Central Florida Memory
Collection
Browse All
Maps
Photographs
Postcards
Most Recent
More...
Advanced Search
Preferences
My Favorites
Help
Share
About the Project
Additional Resources
Credits & Contact Info
Partners
Tell Us What You Think
More Info...
Learn
Florida Stories
Teachers
Exhibits
More Info...
add to favorites
:
reference url
back to results
:
previous
:
next
PART I : ISOLATION OF DIPENTYL 2-(4-(PENTAN-3-YL) PHENYL) MALONATE FROM SANGUISORBA OFFICINALIS LABILL PART II: SYNTHESIS OF A NOVEL FAMILY OF ETHERS OF PODOCARPIC ACID
Access this item.
Title
PART
I
:
ISOLATION
OF
DIPENTYL
2-(4-(PENTAN-3-YL)
PHENYL)
MALONATE
FROM
SANGUISORBA
OFFICINALIS
LABILL
PART
II:
SYNTHESIS
OF A
NOVEL
FAMILY
OF
ETHERS
OF
PODOCARPIC
ACID
Author
Yalavarty, Manjeera
Keywords
podocarpic acid
sanguisorba officinalis
leukemia
Abstract
The
goal
of
part
I
of this
thesis
was to
isolate
pure
anti
cancer
compounds
from the
Russian
plant
Sanguisorba
officinalis.
This
plant
was
selected
for
investigation
because
it
showed
100%
activity
against
leukemia
(L1210
mouse
leukemia
cells)
during
the
preliminary
screening
of
approximately
100
Russian
plant
extracts.
This
work
has
resulted
in the
isolation
of
novel
compound
11
using
traditional
chromatography
techniques.
Compound
11
was
characterized
with
spectroscopic
techniques
such
as
IR
,
1H
NMR
,
13C
NMR
,
DEPT
,
DQCOSY
and
MS.
Compound
11
was
assigned
the
structure
dipentyl
2-(4-(pentan-3-yl)
phenyl)
malonate.
The
goal
of
part
II
of this
thesis
was to
synthesize
novel
ethers
of
podocarpic
acid.
Ethers
are of
great
interest
in
biological
studies
and
pharmaceutical
applications
because
of their
wide
variety
of
uses
in the
treatment
of
various
diseases.
A
novel
family
of
ether
derivatives
was
synthesized
using
podocarpic
acid
(a
natural
tricyclic
diterpene
derived
from
podocarpus
species)
as a
template.
Novel
ether
derivatives
of
podocarpic
acid
were
synthesized
from
podocarpic
acid
in
three
steps.
The
first
step
involved
methylation
of
podocarpic
acid
with
dimethyl
sulfate
to
form
methyl-o-methyl
podocarpate.
The
second
step
was
iodination
of
methyl-o-methyl
podocarpate
with
iodine
in
presence
of a
mercury
catalyst
to
form
13-iodo
methyl-o-methyl
podocarpate.
This was
followed
by
formation
of
novel
aliphatic
ethers
using
a
copper
catalyst.
Thus
this
research
had
led
to the
discovery
of
new
methodology
for
synthesis
of
three
novel
aliphatic
ether
derivatives
of
podocarpic
acid.
These
ethers
will be
tested
for their
biological
activity
against
various
types
of
cancer
,
tuberculosis
by
National
Institutes
of
Health.
Adviser
Miles, Howard
Publisher
University
of
Central
Florida
Degree
M.S.
Degree Discipline
Department of Chemistry
Degree Program
Industrial Chemistry
Graduation Date
2005-08-01
Type
Master's thesis
Access Level
Public - Allow Worldwide Access
Release Date
2008-08-01
Repository
University Archives
Repository Collection
Electronic Theses and Dissertations
Identifier
CFE0000625
Access Link
http://purl.fcla.edu/fcla/etd/CFE0000625
add to favorites
:
reference url
back to results
:
previous
:
next
powered by CONTENTdm
®
|
contact us
^ to top ^
About
Partners
Contact Us
LSTA
IMLS