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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 25, 1995 - Issue 19
128
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Original Articles

Allylation of Aldehydes and Ketones with Allyl Bromide and Tin Promoted by Me3SiCI and Alcohol

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Pages 3081-3087 | Received 31 Jan 1995, Published online: 16 Feb 2007
 

Abstract

Allylation of aldehydes and ketones to give homoallylic alcohols can be carried out successfully with allyl bromide and metallic tin under anhydrous condition. The 64–89% yields of homoallyl alcohols are obtained by addition of chlorotrimethylsilane as a promoter in anhydrous methanol.

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