Zhao, A., Lee, S.H., Moiena, M., Jenkins, R.G., Patrick, D.R., Huber, H.E., Goetz, M.A., Hensens, O.D., Zink, D.L., Viella, D., Dombrowski, A.W., Lingham, R.B. and Huang, L. (1999) Resorcylic Acid Lactones: Naturally Occurring Potent and Selective Inhibitors of MEK. The Journal of Antibiotics, 52, 1086-1094.
https://doi.org/10.7164/antibiotics.52.1086

has been cited by the following article:

• TITLE: Progress toward the Synthesis of Pochonin J

  AUTHORS: Sydney N. Jackson, Rongson Pongdee

  KEYWORDS: Natural Products, Pochonin J, Resorcylic Acid Lactones

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.9 No.2, June 13, 2019

  ABSTRACT: The construction of the C(1) - C(5) fragment of the resorcylic acid lactone pochonin J is described. The synthesis is marked by the installation of the cis-1,3-diol moiety in a highly stereoselective manner using Evans’ intra-molecular base-catalyzed oxyconjugate addition of a hemiacetal-derived nucleophile. The synthetic route presented affords an efficient pathway to the preparation of this critical architectural feature that should facilitate the development of this secondary metabolite as a potential drug candidate.