Issue 42, 2013
From the journal:

Organic & Biomolecular Chemistry

Synthesis and C2-functionalization of indoles with allylic acetates under rhodium catalysis†

Mirim Kim,a   Jihye Park,a   Satyasheel Sharma,a   Sangil Han,a   Sang Hoon Han,a   Jong Hwan Kwak,a   Young Hoon Junga  and  In Su Kim*a  

* Corresponding authors

a School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Republic of Korea
E-mail: insukim@skku.edu
Fax: +82 31 299 4373
Tel: +82 31 290 7788

Abstract

Tandem rhodium-catalyzed oxidative allylation and annulation of acetanilides with allyl acetate to afford the corresponding indoles are described. In addition, the site-selective C2 allylation, crotylation and prenylation of indoles using allylic acetates under rhodium catalysis are reported.

Graphical abstract: Synthesis and C2-functionalization of indoles with allylic acetates under rhodium catalysis

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C3OB41828F
Article type
Paper
Submitted
27 Aug 2013
Accepted
17 Sep 2013
First published
17 Sep 2013

Org. Biomol. Chem., 2013,11, 7427-7434

Permissions

Request permissions

Synthesis and C2-functionalization of indoles with allylic acetates under rhodium catalysis

M. Kim, J. Park, S. Sharma, S. Han, S. H. Han, J. H. Kwak, Y. H. Jung and I. S. Kim, Org. Biomol. Chem., 2013, 11, 7427 DOI: 10.1039/C3OB41828F

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