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Pure Appl. Chem., 2007, Vol. 79, No. 4, pp. 667-676

http://dx.doi.org/10.1351/pac200779040667

Progress toward a total synthesis of spirastrellolide A

Ian Paterson, Edward A. Anderson, Stephen M. Dalby, Jong Ho Lim, Olivier Loiseleur, Philip Maltas and Christian Moessner

University Chemical Laboratory, Lensfield Road, Cambridge CB2 1EW, UK

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  • Paterson Ian, Maltas Philip, Dalby Stephen M., Lim Jong Ho, Anderson Edward A.: A Second-Generation Total Synthesis of Spirastrellolide A Methyl Ester. angew chemie 2012, n/a. <http://dx.doi.org/10.1002/ange.201108594>
  • Paterson Ian, Maltas Philip, Dalby Stephen M., Lim Jong Ho, Anderson Edward A.: A Second-Generation Total Synthesis of Spirastrellolide A Methyl Ester. Angew Chem Int E 2012, n/a. <http://dx.doi.org/10.1002/anie.201108594>
  • Kobayashi Shū, Endo Toshimitsu, Ueno Masaharu: Chiral Zinc-Catalyzed Asymmetric α-Alkylallylation and α-Chloroallylation of Aldehydes. angew chemie 2011, 123, 12470. <http://dx.doi.org/10.1002/ange.201106433>
  • Kobayashi Shū, Endo Toshimitsu, Ueno Masaharu: Chiral Zinc-Catalyzed Asymmetric α-Alkylallylation and α-Chloroallylation of Aldehydes. Angew Chem Int E 2011, 50, 12262. <http://dx.doi.org/10.1002/anie.201106433>
  • Paterson Ian, Dalby Stephen M., Maltas Philip: Strategy Evolution in the Total Synthesis of Spirastrellolide A Methyl Ester. Isr J Chem 2011, 51, 406. <http://dx.doi.org/10.1002/ijch.201100007>
  • Paterson Ian, Dalby Stephen M.: Synthesis and stereochemical determination of the spirastrellolides. Nat Prod Rep 2009, 26, 865. <http://dx.doi.org/10.1039/b906991g>
  • Paterson Ian, Anderson Edward A., Dalby Stephen M., Lim Jong Ho, Genovino Julien, Maltas Philip, Moessner Christian: Total Synthesis of Spirastrellolide A Methyl Ester—Part 1: Synthesis of an Advanced C17–C40 Bis-spiroacetal Subunit. Angew Chem 2008, 120, 3058. <http://dx.doi.org/10.1002/ange.200705565>
  • Paterson Ian, Anderson Edward A., Dalby Stephen M., Lim Jong Ho, Genovino Julien, Maltas Philip, Moessner Christian: Total Synthesis of Spirastrellolide A Methyl Ester—Part 1: Synthesis of an Advanced C17–C40 Bis-spiroacetal Subunit. Angew Chem Int Ed 2008, 47, 3016. <http://dx.doi.org/10.1002/anie.200705565>
  • Paterson Ian, Anderson Edward A., Dalby Stephen M., Lim Jong Ho, Loiseleur Olivier, Maltas Philip, Moessner Christian: Progress Toward a Total Synthesis of Spirastrellolide A. ChemInform 2007, 38. <http://dx.doi.org/10.1002/chin.200738251>