The enantiomers (+)- and (−)-alternarilactone A (1), the first examples of dibenzo-α-pyrones bearing a diepoxy-cage-like moiety, were isolated from the endophytic fungus Alternaria sp. hh930. The deficiency in 1H–1H COSY and HMBC correlations caused by the highly oxidized caged system of 1 and the deceptive and ambiguous signals such as “W” couplings in NMR data increased the risk of structure misassignment of 1. By performing a quantum chemical calculation of the NMR chemical shifts together with a DP4+ probability analysis and single-crystal X-ray crystallographic experiment, their structures were unambiguously determined, and their absolute configurations were determined by ECD calculations
Six new dibenzo-α-pyrones, rhizopycnolides A (<b>1</b>) and B (<b>2</b>) and rhizopycnins A–D (<b>3<...
A new azaphilone derivative, named fusarone (1), has been isolated from the ethyl acetate soluble ex...
Programs of drug discovery generally exploit one enantiomer of a chiral compound for lead developmen...
The enantiomers (+)- and (−)-alternarilactone A (1), the first examples of dibenzo-α-pyrones bearing...
A pair of enantiomeric polyketides, (+)- and (−)-alternamgin (1), featuring an unprecedented 6/6/6/6...
<p>One pair of new cyclopentaisochromenone derivatives, (+)-(<i>S</i>)-6-hydroxy-1,8-dimethoxy-3a-me...
Fifteen meroterpenoids (<b>1</b>–<b>15</b>) with diverse ring systems including an unprecedented oxa...
α-Pyrones and furanones are metabolites produced by <i>Diplodia corticola</i>, a pathogen of cork oa...
Four new 2-pyrone derivatives, two pairs of enantiomers, (±)-egypyrone A [(±)-1] and (±)-egypyrone B...
-Pyrones and furanones are metabolites produced by Diplodia corticola, a pathogen of cork oak. Previ...
Fig. 2. Key COSY, HMBC and NOESY correlations of 1.Published as part of Yan, Wei, Ji, Wenxia, Ping, ...
The exciton coupled CD method has been applied to determine the absolute configuration of the diepox...
Fig. 1. (A) Chemical structure and (B) X-ray crystallographic structure of trichodermatrione A (1).P...
Fig. 3. X-ray structures of (+)-1 (A) and ()-1 (B), and experimental and calculated ECD spectra of (...
R factor = 0.033; wR factor = 0.096; data-to-parameter ratio = 11.2. The title compound (AME; system...
Six new dibenzo-α-pyrones, rhizopycnolides A (<b>1</b>) and B (<b>2</b>) and rhizopycnins A–D (<b>3<...
A new azaphilone derivative, named fusarone (1), has been isolated from the ethyl acetate soluble ex...
Programs of drug discovery generally exploit one enantiomer of a chiral compound for lead developmen...
The enantiomers (+)- and (−)-alternarilactone A (1), the first examples of dibenzo-α-pyrones bearing...
A pair of enantiomeric polyketides, (+)- and (−)-alternamgin (1), featuring an unprecedented 6/6/6/6...
<p>One pair of new cyclopentaisochromenone derivatives, (+)-(<i>S</i>)-6-hydroxy-1,8-dimethoxy-3a-me...
Fifteen meroterpenoids (<b>1</b>–<b>15</b>) with diverse ring systems including an unprecedented oxa...
α-Pyrones and furanones are metabolites produced by <i>Diplodia corticola</i>, a pathogen of cork oa...
Four new 2-pyrone derivatives, two pairs of enantiomers, (±)-egypyrone A [(±)-1] and (±)-egypyrone B...
-Pyrones and furanones are metabolites produced by Diplodia corticola, a pathogen of cork oak. Previ...
Fig. 2. Key COSY, HMBC and NOESY correlations of 1.Published as part of Yan, Wei, Ji, Wenxia, Ping, ...
The exciton coupled CD method has been applied to determine the absolute configuration of the diepox...
Fig. 1. (A) Chemical structure and (B) X-ray crystallographic structure of trichodermatrione A (1).P...
Fig. 3. X-ray structures of (+)-1 (A) and ()-1 (B), and experimental and calculated ECD spectra of (...
R factor = 0.033; wR factor = 0.096; data-to-parameter ratio = 11.2. The title compound (AME; system...
Six new dibenzo-α-pyrones, rhizopycnolides A (<b>1</b>) and B (<b>2</b>) and rhizopycnins A–D (<b>3<...
A new azaphilone derivative, named fusarone (1), has been isolated from the ethyl acetate soluble ex...
Programs of drug discovery generally exploit one enantiomer of a chiral compound for lead developmen...