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David J Lapinsky, Ph.D.
Assistant Professor of Medicinal Chemistry
422B Mellon Hall
T 412.396.6069
L 412.396.1973 (450 Mellon Hall)
F 412.396.5593
E lapinskyd@duq.edu
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| Educational Background |
B.S.(Pharmacy)--Duquesne University
Ph.D. -- The Ohio State University
Publications
- Ring E analogs of methyllycaconitine (MLA) as novel nicotinic antagonists. S.C. Bergmeier, D.J. Lapinsky, R.B. Free, and D.B. McKay; Bioorganic & Medicinal Chemistry Letters 1999, 9, 2263-2266.
- A Suzuki cross-coupling route to substituted aziridines. D.J. Lapinsky and S.C. Bergmeier; Tetrahedron Letters 2001, 42, 8583-8586.
- Structure-activity studies with ring E analogues of methyllycaconitine on bovine adrenal α3β4* nicotinic receptors. D.L. Bryant, R.B. Free, S.M. Thomasy, D.J. Lapinsky, K.A. Ismail, S.B. McKay, S.C. Bergmeier, and D.B. McKay;
- Neuroscience Research 2002, 42, 57-63.
- Effects of methyllycaconitine and related analogues on bovine adrenal α3β4* nicotinic acetylcholine receptors. D.L. Bryant, R.B. Free, S.M. Thomasy, D.J. Lapinsky, K.A. Ismail, K.M. Arason, S.C. Bergmeier, and D.B. McKay; Annals of the New York Academy of Sciences 2002, 971, 139-141.
- Aziridine-allylsilane-mediated synthesis of exocyclic γ-amino olefins and azabicyclo[x.y.1]-systems. D.J. Lapinsky and S.C. Bergmeier; Tetrahedron 2002, 58, 7109-7117.
- Studies in aziridine-allylsilane chemistry: Extension of Scope. D.J. Lapinsky; Dissertation, 2002, The Ohio State University.
- Substitution effects in intramolecular aziridine-allylsilane cyclizations. D.J. Lapinsky, A.B. Pulipaka, and S.C. Bergmeier; submitted to J. Org. Chem. 2/2008.
- Chapter 3: Three-membered ring systems. S.C. Bergmeier and D.J. Lapinsky; Progress in Heterocyclic Chemistry 2008, 20, submitted 3/2008.
Research Presentations
- Isosteric replacement of bisphosphonates in the development of myo-inositol monophosphatase inhibitors. D.J. Lapinsky, D. Gaitonde, and M.W. Harrold; 18th Annual Undergraduate Research Seminar, Oral Presentation, West Virginia University, 11 / 1996.
- Ring E analogs of methyllycaconitine (MLA) as novel nicotinic antagonists. S.C. Bergmeier, D.J. Lapinsky, R.B. Free, and D.B. McKay; 36th National Organic Chemistry Symposium, Poster #148, University of Wisconsin-Madison, 6 / 1999. 4
- Ring E analogs of methyllycaconitine (MLA) as novel nicotinic antagonists. S.C. Bergmeier, D.J. Lapinsky, R.B. Free, and D.B. McKay; 32nd Graduate Student Symposium in Medicinal Chemistry, Poster, SUNY at Buffalo, 6 / 1999.
- Synthesis of azabicyclo[x.2.1]-systems using an intramolecular aziridineallylsilane cyclization reaction. D.J. Lapinsky and S.C. Bergmeier; 37th National Organic Chemistry Symposium, Poster #115, Montana State University, 6 / 2001.
- Synthesis of azabicyclo[x.2.1]-systems using an intramolecular aziridineallylsilane cyclization reaction. D.J. Lapinsky and S.C. Bergmeier; 34th Graduate Student Symposium in Medicinal Chemistry, Oral Presentation, Ohio State University, 6 / 2001.
Teaching
Duquesne University
Fall Semester 2007
- PHBMS 425: Endocrine Module
GPHSC 691: Medicinal Chemistry Seminar I
Spring Semester 2008
- PHBMS 423: GI / Rheumatology Module
- GPHSC 527: Advanced Medicinal Chemistry
- GPHSC 623: Selected Topics in Medicinal Chemisty
Rice University (Department of Chemistry, 8 / 2004 to 8/2007)
- CHEM 211 & 212: Organic Chemistry I & II
- CHEM 251& 252: Honors Organic Chemistry I & II
- CHEM 442 & 443: Principles of Medicinal Chemistry I & II
- CHEM 352: Introductory Module in Experimental
- Chemistry II (Organic Synthesis)
- CHEM 374: Advanced Module in Synthetic Organic Chemistry
- CHEM 384: Advanced Module in Instrumental Analysis
- CHEM 401 & 562: Advanced Organic Chemistry I & II
Service
- Duquesne University School of Pharmacy Committees
Pharmacy Safety
- Pharmacy Faculty Excellence Award
- Duquesne University Student Organizations: Faculty Advisor
- Graduate Student Association (GSA)
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