Embed
Email

CURRICULUM VITAE

Document Sample
CURRICULUM VITAE
Shared by: HC111207235434
Categories
Tags
Stats
views:
10
posted:
12/7/2011
language:
pages:
6
Jason Anthony Deck



RESIDENCE: 4523 Cheltenham Dr

Bethesda, MD 20814

Phone: 512-699-5358

Email: jadeck@gmail.com



TITLE: Post Doctoral Intramural Research Training Awardee

Drug Design and Synthesis Section

Chemical Biology Research Branch

National Institute on Drug Abuse

National Institutes of Health

5625 Fishers Ln, Rm 4N-03, MSC 9415

Bethesda, MD 20892-9415

Phone: 301-435-1922

Fax: 301-402-0589

Email: deckj@nida.nih.gov

Website: www.jasondeck.com/career





CITIZENSHIP: United States Citizen





EDUCATION: PhD, Organic Chemistry, University of Texas at Austin, Austin, TX,

May 2007

Advisor: Professor Stephen F. Martin

Dissertation: “Studies Towards the Total Synthesis of

Condylocarpine and Studies Towards the Enantioselective

Synthesis of (+)-Methyl Lysergate”



MS, Organic Chemistry, University of New Mexico, Albuquerque, NM,

June 2000

Advisor: Professor David L. Vander Jagt



BS, Chemistry, Fort Lewis College, Durango, CO, June 1997





OTHER TRAINING: Principles of Clinical Pharmacology – NIH Clinical Center‟s Office of

Clinical Research Training and Medical Education (OCRTME)



Pharmacology – Foundation for Advanced Education in the Sciences

(FAES), NIH



Gordon Research Conference on Natural Products, 2010



9th Annual Florida Heterocyclic and Synthetic IUPAC-Sponsored

Conference (FloHet IX)



Searching the Beilstein Database with Crossfire/Reaxys – NIH Library



Searching the Chemical Abstracts Service (CAS) database with

SciFinder – NIH Library



Endnote Bibliography Software – UT Austin Library







1

PROFESSIONAL EXPERIENCE:



6/07 – Present: Postdoctoral Fellow IRTA, National Institute on Drug Abuse, Bethesda

and Rockville, MD

Advisor: Dr. Kenner C. Rice

Designed and synthesized novel phenylmorphans to evaluate as

potential high affinity ligands for selective opioid receptors and

analgesics. Identified critical parameters and optimized synthetic route

for chromatography free scale up and production of 5-(3-

methoxyphenyl)-2-methyl-9-oxo-2-azabicyclo[3.3.1]nonane.



8/00 – 5/07: Graduate Assistant, University of Texas at Austin, Austin, TX

Advisor: Professor Stephen F. Martin

Performed synthetic studies towards the total synthesis of the polycyclic,

cage like, indole alkaloid natural product condylocarpine via a dual

cyclization cascade.

Completed the first enantioselective total synthesis of the ergot alkaloid

natural product (+)-isolysergol featuring an unprecedented late stage

microwave mediated asymmetric ring closing metathesis (ARCM).



5/98 – 7/00: Graduate Assistant, University of New Mexico, Albuquerque, NM

Advisor: Professor David L. Vander Jagt

Designed and synthesized non-natural products as inhibitors of lactate

dehydrogenase (LDH) enzymes from the malaria parasite P. falciparum,

and protozoan parasite T. gondii.

Synthesized and characterized (via 2d-multinuclear NMR spectroscopy)

the moderately complex multicyclic heterocycles 2-thienyl-4(3H)-

quinazolinones.

Designed and implemented NMR spectroscopy lab course for organic

laboratory II with both practical instrument use and web based „canned‟

NMR assignments.



5/97 – 11/97: Lab Technician, University of New Mexico, Albuquerque, NM

Supervisor: Professor David L. Vander Jagt

Designed and modeled inhibitors of lactate dehydrogenase (LDH)

enzymes from both humans and the malaria parasite P. falciparum.

Synthesized dihydroxynaphthoic acids structurally related to the

cottonseed oil derived natural product gossypol for LDH inhibition

studies.



6/96 – 9/96: Summer Internship, University of New Mexico, Albuquerque, NM

Supervisor: Professor Mark J. Hampden-Smith

Synthesized organoindium compounds as potential window glass coating

precursors.



