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Issue 1, 2003
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From central to planar chirality, the first example of atropenantioselective cycloetherification

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Abstract

Using chiral quaternary ammonium hydroxide as base, cycloetherification of linear achiral diarylheptanoid 5, by way of an intramolecular SNAr reaction, provides enantiomerically enriched cyclophane 6 in good to excellent yield.

Graphical abstract: From central to planar chirality, the first example of atropenantioselective cycloetherification

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Article information


Submitted
18 Sep 2002
Accepted
07 Oct 2002
First published
08 Nov 2002

Org. Biomol. Chem., 2003,1, 30-32
Article type
Communication

From central to planar chirality, the first example of atropenantioselective cycloetherification

G. Islas-Gonzalez, M. Bois-Choussy and J. Zhu, Org. Biomol. Chem., 2003, 1, 30
DOI: 10.1039/B208905J

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