17839-48-4Relevant academic research and scientific papers
Organoboron-based allylation approach to the total synthesis of the medium-ring dilactone (+)-antimycin A1b
Janetzko, John,Batey, Robert A.
, p. 7415 - 7424 (2014)
The stereoselective synthesis of (+)-antimycin A1b has been accomplished in 12 linear steps and 18% overall yield from (-)-ethyl lactate. A robust, scalable, and highly diastereoselective montmorillonite K10-promoted allylation reaction between
