Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5227456 | Tetrahedron | 2008 | 6 Pages |
Abstract
A simple, stereoselective and efficient method for the hydrothiolation of terminal alkynes with diaryl disulfides and diphenyl diselenide has been developed. In the presence of CuI, rongalite, and Cs2CO3, a variety of disulfides underwent the reaction of terminal alkynes stereoselectively to afford the corresponding (Z)-1-alkenyl sulfides in moderate to excellent yields. It is noteworthy that hydroselenations of 1,2-diphenyldiselane with alkynes are also conducted smoothly to afford (Z)-1-alkenyl selenides in good yields under the standard conditions.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zhang-Lin Wang, Ri-Yuan Tang, Pei-Song Luo, Chen-Liang Deng, Ping Zhong, Jin-Heng Li,