1009044-19-2Relevant academic research and scientific papers
Diastereoselective spiroannulation of phenolic substrates: Advances towards the asymmetric formation of the manumycin m-C7N core skeleton
Plourde, Guy L.,Spaetzel, Randy R.,Kwasnitza, Jolene S.,Scully, Thomas W.
, p. 2215 - 2222 (2007)
The asymmetric syntheses of two new spirolactones prepared in optically pure form from L-3-nitrotyrosine are described. The key step, an oxidative spiroannulation, was carried out on the optically active phenols 11a and 11b and afforded the new spirolacto
