Efficient and selective preparation of organic molecules is critical for the synthesis of therapeutics. Many of the most proficient known processes depend on the availability of catalysts. One of the advantages of organometallic catalysis is the ability to tune the activity and selectivity through modification of the ligands around the metal center. Recently, major advances have been reported thanks to the use of electron-rich phosphines and cyclic diaminocarbenes. We have uncovered several novel families of stable carbenes, such as the cyclic (alkyl)(amino)carbenes and the diaminocyclopropenylidenes, which behave as even more electron-donating ligands. They have already allowed for improving known palladium and ruthenium catalyzed processes, and even for promoting new metal catalyzed reactions. The full catalytic potential of complexes bearing these carbene ligands will be investigated. In order to obtain even more robust and efficient transition-metal catalysts, novel types of carbon-based ligands, which surpass the electron donating properties imposed by any other ligands, will be prepared. Special attention will be drawn on families of ligands for which it will be possible to precisely tune the steric and electronic parameters. There is a high demand for technology to produce therapeutics in a pure enantiomeric form, thus optically active versions of our new ligands will be prepared. The studies will be focused on catalytic processes for which real difficulties remain, and on chemical transformations, which have not yet been achieved, but are of critical importance for building the skeleton of complex molecules. Cascade reactions that involves several reactants, yet a single catalyst, and which lead to biologically relevant heterocycles and to important synthons will be developed. To accelerate the widespread implementation of our ligands, we have already formalized a collaboration with Robert Grubbs at Caltech, and we are looking forward to further partnerships. The ultimate goal of this research effort is to find truly practical catalysts, and catalytic reactions, which will find applications in both industry and academia for the selective synthesis of biologically important compounds.

Public Health Relevance

The success of homogeneous catalysis can largely be attributed to the development of a diverse range of ligand frameworks that have been used to tune the behavior of the various catalysts. In order to obtain robust and efficient transition-metal catalysts, we wish to develop novel types of carbon-based ligands. The ultimate goal of this research effort is to find truly practical catalysts, and catalytic reactions, which will find applications in both industry and academia for the selective synthesis of biologically important compounds.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM068825-05
Application #
7736977
Study Section
Synthetic and Biological Chemistry B Study Section (SBCB)
Program Officer
Schwab, John M
Project Start
2005-08-01
Project End
2013-07-31
Budget Start
2009-08-01
Budget End
2010-07-31
Support Year
5
Fiscal Year
2009
Total Cost
Indirect Cost
Name
University of California Riverside
Department
Chemistry
Type
Earth Sciences/Resources
DUNS #
627797426
City
Riverside
State
CA
Country
United States
Zip Code
92521
Marx, Vanessa M; Sullivan, Alexandra H; Melaimi, Mohand et al. (2015) Cyclic alkyl amino carbene (CAAC) ruthenium complexes as remarkably active catalysts for ethenolysis. Angew Chem Int Ed Engl 54:1919-23
Ung, Gaël; Bertrand, Guy (2013) ?- and ?-Hydride abstraction in Gold(I) alkyl complexes. Angew Chem Int Ed Engl 52:11388-91
Ruiz, David A; Ung, Gaël; Melaimi, Mohand et al. (2013) Deprotonation of a borohydride: synthesis of a carbene-stabilized boryl anion. Angew Chem Int Ed Engl 52:7590-2
Back, Olivier; Henry-Ellinger, Martin; Martin, Caleb D et al. (2013) 31P NMR chemical shifts of carbene-phosphinidene adducts as an indicator of the ?-accepting properties of carbenes. Angew Chem Int Ed Engl 52:2939-43
Ung, Gael; Soleilhavoup, Michele; Bertrand, Guy (2013) Gold(III)- versus gold(I)-induced cyclization: synthesis of six-membered mesoionic carbene and acyclic (aryl)(heteroaryl) carbene complexes. Angew Chem Int Ed Engl 52:758-61
Martin, Caleb D; Soleilhavoup, Michele; Bertrand, Guy (2013) Carbene-Stabilized Main Group Radicals and Radical Ions. Chem Sci 4:3020-3030
Yan, Xiaoyu; Bouffard, Jean; Guisado-Barrios, Gregorio et al. (2012) Anionic 1,2,3-triazole-4,5-diylidene: a 1,2-dihapto ligand for the construction of bimetallic complexes. Chemistry 18:14627-31
Ung, Gael; Bertrand, Guy (2012) C-F bond activation with an apparently benign ethynyl dithiocarbamate, and subsequent fluoride transfer reactions. Chemistry 18:12955-7
Martin, David; Lassauque, Nicolas; Donnadieu, Bruno et al. (2012) A cyclic diaminocarbene with a pyramidalized nitrogen atom: a stable N-heterocyclic carbene with enhanced electrophilicity. Angew Chem Int Ed Engl 51:6172-5
Mendoza-Espinosa, Daniel; Ung, Gael; Donnadieu, Bruno et al. (2011) Mesoionic thiazol-5-ylidenes as ligands for transition metal complexes. Chem Commun (Camb) 47:10614-6

Showing the most recent 10 out of 58 publications