Features of the aminomethylation of 7-hydroxy-4′-fluoroisoflavones with primary amines
摘要:
The behavior of 7-hydroxy-4'-fluoroisoflavones under the conditions of the Mannich reaction with primary amines was studied. New 9-alkyl-substituted 3-(4-fluorophenyl)-9,10-dihydro-4H,8H-chromeno-[8,7-e][1,3]oxazin-4-ones were synthesized. A method was developed for the synthesis of 8-amino- methyl derivatives of isoflavones.
Features of the aminomethylation of 7-hydroxy-4′-fluoroisoflavones with primary amines
作者:S. P. Bondarenko、M. S. Frasinyuk、V. P. Khilya
DOI:10.1007/s10593-010-0485-2
日期:2010.6
The behavior of 7-hydroxy-4'-fluoroisoflavones under the conditions of the Mannich reaction with primary amines was studied. New 9-alkyl-substituted 3-(4-fluorophenyl)-9,10-dihydro-4H,8H-chromeno-[8,7-e][1,3]oxazin-4-ones were synthesized. A method was developed for the synthesis of 8-amino- methyl derivatives of isoflavones.