Synthesis of Functionalized Heterocycles by C-H Activation Hydrocarbons are the simplest and most abundant chemical feedstock available on the planet. Despite this, few efficient methods exist for their selective functionalization. Much attention is being focused on C-H activation problems in contexts ranging from methane to complex molecule total synthesis. Obvious problems include issues of reactivity, selectivity, and functional group compatibility. Recognizing the synthetic potential of the C-H activation process, this proposal seeks to elucidate mechanistic details relevant to its use. Particularly, the metal-catalyzed oxidative dimerization of heteroarenes and related substrates will be investigated.
The specific aims are 1. Establish the factors governing the selectivity of dehydrogenative C-C coupling and elucidate additional details of its mechanism; 2. Determine practical and efficient conditions for the reoxidation of the catalytic species in this process described above; 3. Establish conditions for the oxidative heterodimerization of N-heterocycles with other arenes and related substrates.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM075691-02
Application #
7102756
Study Section
Special Emphasis Panel (ZRG1-F04A (20))
Program Officer
Marino, Pamela
Project Start
2005-07-19
Project End
2007-07-18
Budget Start
2006-07-19
Budget End
2007-07-18
Support Year
2
Fiscal Year
2006
Total Cost
$45,976
Indirect Cost
Name
California Institute of Technology
Department
Chemistry
Type
Schools of Engineering
DUNS #
009584210
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Williams, Travis J; Caffyn, Andrew J M; Hazari, Nilay et al. (2008) C-H bond activation by air-stable [(diimine)M(II)(mu2-OH)]2(2+) dimers (M = Pd, Pt). J Am Chem Soc 130:2418-9