Hydroborations: A new route for the preparation of 1-alkyl- (or aryl) 2-tetralones

Article abstract of DOI:10.1080/00397919308009833

The hydroboration followed by chromic acid oxidation of 1-alkyl- and 1-aryl-3,4-dihydronaphthalenes leads to the corresponding 1-alkyl- (or aryl)2-tetralones (1-substituted 3,4-dihydronaphthalen-2(1H)-ones.

Full text of DOI:10.1080/00397919308009833

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Synthetic Communications: An
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Organic Chemistry
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Hydroborations: A New Route
for the Preparation of 1-Alkyl-
(or Aryl) 2-Tetralones
B. Serge Kirkiacharian a & Pantelis G. Koutsourakis a
a Laboratoire de Chimie Thérapeutique - Faculté
de Pharmacie de Paris - Sud - 5, rue J. B. Clément,
92296, Chatenay-Malabry - Cedex, France
Published online: 23 Sep 2006.
To cite this article: B. Serge Kirkiacharian & Pantelis G. Koutsourakis (1993):
Hydroborations: A New Route for the Preparation of 1-Alkyl- (or Aryl) 2-Tetralones,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 23:6, 737-742
To link to this article: http://dx.doi.org/10.1080/00397919308009833
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