Paul Wender

Born in 1947,[3] Wender received his B.S. from Wilkes University in 1969, and his Ph.D. degree from Yale University in 1973.[4] At Yale he worked with Frederick E. Ziegler, graduating with a thesis on the transformation of ketones into nitriles, and the total synthesis of eremophilone. He was a post-doctoral fellow at Columbia University in 1974. In 1974, he began his independent career as an assistant professor and later associate professor at Harvard University. In 1982, he became a professor at Stanford University. He is currently the Francis W. Bergstrom Professor of Chemistry there.

His research involves the targeted synthesis of complex biologically interesting molecules. He coined the term "function-oriented synthesis." He pursues applications for drugs in cancer therapy, for example, and synthesized phorbol, taxol, resiniferatoxin and prostatin, among others. Because of his work on the synthesis of indole derivatives, the Wender indole synthesis he described in 1981 was named after him.

• Ernest Guenther Award, 1988
• Arthur C. Cope Scholar Award, 1990
• Fellow, American Academy of Arts and Sciences, 1992
• American Chemical Society Award for Creative work in Synthetic Organic Chemistry, 1998
• Fellow, American Association for the Advancement of Science, 2001[1]
• American Chemical Society H.C. Brown Award for Creative Research in Synthetic Methods, 2003
• Member of the National Academy of Sciences, 2003;[5]
• Tetrahedron Prize for Creativity in Organic Chemistry, 2012
• Foreign member - Spanish Royal Academy of Sciences, 2013
• ACS Arthur C. Cope Award, 2015

• Wender Taxol total synthesis