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Updated: Feb 15, 2026

Solid-phase Submonomer Synthesis of Peptoid Polymers and their Self-Assembly into Highly-Ordered Nanosheets
Published on: November 2, 2011
Synthesis of Highly Functionalized Indoles and Indolones via Selectivity-Switchable Olefinations
Ting-Hui Ding1, Zu-Feng Xiao1, Jian-Ping Qu2
1Department of Chemistry, University of Science and Technology of China , Hefei, Anhui 230026, China.
Abstract:
Highly functionalized indoles and indolones were prepared via selectivity-switchable mono- or diolefinations. The Julia olefination of the products followed by a Brønsted acid-prompted cyclization afforded indolones, whereas the indoles were obtained by a sequential Wittig olefination and electrocyclization. This method opens divergent access to highly functionalized nitrogen-containing bicyclic or tricyclic heterocycles.
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