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Syntheses related to some naturally occurring naphthopyranquinones

Bibliography: pages 248-257.

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Main Author: Hugo, Victor Ignatius
Other Authors: Giles, R G F
Format: Thesis
Language:English
Published: Department of Chemistry 2016
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access_status_str Open Access
author Hugo, Victor Ignatius
author2 Giles, R G F
author_browse Giles, R G F
Hugo, Victor Ignatius
author_facet Giles, R G F
Hugo, Victor Ignatius
author_sort Hugo, Victor Ignatius
collection Thesis
description Bibliography: pages 248-257.
format Thesis
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institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:36.207Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2016
publishDateRange 2016
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publisher Department of Chemistry
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/17036 Syntheses related to some naturally occurring naphthopyranquinones Hugo, Victor Ignatius Giles, R G F Organic Chemistry Bibliography: pages 248-257. The naphtho[2,3-c]pyran ring system occurs not infrequently in Nature as derivatives of the 5,10-quinone. Examples include the eleutherins, the nanaomycins and the protoaphins some of which have been shown to possess antibiotic activity. The synthesis of these natural products requires appropriate regiospecific aromatic oxygenation of 2- acetylnaphthoquinone. Syntheses of 3-acetyl-5-methoxy-1, 4- naphthoquinone and the corresponding 5,7-dimethoxy analogue are described and the use of these in the syntheses of several naturally occurring pyranquinones or their derivatives, has been investigated. In the course of this work, an unusual Fries rearrangement and a novel baseinduced cyclisation were discovered - the latter affording several naphtho[2,3-c]pyrans in high yield. Previous routes to (±)-isoeleutherin and (±)-deoxyquinone A dimethyl ether have been recorded, but they give rise to a mixture of eleutherin and isoeleutherin in the first case, and a mixture of deoxyquinone A dimethyl ether and its cisdimethyl isomer. The synthetic routes to isoeleutherin and deoxyquinone A dimethyl ether developed during this investigation are highly stereoselective. The formation of the dimethyl ethers of quinones A and A', which is also highly stereoselective represents the first reported synthesis of the degradation products of the aphid pigments, protoaphin-fb and protoaphin-s1. The synthesis of 7-methoxyeleutherin is also described. The reaction of trifluoroacetic anhydride with various naphthalene derivatives is described and the potential of some of these acylated naphthalenes to be employed in the syntheses of naphtho[2, 3-c]pyrans and naturally occurring quinones has been investigated. 2016-02-15T07:15:37Z 2016-02-15T07:15:37Z 1986 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/17036 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Organic Chemistry
Hugo, Victor Ignatius
Syntheses related to some naturally occurring naphthopyranquinones
thesis_degree_str Doctoral
title Syntheses related to some naturally occurring naphthopyranquinones
title_full Syntheses related to some naturally occurring naphthopyranquinones
title_fullStr Syntheses related to some naturally occurring naphthopyranquinones
title_full_unstemmed Syntheses related to some naturally occurring naphthopyranquinones
title_short Syntheses related to some naturally occurring naphthopyranquinones
title_sort syntheses related to some naturally occurring naphthopyranquinones
topic Organic Chemistry
url http://hdl.handle.net/11427/17036
work_keys_str_mv AT hugovictorignatius synthesesrelatedtosomenaturallyoccurringnaphthopyranquinones