Utilisation du N,N-diméthylamino-acétonitrile pour la synthèse régiosélective de diallylcétones masquées. Application à la synthèse de al γ-damascone = Use of N,N-dimethylamino acetonitrile for the regioselective synthesis of protected diallylketones. Application in the synthesis of γ-damasconeAMROLLAH-MADJDABADI, A; STELLA, L.Bulletin de la Société chimique de France. 1987, Num 2, pp 350-354, issn 0037-8968Article

Another challenge to the validity of the use of cyclizable probes as evidence for single-electron transfer in nucleophilic aliphatic substitution: the reaction of LiAlH₄ with alkyl iodidesASHBY, E. C; TUNG PHAM; AMROLLAH MADJDABADI, A et al.Journal of organic chemistry. 1988, Vol 53, Num 26, pp 6156-6158, issn 0022-3263Article

A convenient method for the preparation of gem-halonitro compoundsAMROLLAH-MADJDABADI, A; BEUGELMANS, R; LECHEVALLIER, A et al.Synthesis (Stuttgart). 1986, Num 10, pp 828-830, issn 0039-7881Article

Direct and efficient preparation of gem-chloronitro compounds or nitro compounds from gen-bromonitro compoundsAMROLLAH-MADJDABADI, A; BEUGELMANS, R; LECHEVALLIER, A et al.Synthesis (Stuttgart). 1986, Num 10, pp 826-828, issn 0039-7881Article

A simple method for the conversion of adamantyl, benzyl and benzyhydryl alcohols to their corresponding bromides and chlorides and the transhalogenation of adamantyl, benzyl, benzhydryl and tertiary alkyl bromides and chloridesAMROLLAH-MADJDABADI, A; PHAM, T. N; ASHBY, E. C et al.Synthesis (Stuttgart). 1989, Num 8, pp 614-616, issn 0039-7881Article

Concerning the mechanism of the reaction of LiAlH₄ with alkyl halidesASHBY, E. C; PHAM, T. N; AMROLLAH-MADJDABADI, A et al.Journal of organic chemistry. 1991, Vol 56, Num 4, pp 1596-1603, issn 0022-3263, 8 p.Article