1379188-47-2Relevant academic research and scientific papers
Stereoselective Total Synthesis of (±)-Pleurospiroketals A and B
Thorat, Sagar S.,Rama Krishna, Gamidi,Kontham, Ravindar
, p. 13572 - 13582 (2021/10/12)
A full account of our efforts toward the stereoselective total synthesis of sesquiterpenoid-derived natural products (±)-pleurospiroketals A and B is described. Commercially available 3-methyl-2-cyclohexenone and 2,2-dimethyloxirane were used as key build
Convergent total synthesis of the racemic HIF-1 inhibitor laurenditerpenol
Jung, Michael E.,Im, G-Yoon J.
, p. 4962 - 4964 (2008/09/21)
The convergent total synthesis of the HIF-1 inhibitor laurenditerpenol 1a is reported. The key step is the Julia olefination-reduction process between the two components, the sulfone 4 (prepared from the dimethylfuran-maleic anhydride Diels-Alder adduct)
