An efficient, one-pot, domino synthesis of quinolines via the coupling of iodoanilines with allylic alcohols facilitated by palladium catalysis is described. The overall synthetic process involves an intermolecular Heck coupling between 2-iodoanilines and allylic alcohols, intramolecular condensation of in situ generated ketones with an internal amine functional group, and a dehydrogenation sequence. Notably, this protocol occurs in water as a green solvent. Significantly, the method exhibits broad substrate scope and is applied for the synthesis of deuterated quinolines through a deuterium-exchange process. © 2021. Thieme. All rights reserved
A two-stage “tandem strategy” for the regiocontrolled synthesis of very highly substituted quinoline...
One-pot sequential Heck reduction–cyclization (HRC) reactions leading to the synthesis of substitute...
Palladium-catalyzed Suzuki-Miyaura cross-coupling of 2-aryl-4-azido-3-iodo-quinolines with arylboron...
An efficient, one-pot, domino synthesis of quinolines via the coupling of iodoanilines with allylic ...
Palladium catalyzed efficient one-pot synthesis of quinolones starting from iodoanilines and allylic...
Palladium-catalyzed dehydrogenative coupling is an efficient synthetic strategy for the construction...
Palladium-catalyzed dehydrogenative coupling is an efficient synthetic strategy for the construction...
Palladium-catalyzed dehydrogenative coupling is an efficient synthetic strategy for the construction...
Palladium-catalyzed dehydrogenative coupling is an efficient synthetic strategy for the construction...
An efficient domino process involving palladium-catalyzed amination of an alkenyl bromide, 1,5-H tra...
A two-stage “tandem strategy” for the regiocontrolled synthesis of very highly substituted quinoline...
[Pd]-catalyzed direct acylation of iodoacetanilides/iodophenyl acetates with aldehydes, was presente...
An efficient palladium-catalyzed synthesis of 1,2-dihydroquinolines has been developed via the react...
A review of the recent literature is given focusing on synthetic approaches to 1,2,3,4-tetrahydroqui...
A review of the recent literature is given focusing on synthetic approaches to 1,2,3,4-tetrahydroqui...
A two-stage “tandem strategy” for the regiocontrolled synthesis of very highly substituted quinoline...
One-pot sequential Heck reduction–cyclization (HRC) reactions leading to the synthesis of substitute...
Palladium-catalyzed Suzuki-Miyaura cross-coupling of 2-aryl-4-azido-3-iodo-quinolines with arylboron...
An efficient, one-pot, domino synthesis of quinolines via the coupling of iodoanilines with allylic ...
Palladium catalyzed efficient one-pot synthesis of quinolones starting from iodoanilines and allylic...
Palladium-catalyzed dehydrogenative coupling is an efficient synthetic strategy for the construction...
Palladium-catalyzed dehydrogenative coupling is an efficient synthetic strategy for the construction...
Palladium-catalyzed dehydrogenative coupling is an efficient synthetic strategy for the construction...
Palladium-catalyzed dehydrogenative coupling is an efficient synthetic strategy for the construction...
An efficient domino process involving palladium-catalyzed amination of an alkenyl bromide, 1,5-H tra...
A two-stage “tandem strategy” for the regiocontrolled synthesis of very highly substituted quinoline...
[Pd]-catalyzed direct acylation of iodoacetanilides/iodophenyl acetates with aldehydes, was presente...
An efficient palladium-catalyzed synthesis of 1,2-dihydroquinolines has been developed via the react...
A review of the recent literature is given focusing on synthetic approaches to 1,2,3,4-tetrahydroqui...
A review of the recent literature is given focusing on synthetic approaches to 1,2,3,4-tetrahydroqui...
A two-stage “tandem strategy” for the regiocontrolled synthesis of very highly substituted quinoline...
One-pot sequential Heck reduction–cyclization (HRC) reactions leading to the synthesis of substitute...
Palladium-catalyzed Suzuki-Miyaura cross-coupling of 2-aryl-4-azido-3-iodo-quinolines with arylboron...