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 …

Propargyl alcohols are widely used in organic reactions. Their great success is rooted in the
presence of multiple functional groups. This review will focus on six types of mechanisms:(i) …

Indole derivatives are important heterocycles in organic synthesis for serving as privileged
building blocks for functional material and as key components in a lot of bioactive …

A wide range of 3-selenylindoles were synthesized via an eco-friendly approach that uses
Oxone® as the oxidant in the presence of a catalytic amount of iodine. This mild and …

Iodocyclization of propargyl alcohols is an active area for the construction of
hetero/carbocyclic iodides. Ambiphilic reactivity of propargyl alcohols made it more attractive …

Recently, we have demonstrated that N-((trans)-4-(2-(7-cyano-3, 4-dihydroisoquinolin-2 (1
H)-yl) ethyl) cyclohexyl)-1 H-indole-2-carboxamide (SB269652)(1) adopts a bitopic pose at …

Iodine-Mediated Intramolecular Electrophilic Aromatic Cyclization in Allylamines: A General
Route to Synthesis of Quinolines, Pyrazolo[4,3-b]pyridines, and Thieno[3,2-b]pyridines | Organic …

A rapid one-pot protocol for the synthesis of indole-based polyheterocycles via a sequential
Lewis acid catalyzed intermolecular Michael addition and an intramolecular azide/internal …

Iodocyclization reactions are acquiring an increasing importance in organic synthesis, in
view of the possibility to obtain iodine-containing heterocycles starting from readily available …

Platinum pincer complexes featuring an SCS indenediide backbone have been prepared
and evaluated in the catalytic cycloisomerization of alkynoic acids and N‐tosyl …