FIELD: organic synthesis.
SUBSTANCE: invention provides a method of preparing 3-indolylphenylmethyl-2-substituted cyclic alpha-ketones having general formula:
, in which R represents 1 or 2 carbon atoms with annelated benzene ring or substituted methylidene group, in particular 2-methylpropylidene or 2-phenylmethylidene group, and consists in that α-phenyl-norgramine is brought into reaction with cyclic ketone of general formula:
, wherein R is defined above, in boiling isopropyl alcohol in presence of sodium acetate, pyridine, triethylamine, alkali, or chiral amine as base.
EFFECT: expanded synthetic possibilities in a series of indolyl derivatives.
3 tbl, 6 ex
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