An efficient protocol to synthesize substituted benzo[4,5]imidazo[1,2-c]quinazolines starting from N-LG-2-phenylbenzoimidazole and dioxazolones catalyzed by Rh(III) or Ir(III) has been developed. Various substituted benzo[4,5]imidazo[1,2-c]quinazolines could be easily provided in up to 99% yield. A large range of substrates and functional groups are compatible for this transformation. This method features low catalyst loading, acid-free conditions, and low solvent consumption
A general and efficient iodine-catalyzed metal-free oxidative cross-coupling reaction of methyl keto...
A Rh(III)-catalyzed cascade annulation/C–H activation of <i>o</i>-ethynylanilines with diazo compou...
A Rh(III)-catalyzed one-pot reaction of benzamides, ketones, and hydrazines for facile access to is...
A one-pot transition metal-free method for synthesizing benzo[4,5]imidazo[1,2-<i>a</i>]quinazoli...
A Rh(III)-catalyzed reaction of N-methoxybenzamides and 4-diazoisochroman-3-imines is described. Th...
A Rh(II)-catalyzed transannulation of <i>N</i>-sulfonyl-1,2,3-triazoles with 2,1-benzisoxazoles has...
Two operationally simple one-pot protocols have been developed for the synthesis of amino-functional...
A regioselective C3-alkylation based on the reaction of 2-arylimidazo[1,2-a]pyridines with a wide ra...
A simple C–H/N–H bond functionalization of N-aryl amidines with cyclic 2-diazo-1,3-diketones for the...
The benzimidazole core is a common moiety in a large number of natural products and pharmacologicall...
Ir(III)-catalyzed synthesis of benzimidazoles has been realized under redox-neutral conditions by an...
Benzo[4,5]imidazo[1,2-<i>c</i>]quinazoline-6-carbonitriles are prepared in high yields via three...
Benzofused nitrogen heterocycles are prevalent as key core structural motifs in functional molecules...
A novel palladium-catalyzed three-component reaction for the synthesis of quinazolin-4(3<i>H</i>)-o...
<p>An efficient, catalyst-free, microwave-assisted approach has been developed for the synthesis of ...
A general and efficient iodine-catalyzed metal-free oxidative cross-coupling reaction of methyl keto...
A Rh(III)-catalyzed cascade annulation/C–H activation of <i>o</i>-ethynylanilines with diazo compou...
A Rh(III)-catalyzed one-pot reaction of benzamides, ketones, and hydrazines for facile access to is...
A one-pot transition metal-free method for synthesizing benzo[4,5]imidazo[1,2-<i>a</i>]quinazoli...
A Rh(III)-catalyzed reaction of N-methoxybenzamides and 4-diazoisochroman-3-imines is described. Th...
A Rh(II)-catalyzed transannulation of <i>N</i>-sulfonyl-1,2,3-triazoles with 2,1-benzisoxazoles has...
Two operationally simple one-pot protocols have been developed for the synthesis of amino-functional...
A regioselective C3-alkylation based on the reaction of 2-arylimidazo[1,2-a]pyridines with a wide ra...
A simple C–H/N–H bond functionalization of N-aryl amidines with cyclic 2-diazo-1,3-diketones for the...
The benzimidazole core is a common moiety in a large number of natural products and pharmacologicall...
Ir(III)-catalyzed synthesis of benzimidazoles has been realized under redox-neutral conditions by an...
Benzo[4,5]imidazo[1,2-<i>c</i>]quinazoline-6-carbonitriles are prepared in high yields via three...
Benzofused nitrogen heterocycles are prevalent as key core structural motifs in functional molecules...
A novel palladium-catalyzed three-component reaction for the synthesis of quinazolin-4(3<i>H</i>)-o...
<p>An efficient, catalyst-free, microwave-assisted approach has been developed for the synthesis of ...
A general and efficient iodine-catalyzed metal-free oxidative cross-coupling reaction of methyl keto...
A Rh(III)-catalyzed cascade annulation/C–H activation of <i>o</i>-ethynylanilines with diazo compou...
A Rh(III)-catalyzed one-pot reaction of benzamides, ketones, and hydrazines for facile access to is...