Issue 30, 2012

Development of strong Brønsted base catalysis: catalytic direct-type Mannich reactions of non-activated estersvia a product-base mechanism

Abstract

A catalytic Mannich reaction of a simple ester with no activating functionality at the α-position via a product-base mechanism was reported. The desired Mannich adducts were obtained in high yields using a catalytic amount of KH. This is a rare example of a Brønsted base-catalyzed Mannich reaction of unactivated esters as substrates.

Graphical abstract: Development of strong Brønsted base catalysis: catalytic direct-type Mannich reactions of non-activated esters via a product-base mechanism

Supplementary files

Article information

Article type
Communication
Submitted
10 Mar 2012
Accepted
02 Apr 2012
First published
03 Apr 2012

Org. Biomol. Chem., 2012,10, 5750-5752

Development of strong Brønsted base catalysis: catalytic direct-type Mannich reactions of non-activated esters via a product-base mechanism

Y. Yamashita, H. Suzuki and S. Kobayashi, Org. Biomol. Chem., 2012, 10, 5750 DOI: 10.1039/C2OB25522G

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