108124-04-5Relevant academic research and scientific papers
Process for preparing (hetero) aromatic substituted benzene derivatives
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Page column 17, (2008/06/13)
Three processes are described for preparing (hetero)aromatic substituted benzene derivatives which comprise aromatization of cyclohexenone derivatives via (chloro)cyclohexadiene derivatives.
Process for preparing (hetero) aromatic substituted benzene derivatives
-
, (2008/06/13)
Three processes are described for preparing (hetero)aromatic substituted benzene derivatives which comprise aromatization of cyclohexenone derivatives via (chloro)cyclohexadiene derivatives.
Studies on alkylation of Hagemann's ester and its derivatives with alkyl halides and Michael acceptors
Sen, Parimal K.,Das, Tulika,Maiti, Krishnásri,Maiti, Basudeb,Sarkar, Achintya K.
, p. 583 - 587 (2007/10/03)
Alkylation and Michael addition of ethyl 3-methyl-4-oxo-2-phenylcyclohex-2-enecarboxylate (1b) have been studied under basic conditions. Similar reactions with Hagemann's ester (1c) have been carried out using phase transfer catalysts as well as solid supports. The ratio of the C-1 to C-3 alkylated products have been determined. A probable explanation for the regioselectivity observed has been given.
Aromatization of Cyclohexenones with Iodine/sodium alkoxide. A Regioselective synthesis of 2-Iodophenols
Hegde, Shridhar G.,Kassim, Amude M.,Ingrum, April I.
, p. 8395 - 8398 (2007/10/02)
Aromatizations of a wide variety of easily accessible 2-cyclohexenone-4-carboxylates with iodine and sodium ethoxide give the corresponding 2-iodophenols in good yield and high regioselectivity.
