A novel series of N-functionalized 4-aryl-tetrahydrobiquinoline-2,5-(1H,3H)-diones were synthesized in high yields by a one-pot three-component reaction involving 2-chloroquinoline-3-carbaldehydes, Meldrum's acid, and enaminones (dimedone-based enaminones) in the presence of K2CO3 in CH3CN under reflux condition. To gain a deep insight on the mechanism of the reaction, an extensive series of quantum mechanics calculations in the framework of density functional theory (DFT) were carried out for supporting the suggested reaction pathway
A one-pot, three-component method incorporating a domino Heck–aza-Michael reaction has been de...
An efficient three-component tandem reaction of aryl azides, propargylic alcohols, and iodine has be...
The Lautens group has a long-standing interest in developing novel approaches to heterocycle synthes...
In this thesis, Density Functional Theory (DFT) methods have been applied to study the mechanisms of...
An efficient, high yielding and environmentally benign strategy to the synthesis of new 2-amino-3-cy...
193 p.In this thesis, Density Functional Theory (DFT) methods have been applied to study the mechani...
A set of 3-carboethoxy-quinolin-4-ones has been synthesized from diethyl 2-((arylamino)methylene) ma...
In an attempt to further exploit multicomponent reactions in the field of 1,4 naphthoquinone-based c...
A palladium‐catalysed intramolecular nucleophilic addition of aryl iodides to aldehydes leading to t...
A mechanistic study of three-component reactions of various aromatic amines with a number of aldehyd...
The palladium-catalyzed cross-coupling reaction of aryl halides with isoquinoline-1,3(2<i>H</i>,4<i...
C−H bond functionalization is a powerful method in organic synthesis, since it avoids prefunctionali...
The three-component reactions of isoquinoline and acetylenic esters in the presence of 2-tert-butyl-...
Ugi-adducts were obtained via a one-pot four-component reaction of divergent aldehydes, amines, aroy...
This article describes an experimental and computational investigation on the possible aryne reactiv...
A one-pot, three-component method incorporating a domino Heck–aza-Michael reaction has been de...
An efficient three-component tandem reaction of aryl azides, propargylic alcohols, and iodine has be...
The Lautens group has a long-standing interest in developing novel approaches to heterocycle synthes...
In this thesis, Density Functional Theory (DFT) methods have been applied to study the mechanisms of...
An efficient, high yielding and environmentally benign strategy to the synthesis of new 2-amino-3-cy...
193 p.In this thesis, Density Functional Theory (DFT) methods have been applied to study the mechani...
A set of 3-carboethoxy-quinolin-4-ones has been synthesized from diethyl 2-((arylamino)methylene) ma...
In an attempt to further exploit multicomponent reactions in the field of 1,4 naphthoquinone-based c...
A palladium‐catalysed intramolecular nucleophilic addition of aryl iodides to aldehydes leading to t...
A mechanistic study of three-component reactions of various aromatic amines with a number of aldehyd...
The palladium-catalyzed cross-coupling reaction of aryl halides with isoquinoline-1,3(2<i>H</i>,4<i...
C−H bond functionalization is a powerful method in organic synthesis, since it avoids prefunctionali...
The three-component reactions of isoquinoline and acetylenic esters in the presence of 2-tert-butyl-...
Ugi-adducts were obtained via a one-pot four-component reaction of divergent aldehydes, amines, aroy...
This article describes an experimental and computational investigation on the possible aryne reactiv...
A one-pot, three-component method incorporating a domino Heck–aza-Michael reaction has been de...
An efficient three-component tandem reaction of aryl azides, propargylic alcohols, and iodine has be...
The Lautens group has a long-standing interest in developing novel approaches to heterocycle synthes...