Site selective functionalizations of fluorinated heterocycles

Heterocyclic chem. continues to be in the focus of life science-oriented research. Fluorine, a unique tool for finetuning biol. properties, offers an extra bonus in this context. The lecture features three pertinent issues. First, proven and novel routes to F-, CF3- and OCF3-substituted heterocycles will be reviewed. Next, the specific merits of the organometallic approach to the functionalization of "naked" core structures will be portrayed. Finally, it will be demonstrated how any vacant position in pyridines, quinolines, pyrimidines, pyrazoles and indoles can be substituted and, in particular, functionalized selectively and reliably. [on SciFinder (R)]

Published in:
Abstracts of Papers, 232nd ACS National Meeting, San Francisco, CA, United States, Sept. 10-14, 2006, FLUO-010
Institute for Chemical Sciences and Engineering,Ecole Polytechnique Federale,CH-Lausanne,Switz.
Conference; Meeting Abstract; Computer Optical Disk
written in English.

 Record created 2007-03-07, last modified 2018-01-27

Rate this document:

Rate this document:
(Not yet reviewed)