69204-28-0Relevant academic research and scientific papers
Simple Approach to O-Protected Deaminotunicaminyluracil
Karpiesiuk, Wojciech,Banaszek, Anna
, p. 2965 - 2974 (1994)
A five-step synthesis of deaminotunicaminyluracil is presented.Coupling of the ylide, generated from the phosphonium salt 4, with the aldehyde 5 afforded the undecose 6 in high yield.The key step in this synthesis was the hydroboration-oxidation reaction of the olefin 6.For this purpose several hydroborating reagents were examined.The diborane-THF reagent led to the desired deaminotunicamine derivative 8, as the predominant product.Condensation of undecose 8c with 1,3-di-O-trimethylsilyluracil gave the title compound.
