Issue 46, 2008
From the journal:

Chemical Communications

Primary amino acidlithium salt as a catalyst for asymmetric Michael addition of isobutyraldehyde with β-nitroalkenes†

Atsushi Sato,a   Masanori Yoshida*a  and  Shoji Haraa  

* Corresponding authors

a Division of Chemical Process Engineering, Graduate School of Engineering, Hokkaido University, Sapporo, Japan
E-mail: myoshida@eng.hokudai.ac.jp
Fax: +81 11 706 6557
Tel: +81 11 706 6557

Abstract

Phenylalanine lithium salt was found to be an effective catalyst for asymmetric Michael addition of isobutyraldehyde with β-nitroalkenes to give quaternary carbon-containing nitroalkanes.

Graphical abstract: Primary amino acidlithium salt as a catalyst for asymmetric Michael addition of isobutyraldehyde with β-nitroalkenes

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Article information

DOI
https://doi.org/10.1039/B814804J
Article type
Communication
Submitted
26 Aug 2008
Accepted
30 Sep 2008
First published
16 Oct 2008

Chem. Commun., 2008, 6242-6244

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Primary amino acidlithium salt as a catalyst for asymmetric Michael addition of isobutyraldehyde with β-nitroalkenes

A. Sato, M. Yoshida and S. Hara, Chem. Commun., 2008, 6242 DOI: 10.1039/B814804J

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