877454-86-9Relevant academic research and scientific papers
Utilization of a 1,2-dioxine for the synthesis of the four possible stereoisomers of oak lactone
Brown, Rachel C.,Taylor, Dennis K.,Elsey, Gordon M.
, p. 463 - 466 (2007/10/03)
The natural products cis- and trans-oak lactone (1) have been prepared, along with their enantiomeric counterparts, from furanone 12, which was itself prepared from racemic 1,2-dioxine 9 and a chiral malonate diester. The key steps in the synthesis of 1 a
