z-logo
Premium
Dearomatization of 3‐Nitroindoles by a Phosphine‐Catalyzed Enantioselective [3+2] Annulation Reaction
Author(s) -
Li Kaizhi,
Gonçalves Théo P.,
Huang KuoWei,
Lu Yixin
Publication year - 2019
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201900248
Subject(s) - annulation , enantioselective synthesis , phosphine , chemistry , catalysis , combinatorial chemistry , organic chemistry
The dearomatization of 3‐nitroindoles through a chiral‐phosphine‐mediated [3+2] annulation reaction is described. This method makes use of readily available 3‐nitroindoles as an aromatic feedstock and rapidly delivers a wide range of cyclopentaindoline alkaloid scaffolds in a highly enantioselective manner. Notably, phosphine‐triggered cyclization has not been utilized previously in a dearomatization process.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here