Synthesis 2004(17): 2787-2798  
DOI: 10.1055/s-2004-831257
PAPER
© Georg Thieme Verlag Stuttgart · New York

Rhodium(II)-Catalyzed Reaction of Iodonium Ylides with Conjugated Compounds: Efficient Synthesis of Dihydrofurans, Oxazoles, and Dihydrooxepines

Yong Rok Lee*a, Sang Heum Yoona, Youngwan Seob, Bong Sik Kima
a School of Chemical Engineering and Technology, College of Engineering, Yeungnam University, Kyongsan 712-749, Korea
Fax: +82(53)8104631; e-Mail: yrlee@yu.ac.kr;
b Division of Ocean Science, Korea Maritime University, Busan 606-791, Korea
Further Information

Publication History

Received 19 May 2004
Publication Date:
07 October 2004 (online)

Abstract

The rhodium(II)-catalyzed reaction of iodonium ylides with a variety of conjugated compounds has been examined. With α,β-unsaturated esters and α,β-unsaturated ketones, dihydrofurans were produced in moderate yields. Reactions with acrylonitriles yield oxazoles and dihydrofurans in moderate yields, whereas reactions with 1,3-butadienes result in dihydrofurans and dihydrooxepines in good yields, respectively. The mechanistic pathway for the formation of these products has been described in terms of a cyclopropane intermediate or a 1,3-dipolar cycloaddition mechanism.