Gore, Sangram and Baskaran, Sundarababu and König, Burkhard (2012) Fischer Indole Synthesis in Low Melting Mixtures. Organic Letters 14 (17), pp. 4568-4571.
Full text not available from this repository.
Functionalized indoles are synthezised under mild conditions in a tartaric acid-dimethylurea melt. The melt serves as the solvent and as the catalyst. Under these reaction conditions, sensitive functional groups such as N-Boc, N-Cbz, or azides are stable, and indolenines are obtained regioselectively in excellent yields. The practical use of the method is demonstrated in the synthesis of the hormone melatonin.
Export bibliographical data
|Institutions:||Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König|
|Dewey Decimal Classification:||500 Science > 540 Chemistry & allied sciences|
|Refereed:||Yes, this version has been refereed|
|Created at the University of Regensburg:||Yes|
|Deposited on:||23 Aug 2012 09:25|
|Last modified:||28 Sep 2012 10:06|