Selective hydrogenation of nitro compounds to amines by coupled redox reactions over a heterogeneous biocatalyst. [PDF]
Sokolova D +7 more
europepmc +1 more source
Water-soluble gold nanoparticles: recyclable catalysts for the reduction of aromatic nitro compounds in water. [PDF]
Monti GA +4 more
europepmc +1 more source
Tandem imine formation via auto-hydrogen transfer from alcohols to nitro compounds catalyzed by a nanomagnetically recyclable copper catalyst under solvent-free conditions. [PDF]
Sobhani S +3 more
europepmc +1 more source
Self‐Complementary Dimers Based on Zwitterionic Halogen Bond Donors
In this study we present the first isolated zwitterionic homodimers based on halogen bonding (XB). After optimization of the structures by changing the Lewis base (LB) and the backbone, their dimerization was observed in gas phase, as well as, in solid state.
Dana Kutzinski +5 more
wiley +1 more source
Synthetic and Mechanistic Studies into the Reductive Functionalization of Nitro Compounds Catalyzed by an Iron(salen) Complex. [PDF]
Pocock E +6 more
europepmc +1 more source
Effects of Preparation Parameters of NiAl Oxide-Supported Au Catalysts on Nitro Compounds Chemoselective Hydrogenation. [PDF]
Zhao J +9 more
europepmc +1 more source
Efficient reduction of nitro compounds and domino preparation of 1-substituted-1H-1,2,3,4-tetrazoles by Pd(ii)-polysalophen coated magnetite NPs as a robust versatile nanocomposite. [PDF]
Xu D, Xiong M, Kazemnejadi M.
europepmc +1 more source
Over the past decade, the interest in azetidines has continuously risen, by virtue of their highly appealing pharmaceutical properties. Monocyclic, spirocyclic, and bridged azetidines can be accessed by leveraging 1‐azabicyclo[1.1.0]butanes as precursors.
Yuri Gelato +3 more
wiley +1 more source
How Do Aromatic Nitro Compounds React with Nucleophiles? Theoretical Description Using Aromaticity, Nucleophilicity and Electrophilicity Indices. [PDF]
Błaziak K, Danikiewicz W, Mąkosza M.
europepmc +1 more source
Flipping the Card With Enantiodivergent Organocatalysis
This minireview elaborates on recent organocatalytic strategies for achieving enantiodivergence—the ability to access both product enantiomers using a single chiral catalyst. It highlights how achiral stimuli, such as solvent polarity and chemical additives, along with minimal catalyst modifications, trigger stereochemical inversions in reactions ...
Debora Iapadre +3 more
wiley +1 more source

