Novel reductive cleavage reaction of thiobenzoates with samarium diiodide: Convenient synthesis of disulfides

Article abstract of DOI:10.1080/00397910008087054

The reductive cleavage of thiobenzoates promoted by samarium diiodide afforded various kinds of disulfides in good yields under mild and neutral conditions.

Full text of DOI:10.1080/00397910008087054

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Synthetic Communications: An
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Novel Reductive Cleavage
Reaction of Thiobenzoates with
Samarium Diiodide: Convenient
Synthesis of Disulfides
Byung Woo Yoo a , Heung Soo Baek a , Sam Rok Keum
a , Cheol Min Yoon a , Ghil Soo Nam b , Sung Hoon
Kim b & Joong Hyup Kim b
a Department of Chemistry , Korea University ,
Chochiwon, Chungnam, 339--700, Korea
b Biochemical Research Center , Korea Institute
of Science and Technology , Cheongryang, Seoul,
130--650, Korea
Published online: 04 Dec 2007.
To cite this article: Byung Woo Yoo , Heung Soo Baek , Sam Rok Keum , Cheol Min
Yoon , Ghil Soo Nam , Sung Hoon Kim & Joong Hyup Kim (2000) Novel Reductive
Cleavage Reaction of Thiobenzoates with Samarium Diiodide: Convenient
Synthesis of Disulfides, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 30:23, 4317-4322, DOI:
10.1080/00397910008087054
To link to this article: http://dx.doi.org/10.1080/00397910008087054
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