La vinflunine, nouvel agent anticancéreux fluoré dérivé des alcaloïdes de Vinca = Vinflunine: a new anti-cancer fluorinated agent derived from vinca-alkaloïdsJACQUESY, J. C; JOUANNETAUD, M. P.Annales pharmaceutiques françaises. 2005, Vol 63, Num 1, pp 28-34, issn 0003-4509, 7 p.Article

Fonctionnalisation de liaisons non activées en milieu superacide = Functionalization of nonactivated bonds in superacidic mediaJACQUESY, J.-C; JOUANNETAUD, M.-P; MARTIN, A et al.Bulletin de la Société chimique de France. 1997, Vol 134, Num 5, pp 425-438, issn 0037-8968Article

Hydroxylation de l'estrone et de son acétate par le peroxyde d'hydrogène en milieu superacide = Hydroxylation of estrone and its acetate with hydrogen peroxide in superacid mediaBERRIER, C; JACQUESY, J. C; JOUANNETAUD, M. P et al.Tetrahedron (Oxford. Print). 1984, Vol 40, Num 24, pp 5135-5141, issn 0040-4020Article

Hydroxylation directe d'esters de phényle et d'anilides par le peroxyde d'hydrogène en milieu superacide = Direct hydroxylation of phenyl esters and anilides by hydrogen peroxide in superacid mediumBERRIER, C; JACQUESY, J.-C; JOUANNETAUD, M.-P et al.Bulletin de la Société chimique de France. 1987, Num 1, pp 158-164, issn 0037-8968Article

Direct conversion of anilines into aminophenolsJACQUESY, J.-C; JOUANNETAUD, M.-P; MORELLET, G et al.Tetrahedron letters. 1984, Vol 25, Num 14, pp 1479-1482, issn 0040-4039Article

Synthesis of fluorohydrins and of bromofluoroderivatives by anti addition on the 14,15 double bond of tabersonine in superacidsBERRIER, C; JACQUESY, J. C; JOUANNETAUD, M. P et al.Tetrahedron (Oxford. Print). 1990, Vol 46, Num 3, pp 815-826, issn 0040-4020, 12 p.Article

Direct bromination or hydroxylation AT C-11 in vincadifformine and tabersonine derivatives in superacidsBERRIER, C; JACQUESY, J. C; JOUANNETAUD, M. P et al.Tetrahedron (Oxford. Print). 1990, Vol 46, Num 3, pp 827-832, issn 0040-4020, 6 p.Article

Protonated phenol derivatives as reactive speciesJACQUESY, J.-C; GESSON, J.-P; JOUANNETAUD, M.-P et al.Reviews of chemical intermediates. 1988, Vol 9, Num 1, pp 1-26, issn 0162-7546Article

Direct hydroxylation of indoles in superacids: application to the hydroxylation of tryptophan and tryptamine derivativesBERRIER, C; JACQUESY, J. C; JOUANNETAUD, M. P et al.New journal of chemistry (1987). 1987, Vol 11, Num 8-9, pp 611-615, issn 1144-0546Article

Hydroxylation and bromination of indolines and tetrahydroquinoline in superacidsBERRIER, C; JACQUESY, J. C; JOUANNETAUD, M. P et al.New journal of chemistry (1987). 1987, Vol 11, Num 8-9, pp 605-609, issn 1144-0546Article

Hydroxylation directe d'anilines en aminophénols = Direct hydroxylation of anilines to aminophenolsJACQUESY, J.-C; JOUANNETAUD, M.-P; MORELLET, G et al.Bulletin de la Société chimique de France. 1986, Num 4, pp 625-629, issn 0037-8968Article

Nouvelle synthèse de 2-aryl ou 4-arylcyclohexénones = Novel synthesis of 2-aryl or 4-arylcyclohexenonesBERRIER, C; GAILLARD, E; JACQUESY, J. C et al.Bulletin de la Société chimique de France. 1991, Num 4, pp 537-543, issn 0037-8968Article

Nouvelles voies de synthèses en milieux superacides = New syntheses in superacidsJACQUESY, J. C; BERRIER, C; GESSON, J. P et al.Annales de chimie (Paris. 1914). 1984, Vol 9, Num 6, pp 641-648, issn 0151-9107Conference Paper

Ipso-chloration des éthers de para-alkylphénols par SbF₅-CH₂Cl₂(CHCl₃,CCl₄) : une nouvelle voie d'accès aux 4-chlorocyclohexa-2,5-diénones = Ipso-chlorination of para-alkylphenols ethers with SbF₅-CH₂Cl₂(CHCl₃,CCl₄) : a nouvel route to 4-chlorocyclohexa-2,5-dienonesJOUANNETAUD, M.-P; JACQUESY, J.-C; KARAM, O et al.Bulletin de la Société chimique de France. 1994, Vol 131, Num 3, pp 284-290, issn 0037-8968Article

Electrophilic hydroxylation of aromatics in superacidsJACQUESY, J.-C; BERRIER, C; GESSON, J.-P et al.Bulletin de la Société chimique de France. 1994, Vol 131, Num 6, pp 658-664, issn 0037-8968Article

Ipso-chlorination of 4-alkylphenols ethers a novel route to 4-chlorocyclohexa-2,5-dienonesFERRON, B; JACQUESY, J.-C; JOUANNETAUD, M.-P et al.Tetrahedron letters. 1993, Vol 34, Num 18, pp 2949-2952, issn 0040-4039Article