An improved synthesis of camphorquinone-3-oxime

Article abstract of DOI:10.1080/00397919908086451

Camphorquinone 3-oxime is prepared in 77% yield in one step from camphor. The synthesis avoids the use of toxic selenium reagents, and provides the syn compound as the major stereoisomer.

Full text of DOI:10.1080/00397919908086451

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic Organic
Chemistry
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An Improved Synthesis of
Camphorquinone-3-Oxime
a
a
Brian E. Love & Edward G. Jones
a
Department of Chemistry, East Carolina University,
Greenville, NC, 27858
Published online: 25 Sep 2007.
To cite this article: Brian E. Love & Edward G. Jones (1999) An Improved Synthesis
of Camphorquinone-3-Oxime, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 29:16, 2831-2840, DOI:
10.1080/00397919908086451
To link to this article: http://dx.doi.org/10.1080/00397919908086451
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