K. R. Knudsen

发表

The Use of a Continuous Flow‐Reactor Employing a Mixed Hydrogen—Liquid Flow Stream for the Efficient Reduction of Imines to Amines.

S. Ley, S. Saaby, K. R. Knudsen, 2005 .

Effect of Precursor Ligands and Oxidation State in the Synthesis of Bimetallic Nano-Alloys

K. R. Knudsen, D. Anjum, O. Bakr, 2015 .

A chiral molecular recognition approach to the formation of optically active quaternary centres in aza-Henry reactions.

K. R. Knudsen, K. Jørgensen, Kristian Rahbek Knudsen, 2005, Organic & biomolecular chemistry.

The First Catalytic Asymmetric Aza-Henry Reaction of Nitronates with Imines: A Novel Approach to Optically Active β-Nitro-α-Amino Acid- and α,β-Diamino Acid Derivatives

K. R. Knudsen, K. Jørgensen, Kristian Rahbek Knudsen, 2001 .

A general organocatalytic enantioselective malonate addition to alpha,beta-unsaturated enones.

S. Ley, K. R. Knudsen, V. Wascholowski, 2008, Chemistry.

Asymmetric organocatalytic conjugate addition of malonates to enones using a proline tetrazole catalyst.

S. Ley, K. R. Knudsen, Kristian Rahbek Knudsen, 2006, Chemical communications.

Catalytic enantioselective transaminiation of α-keto esters: an organic approach to enzymatic reactions

K. R. Knudsen, K. Jørgensen, S. Bachmann, 2003 .

Mimicking enzymatic transaminations: attempts to understand and develop a catalytic asymmetric approach to chiral alpha-amino acids.

K. R. Knudsen, K. Jørgensen, S. Bachmann, 2004, Organic & biomolecular chemistry.

Diastereoselective aldol reactions with butane-2,3-diacetal protected glyceraldehyde derivatives.

A. Stepan, S. Ley, K. R. Knudsen, 2006, Organic & biomolecular chemistry.

Enantioselective synthesis of optically active carbocyclic sugars.

K. R. Knudsen, K. Jørgensen, N. Gathergood, 2001, The Journal of organic chemistry.

Optimisation of Conditions for O‐Benzyl and N‐Benzyloxycarbonyl Protecting Group Removal using an Automated Flow Hydrogenator

Steven V. Ley, S. Ley, K. R. Knudsen, 2007 .

The use of a continuous flow-reactor employing a mixed hydrogen-liquid flow stream for the efficient reduction of imines to amines.

Steven V Ley, S. Ley, S. Saaby, 2005, Chemical communications.

Fully Automated Sequence-Specific Synthesis of α-Peptides Using Flow Chemistry

S. Ley, K. R. Knudsen, M. Ladlow, 2015, Journal of Flow Chemistry.