A facile route to olefins from vic-diols via cyclic sulfates with triphenylphosphine and iodine

Article abstract of DOI:10.1080/00397919708004099

Treatment of cyclic sulfates of vic-diols with triphenylphosphine and iodine offers the corresponding olefins in high yields at room temperature. Both cyclic sulfates of d,l-hydrobenzoin and meso-hydrobenzoin give trans- stilbene.

Full text of DOI:10.1080/00397919708004099

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Facile Route to Olefins from
Vic-Diols Via Cyclic Sulfates
with Triphenylphosphine and
Iodine
a
b
a
Doo Ok Jang , Yung Hyup Joo & Dae Hyan Cho
a
Department of Chemistry , Yonsei University ,
Wonju, 222-710, Korea
b
Pacific Corporation, Pharmaceutical Research
Institute , Kyounggi-do, 449-900, Korea
Published online: 21 Aug 2006.
To cite this article: Doo Ok Jang , Yung Hyup Joo & Dae Hyan Cho (1997) A Facile
Route to Olefins from Vic-Diols Via Cyclic Sulfates with Triphenylphosphine and Iodine,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 27:14, 2379-2386, DOI: 10.1080/00397919708004099
To link to this article: http://dx.doi.org/10.1080/00397919708004099
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