Allylation of novel β-phenylthio substituted gem-difluoroallylic bromide to carbonyl compounds

Article abstract of DOI:10.1080/00397919908085762

The reaction of β-phenylthio substituted gem-difluoroallylic bromide 3 with aldehydes and ketones in the presence of Zn(Cu) in THF at reflux temperature afforded the corresponding homoallylic alcohols 4 in good yields.

Full text of DOI:10.1080/00397919908085762

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Allylation Of Novel β-
Phenylthio Substituted gem-
Difluoroallylic Bromide to
Carbonyl Compounds
In Howa Jeong a , Myong Sang Kim a & Bum Tae Kim b
a Department of Chemistry , Yonsei University ,
Wonju, 220-710, Korea
b Korea Research Institute of Chemical Technology ,
Daejeon, 305-606, Korea
Published online: 17 Sep 2007.
To cite this article: In Howa Jeong , Myong Sang Kim & Bum Tae Kim (1999)
Allylation Of Novel β-Phenylthio Substituted gem-Difluoroallylic Bromide to
Carbonyl Compounds, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 29:2, 235-241, DOI:
10.1080/00397919908085762
To link to this article: http://dx.doi.org/10.1080/00397919908085762
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