Synthetic strategies towards pyranonaphthoquinone antibiotics

Brimble, MA; Nairn, MR; Prabaharan, H

dc.contributor.author	Brimble, MA	en
dc.contributor.author	Nairn, MR	en
dc.contributor.author	Prabaharan, H	en
dc.date.accessioned	2011-09-21T23:09:41Z	en
dc.date.issued	2000	en
dc.identifier.citation	TETRAHEDRON 56(14):1937-1992 31 Mar 2000	en
dc.identifier.issn	0040-4020	en
dc.identifier.uri	http://hdl.handle.net/2292/8235	en
dc.description.abstract	The class of compounds known as the pyranonaphthoquinone antibiotics are isolated from various strains of bacteria and fungi, the majority being microbial in origin.1 The basic skeleton of these antibiotics is the naphtho[2,3-c]pyran-5,10-dione ring system (Fig. 1), with some members of the family containing an additional γ-lactone ring fused to the dihydropyran moiety as the basic subunit. This substituted benzoisochromane skeleton represents a biosynthetic product common to all members of this class and is built up from acetate/malonate units via a polyketide pathway	en
dc.language	EN	en
dc.relation.ispartofseries	Tetrahedron	en
dc.rights	Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/0040-4020/	en
dc.rights.uri	https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm	en
dc.subject	NATURALLY-OCCURRING QUINONES	en
dc.subject	ENANTIOSELECTIVE TOTAL SYNTHESIS	en
dc.subject	ENANTIODIVERGENT TOTAL SYNTHESES	en
dc.subject	POTASSIUM TERT-BUTOXIDE	en
dc.subject	DIELS-ALDER REACTION	en
dc.subject	NAPHTHOQUINONE ANTIBIOTICS	en
dc.subject	NANAOMYCIN-A	en
dc.subject	METHYL-ESTER	en
dc.subject	STEREOSELECTIVE FORMATION	en
dc.subject	FUROFURAN ANNULATION	en
dc.title	Synthetic strategies towards pyranonaphthoquinone antibiotics	en
dc.type	Journal Article	en
dc.identifier.doi	10.1016/S0040-4020(99)01021-2	en
pubs.issue	14	en
pubs.begin-page	1937	en
pubs.volume	56	en
dc.rights.holder	Copyright: 2000 Elsevier Science Ltd.	en
pubs.end-page	1992	en
dc.rights.accessrights	http://purl.org/eprint/accessRights/RestrictedAccess	en
pubs.subtype	Article	en
pubs.elements-id	2485	en
pubs.org-id	Science	en
pubs.org-id	Chemistry	en
pubs.org-id	Science Research	en
pubs.org-id	Maurice Wilkins Centre (2010-2014)	en
pubs.record-created-at-source-date	2010-09-01	en