This NIH R15 proposal is intended to develop novel X-C/C-C bond formation reactions and Diels-Alder cyclization using 1-iodo-3-siloxy-l,3-butadiene (Danishefsky-type diene). The asymmetric catalytic versions of these reaction will be investigated. These reactions can provide efficient approaches to numerous chemically and biologically important compound. For example, a novel lead structure made by the Pl's group has been found to be active toward colon cancer, non-small cell lung cancer and Melanoma as tested by NCI. In the past few years, the PI's group have obtained a substantial amount of preliminary results for the multiple-component X-C/C-C bond formation reaction. The asymmetric halo aldol reaction is the first asymmetric catalytic carbonyl addition of allenolates to aldehydes. Based on our preliminary results, the new asymmetric halo aldol reactions will be carried out by 1,4-robust activation and 1,2-tandem functionalization of alpha,beta-alkylenic ketones. New chiral phosphoramides and polymer beads-attached chiral phosphoramides are designed and will be synthesized as the Lewis base catalysts. Meanwhile, a series of chiral Lewis acid catalysts will be obtained and utilized to control the chirality for the halo aldol and Diels-Alder reactions. The 1,2-difuctionalization of alpha,beta-acetylenic ketones and esters will result in beta-halo Baylis-Hillman adducts which are multiple functionalized. The new catalysts and catalytic systems will result in high regioselectivity, stereoselectivity, chemoselectivity, as well as the scope of substrates for the new reactions. Besides the asymmetric catalysis, chiral p-toluene and tert-butanesulfinimines will also be utilized as the chiral auxiliaries and electrophiles for the novel X-C/C-C bond formation reactions. So far, the PI has trained 21 undergraduates, and fourteen of them achieved publications as co-authors. Most of these students have successfully entered medical or graduate schools in the US. In addition, 6 graduate students have been or are still being trained by PI's synthesis projects. This R15 grant application is very important for the PI to continue his teaching and research activities at Texas Tech.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15CA099995-01
Application #
6596483
Study Section
Medicinal Chemistry Study Section (MCHA)
Program Officer
Lees, Robert G
Project Start
2003-06-06
Project End
2007-05-31
Budget Start
2003-06-06
Budget End
2007-05-31
Support Year
1
Fiscal Year
2003
Total Cost
$143,904
Indirect Cost
Name
Texas Tech University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
041367053
City
Lubbock
State
TX
Country
United States
Zip Code
79409
Han, Jianlin; Ai, Teng; Nguyen, Thao et al. (2008) Chiral N-phosphonyl imine chemistry: asymmetric additions of ester enolates for the synthesis of beta-amino acids. Chem Biol Drug Des 72:120-6
Saibabu Kotti, S R S; Timmons, Cody; Li, Guigen (2006) Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry. Chem Biol Drug Des 67:101-14
Kattuboina, Adiseshu; Kaur, Parminder; Timmons, Cody et al. (2006) Novel approach to multifunctionalized homoallylic alcohols via regioselective ring opening of aryl oxiranes with 3-iodo allenoates. Org Lett 8:2771-4
Timmons, C; McPherson, L M; Chen, D et al. (2005) Manganese (IV) oxide-catalyzed electrophilic diamination of electron-deficient alkenes provides an easy synthesis of alpha,beta-diamino acid and ketone derivatives for peptidomimetic studies. J Pept Res 66:249-54
Chen, Dianjun; Guo, Li; Liu, Junying et al. (2005) Functionalization of alpha,beta-unsaturated esters and ketones: a facile and highly stereoselective one-pot approach to N-protected alpha,beta-dehydroamino acid derivatives. Org Lett 7:921-4
Timmons, Cody; Guo, Li; Liu, Junying et al. (2005) Asymmetric halo-Mannich-type reaction provides access to pyrrolidines and beta-proline derivatives. J Org Chem 70:7634-9
Timmons, Cody; Chen, Dianjun; Cannon, John F et al. (2004) New asymmetric halo aldol reaction provides a novel approach to biologically important chiral cyclothers and cycloamines. Org Lett 6:2075-8
Wei, Han-Xun; Timmons, Cody; Farag, Mohamed Ali et al. (2004) MgI2-catalyzed halo aldol reaction: a practical approach to (E)-beta-iodovinyl-beta'-hydroxyketones. Org Biomol Chem 2:2893-6
Xu, Xin; Kotti, S R S Saibabu; Liu, Junying et al. (2004) Ionic liquid media resulted in the first asymmetric aminohalogenation reaction of alkenes. Org Lett 6:4881-4
Karur, Subramanian; Kotti, S R S Saibabu; Xu, Xin et al. (2003) A catalytic reaction of alkynes via multiple-site functionalization. J Am Chem Soc 125:13340-1