A stereoselective access to the basic skeleton of phyllocladane type diterpenes: [3+2], [2+2+2], and [4+2] cycloadditionGOTTELAND, J.-P; MALACRIA, M.Tetrahedron letters. 1989, Vol 30, Num 19, pp 2541-2544, issn 0040-4039, 4 p.Article

Ulipristal acetate - safety and pharmacokinetics following multiple doses of 10-50 mg per dayPOHL, O; OSTERLOHT, I; GOTTELAND, J.-P et al.Journal of clinical pharmacy and therapeutics (Print). 2013, Vol 38, Num 4, pp 314-320, issn 0269-4727, 7 p.Article

Effects of erythromycin at steady-state concentrations on the pharmacokinetics of ulipristal acetatePOHL, O; OSTERLOH, I; GOTTELAND, J.-P et al.Journal of clinical pharmacy and therapeutics (Print). 2013, Vol 38, Num 6, pp 512-517, issn 0269-4727, 6 p.Article

Design and synthesis of new potential photoaffinity labels for mammalian squalene epoxidaseGOTTELAND, J.-P; DAX, C; HALAZY, S et al.Bioorganic & medicinal chemistry letters (Print). 1997, Vol 7, Num 9, pp 1153-1156, issn 0960-894XArticle

Structure of dimethyl (±)-1,2,3,4,4aα,4b,9,10-octahydro-6,7-bis(trimethylsilyl)-2β,10aβ-ethanophenanthrene-12,12-dicarboxylateGOTTELAND, J.-P; MALACRIA, M; FAURE, R et al.Acta crystallographica. Section C, Crystal structure communications. 1990, Vol 46, Num 7, pp 1271-1273, issn 0108-2701, 3 p.Article

Stereoselective access to the basic skeleton of tetracyclic diterpenes via a sequence of consecutive [3 + 2], [2 + 2 + 2], and [4 + +2] cycloaddition reactionsAUBERT, C; GOTTELAND, J.-P; MALACRIA, M et al.Journal of organic chemistry. 1993, Vol 58, Num 16, pp 4298-4305, issn 0022-3263Article

Asymmetric induction in the palladium catalyzed [3+2] cycloaddition reaction of trimethylenemethane with homochiral vinylsulfoxidesCHAIGNE, F; GOTTELAND, J.-P; MALACRIA, M et al.Tetrahedron letters. 1989, Vol 30, Num 14, pp 1803-1806, issn 0040-4039, 4 p.Article

Synthetic approach to aphidicolan and stemodan basic skeletons using a tandem principle [2+2+2] and [4+2] cycloaddition reactionsSTAMMLER, R; HALVORSEN, K; GOTTELAND, J.-P et al.Tetrahedron letters. 1994, Vol 35, Num 3, issn 0040-4039, 345, 417-420 [5 p.]Article

Sulfonamide derivatives of benzylamine block cholesterol biosynthesis in HepG₂ cells : A new type of potent squalene epoxidase inhibitorsGOTTELAND, J.-P; LOUBAT, C; PLANTY, B et al.Bioorganic & medicinal chemistry letters (Print). 1998, Vol 8, Num 11, pp 1337-1342, issn 0960-894XArticle

(Aryloxy)methylsilane derivatives as new cholesterol biosynthesis inhibitors : synthesis and hypocholesterolemic activity of a new class of squalene epoxidase inhibitorsGOTTELAND, J.-P; BRUNEL, I; GENDRE, F et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 17, pp 3207-3216, issn 0022-2623Article