An abnormal fries rearrangement induced by a -methoxyl group in monoacetates of naphthohydroquinones.

Journal article

Peer reviewed

T.A. Chorn, R.G.F. Giles, I.R. Green, V.I. Hugo and P.R.K. Mitchell

Tetrahedron Letters, Vol.23(32), pp.3299-3300

1982

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The acetyl group of two I-acetoxy-4-hydroxy-S methoxynaphthalenes migrates to C-3 on treatment with boron trifZuoride etherate.

Title: An abnormal fries rearrangement induced by a -methoxyl group in monoacetates of naphthohydroquinones.
Authors/Creators: T.A. Chorn (Author/Creator) - University of Cape Town
R.G.F. Giles (Author/Creator) - University of Cape Town
I.R. Green (Author/Creator) - University of Cape Town
V.I. Hugo (Author/Creator) - University of Cape Town
P.R.K. Mitchell (Author/Creator) - University of Cape Town
Publication Details: Tetrahedron Letters, Vol.23(32), pp.3299-3300
Publisher: Elsevier BV
Identifiers: 991005545300907891
Copyright: © 1982 Published by Elsevier Ltd.
Murdoch Affiliation: Murdoch University
Language: English
Resource Type: Journal article

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Citation topics: 1 Clinical & Life Sciences; 1.219 Cancer Drugs; 1.219.1527 Naphthoquinone Derivatives
Web Of Science research areas: Chemistry, Organic
ESI research areas: Chemistry