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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…
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Keywords:
esters methyl;
naphthalate esters;
isophthalates naphthalate;
pathways isophthalates ... See more keywords