The number and importance of polyquinane natural products continues to grow and a diverse range of biological activities have been identified. The proposal outlines the continued development of a general strategy toward this class of compounds which permits entry to both natural products and synthetic analogues of widely differing structural types. The main focus of the proposal is on the development of new free radical-based methods for carbon-carbon bond formation. The unique ability to sequence free radical reactions to form several C-C bonds in one step is highlighted and a variety of new methods based on this concept are proposed. In all cases, the new chemistry to be developed is illustrated in the context of the synthesis of one or more important natural products, although more general utility is always implied. New methods to generate radicals and control both regio- and stereoselectivity in radical reactions are also proposed. The chemistry outlined int his proposal will contribute both to the understanding of free radical reactions and to the ability to prepare important cyclopentanoid natural products.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM033372-04
Application #
3283012
Study Section
Medicinal Chemistry Study Section (MCHA)
Project Start
1984-04-01
Project End
1992-03-31
Budget Start
1987-04-01
Budget End
1988-03-31
Support Year
4
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Type
Schools of Arts and Sciences
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Moretti, Jared D; Wang, Xiao; Curran, Dennis P (2012) Minimal fluorous tagging strategy that enables the synthesis of the complete stereoisomer library of SCH725674 macrolactones. J Am Chem Soc 134:7963-70
Gudipati, Venugopal; Curran, Dennis P (2011) Synthesis of C1-C20 and C21-C40 fragments of tetrafibricin. Tetrahedron Lett 52:2254-2257
Moura-Letts, Gustavo; Curran, Dennis P (2007) Selective synthesis of (2Z,4E)-dienyl esters by ene-diene cross metathesis. Org Lett 9:5-8
Du, Wu; Curran, Dennis P; Bevins, Robert L et al. (2002) Synthesis and evaluation of a novel E-ring modified alpha-hydroxy keto ether analogue of camptothecin. Bioorg Med Chem 10:103-10