Bromination is one of the most important transformations in organic synthesis and can be
carried out using bromine and many other bromo compounds. Use of molecular bromine in …

In the last two or three decades the emphasis on and applications of green chemical
principles, introduced some significant advances in organic synthesis, such as combinatorial …

The aza-alkylation reaction at indole's C3 position allows the introduction of a differently
substituted aminomethyl group, with the formation of a new stereogenic centre. The reaction …

Heterocyclic compounds having a nitrogen atom in the ring exhibit very interesting biological
activities. Indole is the core structure of many bioactive compounds owing to its high affinity …

Amine‐terminated ionic liquid has been covalently fabricated over the surface of Magnetic
graphene oxide nanosheets. The structure of prepared material has been confirmed by …

An efficient micelle promoted one-pot synthesis of 3-amino alkylated indoles has been
developed via a three-component Mannich-type reaction from secondary amines, aldehydes …

A one-pot multicomponent aza-Friedel–Crafts reaction was performed under green, neat
and heterogeneous conditions in the presence of 1.25 mmol% of 30% w/w silicotungstic …

An efficient and rapid synthetic strategy for the naturally occurring indoloazepinone scaffold
via a three-component reaction of indole-2-carboxamides, 1, 3-disubstituted propargyl …

A highly efficient and sustainable approach for the multi-component synthesis of biologically
important 3-amino alkylated indoles has been investigated via Mannich-type reaction under …

Bromodimethylsulfonium bromide (BDMS) was found to be a very efficient reagent for
Lossen rearrangement of hydroxamic acids to the corresponding isocyanates which were …