A variety of substituted isocoumarins and α-pyrones are readily prepared in excellent yields
under very mild reaction conditions by the reaction of o-(1-alkynyl) benzoates and (Z)-2 …

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A variety of substituted isoindolin-1-ones are readily prepared in good to excellent yields
under very mild reaction conditions by the reaction of o-(1-alkynyl) benzamides with ICl, I2 …

A catalyst-free oxyboration reaction of alkynes is developed. The resulting borylated
isocoumarins and 2-pyrones are isolated as boronic acids, pinacolboronate esters, or …

A large number of functionally substituted 2-alkyn-1-one O-methyl oximes have been
cyclized under mild reaction conditions in the presence of ICl to give the corresponding 4 …

3-Iodoindoles have been prepared in excellent yields by coupling terminal acetylenes with
N, N-dialkyl-o-iodoanilines in the presence of a Pd/Cu catalyst, followed by an electrophilic …

A variety of substituted polycyclic aromatics are readily prepared in good to excellent yields
under very mild reaction conditions by the reaction of 2-(1-alkynyl) biphenyls with ICl, I2 …

The ICl-induced cyclization of heteroatom-substituted alkynones provides a simple, highly
efficient approach to various 3-iodochromones and analogues. This process is run under …

The coupling reaction of o-iodobenzoic acid with terminal alkynes by using a catalyst system
of 10% Pd/C− Et3N− CuI− PPh3 has been studied in a variety of solvents. 3-Substituted …

Highly substituted 3-iodoquinolines bearing different alkyl and aryl moieties can be
synthesized in moderate to excellent yields (up to 99%) by 6-endo-dig iodocyclization of 2 …