Lambertellols A and B, Novel 3,4-Dihydronaphthalen-1(2H)-ones with Spiro-butenolide Produced by Lambertella sp.1346
Organic Letters2003Vol. 6(2), pp. 157–160
Citations Over TimeTop 17% of 2003 papers
Abstract
[structure: see text] Lambertella sp. 1346 was found to produce lambertellols A (1) and B (2) carrying a novel dihydronaphthalen-1(2H)-ones with spiro-1-furan-2(5'H)-one. The spiro-lactone ring moiety of both 1 and 2 were easily migrated to afford lambertellin, a known metabolite of Lambertella corni-maris. The absolute stereochemistry of these compounds was established on the basis of CD spectrum after chemical derivatization.
Related Papers
- → Organic Dyes Containing Furan Moiety for High-Performance Dye-Sensitized Solar Cells(2008)209 cited
- → New entry to chiral butenolide synthons. Application to expeditious syntheses of (+)-nephrosteranic acid, (+)-trans-whisky lactone, and (+)-trans-cognac lactone(1994)37 cited
- → Competition between π–π or furan–perfluorophenyl stacking interactions in conjugated compounds prepared from azomethine connections(2011)17 cited
- → Asymmetric Vinylogous Michael Reaction of α,β-Unsaturated Aldehyde with Buteno-4-lactone(2011)11 cited
- → Novel photochromic indolinospiropyrans containing phenyl substituents in the condensed furan moiety(2006)2 cited