1344153-75-8Relevant academic research and scientific papers
Enantioselective synthesis of (-)-exiguolide by iterative stereoselective dioxinone-directed prins cyclizations
Crane, Erika A.,Zabawa, Thomas P.,Farmer, Rebecca L.,Scheidt, Karl A.
, p. 9112 - 9115 (2011)
Three become one: The title compound can be prepared in 26 steps by employing a unified Prins cyclization strategy to construct both tetrahydropyran rings (see scheme). The route combines two similar dioxinone fragments and one aldehyde component to gener
