Abstract
Reformatsky reagent generated from methyl 1-bromocyclohexane-1-carboxylate reacted with N-aryl-2-oxochromene-3-carboxamides and N-aryl-6-bromo-2-oxochromene-3-carboxamides to give, depending on the conditions, the corresponding N-aryl-(6-bromo)-4-(1-methoxycarbonylcyclohexyl)-2-oxochroman-3-carboxamides or 3-aryl-(9-bromo)-1,1-pentamethylene-2,3,4,4a,5,10b-hexahydro-1H-chromeno[3,4-c]pyridine-2,4,5-triones. The products were isolated as a single diastereoisomer.
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Original Russian Text © V.V. Shchepin, N.F. Kirillov, M.I. Vakhrin, O.B. Bayanova, S.N. Shurov, P.S. Silaichev, 2006, published in Zhurnal Obshchei Khimii, 2006, Vol. 76, No. 7, pp. 1194–1197.
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Shchepin, V.V., Kirillov, N.F., Vakhrin, M.I. et al. Reformatsky reaction of methyl 1-bromocyclohexane-1-carboxylate with N-aryl-2-oxochromene-3-carboxamides. Russ J Gen Chem 76, 1146–1149 (2006). https://doi.org/10.1134/S1070363206070255
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DOI: https://doi.org/10.1134/S1070363206070255