The principal goal of this research program is to improve the efficiency by which relatively small organic compounds are synthesized. Large numbers of relatively small organic compounds are screened annually by the National Institutes of Health as a part of their mission to address specific public health concerns and to develop new therapeutic agents. For example, new therapeutic agents are constantly being developed and evaluated as effective agents to control and possibly to eradicate the HIV virus. The design and the reduction to practice of in vitro chemical syntheses of every small molecule in the NCI publication Chemical Structures of Interest to the Division of Cancer Treatment is critically dependent upon the availability of preparative synthetic methodology. Hence, procedures which decrease the effort required for in vitro chemical synthesis will assist the ongoing development and syntheses of physiologically active, small organic molecules. Synthetic efficiency of both naturally occurring and of non-naturally occurring analogs of small organic molecules will be improved through understanding of the precise details which control the key carbon-carbon bond forming reactions utilized in their preparation. The protocol utilized in this research project will be to complete a thorough structural analysis of common reactive intermediates which are utilized extensively in every synthetic organic chemistry laboratory. Most but not all of the compounds proposed for study in this project are organolithium compounds. The structural results are obtained for these species thorough a combination of techniques which include NMR spectroscopy, x-ray diffraction analysis and computational chemistry. The structural results manifest themselves as three dimensional pictures of aggregated species which have been shown by others to be reactive intermediates. The structural information will also be utilized to design synthetic methods and to explain, to control, and to predict the outcome of chemical reactions which are required to synthesize physiologically active compounds. Structural information will also be utilized to develop and to improve certain specific synthetic reagents for the asymmetric synthesis of organic chemicals. This research project is designed to complement the development of new synthetic reactions with a thorough understanding of the reaction processes themselves. Overall, a strict emphasis will be focused on those specific reactive species and reaction processes deemed most relevant to the development of synthetic organic chemistry used for the total synthesis of medicinal chemicals.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM035982-16A1
Application #
6478564
Study Section
Medicinal Chemistry Study Section (MCHA)
Program Officer
Schwab, John M
Project Start
1986-01-01
Project End
2006-04-30
Budget Start
2002-03-01
Budget End
2003-04-30
Support Year
16
Fiscal Year
2002
Total Cost
$311,843
Indirect Cost
Name
Brown University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
001785542
City
Providence
State
RI
Country
United States
Zip Code
02912
Annese, Cosimo; Fanizza, Immacolata; Calvano, Cosima D et al. (2011) Selective synthesis of hydroxy analogues of valinomycin using dioxiranes. Org Lett 13:5096-9
Annese, Cosimo; D'Accolti, Lucia; De Zotti, Marta et al. (2010) Concerning selectivity in the oxidation of peptides by dioxiranes. Further insight into the effect of carbamate protecting groups. J Org Chem 75:4812-6
Li, Deyu; Keresztes, Ivan; Hopson, Russell et al. (2009) Characterization of reactive intermediates by multinuclear diffusion-ordered NMR spectroscopy (DOSY). Acc Chem Res 42:270-80
Li, Deyu; Kagan, Gerald; Hopson, Russell et al. (2009) Formula weight prediction by internal reference diffusion-ordered NMR spectroscopy (DOSY). J Am Chem Soc 131:5627-34
Liu, Jia; Li, Deyu; Sun, Chengzao et al. (2008) Analysis of an asymmetric addition with a 2:1 mixed lithium amide/n-butyllithium aggregate. J Org Chem 73:4045-52
Li, Deyu; Sun, Chengzao; Williard, Paul G (2008) Characterization of a chiral enolate aggregate and observation of 6Li-1H scalar coupling. J Am Chem Soc 130:11726-36
Li, Deyu; Sun, Chengzao; Liu, Jia et al. (2008) Aggregation studies of complexes containing a chiral lithium amide and n-Butyllithium. J Org Chem 73:2373-81
Li, Deyu; Hopson, Russell; Li, Weibin et al. (2008) 13C INEPT diffusion-ordered NMR spectroscopy (DOSY) with internal references. Org Lett 10:909-11
Rella, Maria Rosaria; Williard, Paul G (2007) Oxidation of peptides by methyl(trifluoromethyl)dioxirane: the protecting group matters. J Org Chem 72:525-31
Ma, Lili; Williard, Paul G (2006) Synthesis of Polymer-supported Chiral Lithium Amide Bases and Application in Asymmetric Deprotonation of Prochiral Cyclic Ketones. Tetrahedron Asymmetry 17:3021-3029

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