There has been considerable interest in the development of novel heterocyclic compounds
with varied biological activities. Triazoles are a special class of heterocyclic compounds with …

An efficient domino approach to assemble benzoxazoles and anthranilamides bearing
dithiocarbamate moieties has been developed. The proposed route represents a Cu …

Mixing copper (II) perchlorate and sodium iodide solutions results in copper (I) species and
the electrophilic triiodide ions, which collectively mediate the cycloaddition reaction of …

A systematic series of anion receptors based on bidentate halogen bonding by halo-
triazoles and-triazoliums is presented. The influence of the halogen bond donor atom, the …

Fluorinated molecules are omnipresent in pharmaceuticals and agrochemicals,[1]
materials,[2] and as imaging agents for positron emission tomography (PET) scanning.[3] …

The combination of CuI and glycerol exhibits a versatile and high catalytic activity in the
Huisgen cycloaddition of azides and terminal or 1-iodoalkynes under standard bench …

We report the gold‐catalyzed synthesis of highly functionalized iodofulvenes from
iododialkynes under mild conditions. The catalytic cycle involves the formation of gold …

The iodination of terminal alkynes for the synthesis of 1‐iodoalkynes using N‐
iodosuccinimide in the presence of a AuI‐NHC (NHC= N‐heterocyclic carbene) catalyst is …

Base-mediated cyclization of (5-iodo-1, 2, 3-triazolyl) phenols was proposed as a new
synthetic strategy for the in situ generation of diazoimines via electrocyclic ring opening of …

Cu-catalyzed 1, 3-dipolar cycloaddition of iododiacetylenes with organic azides using
iodotris (triphenylphosphine) copper (I) as a catalyst was found to be an efficient one-step …