Divergent pathways to isophthalates and naphthalate esters from methyl coumalate
Sign Up to like & getrecommendations! Published in 2018 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2018.09.058
Abstract: Abstract Methyl coumalate readily reacts with enamines at ambient temperature to give lactones, which can be further transformed into isophthalates and tetrahydronaphthoates. Both cyclic and acyclic enamines show good reactivity. Dehydrogenation of tetrahydronaphthoate 4a was… read more here.
Keywords: esters methyl; naphthalate esters; isophthalates naphthalate; pathways isophthalates ... See more keywords