6/95 – 6/96: Undergraduate Research, Fort Lewis College, Durango, CO

Supervisor: Professor Irwin (Ike) L. Klundt

Synthesized pyrrole precursors for use as singlet oxygen traps.





TECHNICAL SKILLS:

Synthesis

Multistep organic and organometallic synthesis.

Bench top and air sensitive techniques.

Milligram to multigram scale.





2

Asymmetric enantioselective synthesis.

Optical resolution via chiral salts.

Chiral HPLC.

Compound Isolation and purification

Flash chromatography

HPLC

Distillation

Recrystallization

Sublimation

Liquid-liquid extraction

TLC

Preparative TLC

Radial chromatography

Compound Identification/Spectroscopy

1 13

NMR spectroscopy: H, C, COSY, HMQC, HMBC, NOESY,

VT, etc.

FT-IR

LRMS, GC-MS, HRMS

TLC

Chiral HPLC

Optical rotation

Computer skills

Windows, Mac OS, Linux, MS Office, ChemOffice, ISIS, MDL

Crossfire/Reaxys, SciFinder, Waters‟ Breeze and Empower,

Photoshop, GIMP, HTML/webpage construction and

deployment, internet and database searching





LEADERSHIP/MENTORSHIP:



Invented, prepared, and developed new chemical products utilizing

advanced chemical knowledge, data, modeling and statistical tools to

solve technical challenges.



Served as a team leader and advisor to other scientists.



Trained and supported chemists in instrument use and bench

techniques.



Purchased, set up, and maintained laboratory equipment, including

instruments such as HPLC, and trained researchers in their use.



Provided expert advice to other chemists on sampling, and instructed

other laboratory personnel in analysis techniques.



Strong interpersonal skills, and excellent organizational and

communication (written and verbal) skills.



Developed and implemented group meeting schedule to foster

communication between researchers.



Edited technical documents for content, grammar, and language for both

native and non-native English speakers.



Documented, interpreted and communicated results to colleagues and

supervisors.





3

Prepared summaries and reports addressing problems, deficiencies,

corrective actions taken, and recommendations for strengthening and

improving programs.



Worked both independently and cooperatively in a multidisciplinary

environment, collaborating with colleagues to develop innovative new

technology.



Attended technical meetings, read relevant reports and publications, and

provided technical assistance to researchers, supervisors, and the

public.



Lecture teaching assistant for organic 1 and 2.



Lab teaching assistant for general chemistry 1 and organic 2.



Designed and implemented NMR spectroscopy lab course for

undergraduates including web based assignments, UNM 1998-2000.



Directed the research of undergraduate students, UNM 1997-2000.



Fort Lewis College Chemistry Club, president, 1996-1997.





MEMBERSHIP IN PROFESSIONAL SOCIETIES:



1996 – Present American Chemical Society



2007 – Present Texas Exes, University of Texas alumni association





AWARDS AND OTHER SPECIAL RECOGNITION:



Dean's Excellence Award – UT Austin, 2000



Army Corps of Engineers Pre-Doctoral Fellowship – UNM, 1999



Clark Graduate Teaching Award – UNM, 1997





ORAL PRESENTATIONS:



“Enantioselective synthesis of (+)-isolysergol via ring closing metathesis”,

American Chemical Society Fall National Meeting, Boston, MA, 8/2010.



“Synthesis and structure-activity relationship of 5-(3-

hydroxy)phenylmorphans: Probes for narcotic receptor mediated

phenomena”, American Chemical Society Fall National Meeting,

Philadelphia, PA, 8/2008.









4

PUBLICATIONS:



Deck, J. A.; Rice, K. C. Synthesis and structure-activity relationship of 5-(3-

hydroxy)phenylmorphans: Probes for narcotic receptor mediated

phenomena. In Preparation.



Deck, J. A.; Martin, S. F. Enantioselective Total Synthesis of (+)-Isolysergol

via Asymmetric Ring Closing Metathesis. Organic Letters 2010, 12, 11, 2610-

2613.



Lee, S. B.; Park, J. H; Folk, J. E.; Deck, J. A.; Pegg, A. E.; Sokabe, M.;

Fraser, C. S.; Park, M. H. Inactivation of Eukaryotic Initiation Factor 5A

(eIF5A) by Specific Acetylation of its Hypusine Residue by

Spermidine/Spermine Acetyltransferase 1 (SSAT1). Submitted.



