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Towards a synthesis of naphthalene derived natural products

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Date

2005-10-31

Authors

McCulloch, Malcolm
Barrow, Russell

Journal Title

Journal ISSN

Volume Title

Publisher

Molecular Diversity Preservation International

Abstract

Dieckmann-type cyclization reactions have been employed in the synthesis of the alkyl substituted naphthoquinone 11 and the naphthalenes 10 and 12. Various conditions for the benzylic oxidation of these compounds have been investigated with a view towards the synthesis of some naphthalene based natural products.

Description

Keywords

Naphthalenes, benzylic oxidation, naphtho-γ-pyrone

Citation

Molecules 10.10 (2005): 1272-1278

URI

http://hdl.handle.net/10440/296
 http://digitalcollections.anu.edu.au/handle/10440/296

Collections

ANU Research Publications

Source

Molecules: a journal of synthetic organic and natural products

Type

Journal article

Book Title

Entity type

Access Statement

License Rights

DOI

10.3390/10101272

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