Chemical modification of rapamycin: the discovery of SDZ RAD von Sedrani, R, Cottens, S, Kallen, J, Schuler, W

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SDZ RAD, a new rapamycin derivative : Pharmacological properties in vitro and in vivo von SCHULER, W, SEDRANI, R, COTTENS, S, HÄBERLIN, B, SCHULZ, M, SCHUURMAN, H.-J, ZENKE, G, ZERWES, H.-G, SCHREIER, M. H

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Sanglifehrin−Cyclophilin Interaction:  Degradation Work, Synthetic Macrocyclic Analogues, X-ray Crystal Structure, and Binding Data von Sedrani, Richard, Kallen, Jörg, Martin Cabrejas, Luisa M, Papageorgiou, Charles D, Senia, Francesco, Rohrbach, Stefan, Wagner, Dieter, Thai, Binh, Jutzi Eme, Anne-Marie, France, Julien, Oberer, Lukas, Rihs, Grety, Zenke, Gerhard, Wagner, Jürgen

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SDZ RAD, a new rapamycin derivative : Synergism with cyclosporine von SCHUURMAN, H.-J, COTTENS, S, FUCHS, S, JOERGENSEN, J, MEERLOO, T, SEDRANI, R, TANNER, M, ZENKE, G, SCHULER, W

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Toward a Total Synthesis of the Immunosuppressant Sanglifehrin A. Preparation of Two Relay Compounds by Degradation and Their Use in the Reassembly of the Natural Product von Metternich, Rainer, Denni, Donatienne, Thai, Binh, Sedrani, Richard

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The Direct Conversion of Olefins into Esters Through Ozonolysis von Marshall, James A., Garofalo, Albert W., Sedrani, Richard C.

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Stereochemical effects of trimethylsilyl chloride (TMSCl) on the conjugate addition of organocopper reagents von Alexakis, A., Sedrani, R., Mangeney, P.

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Chiral aminal templates 3 diastereoselectivity of organometallic attack on aldehydes bearing a chiral imidazolidine group von Alexakis, A., Sedrani, R., Normant, J.F., Mangeney, P.

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Chiral acetals in enantio- and diastereoselective substitution or elimination reactions von Alexakis, A., Mangeney, P., Ghribi, A., Marek, I., Sedrani, R., Guir, C., Normant, J.

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Diastereoselective conjugate addition with acetals, oxazolidines and imidazolidines as chiral auxiliaries von Alexakis, A., Sedrani, R., Mangeney, P., Normant, J.F.

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A convergent, highly stereoselective synthesis of a C-11-C-21 subunit of the macbecins von Marshall, James A, Sedrani, Richard

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Dihydroxylation of the Triene Subunit of Rapamycin von Sedrani, Richard, Thai, Binh, France, Julien, Cottens, Sylvain

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X-ray Crystal Structure of 28-O-Methylrapamycin complexed with FKBP12:  Is the Cyclohexyl Moiety Part of the Effector Domain of Rapamycin? von Kallen, Joerg A, Sedrani, Richard, Cottens, Sylvain

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Cleavage of the cyclohexyl-subunit of rapamycin results in loss of immunosuppressive activity von Sedrani, Richard, Jones, Lyn H., Jutzi-Eme, Anne-Marie, Schuler, Walter, Cottens, Sylvain

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A convergent, highly stereroselectiv synthesis of a C-11-C21 subunit of the Macbenins von MARSHALL, J. A, SEDRANI, R

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Rapamycin derivatives von S. COTTENS, R. SEDRANI

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Rapamycin derivatives von S. COTTENS, R. SEDRANI

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Rapamycin derivatives von S. COTTENS, R. SEDRANI

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Diastereoselective conjugate addition with acetals, oxazolidines and imidazolidines as chiral auxiliaires von ALEXAKIS, A, SEDRANI, R, MANGENEY, P, NORMANT, J. F

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Rapamycin derivatives useful as immunosuppressants von S. COTTENS, R. SEDRANI

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