| abstract |
The invention relates to compounds of formula (I): wherein n is an integer from 0 to 3, p is 0 or 1, D is an oxygen atom or a bond, X is a heteroatom chosen from an oxygen atom or a sulfur atom, R1, R2 represent, independently of one another, a hydrogen atom or a (C1-6) alkyl group or R1, R2 may form a cycloalkyl group, Y is an aryl, heteroaryl, aryloxy, (C1-6) alkyl, (C3-10) cycloalkyl group, said groups being optionally substituted by one or more substituents selected from a halogen atom, a (C1-6) alkyl group or (C1-6) alkoxy. Preparation process and therapeutic application |