QDIS was founded in 2003 by Edward Vawter, PhD. We offer a variety of services including consulting, informational searches, and training courses. For those interested, the name comes from the Library of Congress classification code for chemistry information; QD.
Edward Vawter brings well over a decade of experience in research and development in the pharmaceutical industry with both large and small companies. He has a PhD in organic chemistry from Purdue University and has been involved in the synthesis of multi-step complex pharmaceuticals including polymer drug conjugates through all stages of development. He has managed the outsourcing of development and manufacturing for multi-million dollar projects on an international basis. Edward also has five years of experience with development of polymer based drug conjugates as well as extensive analytical development knowledge related to polymers. He has experience with experimental design and data analysis; not only statistical analysis but also exploratory data analysis and building of models to represent behavior of chemical systems. His business experience as well as his solid technical background can help your company succeed.
Patent Application Pub No.: US 20030054977 A1, Pub Date: Mar. 20, 2003. Manufacture of Polyglutamate-Therapeutic Agent Conjugates; Anil Kumar, J. Peter Klein, Rama Bhatt, Edward Vawter.
Book chapter from Polymer Drugs in the Clinical Stage Hiroshi Maeda, et. al. (Editors) "Poly-(L)-Glutamic Acid-Paclitaxel (CT-2103) [Xyotax®], a Biodegradable Polymeric Drug Conjugate: Characterization, Preclinical Pharmacology, and Preliminary Clinical Data" by Jack Singer, Brian Baker, Peter De Vries, Anil Kumar, Scott Shaffer, Ed Vawter, Mary Bolton, and Pamela Garzone.
Efficient Asymmetric Synthesis of the Vasopeptidase Inhibitor BMS-189921 Singh, J.; Kronenthal, D. R.; Schwinden, M.; Godfrey, J. D.; Fox, R.; Vawter, E. J.; Zhang, B.; Kissick, T. P.; Patel, B.; Mneimne, O.; Humora, M.; Papaioannou, C. G.; Szymanski, W.; Wong, M. K. Y.; Chen, C. K.; Heikes, J. E.; DiMarco, J. D.; Qiu, J.; Deshpande, R. P.; Gougoutas, J. Z.; Mueller, R. H.; Org. Lett., 2003, 5(17), 3155-3158.
Book chapter from Process Chemistry in the Pharmaceutical Industry Kumar G. Gadamasetti (Editor) "A Practical Synthesis of Ifetroban Sodium" by Richard M. Mueller.
Apparent endo-mode cyclic carbopalladation with inversion of alkene configuration via exo-mode cyclization-cyclopropanation rearrangement Zbyslaw Owczarczyk, Frederic Lamaty, Edward J. Vawter, Ei-ichi Negishi; J. Am. Chem. Soc. 1992, 114(25), 10091-10092.
Effects of Oragonmetals on the Palladium-Catalyzed Tandem Carbopalladation–Cross Coupling for Preparing Stereodefined Exocyclic Alkenes Negishi E.; Noda, Y.; Lamaty, F.; Vawter E. J.; Tetrahedron Lett. 1990, 31, 4393
Steroselective Cyclic Carbolithiation of Alkyne Derivatives. A Stereoselective Synthesis of Exocyclic Alkenes Guangzhong Wu, Fredrick E. Cedarbaum, and Ei-ichi Negishi; Tetrahedron Lett. 1990, 31, 493.
Regioselective 1,4-Addition to alpha,beta-Unsaturated Ketones with Grignard Reagents Mediated by (N,N,N',N'-tetramethylethylenediamine)zinc(II) chloride Richard A. Kjonaas, Edward J. Vawter; J. Org. Chem. 1986, 51(21), 3993-3996.

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