This proposal is being submitted in response to RFA-RM-05-013 (New Methodologies for Natural Products Chemistry). The hypothesis of this proposal is that cycloadducts and ene products derived from reactions of diene- and alkene-containing natural products with nitroso moieties, will provide novel derivatives that can serve as versatile building blocks (evolvable scaffolds) for syntheses of a number of important and often new bioactive molecules.
Specific Aims Are: 1. Generate novel scaffolds from diene and alkene-containing natural products by simple one step cycloaddition and ene reactions with a variety of nitroso compounds, even those that contain extensive additional functionality. Both solution phase chemistry and novel """"""""natural product solid phase capture"""""""" methods will be described. 2. Demonstrate that the newly functionalized natural product scaffolds are """"""""evolvable platforms"""""""" that can be elaborated to both conformationally restricted and more flexible libraries using novel chemistry developed in the PI's laboratory and classical chemistry in the labs of the described collaborators as well as in the PI's labs. 3. Broadly test the scaffold and derived libraries of novel compounds using the extensive set of assays in place at the Hans-Knoll Institute for Natural Products Research (HKI).

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM075855-03
Application #
7270478
Study Section
Special Emphasis Panel (ZRG1-BCMB-R (50))
Program Officer
Schwab, John M
Project Start
2005-09-23
Project End
2008-07-31
Budget Start
2007-08-01
Budget End
2008-07-31
Support Year
3
Fiscal Year
2007
Total Cost
$319,817
Indirect Cost
Name
University of Notre Dame
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
824910376
City
Notre Dame
State
IN
Country
United States
Zip Code
46556
Carosso, Serena; Miller, Marvin J (2014) Nitroso Diels-Alder (NDA) reaction as an efficient tool for the functionalization of diene-containing natural products. Org Biomol Chem 12:7445-68
Ji, Cheng; Lin, Weimin; Moraski, Garrett C et al. (2012) Syntheses and biological studies of novel spiropiperazinyl oxazolidinone antibacterial agents using a spirocyclic diene derived acylnitroso Diels-Alder reaction. Bioorg Med Chem 20:3422-8
Wencewicz, Timothy A; Yang, Baiyuan; Rudloff, James R et al. (2011) N-O chemistry for antibiotics: discovery of N-alkyl-N-(pyridin-2-yl)hydroxylamine scaffolds as selective antibacterial agents using nitroso Diels-Alder and ene chemistry. J Med Chem 54:6843-58
Bodnar, Brian S; Miller, Marvin J (2011) The nitrosocarbonyl hetero-Diels-Alder reaction as a useful tool for organic syntheses. Angew Chem Int Ed Engl 50:5630-47
Krchnak, Viktor; Zajicek, Jaroslav; Miller, Patricia A et al. (2011) Selective molecular sequestration with concurrent natural product functionalization and derivatization: from crude natural product extracts to a single natural product derivative in one step. J Org Chem 76:10249-53
Yang, Baiyuan; Miller, Marvin J (2010) Indium triflate-assisted nucleophilic aromatic substitution reactions of nitrosobezene-derived cycloadducts with alcohols. Org Lett 12:392-5
Yang, Baiyuan; Zhu, Zhiqing C; Goodson, Holly V et al. (2010) Syntheses and biological evaluation of ring-C modified colchicine analogs. Bioorg Med Chem Lett 20:3831-3
Yan, Shanshan; Miller, Marvin J; Wencewicz, Timothy A et al. (2010) Syntheses and antibacterial activity studies of new oxazolidinones from nitroso Diels-Alder chemistry. Bioorg Med Chem Lett 20:1302-5
Yang, Baiyuan; Miller, Marvin J (2010) Iminonitroso ene reactions: experimental studies on reactivity, regioselectivity and enantioselectivity. Tetrahedron Lett 51:328-331
Yang, Baiyuan; Miller, Marvin J (2010) Regio- and stereochemically controlled formation of hydroxamic acids from indium triflate-mediated nucleophilic ring-opening reactions with acylnitroso-Diels-Alder adducts. Tetrahedron Lett 51:889-891

Showing the most recent 10 out of 26 publications