novel chemistry from which
to derivatize enaminones, and additionally I utilized cyclic enaminones as synthons for
the preparation of natural product derivatives.
I discovered that α,β-unsaturated aldehydes add to the α-carbon of enaminones in
the presence of organocatalysts and thereby, introduce aliphatic α-branched substituents;
a reaction that was previously very difficult to accomplish. The chiral reaction products
were obtained in good- to excellent yields and with high enantiopurity. The absolute
stereochemistry of the reaction products was also determined.
I prepared analogues of the cytotoxic phenanthropiperidines tylophorine and
boehmeriasin A, and I synthesized dihydrolyfoline, a member of a group of natural
biphenylquinolizidine lactone alkaloids that posses a wide variety of bioactivities. The
natural occurring cytotoxic phenanthropiperidines suffer from poor physiochemical
properties and adverse side effects. Thus, the target molecules were designed to mitigate
the unwanted side effects by improving their physiochemical properties. I devised short,
concise routes toward the synthesis of a library of simplified tylophorine analogs, as well as 15-hydroxyboehmeriasin A. The tylophorine analog library was screened for
antiproliferative activity against several cancer cell lines and thus, insight was gained into
the structure-activity relationships of this class of compounds including the indication
that an intact indolizidine moiety is critical for high potency of tylophorine analogues.
15-Hydroxyboehmeriasin A was prepared and evaluated for cytotoxicity against the
A549 human lung carcinoma cell line. An observed GI50 of 81 nM demonstrates that the
addition of the 15-hydroxyl group was not detrimental to cytotoxicity and that this
position should be explored for further modifications in efforts to improve the
physicochemical properties. In addition I prepared (±)-dihydrolyfoline in a concise
manner from a bicyclic enaminone precursor using a biomimetic oxidative biaryl coupling approach as the key reaction step.
Description
University of Minnesota Ph.D. dissertation. December 2012. Major: Medicinal Chemistry. Advisor: Gunda I. Georg. 1 computer file (PDF); xx, 282 pages.
Suggested Citation
Gay, Bryant Charles.
(2012).
Cyclic enaminones: synthons for piperidine containing natural products and natural product analogs..
Retrieved from the University of Minnesota Digital Conservancy,
https://hdl.handle.net/11299/143196.