An effective electrophilic annulation reaction of azacyclic ynones was reported, divergently
affording various functionalized 3-iodo-2H-quinolizin-2-ones and 1, 3-diiodo-2H-quinolizin-2 …

A simple and effective annulation of ynediones and (iso) quinoline N-oxides was developed
to afford various functionalized pyrrolo [2, 1-a] isoquinolines and pyrrolo [1, 2-a] quinolines …

An effective annulation of ynones and (iso) quinoline N-oxides was developed to deliver
various functionalized 3-((iso) quinolin-1-yl)-4H-chromen-4-ones and 13H-isoquinolino [2, 1 …

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 …

Polysubstituted quinolines are synthesized through an unprecedented cascade annulation
of ω-azido-1-alkynes with diaryliodonium salts, which serve as C2-building blocks. The …

An efficient synthesis of C4-functionalized quinolines through copper-catalyzed tandem
annulation of alkynyl imines with diazo compounds is described. This transformation …

A rapid growth in synthetic methods for the preparation of diverse organic molecules using N‐
sulfonyl‐1, 2, 3‐triazoles is of great interest in organic synthesis. Transition metals are …

An efficient single-step approach toward the synthesis of 2-alkylquinolines is described.
Through a Lewis acid mediated [3+ 3] annulation reaction between 3-ethoxycyclobutanones …

A novel tandem intermolecular ammonium ylide formation/intramolecular Mannich-type [5+
1] cyclization reaction of aryl diazoacetates and ortho-aminophenyl imine derivatives was …

An efficient strategy for the synthesis of pyrrolo [1, 2-a] quinolines and indolizines from
pyranoquinolines via site-selective electrophilic cyclization and subsequent opening of …