Synthesis of 3-acetyl-5-methoxy-1,4-naphthoquinone. A new approach

Article abstract of DOI:10.1080/00397919408012620

A new and efficient synthesis for 3-acetyl-5-methoxy-1,4- naphthoquinone has been developed. The synthesis involves inter alia pyrolysis of an acetylated Diels-Alder adduct and a regiospecific Fries rearrangement reaction.

Full text of DOI:10.1080/00397919408012620

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Synthetic Communications: An
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Synthesis of 3-Acetyl-5-
methoxy-1,4-naphthoquinone.
A New Approach
a
a
Victor I. Hugo , Joanne L. Nicholson , Petra W.
a
b
Snijman & Ivan R. Green
a
Department of Chemistry , Cape Technikon , P O
Box 652, Cape Town, 8000, Republic of South Africa
b
Department of Chemistry , University of the
Western Cape , Private Bag X17, Bellville, 7530,
Republic of South Africa
Published online: 23 Sep 2006.
To cite this article: Victor I. Hugo , Joanne L. Nicholson , Petra W. Snijman & Ivan R.
Green (1994) Synthesis of 3-Acetyl-5-methoxy-1,4-naphthoquinone. A New Approach,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 24:1, 23-28, DOI: 10.1080/00397919408012620
To link to this article: http://dx.doi.org/10.1080/00397919408012620
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