Novel reactions of ethylene acetals with silyl-substituted nucleophiles. A mild and efficient procedure for the synthesis of homoallyl alkyl ethers and unsymmetrical dialkyl ethers

Article abstract of DOI:10.1080/00397919908086101

Efficient one-pot synthesis of homoallyl alkyl ethers and dialkyl ethers was performed by the allylation and reduction of ethylene acetals with allyltrimethylsilane and t-butyldimethylsilane, respectively, in the presence of alkoxytrimethylsilane.

Full text of DOI:10.1080/00397919908086101

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Novel Reactions of Ethylene
Acetals with Silyl-Substituted
Nucleophiles. A Mild and
Efficient Procedure for the
Synthesis of Homoallyl Alkyl
Ethers and Unsymmetrical
Dialkyl Ethers
Takeshi Suzuki a & Takeshi Oriyama a
a Faculty of Science, Ibaraki University , Bunkyo,
Mito, 310-8512, Japan
Published online: 17 Sep 2007.
To cite this article: Takeshi Suzuki & Takeshi Oriyama (1999) Novel Reactions of
Ethylene Acetals with Silyl-Substituted Nucleophiles. A Mild and Efficient Procedure
for the Synthesis of Homoallyl Alkyl Ethers and Unsymmetrical Dialkyl Ethers,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 29:8, 1263-1269, DOI: 10.1080/00397919908086101
To link to this article: http://dx.doi.org/10.1080/00397919908086101
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