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Communication | Regular issue | Vol 51, No. 3, 1999, pp.489-492
Published online, 1st January, 1970
DOI: 10.3987/COM-98-8427
Radical Cyclizations of Vinylogous Systems Involving Oxime Ethers Connected with Carbonyl Groups

Takeaki Naito,* Daisuke Fukumoto, Kumiko Takebayashi, and Toshiko Kiguchi

*Kobe Pharmaceutical University, Motoyamakita, Higashinada, Kobe 658-8558, Japan

Abstract

Stannyl radical addition-cyclization of the isolated oximeethers or α,β-unsaturated oxime ethers connected by a tether to α,β -unsaturated aldehydes or ketones provides a new entry to the adjacently functionalized heterocycles.