G. Malik

A masked 1,3-dipole revealed from aziridines.

P. Dauban, G. Malik, 2009, Angewandte Chemie.

A thiocyanopalladation/carbocyclization transformation identified through enzymatic screening: stereocontrolled tandem C–SCN and C–C bond formation† †Electronic supplementary information (ESI) available: Enzymatic screening procedures, detailed synthetic procedures and compilations of spectroscopic

D. Berkowitz, V. Tiwari, G. Malik, 2017, Chemical science.

Combining a Clostridial enzyme exhibiting unusual active site plasticity with a remarkably facile sigmatropic rearrangement: rapid, stereocontrolled entry into densely functionalized fluorinated phosphonates for chemical biology.

D. Berkowitz, G. Malik, G. A. Applegate, 2015, Journal of the American Chemical Society.

Total synthesis of indolizidine alkaloid (-)-209D: overriding substrate bias in the asymmetric rhodium-catalyzed [2+2+2] cycloaddition.

T. Rovis, G. Malik, Ernest E. Lee, 2009, Angewandte Chemie.

Enantioselective rhodium-catalyzed [2 + 2 + 2] cycloadditions of terminal alkynes and alkenyl isocyanates: mechanistic insights lead to a unified model that rationalizes product selectivity.

T. Rovis, G. Malik, M. L. Pease, 2009, Journal of the American Chemical Society.

General Linker Diversification Approach to Bivalent Ligand Assembly: Generation of an Array of Ligands for the Cation-Independent Mannose 6-Phosphate Receptor.

D. Berkowitz, R. Macdonald, G. Malik, 2017, Organic letters.

Aziridines from intramolecular alkene aziridination of sulfamates: reactivity toward carbon nucleophiles. application to the synthesis of spisulosine and its fluoro analogue.

P. Dauban, P. Retailleau, G. Malik, 2011, The Journal of organic chemistry.