Acyclic α-tertiary ethers represent a highly prevalent functionality, common to high-value
bioactive molecules, such as pharmaceuticals and natural products, and feature as crucial …

Presently, the major cornerstone of the research community is to develop green as well as
sustainable protocols involving inexpensive catalysts and/or reagents without the usage of …

A convenient synthesis of a privileged pharmaceutical motif, thiazoline is accomplished. This
reaction utilizes simple and readily available alkene and thioamide substrates in an …

We have demonstrated a protocol to generalize regioselective 1, 2-difunctionalization of
alkenes, which is a simple and efficient method for the preparation of haloethers, haloesters …

In this study, novel 3-O-methoxy-4-halo, disubstituted-5, 7-dimethoxy chromans with
bacterial cell wall degrading potentials were synthesized, characterized and evaluated as …

The halogenation of alkenes is a crucial pathway in forming CX bonds, with a significant
impact on organic synthesis and pharmaceuticals. However, traditional methodologies …

Difunctionalization of alkene conceptually serves as an appealing way to generate
molecular complexity and synthesis of functional molecules. Bromoalkoxylation is an …

A novel protocol for the synthesis of α-iodoketones from alcohols has been developed.
Using water as the reaction medium, ammonium iodide and Oxone® was proven to be an …

A facile entry to α-chloro-β-hydroxy ketone derivatives via SnCl 4· 5H 2 O-catalyzed
regioselective chlorohydroxylation of α, β-unsaturated carbonyl compounds is described …

An organocatalytic Markovnikov-type bromo-aminoxidation of styrene derivatives was
achieved by using in-situ-generated bromine and N-oxyl radicals, and the desired products …