The principal investigator notes that although the fundamental chemistry of silacyclopropanes has been explored, these compounds have not been utilized in organic synthesis. He reports that preliminary data suggest that these strained-ring silanes are useful building blocks for the construction of polyoxygenated organic compounds. It is stated that the silacyclopropane acts as a masked 1,3-diol, and new carbon-carbon bonds are formed with high stereoselectivity (greater than 98 percent). The principal investigator indicates that the proposal details methods for the construction of propionate (and dipropionate) units terminated by an acetyaldehyde unit and that this architectural feature, which can be difficult to install if it possesses anti stereochemistry, is shared by many therapeutically important compounds, such as amphotericin B and nystatin A1, representatives of the polyene macrolide antibiotics. It is noted that these compounds are the most effective drugs for combating systemic fungal infections, which occur in immuno-compromised patients undergoing cancer chemotherapy and transplants, as well as AIDS patients and that new methods which facilitate the preparation of the polyene macrolides and their analogs for conducting structure-activity studies are important to the progress of the health sciences. The principal investigator states that in particular, the following will be demonstrated: (1) the insertion of formamides into silacyclopropanes will lead to new methods for the synthesis of polyoxygenated compounds, culminating in the total synthesis of stegobiol, the sex pheromone of a pest responsible for the destruction of stored grain; (2) metal-catalyzed reactions such as silylene transfer reactions will provide new syntheses of silacyclopropanes, and metal-catalyzed insertion reactions will generate useful polyol substructures; (3) silacyclopropanes with aromatic substituents on the silicon atom will be investigated to determine their reactivity; and (4) the generality of a modified oxidation of silanes to alcohols will be determined.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
1R29GM054909-01
Application #
2194222
Study Section
Medicinal Chemistry Study Section (MCHA)
Project Start
1996-07-01
Project End
2001-06-30
Budget Start
1996-07-01
Budget End
1997-06-30
Support Year
1
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
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