The nucleophilic addition of alpha-metallated 1,3-dioxanes to planar chiral cationic eta3-allylmolybdenum complexes. Synthesis of (2E,5S,6R,7E)-6-methyl-8-phenylocta-2,7-dienoic acid methyl ester, a key component of the Cryptophycins

Org Biomol Chem. 2004 Jun 21;2(12):1719-31. doi: 10.1039/b400242c. Epub 2004 May 25.

Abstract

Two adjacent stereogenic centres and a pendant alkene were constructed via nucleophilic addition of a 1,3-dioxan-4-ylcopper(I) reagent to a cationic eta3-allylmolybdenum complex as part of a synthesis of (2E,5S,6R,7E)-6-methyl-8-phenylocta-2,7-dienoic acid, a key component of the Cryptophycins. Oxidative addition of Mo(CO)(4)(THF)(2) to allyl benzoates provides an efficient synthesis of eta3-allylmolybdenum(dicarbonyl) complexes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allyl Compounds / chemistry
  • Antineoplastic Agents / chemistry
  • Cations / chemistry
  • Copper / chemistry*
  • Depsipeptides
  • Dioxanes / chemistry*
  • Esters / chemical synthesis
  • Esters / chemistry
  • Molecular Structure
  • Molybdenum / chemistry*
  • Organometallic Compounds / chemistry*
  • Oxidation-Reduction
  • Peptides, Cyclic / chemistry*
  • Stereoisomerism

Substances

  • Allyl Compounds
  • Antineoplastic Agents
  • Cations
  • Depsipeptides
  • Dioxanes
  • Esters
  • Organometallic Compounds
  • Peptides, Cyclic
  • cryptophycin
  • Copper
  • Molybdenum