Stereoselective synthesis of (R)-(−) and (S)-(+)-phoracantholide I from (R)-(+)-γ-valerolactone
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V. Siddaiah | H. Mohan | T. Pratap | V. Gajare | Sandip R. Khobare | Rajender Datrika | Srinivasa Reddy Kallam | Muralikrishna Kommi
[1] I. Lavandera,et al. Stereodivergent Preparation of Valuable γ- or δ-Hydroxy Esters and Lactones through One-Pot Cascade or Tandem Chemoenzymatic Protocols , 2014 .
[2] M. Vences,et al. Macrolides and alcohols as scent gland constituents of the Madagascan frog Mantidactylus femoralis and their intraspecific diversity. , 2013, Journal of natural products.
[3] J. Campagne,et al. Update 1 of: macrolactonizations in the total synthesis of natural products. , 2013, Chemical reviews.
[4] T. Jamison,et al. Recent progress in the synthesis of oxepanes and medium ring ethers , 2012 .
[5] M. Raggi,et al. Selective serotonin reuptake inhibitors (SSRIs): therapeutic drug monitoring and pharmacological interactions. , 2012, Current medicinal chemistry.
[6] M. Vences,et al. Volatile amphibian pheromones: macrolides from mantellid frogs from Madagascar. , 2012, Angewandte Chemie.
[7] R. Bauer,et al. Design, synthesis and antimycobacterial activities of 1-methyl-2-alkenyl-4(1H)-quinolones , 2011, Bioorganic & medicinal chemistry.
[8] N. N. Rao,et al. An efficient total synthesis of (+)-Cladospolide C , 2009 .
[9] M. Struchkova,et al. A convenient route to chiral γ-lactones via asymmetric hydrogenation of γ-ketoesters using the RuCl3–BINAP–HCl catalytic system , 2008 .
[10] P. Krishna,et al. Stereoselective First TotalSynthesis of a Ten-Membered Macrolide from l-MalicAcid and (2R)-2,3-O-Cyclohexylideneglyceraldehyde , 2008 .
[11] J. Rokach,et al. Enantio- and stereospecific syntheses of 15(R)-Me-PGD2, a potent and selective DP2-receptor agonist. , 2008, The Journal of organic chemistry.
[12] J. Yadav,et al. Stereoselective formal total synthesis of (+)-methynolide. , 2007, The Journal of organic chemistry.
[13] Isamu Shiina. Total synthesis of natural 8- and 9-membered lactones: recent advancements in medium-sized ring formation. , 2007, Chemical reviews.
[14] B. Lipshutz,et al. Applications of asymmetric hydrosilylations mediated by catalytic (DTBM-SEGPHOS)CuH. , 2006, Organic letters.
[15] T. Sammakia,et al. Use of thiazoles in the halogen dance reaction: application to the total synthesis of WS75624 B. , 2004, The Journal of organic chemistry.
[16] H. Hara,et al. Synthesis of the highly potent prostanoid FP receptor agonist, AFP-168: a novel 15-deoxy-15,15-difluoroprostaglandin F2α derivative , 2004 .
[17] Arun K. Ghosh,et al. Enantioselective synthesis of (+)-cryptophycin 52 (LY355703), a potent antimitotic antitumor agent. , 2003, The Journal of organic chemistry.
[18] W. A. Donaldson,et al. Synthesis of (+)-decarestrictine L , 2003 .
[19] V. Roussis,et al. New sesterterpene metabolites from the Mediterranean sponge Cacospongia scalaris. , 2003, Journal of natural products.
[20] P. Ramachandran,et al. Selective Reductions. 59. Effective Intramolecular Asymmetric Reductions of α-, β-, and γ-Keto Acids with Diisopinocampheylborane and Intermolecular Asymmetric Reductions of the Corresponding Esters with B-Chlorodiisopinocampheylborane , 2002 .
[21] Chi-Tang Ho,et al. New type sesquiterpene lactone from almond hulls (Prunus amygdalus Batsch) , 2002 .
[22] C. Senanayake,et al. A practical asymmetric synthesis of (R)-fluoxetine and its major metabolite (R)-norfluoxetine , 2001 .
[23] F. Molinari,et al. Microbial bioreductions of γ- and δ-ketoacids and their esters , 2001 .
[24] T. LaPorte,et al. Biochemical approaches to the synthesis of ethyl 5-(s)-hydroxyhexanoate and 5-(s)-hydroxyhexanenitrile. , 2001, Enzyme and microbial technology.
[25] H. Ohta,et al. BIOCATALYST-MEDIATED EFFICIENT PREPARATION OF HIGHLY ENANTIOMERICALLY ENRICHED (R)-5-HEXANOLIDE , 1997 .
[26] T. Katsuki,et al. Insect pheromone synthesis using Mn-salen catalyzed asymmetric epoxidation as a key step , 1995 .
[27] G. Rousseau,et al. Medium ring lactones , 1995 .
[28] L. Bito,et al. Phenyl-substituted prostaglandins: potent and selective antiglaucoma agents. , 1993, Journal of medicinal chemistry.
[29] Y. Ban,et al. A synthesis of novel nine-membered dienones through a cyclic acetylenic oxy-cope rearrangement: The synthesis of dl-phoracantholide I , 1986 .
[30] S. Yamada,et al. New general synthesis of medium-sized lactones: A new entry tothe synthesis of (+−)-phoracantholide I [(+−)-decan-9-olide]☆ , 1985 .
[31] T. Katsuki,et al. A rapid esterification by means of mixed anhydride and its application to large-ring lactonization. , 1979 .
[32] B. Trost,et al. Influence of a transition metal on the regiochemistry of ring closures. An approach to medium-ring compounds , 1979 .
[33] H. Gerlach,et al. Synthese von zwei natürlich vorkommenden Lactonen mit 10gliedrigen Ringen: (±)-Phoracantholid J und I , 1978 .
[34] O. Mitsunobu,et al. Synthesis of lactones and cycloalkanes. Cyclization of ω-hydroxy acids and ethyl α-cyano-ω-hydroxycarboxylates , 1976 .