Scripps Florida

Links

Micalizio Website 

















 

Florida Faculty and Professional Staff

Glenn Micalizio

Associate Professor
Department of Chemistry
TSRI - 2008

Education 

Harvard University, 2001-2003: postdoctoral fellow of the Helen Hay Whitney Foundation
University of Michigan, 1997-2001: Ph.D. in Chemistry
Ramapo College of NJ, 1992-1996: B.S. in Chemistry

Awards & Activities 

2007 - University of Michigan Department of Chemistry Kasimir Fajans Award
2007 - Boehringer Ingelheim New Investigator Award
2006 - Yale University Junior Faculty Fellowship in the Natural Sciences
2006 - Lilly Grantee Award
2006 - American Cancer Society Research Scholar Award
2005 - Beckman Young Investigator Award
2003 - Lilly New Faculty Award

Research Focus 

A central focus of modern synthetic organic chemistry is the design of new reactions and synthesis strategies that will facilitate the construction of complex molecules. We are interested in developing fundamental approaches to the assembly of stereochemically dense architecture that have the potential to facilitate investigations aimed at discovery of biologically active small molecules. Areas of active investigation include the development of new convergent C–C bond forming reactions and the application of these methods to target- and diversity-oriented synthesis.

Selected References 

H. A. Reichard, J. C. Rieger, G. C. Micalizio Total Synthesis of Callystatin A by Titanium-mediated Reductive Alkyne–Alkyne Cross-Coupling Angew. Chem. Int. Ed. 2008, 47, in press.

J. K. Belardi, G. C. Micalizio Total Synthesis of Macbecin I Angew. Chem. Int. Ed. 2008, 47, 4069-4072.

M. Takahashi, G. C. Micalizio Regio- and Stereoselective Cross Coupling of Substituted Olefins and Imines. A Convergent Stereoselective Synthesis of Saturated 1,5-Aminoalcohols and Substituted Piperidines. J. Am. Chem. Soc. 2007, 129, 7514-7516.

F. Kolundzic, G. C. Micalizio Synthesis of Substituted 1,4-Dienes by Direct Alkylation of Allylic Alcohols. J. Am. Chem. Soc. 2007, 129, 15112-15113.