Issue 9, 2001
From the journal:

Chemical Communications

Solid-phase tandem radical addition–cyclisation reaction of oxime ethers

Hideto Miyabe,a   Kayoko Fujii,a   Hirotaka Tanakaa  and  Takeaki Naito*a  

* Corresponding authors

a Kobe Pharmaceutical University, Motoyamakita, Higashinada, Kobe, Japan.
E-mail: taknaito@kobepharma-u.ac.jp

Abstract

The solid-phase tandem C–C bond-forming reactions of oxime ethers connected with α,β-unsaturated carbonyl groups proceeded effectively under iodine atom-transfer reaction conditions to give the azacycles or chiral oxacycles after cleavage of the resin.

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Article information

DOI
https://doi.org/10.1039/B101074N
Article type
Communication
Submitted
31 Jan 2001
Accepted
20 Mar 2001
First published
10 Apr 2001

Chem. Commun., 2001, 831-832

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Solid-phase tandem radical addition–cyclisation reaction of oxime ethers

H. Miyabe, K. Fujii, H. Tanaka and T. Naito, Chem. Commun., 2001, 831 DOI: 10.1039/B101074N

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