A divergent and stereoselective approach to phenolic 1,7-dihydroxy-bisabolane sesquiterpenes: asymmetric total synthesis of (+)-curcutetraol, (+)-sydonol, (+)-sydonic acid, and (+)-7-O-methylsydonic acid

[1]  K. Hong,et al.  Cytotoxic Polyphenols from the Fungus Penicillium expansum 091 006 Endogenous with the Mangrove Plant Excoecaria agallocha , 2012, Planta Medica.

[2]  S. Serra,et al.  Unambiguous Characterization of the Sesquiterpene (7R,9E)‐1,2,11‐Trihydroxy‐1,3,5,9‐bisabolatetraene through Its Enantioselective Synthesis , 2012 .

[3]  S. Serra.  Enantioselective Synthesis of the Bisabolane Sesquiterpene (+)-1-Hydroxy-1,3,5-Bisabolatrien-10-one and Revision of its Absolute Configuration , 2012, Natural product communications.

[4]  C. Shao,et al.  New bisabolane sesquiterpenoids from a marine-derived fungus Aspergillus sp. isolated from the sponge Xestospongia testudinaria. , 2012, Bioorganic & medicinal chemistry letters.

[5]  P. Qian,et al.  Antibacterial Bisabolane-Type Sesquiterpenoids from the Sponge-Derived Fungus Aspergillus sp. , 2012, Marine drugs.

[6]  J. Sakayaroj,et al.  Sesquiterpene and xanthone derivatives from the sea fan-derived fungus Aspergillus sydowii PSU-F154. , 2011, Journal of natural products.

[7]  S. Serra.  Lipase-mediated resolution of substituted 2-aryl-propanols: application to the enantioselective synthesis of phenolic sesquiterpenes , 2011 .

[8]  K. Hong,et al.  Cytotoxic polyphenols from the marine-derived fungus Penicillium expansum. , 2010, Journal of natural products.

[9]  C. Shao,et al.  Five Sesquiterpenoids from a Marine-Derived Fungus Aspergillus sp. Isolated from a Gorgonian Dichotella gemmacea , 2010, Marine drugs.

[10]  R. J. Thomson,et al.  Triflimide-catalysed sigmatropic rearrangement of N-allylhydrazones as an example of a traceless bond construction , 2010, Nature Chemistry.

[11]  Kazuaki Tanaka,et al.  Isolation and Absolute Stereochemistry of Optically Active Sydonic Acid from Glonium sp. (Hysteriales, Ascomycota) , 2009, Bioscience, biotechnology, and biochemistry.

[12]  Suguru Ito,et al.  Asymmetric total synthesis of (+)-curcutetraol and (+)-sydonol , 2008 .

[13]  M. Chorghade,et al.  A Short and Efficient Synthetic Strategy for the Total Syntheses of (S)‐(+)‐ and (R)‐(–)‐Plakolide A , 2007 .

[14]  Elisabetta Brenna,et al.  Recent advances in the benzannulation of substituted 3-alkoxycarbonyl-3,5-hexadienoic acids and 3-alkoxycarbonylhex-3-en-5-ynoic acids to polysubstituted aromatics. , 2007, Chemistry.

[15]  G. Bringmann,et al.  Isolation, Structural Elucidation, and Synthesis of Curcutetraol , 2005 .

[16]  C. Fuganti,et al.  CUPARENE SESQUITERPENES: SYNTHESIS OF (+)-3-HYDROXYCUPARENE AND (+)-CUPARENE , 1999 .

[17]  C. Fuganti,et al.  A Concise Synthesis of 3-Hydroxy-4-(β-glucopyranosyl) Benzoate: A New Route to β-C-Aryl Glycosides , 1999 .

[18]  A. Zeeck,et al.  Secondary Metabolites by Chemical Screening, 23. Waraterpols, New Penicillium Metabolites and Their Derivatives , 1993 .

[19]  S. Takano,et al.  Asymmetric construction of optically active 3-hydroxyalkyne functionalities , 1989 .

[20]  S. Denmark,et al.  (E)-3-(Trimethylsilyl)-2-propen-1-ol. An Improved Preparation , 1983 .

[21]  Yoshifumi Sato,et al.  Sydonol, a new fungal morphogenic substance produced by an unidentified Aspergillus sp. , 1981 .

[22]  T. Hamasaki,et al.  Two New Metabolites, Sydonic Acid and Hydroxysydonic Acid, from Aspergillus sydowi , 1978 .

[23]  R. Hudson,et al.  Structure et réactions du composé d'addition: triphénylphosphine ‐ anhydride maléique , 1963 .