An efficient and stereoselective dearylation of asarinin and sesamin tetrahydrofurofuran lignans to acuminatolide by methyltrioxorhenium/H(2)O(2) and UHP systems

J Nat Prod. 2007 Jan;70(1):39-42. doi: 10.1021/np060479u.

Abstract

The synthesis of stereoisomers of acuminatolide is rare and requires complex and time-consuming multistep procedures. Asarinin (1) and sesamin (2), two diasteromeric tetrahydrofurofuran lignans, are efficiently mono-dearylated by methyltrioxorhenium (MTO, I) and hydrogen peroxide (H2O2) or urea hydrogen peroxide adduct (UHP) as primary oxidant to give (-)-(7R,8'R,8R)-acuminatolide (3A) and (+)-(7S,8R,8'R)-acuminatolide (3B), respectively, in high yield and diastereoselectivity (de >98%). The oxidation of 1 was also performed with novel heterogeneous catalysts based on the heterogenation of MTO on poly(4-vinylpyridine) and polystyrene resins. In these latter cases 3A was obtained with a different yield and selectivity depending on the physical-chemical properties of the support. Cytotoxic effects of 3A and 3B in mammalian cell lines in vitro are also reported.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / isolation & purification
  • Antineoplastic Agents / pharmacology
  • Dioxoles / chemistry*
  • Dioxoles / isolation & purification
  • Dioxoles / pharmacology
  • Drug Screening Assays, Antitumor
  • Humans
  • Lignans / chemistry*
  • Lignans / isolation & purification
  • Lignans / pharmacology
  • Mice
  • Molecular Structure
  • Organometallic Compounds / chemistry
  • Oxidation-Reduction
  • Rhenium / chemistry
  • Stereoisomerism
  • Zanthoxylum / chemistry*

Substances

  • Antineoplastic Agents
  • Dioxoles
  • Lignans
  • Organometallic Compounds
  • acuminatolide
  • Rhenium
  • methyltrioxorhenium VII
  • sesamin