The first total synthesis of a bioactive metabolite, a spirobenzofuran isolated from the fungi Acremonium sp. HKI 0230
- 1 October 2005
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 46 (41) , 7029-7031
- https://doi.org/10.1016/j.tetlet.2005.08.049
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Facial selectivity of the Ireland–Claisen rearrangement of allylic esters of 2-methyl and 2-methoxycyclopentanecarboxylic acidsTetrahedron, 2004
- Spirobenzofuran, a new bioactive metabolite from Acremonium sp.HKI 0230.The Journal of Antibiotics, 2001
- The Development of L2X2RuCHR Olefin Metathesis Catalysts: An Organometallic Success StoryAccounts of Chemical Research, 2000
- Baker’s yeast-mediated enantioselective synthesis of the bisabolane sesquiterpenes (+)-curcuphenol, (+)-xanthorrhizol, (−)-curcuquinone and (+)-curcuhydroquinoneJournal of the Chemical Society, Perkin Transactions 1, 2000
- Olefin Metathesis and BeyondPublished by Wiley ,2000
- Recent advances in olefin metathesis and its application in organic synthesisTetrahedron, 1998
- Stereochemical control in the ester enolate Claisen rearrangement. 1. Stereoselectivity in silyl ketene acetal formationThe Journal of Organic Chemistry, 1991
- Lagopodin metabolites and artefacts in cultures of CoprinusPhytochemistry, 1976
- Hydroxylagopodin B, A sesquiterpenoid quinone from a mutant strain of Coprinus macrorhizus var. MicrosporusPhytochemistry, 1975
- Claisen rearrangement of allyl estersJournal of the American Chemical Society, 1972