The specific goal of this research proposal is the total synthesis of the indoline alkaloid communesin B. Communesin B is a broadly biologically active natural product that posseses two vicinal quaternary centers and two aminal moeities embedded within a heptacyclic framework. There have been no reported total syntheses to date. The successful synthesis of this compound would represent an important advance in the field of alkaloid synthesis. The key step in the synthesis of communesin B would be a Mo-, Ir-, or W- catalyzed asymmetric allylic alkylation (AAA) reaction which will employ indole derivatives as the nucleophile. The use of indoles nucleophiles in the AAA reaction has not been precedented and would be a significant extension of the current AAA technology. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32GM077734-01
Application #
7108887
Study Section
Special Emphasis Panel (ZRG1-F04A-D (20))
Program Officer
Fabian, Miles
Project Start
2006-02-28
Project End
2008-02-27
Budget Start
2006-02-28
Budget End
2007-02-27
Support Year
1
Fiscal Year
2006
Total Cost
$43,996
Indirect Cost
Name
Stanford University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305