Since the first natural carbazole alkaloid, murrayanine, was isolated from Mwraya Spreng,
carbazole alkaloid derivatives have been widely concerned for their anti-tumor, anti-viral …

Organoalkali compounds have undergone a far‐reaching transformation being a coupling
partner to a mediator in unusual organic conversions which finds its spot in the field of …

Due to the single target but extensive application of commercialized succinate
dehydrogenase inhibitors (SDHIs), resistance problems have gradually become apparent in …

The development of new green fungicides is an effective way to solve the resistance of
agricultural pathogens and plays an important role in promoting high-quality and …

We report the first Suzuki–Miyaura cross-coupling of 2-pyridyl ammonium salts by highly
selective N–C activation catalyzed by air-and moisture-stable Pd (II)–NHC (NHC= N …

A microwave-promoted, one-pot, three-component synthesis of N-arylindoles has been
developed, utilising sequential Fischer indolisation then copper (I)-catalysed indole N …

2-Arylindoles are privileged structures widely present in biologically active molecules. New
sustainable synthetic routes toward their synthesis are, therefore, in high demand. Herein, a …

A convenient method is proposed for the synthesis of isoquinolone derivatives from 2-
methylaryl aldehydes and nitriles through LiN (SiMe3) 2/KO t Bu-promoted formal [4+ 2] …

Pd (OAc) 2/Nixantphos or CoI2/Nixantphos catalyzed allylic substitutions with weakly acidic
C (sp) 3–H bonds of azaarylmethylamines are described. This method facilitates access to …

A tandem Madelung indole synthesis by the reaction of methyl benzoate and N-methyl-o-
toluidine has been discovered. The combination of LiN (SiMe3) 2 with CsF is the key factor …