Comprehensive Summary Fused polycyclic N‐heterocycles are very important scaffolds in
biomedicinal chemistry and materials science. Intramolecular alkyne hydroamination is a …

1, 3-butadiynamides—the ethynylogous variants of ynamides—receive considerable
attention as precursors of complex molecular scaffolds for organic and heterocyclic …

A one-pot copper-catalyzed [4+ 1] annulation reaction of primary amines with ynamide-
derived buta-1, 3-diynes for the synthesis of 2, 5-diamido bearing N-aryl/alkyl pyrroles in up …

Herein, we present a Zn (II)-catalyzed (3+ 3) heteroannulation reaction between aromatic
amines and 1, 3-diynamides for the synthesis of amidoquinolines. A large number of …

Herein, a catalytic synthetic transformation offering a series of-NH2 group-bearing
aminoisoquinolines with moderate to good yields has been showcased. Interestingly, the …

Herein, a one-pot desulfonylative protocol enabled by copper (II)/zinc (II) salts to access
pyrrolo [2, 3-b] quinolines in good to excellent yields from 2-carbonylanilines and ynamide …

1-Alkynyl triazenes are versatile reagents in synthetic organic chemistry, but the structural
diversity of this compound class has so far been limited. Herein, we describe the synthesis of …

Abstract The zinc‐catalyzed [4+ 2] annulation of 2‐aminoarylnitriles with ynamides offers an
easy one‐step access to polysubstituted quinolines. In this new protocol, inexpensive ZnCl2 …

A straightforward and atom-economical one-pot protocol catalyzed by gold (I) and zinc (II) for
the synthesis of amine-substituted diaryl [c, h][1, 6] naphthyridines from two different …

Cascade or domino reactions serve as a powerful technique for the synthesis of complex
organic scaffolds in one pot. Herein, a Cu (II)-catalyzed and silica gel-assisted …