Issue 76, 2021

Enantioselective synthesis of 1-aminoindene derivatives via asymmetric Brønsted acid catalysis

Abstract

We describe a catalytic asymmetric iminium ion cyclization reaction of simple 2-alkenylbenzaldimines using a BINOL-derived chiral N-triflyl phosphoramide. The corresponding 1-aminoindenes and tetracyclic 1-aminoindanes are formed in good yields and high enantioselectivities. Further, the chemical utility of the obtained enantiopure 1-aminoindene is demonstrated for the asymmetric synthesis of (S)-rasagiline.

Graphical abstract: Enantioselective synthesis of 1-aminoindene derivatives via asymmetric Brønsted acid catalysis

Supplementary files

Article information

Article type
Communication
Submitted
03 Шіл. 2021
Accepted
24 Там. 2021
First published
24 Там. 2021

Chem. Commun., 2021,57, 9680-9683

Enantioselective synthesis of 1-aminoindene derivatives via asymmetric Brønsted acid catalysis

X. Wu, D. Ding, Y. Zhang, H. Jiang, T. Wang and L. Zhao, Chem. Commun., 2021, 57, 9680 DOI: 10.1039/D1CC03568A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements