Enantioselective Organocatalytic Construction of Spiroindane Derivatives by Intramolecular Friedel–Crafts‐Type 1,4‐Addition | Zendy

Yoshida Keisuke | Zendy; Itatsu Yukihiro | Zendy; Fujino Yuta | Zendy; Inoue Hiroki | Zendy; Takao Kenichi | Zendy

Premium

Enantioselective Organocatalytic Construction of Spiroindane Derivatives by Intramolecular Friedel–Crafts‐Type 1,4‐Addition

Author(s) -

Yoshida Keisuke,

Itatsu Yukihiro,

Fujino Yuta,

Inoue Hiroki,

Takao Kenichi

Publication year - 2016

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.201601683

Subject(s) - stereocenter , enantioselective synthesis , cinchonidine , intramolecular force , friedel–crafts reaction , chemistry , catalysis , organic chemistry , amine gas treating , organocatalysis , michael reaction , quaternary carbon , stereochemistry

The highly enantioselective organocatalytic construction of spiroindanes containing an all‐carbon quaternary stereocenter by intramolecular Friedel–Crafts‐type 1,4‐addition is described. The reaction was catalyzed by a cinchonidine‐based primary amine and accelerated by water and p ‐bromophenol. A variety of spiro compounds containing quaternary stereocenters were obtained with excellent enantioselectivity (up to 95 % ee ). The reaction was applied to the asymmetric formal synthesis of the spirocyclic natural products (−)‐cannabispirenones A and B.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research