Epoxides are valuable intermediates for the stereocontrolled synthesis of complex organic
compounds, and their utility has expanded dramatically with the advent of practical …

ABSTRACT β-Amino alcohols are versatile intermediates in the synthesis of various
biologically potent compounds, which can also be achieved by ring opening of epoxides by …

The present review deals with the ring-opening of epoxides by various carbon, nitrogen,
oxygen, halogen, and sulfur-containing nucleophiles, which most of the resulting products …

The utility of tethered Ru-TsDPEN catalyst has been demonstrated for the asymmetric
transfer hydrogenation of rac-α-heteroaryl amino cycloalkanones to construct biologically …

Single-step and two-steps synthetic procedure for the synthesis of sulfated zirconia (SZ) was
developed, which were calcined at 500, 600 and 700° C and characterized by various …

We report the use of magnetic nano Fe 3 O 4 as a mild heterogeneous catalyst for the
aminolysis of epoxides with amines. The approach constitutes a green method for the …

We describe here a mild and efficient method for the nucleophilic ring-opening of epoxides
with amines, alcohols and water in the presence of nitromethane as a polar solvent without …

An efficient method for the 1, 6‐conjugate addition of para‐quinone methides with readily
available nucleophiles was developed. This protocol provides a straightforward access to a …

The ring opening of epoxides with aromatic and aliphatic amines was carried out under
solvent free conditions using N-fluorobenzenaminium tetrafluoroborate (2 mol%) generated …

We report a solid‐acid catalyzed aminolysis of epoxides under continuous‐flow conditions.
A titania‐zirconia supported molybdenum oxide catalyst demonstrated exceptional substrate …