Abstract
The key steps of a versatile new protocol for the convergent synthesis of 3,4-disubstituted indoles are the addition of an α-lithiated alkylaminofuran to a carbonyl compound, a microwave-accelerated intramolecular Diels-Alder cycloaddition and an in situ double aromatization reaction.
Original language | English |
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Pages (from-to) | 104-106 |
Number of pages | 3 |
Journal | Chemical Communications |
Issue number | 1 |
DOIs | |
Publication status | Published - 2009 |
Externally published | Yes |