F. Dehmel

Trithiocarbonates: exploration of a new head group for HDAC inhibitors.

T. Beckers, T. Ciossek, T. Maier, 2007, Bioorganic & medicinal chemistry letters.

BROMINE-MAGNESIUM-EXCHANGE AS A GENERAL TOOL FOR THE PREPARATION OF POLYFUNCTIONAL ARYL AND HETEROARYL MAGNESIUM-REAGENTS

P. Knochel, M. Abarbri, F. Dehmel, 1999 .

Unexpected endo selectivity of conjugate nucleophilic addition to an arene-Cr(CO)3 complex: enantioselective synthesis of the diterpene 11-epi-helioporin B.

H. Schmalz, F Dehmel, H G Schmalz, 2001, Organic letters.

An approach to serrulatane diterpenes via endo-selective conjugate nucleophilic addition to arene-Cr(CO)3 complexes.

J. Lex, H. Schmalz, F. Dehmel, 2002, Organic letters.

Formal total synthesis of oximidine II via a Suzuki-type cross-coupling macrocyclization employing potassium organotrifluoroborates.

G. Molander, F. Dehmel, 2004, Journal of the American Chemical Society.

Formal total synthesis of oximidine II via a Suzuki-type cross-coupling macrocyclization employing potassium organotrifluoroborates.

G. Molander, F. Dehmel, 2004, Journal of the American Chemical Society.

Trithiocarbonates as a novel class of HDAC inhibitors: SAR studies, isoenzyme selectivity, and pharmacological profiles.

T. Beckers, T. Stengel, T. Ciossek, 2008, Journal of medicinal chemistry.

Preparation of new polyfunctional magnesiated heterocycles using a chlorine-, bromine-, or iodine-magnesium exchange

P. Knochel, L. Bérillon, Abarbri, 2000, The Journal of organic chemistry.