Zinc-promoted Barbier-type reaction of propargyl bromide with aldehydes in aqueous media

Article abstract of DOI:10.1080/00397919508011422

In the presence of metallic zinc, propargyl bromide is found to react with aldehydes at room temperature in tetrahydrofurane-saturated aqueous ammonium chloride (5:2) to afford the corresponding homopropargylic alcohols in moderate to high yields together

Full text of DOI:10.1080/00397919508011422

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Zinc-Promoted Barbier-Type
Reaction of Propargyl Bromide
with Aldehydes in Aqueous
Media
Issa Yavari a & Farhad Riazi-Kermani b
a Chemistry Department , Tarbiat Modarres
University , P. O. BOX 14155-4838, Tehran, Iran
b Chemistry Department , Shahid Beheshti
University, Evin , Tehran, 19834, Iran
Published online: 16 Feb 2007.
To cite this article: Issa Yavari & Farhad Riazi-Kermani (1995) Zinc-Promoted Barbier-
Type Reaction of Propargyl Bromide with Aldehydes in Aqueous Media, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 25:19, 2923-2928, DOI: 10.1080/00397919508011422
To link to this article: http://dx.doi.org/10.1080/00397919508011422
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