Issue 40, 2006
From the journal:

Chemical Communications

The reductive amination of aldehydes and ketones by catalytic use of dibutylchlorotin hydride complex†

Hirofumi Kato,a   Ikuya Shibata,*b   Yuta Yasaka,b   Shinji Tsunoi,b   Makoto Yasudaa  and  Akio Baba*a  

* Corresponding authors

a Department of Applied Chemistry, Center for Atomic and Molecular Technologies (CAMT), Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Japan
Fax: +81 6-6879-7387
Tel: +81 6-6879-7386

b Research Center for Environmental Preservation, Osaka University, 2-4 Yamadaoka, Suita, Japan
E-mail: shibata@epc.osaka-u.ac.jp
Fax: +81 6-6879-8978
Tel: +81 6-6879-8975

Abstract

The reductive amination of aldehydes or ketones using Ph2SiH2 or PhSiH3 has been effectively promoted by the direct use of Bu2SnClH–pyridine N-oxide as a catalyst; this method has advantages in terms of its mild conditions and wide application to various carbonyls and amines, including aliphatic examples.

Graphical abstract: The reductive amination of aldehydes and ketones by catalytic use of dibutylchlorotin hydride complex

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B610614E
Article type
Communication
Submitted
25 Jul 2006
Accepted
14 Aug 2006
First published
29 Aug 2006

Chem. Commun., 2006, 4189-4191

Permissions

Request permissions

The reductive amination of aldehydes and ketones by catalytic use of dibutylchlorotin hydride complex

H. Kato, I. Shibata, Y. Yasaka, S. Tsunoi, M. Yasuda and A. Baba, Chem. Commun., 2006, 4189 DOI: 10.1039/B610614E

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