159691-90-4Relevant academic research and scientific papers
Enantioselective Synthesis of Bis(γ-butyrolactones). Their Oxidative Degradation to Tetraols as a Key Step in Stereoselective Syntheses of 1,3,5,7,9-Pentaol Synthons for Polyhydroxylated Natural Products
Menges, Markus,Brueckner, Reinhard
, p. 365 - 384 (2007/10/02)
The syntheses of two enatiopure skipped-chain pentaol building blocks 51 and 56 are described.They are based on a strategy which derives 1,3,7,9-tetraols from bis(γ-butyrolactones).Two equivalents of γ-lactone 17, readily available from L-glutamic acid, a
