Hypervalent iodine in synthesis 44: Stereoselective synthesis of vinylic selenides by the reaction of sodium selenolates with vinyl (phenyl) iodonium salts

Article abstract of DOI:10.1080/00397910008087118

Vinylic selenides have been prepared stereoselectively by the reaction of sodium selenolates with vinyl(phenyl)iodonium salts with retention or inversion of the configurations.

Full text of DOI:10.1080/00397910008087118

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Hypervalent Iodine in Synthesis
44: Stereoselective Synthesis
of Vinylic Selenides by the
Reaction of Sodium Selenolates
with Vinyl (Phenyl) Iodonium
Salts
Jie Yan a & Zhen-Chu Chen a
a Department of Chemistry , Zhejiang University (Xi-
Xi Campus) , Hangzhou, 310028, P.R China
Published online: 04 Dec 2007.
To cite this article: Jie Yan & Zhen-Chu Chen (2000) Hypervalent Iodine in Synthesis
44: Stereoselective Synthesis of Vinylic Selenides by the Reaction of Sodium
Selenolates with Vinyl (Phenyl) Iodonium Salts, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 30:6,
1009-1015, DOI: 10.1080/00397910008087118
To link to this article: http://dx.doi.org/10.1080/00397910008087118
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