Jeffrey Johnson

Jeffrey Johnson

A. Ronald Gallant Distinguished Professor

    Caudill Laboratories 220
    919-843-4936, 919-962-4358
   Group Website
    Curriculum Vitae

Research Interests

Synthetic Organic Chemistry, Asymmetric Catalysis

Professional Background

B.S., University of Kansas, 1994; Ph.D., Harvard University, 1999; NIH Postdoctoral Fellow, University of California, Berkeley, 1999-2001; Research Corporation Research Innovation Award, 2002; National Science Foundation CAREER Award, 2003-2008; 3M Nontenured Faculty Award, 2003; UNC Junior Faculty Development Award, 2004; Johnson and Johnson Focused Giving Award, 2004-2006; Eli Lilly Grantee, 2004; Amgen Young Investigator Award, 2005; GSK Scholar Award, 2006-2007; Alfred P. Sloan Fellow, 2006-2008; Camille Dreyfus Teacher Scholar, 2006-2009; Ruth and Phillip Hettleman Prize for Artistic and Scholarly Achievement, 2006; Novartis Early Career Award in Organic Chemistry, 2008; American Chemical Society's Arthur C. Cope Scholar Award in Recognition of Excellence in Organic Chemistry, 2010; Elias J. Corey Award, 2012; Society of Synthetic Organic Chemistry, Japan Lectureship Award, 2014; Japanese Society for the Promotion of Science Fellow, 2015; William C. Friday, Class of 1986, Award for Excellence in Teaching, 2016

Research Group

Research Synopsis

My interests lie in the general area of chemical synthesis. I am particularly interested in the discovery of new organic transformations and their application to the total synthesis of architecturally challenging and biologically important natural products. Our criteria for the development of a synthetic method may be summarized by three characteristics:

The reaction should achieve several structural modifications in a single synthetic operation: tandem or domino reactions are optimal;

The reaction should introduce a significant level of stereochemical complexity in a controlled fashion and absolute stereocontrol should arise from a chiral source used in catalytic quantities;

The starting materials should be readily accessed, but be easily transformed into complex products. To meet these challenges, students in my group will learn a full complement of organic and organometallic chemistry.

News & Publications

Molecular Diversity

Benzenoids in principle represent attractive and abundant starting materials for the preparation of...


Molecular Diversity

Benzenoids, in principle, represent attractive and abundant starting materials for the preparation...