Preparation of diallyl ketals

Article abstract of DOI:10.1080/00397919508011393

A general method for the preparation of diallyl acetals and ketals is reported. The reaction is performed well below room temperature, thereby eliminating any competing Claisen rearrangement. These mild reaction conditions also facilitate ketal formation on methyl levulinate 1 with no transesterification.

Full text of DOI:10.1080/00397919508011393

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Preparation of Diallyl Ketals
John B. Brogan a , Judson E. Richard a & Charles K.
Zercher a
a Department of Chemistry , University of New
Hampshire Durham , New Hampshire, 03824
Published online: 23 Sep 2006.
To cite this article: John B. Brogan , Judson E. Richard & Charles K. Zercher (1995)
Preparation of Diallyl Ketals, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 25:4, 587-593, DOI:
10.1080/00397919508011393
To link to this article: http://dx.doi.org/10.1080/00397919508011393
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