Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5281574 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
Indoles undergo smooth alkylation with α- and β-pinenes in the presence of 20 mol % of anhydrous FeCl3 under mild reaction conditions to produce a wide range of the corresponding 3-alkylated indoles in excellent yields with high trans-selectivity. This is the first example of alkylation of indoles with mono-terpenes.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
J.S. Yadav, B.V. Subba Reddy, G. Narasimhulu, N. Sivasankar Reddy, P. Narayana Reddy, K.V. Purnima, P. Naresh, B. Jagadeesh,