Issue 2, 2019

An enantioselective assembly of naphthopyran via NHC-catalyzed [3 + 3] annulation of bromoenal with β-tetralone

Abstract

An asymmetric assembly of naphthopyran was realized via the N-heterocyclic carbene (NHC)-catalyzed formal [3 + 3] annulation of bromoenal and β-tetralone. The key advantages of this protocol include ready availability of starting materials, mild reaction conditions, good yields and excellent enantioselectivities.

Graphical abstract: An enantioselective assembly of naphthopyran via NHC-catalyzed [3 + 3] annulation of bromoenal with β-tetralone

Supplementary files

Article information

Article type
Paper
Submitted
05 Sep 2018
Accepted
04 Dec 2018
First published
05 Dec 2018

Org. Biomol. Chem., 2019,17, 268-274

An enantioselective assembly of naphthopyran via NHC-catalyzed [3 + 3] annulation of bromoenal with β-tetralone

S. Li, Y. Yao, Z. Tang, B. Sun, C. Yu, T. Li and C. Yao, Org. Biomol. Chem., 2019, 17, 268 DOI: 10.1039/C8OB02192A

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