127604-87-9Relevant academic research and scientific papers
CYCLOADDITIONS IN SYNTHESES.PART 41. CHIRAL SPIROCYCLIC 5-ARYL-METHYLENE-1,3-DIOXANE-4,6-DIONES AS NOVEL SYNTHONS FOR ENANTIOMERICALLY PURE 2-ARYLCYCLOPROPANE-1,1-DICARBOXYLATES
Sato, Masayuki,Hisamichi, Hiroyuki,Kaneko, Chikara,Suzaki, Naoko,Furuya, Toshio,Inukai, Noriyoshi
, p. 5281 - 5284 (1989)
E- and Z- isomers of spirocyclic 5-arylmethylene-1,3-dioxane-4,6-dione, useful synthons for enantiomerically pure cyclopropane-1,1-dicarboxylates, have been synthesized from 1-menthone.Their diastereofacial selectivity is explained by a boat conformation in their dioxanedione ring.
