Issue 34, 2007

An asymmetric SNAr reaction using the molecular chirality in a crystal

Abstract

An asymmetric SNAr reaction was performed by using molecular chirality generated and amplified by the spontaneous crystallization of achiral naphthamides; the chirality was retained in a cold solution, caused by slow racemization, and was transferred to stable axially chiral materials with high enantiomeric excesses.

Graphical abstract: An asymmetric SNAr reaction using the molecular chirality in a crystal

Supplementary files

Article information

Article type
Communication
Submitted
27 Apr 2007
Accepted
04 Jul 2007
First published
26 Jul 2007

Chem. Commun., 2007, 3586-3588

An asymmetric SNAr reaction using the molecular chirality in a crystal

M. Sakamoto, A. Unosawa, S. Kobaru, K. Fujita, T. Mino and T. Fujita, Chem. Commun., 2007, 3586 DOI: 10.1039/B706426H

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