Issue 81, 2019

Phosphine-mediated sequential annulations of allenyl ketone and isocyanide: a bicyclization strategy to access a furan-fused eight-membered ring and a spirocycle

Abstract

Phosphine-mediated cascade annulations of allenyl ketone and isocyanide have been disclosed. Two molecular allenyl ketones work as different four-carbon synthons to form two rings, respectively, and thus enables the efficient synthesis of a furan-fused eight-membered ring and a spirocycle.

Graphical abstract: Phosphine-mediated sequential annulations of allenyl ketone and isocyanide: a bicyclization strategy to access a furan-fused eight-membered ring and a spirocycle

Supplementary files

Article information

Article type
Communication
Submitted
13 Aug 2019
Accepted
13 Sep 2019
First published
14 Sep 2019

Chem. Commun., 2019,55, 12180-12183

Phosphine-mediated sequential annulations of allenyl ketone and isocyanide: a bicyclization strategy to access a furan-fused eight-membered ring and a spirocycle

B. Xue, S. Su, Y. Cui, Y. Fei, X. Jia, J. Li and J. Fang, Chem. Commun., 2019, 55, 12180 DOI: 10.1039/C9CC06267J

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