A novel and convenient method has been developed for the regioselective iodination of quinolines at their C3 position under metal-free conditions. Iodinated quinolines, which are popular building blocks in organic and medicinal chemistry, can be prepared in gram quantities and good yields using this method and further derivatized to give increasingly complex compounds. Preliminary mechanistic studies have shown that this reaction most likely occurs via a radical intermediate
An iron-catalyzed, 8-amido-enabled regiodivergent C–H allylation of quinolines is described. This re...
Palladium-catalyzed intermolecular cyclocarbonylation of 2-iodoanilines with diethyl ethoxycarbonylb...
Heterocyclic compounds are indispensable structures that have widespread occurrence in nature and ex...
Reported herein is the metal-catalyzed regioselective C-H functionalization of quinoline N-oxides at...
Reported herein is the metal-catalyzed regioselective C–H functionalization of quinoline <i>N</i>-ox...
A new approach for the regioselective functionalization of the C-3-position of quinolines is describ...
An efficient three-component tandem reaction of aryl azides, propargylic alcohols, and iodine has be...
<p></p><p>Halogenated compounds are valuable substrates for the field of organic synthesis and more ...
Quinolones are important heterocyclic compounds in medicine and materials for DSSC or OLED. This stu...
An I<sub>2</sub>/TBHP-mediated intramolecular dehydrogenative coupling reaction is developed for the...
An expedient and metal-free synthetic protocol for construction of substituted quinolines has been d...
Quinoline is a versatile heterocycle that is part of numerous natural products and countless drugs. ...
An iron(III)-catalyzed method for the rapid and highly regioselective iodination of arenes has been...
The quinoline ring system is one of the most ubiquitous heterocycles in the fields of medicinal and ...
Quinolones are important heterocyclic compounds in medicine and materials for DSSC or OLED. This stu...
An iron-catalyzed, 8-amido-enabled regiodivergent C–H allylation of quinolines is described. This re...
Palladium-catalyzed intermolecular cyclocarbonylation of 2-iodoanilines with diethyl ethoxycarbonylb...
Heterocyclic compounds are indispensable structures that have widespread occurrence in nature and ex...
Reported herein is the metal-catalyzed regioselective C-H functionalization of quinoline N-oxides at...
Reported herein is the metal-catalyzed regioselective C–H functionalization of quinoline <i>N</i>-ox...
A new approach for the regioselective functionalization of the C-3-position of quinolines is describ...
An efficient three-component tandem reaction of aryl azides, propargylic alcohols, and iodine has be...
<p></p><p>Halogenated compounds are valuable substrates for the field of organic synthesis and more ...
Quinolones are important heterocyclic compounds in medicine and materials for DSSC or OLED. This stu...
An I<sub>2</sub>/TBHP-mediated intramolecular dehydrogenative coupling reaction is developed for the...
An expedient and metal-free synthetic protocol for construction of substituted quinolines has been d...
Quinoline is a versatile heterocycle that is part of numerous natural products and countless drugs. ...
An iron(III)-catalyzed method for the rapid and highly regioselective iodination of arenes has been...
The quinoline ring system is one of the most ubiquitous heterocycles in the fields of medicinal and ...
Quinolones are important heterocyclic compounds in medicine and materials for DSSC or OLED. This stu...
An iron-catalyzed, 8-amido-enabled regiodivergent C–H allylation of quinolines is described. This re...
Palladium-catalyzed intermolecular cyclocarbonylation of 2-iodoanilines with diethyl ethoxycarbonylb...
Heterocyclic compounds are indispensable structures that have widespread occurrence in nature and ex...