Kruiswijk, E.; Deck, J. A. Synthesis of Ammonium Compounds including N-

Ylides. In Science of Synthesis; Enders, D. Ed.; Vol 40; Georg Thieme

Verlag, 2008.



Assisted in editing “The Comprehensive E-book of named organic reactions

and their mechanisms” by E. Kruiswijk, edition 2.1

(www.namedorganicreactions.co.uk).



Stoddard Hatch, M.; Brown, W. M.; Deck, J. A.; Hunsaker, L. A.; Deck, L. M.;

Vander Jagt, D. L. Inhibition of yeast lipase (CRL1) and cholesterol esterase

(CRL3) by 6-chloro-2-pyrones: comparison with porcine cholesterol esterase.

Biochimica et Biophysica Acta 2002, 1596(2), 381-391.



Yu, Y.; Deck, J. A.; Hunsaker, L. A.; Deck, L. M.; Royer, R. E.; Goldberg, E.;

Vander Jagt, D. L. Selective active site inhibitors of human lactate

dehydrogenases A4, B4, and C4. Biochemical Pharmacology 2001, 62(1),

81-89.



Deck, L. M.; Turner, S. D.; Deck, J. A.; Papadopoulos, E. P. Synthesis of

derivatives of thiophene using methyl 2-isothiocyanatobenzoate. Journal of

Heterocyclic Chemistry 2001, 38(2), 343-347.





POSTER PRESENTATIONS:



“Studies Towards the Enantiocontrolled Total Synthesis of (+)-Methyl

th

Lysergate”, Stephen F. Martin 60 Birthday Symposium, University of Texas

at Austin, 2006.



“Dihydroxynaphthoic Acids as Inhibitors of Lactate Dehydrogenase”, Sevilleta

Research Symposium, Sevilleta National Wildlife Refuge, NM, 2000.



“Pan-active Site Inhibition: Inhibitor Specificity Through Competitive Binding

at both Substrate and Cofactor Sites”, Sevilleta Research Symposium,

Sevilleta National Wildlife Refuge, NM, 2000.



“Pancreatic Cholesterol Esterase: a Potential Drug Target in the Treatment of

Heart Disease and the Development of Selective Inhibitors”, Sevilleta

Research Symposium, Sevilleta National Wildlife Refuge, NM, 2000.









5

“Synthesis of Selective Inhibitors of Cholesterol Esterase”, Sevilleta

Research Symposium, Sevilleta National Wildlife Refuge, NM, 1999.



“Synthesis of Selective Inhibitors of Lactate Dehydrogenases”, Sevilleta

Research Symposium, Sevilleta National Wildlife Refuge, NM, 1999.



“Dihydroxynaphthoic Acids: A New Class of Active Site Dehydrogenase

Inhibitors.”, Annual Meeting of the American Society for Biochemistry and

Molecular Biology and Satellite Meetings, Washington, DC, 1998.





REFERENCES: Dr. Kenner C. Rice

Chief, Drug Design and Synthesis Section

Chief, Laboratory of Medicinal Chemistry

National Institute on Drug Abuse, National Institutes of health

Phone: 301-496-1856

Email: kennerr@nida.nih.gov



Professor Stephen F. Martin

M. June and J. Virgil Waggoner Regents Chair in Chemistry

Department of Chemistry & Biochemistry

The University of Texas at Austin

Phone: 512-471-3915

Email: sfmartin@mail.utexas.edu



Professor David L. Vander Jagt

Department of Biochemistry & Molecular Biology

The University of New Mexico

Phone: 505-272-5788

Email: dlvanderjagt@salud.unm.edu









6


Related docs
Other docs by HC111207235434
Verandah Lunch
Views: 0  |  Downloads: 0
English Revision Paper Class- II
Views: 9  |  Downloads: 0
IMRT Reimbursement
Views: 11  |  Downloads: 0
Land Resource Economics
Views: 0  |  Downloads: 0
Yolanda A
Views: 8  |  Downloads: 0
GUIA INSTRUCTIVA PARA ARMAR LA ANTENA
Views: 0  |  Downloads: 0
Riepilogando
Views: 0  |  Downloads: 0
products_2011-04-01_14-52
Views: 6  |  Downloads: 0
KENTUCKY FARM BUREAU
Views: 0  |  Downloads: 0
By registering with docstoc.com you agree to our
privacy policy

You are almost ready to download!

You are almost ready to download!