(+)- and (-)-Alternarilactone A: Enantiomers with a Diepoxy-Cage-like Scaffold from an Endophytic Alternaria sp.

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.

[1]  C. Butts,et al.  Synergy of synthesis, computation and NMR reveals correct baulamycin structures , 2017, Nature.

[2]  R. Chen,et al.  Polyketides from the endophytic fungus Phomopsis sp. sh917 by using the one strain/many compounds strategy , 2017 .

[3]  Ariel M. Sarotti,et al.  Computational Chemistry Driven Solution to Rubriflordilactone B. , 2016, Organic letters.

[4]  Yuheng Cao,et al.  Bioactive Dibenzo-α-pyrone Derivatives from the Endophytic Fungus Rhizopycnis vagum Nitaf22. , 2016, Journal of natural products.

[5]  Han-Dong Sun,et al.  Structural Characterization of Kadcoccinin A: A Sesquiterpenoid with a Tricyclo[4.4.0.0(3,10)]decane Scaffold from Kadsura coccinea. , 2016, Organic letters.

[6]  Han-Dong Sun,et al.  Phomopchalasins A and B, Two Cytochalasans with Polycyclic-Fused Skeletons from the Endophytic Fungus Phomopsis sp. shj2. , 2016, Organic letters.

[7]  G. Challis,et al.  LC-MS-Guided Isolation of Penicilfuranone A: A New Antifibrotic Furancarboxylic Acid from the Plant Endophytic Fungus Penicillium sp. sh18. , 2016, Journal of natural products.

[8]  Wei‐Lie Xiao,et al.  LC-UV-Guided Isolation and Structure Determination of Lancolide E: A Nortriterpenoid with a Tetracyclo[5.4.0.0(2,4).0(3,7)]undecane-Bridged System from a "Talented" Schisandra Plant. , 2016, Organic letters.

[9]  Ariel M. Sarotti,et al.  Beyond DP4: an Improved Probability for the Stereochemical Assignment of Isomeric Compounds using Quantum Chemical Calculations of NMR Shifts. , 2015, The Journal of organic chemistry.

[10]  C. Darsih,et al.  Cytotoxic metabolites from the endophytic fungus Penicillium chermesinum: discovery of a cysteine-targeted Michael acceptor as a pharmacophore for fragment-based drug discovery, bioconjugation and click reactions , 2015 .

[11]  Xiaobing Wang,et al.  Bioactive metabolites from the endophytic fungus Alternaria alternata. , 2014, Fitoterapia.

[12]  Jin-Ming Gao,et al.  Secondary metabolites from the endophytic Botryosphaeria dothidea of Melia azedarach and their antifungal, antibacterial, antioxidant, and cytotoxic activities. , 2014, Journal of agricultural and food chemistry.

[13]  D. Lai,et al.  Natural Dibenzo-α-Pyrones and Their Bioactivities , 2014, Molecules.

[14]  J. Rita,et al.  The correct structure of aquatolide-experimental validation of a theoretically-predicted structural revision. , 2012, Journal of the American Chemical Society.

[15]  Shu-Lin Chang,et al.  Illuminating the diversity of aromatic polyketide synthases in Aspergillus nidulans. , 2012, Journal of the American Chemical Society.

[16]  William H Gerwick,et al.  Survey of marine natural product structure revisions: a synergy of spectroscopy and chemical synthesis. , 2011, Bioorganic & medicinal chemistry.

[17]  Xiaobing Wang,et al.  A [2 + 2] cycloaddition dimer and a Diels-Alder adduct from Alpinia katsumadai. , 2011, Organic letters.

[18]  Jonathan M Goodman,et al.  Assigning stereochemistry to single diastereoisomers by GIAO NMR calculation: the DP4 probability. , 2010, Journal of the American Chemical Society.

[19]  F. Jensen The optimum contraction of basis sets for calculating spin–spin coupling constants , 2010 .

[20]  Jason W. Labonte,et al.  Structural basis for biosynthetic programming of fungal aromatic polyketide cyclization , 2009, Nature.

[21]  Ariel M. Sarotti,et al.  A multi-standard approach for GIAO (13)C NMR calculations. , 2009, The Journal of organic chemistry.

[22]  M. Maier,et al.  Structural revisions of natural products by total synthesis. , 2009, Natural product reports.

[23]  J. Goodman,et al.  Assigning the stereochemistry of pairs of diastereoisomers using GIAO NMR shift calculation. , 2009, The Journal of organic chemistry.

[24]  F. Totzke,et al.  Cytotoxic metabolites from the fungal endophyte Alternaria sp. and their subsequent detection in its host plant Polygonum senegalense. , 2008, Journal of natural products.

[25]  C. Birkinshaw,et al.  Antiproliferative xanthones of Terminalia calcicola from the Madagascar rain forest. , 2007, Journal of natural products.

[26]  C. Shearer,et al.  Altenuene derivatives from an unidentified freshwater fungus in the family Tubeufiaceae. , 2006, Journal of natural products.

[27]  K C Nicolaou,et al.  Chasing molecules that were never there: misassigned natural products and the role of chemical synthesis in modern structure elucidation. , 2005, Angewandte Chemie.

[28]  I. Carletti,et al.  Yardenone A and B: new cytotoxic triterpenes from the Indian Ocean sponge Axinella cf. bidderi. , 2003, Journal of natural products.

[29]  J. Staunton,et al.  Polyketide biosynthesis: a millennium review. , 2001, Natural product reports.