State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China

Tel: 8621 6416 7510; Fax: (+86) 21-64167510Search for more papers by this author

Chun-Ling Fu,

Chun-Ling Fu

Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang 310027, China

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Guo-Fei Chen,

Guo-Fei Chen

Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang 310027, China

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You-Qian Deng,

You-Qian Deng

Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang 310027, China

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Xian Huang,

Xian Huang

Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang 310027, China

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Sheng-Ming Ma,

Corresponding Author

Sheng-Ming Ma

[email protected]

Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang 310027, China

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China

Tel: 8621 6416 7510; Fax: (+86) 21-64167510Search for more papers by this author

First published: 26 August 2010

https://doi.org/10.1002/cjoc.20040220922

Citations: 8

^†

Dedicated to Professor Chengye Yuan on the occasion of his 80th birthday.

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Abstract

The E-iodohydroxylation of 1, 2-allenylic sulfoxides with I₂ in the presence of EtOH afforded 3-phenylsulfinyl-2–10do-2(E)-alkenols in good yields and regio/stereo-selectivities under very mild conditions.

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Volume22, Issue9

September 2004

Pages 990-993

Effect of EtOH on the E-Iodohydroxylation of 1,2-allenylic sulfoxides with 1₂^†

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Effect of EtOH on the E-Iodohydroxylation of 1,2-allenylic sulfoxides with 12†

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Effect of EtOH on the E-Iodohydroxylation of 1,2-allenylic sulfoxides with 1₂^†