The Smiles rearrangement is the intramolecular nucleophilic aromatic substitution reaction incorporating a heteroatom as the nucleophilic component and an activated electrophilic arene. One particular variation—the Truce–Smiles rearrangement—utilises a carbon-based nucleophile and an electrophilic arene which does not require additional activation. Such a variation generates a new carbon–carbon bond and the synthetic utility of this relatively under-utilised rearrangement is discussed in this tutorial review
The ring-opening of 3-aminocyclobutanone oximes enables easy generation of primary alkyl radicals, c...
Direct metal-free C-H functionalization of arenes with nucleophiles is a new chapter in the chemistr...
We report the first examples of radical cation Smiles rearrangements. A series of aryloxy alkylamine...
The Smiles rearrangement is the intramolecular nucleophilic aromatic substitution reaction incorpora...
The Truce-Smiles rearrangement is an X â C aryl migration reaction that is achieved by an intramol...
The Truce-Smiles rearrangement is an X â C aryl migration reaction that is achieved by an intramol...
post-printThe Truce–Smiles rearrangement is an X → C aryl migration reaction that is achieved by an ...
Over the decades the Smiles rearrangement and its variants have become essential synthetic tools in ...
AbstractThe Smiles rearrangement has undergone a renaissance in recent years providing new avenues f...
International audienceThe synthesis of new arene and heteroarene scaffolds of therapeutic interest h...
International audienceThe synthesis of new arene and heteroarene scaffolds of therapeutic interest h...
post-printThis report examines the effect of substrate design upon the Truce‐Smiles rearrangement, a...
post-printThe requirement of aryl ring activation by strong-electron withdrawing substituents in sub...
A conceptually new and synthetically valuable radical Smiles rearrangement reaction is reported unde...
Tetraarylmethanes are molecules that contain four aryl groups bonded to a central carbon atom. They ...
The ring-opening of 3-aminocyclobutanone oximes enables easy generation of primary alkyl radicals, c...
Direct metal-free C-H functionalization of arenes with nucleophiles is a new chapter in the chemistr...
We report the first examples of radical cation Smiles rearrangements. A series of aryloxy alkylamine...
The Smiles rearrangement is the intramolecular nucleophilic aromatic substitution reaction incorpora...
The Truce-Smiles rearrangement is an X â C aryl migration reaction that is achieved by an intramol...
The Truce-Smiles rearrangement is an X â C aryl migration reaction that is achieved by an intramol...
post-printThe Truce–Smiles rearrangement is an X → C aryl migration reaction that is achieved by an ...
Over the decades the Smiles rearrangement and its variants have become essential synthetic tools in ...
AbstractThe Smiles rearrangement has undergone a renaissance in recent years providing new avenues f...
International audienceThe synthesis of new arene and heteroarene scaffolds of therapeutic interest h...
International audienceThe synthesis of new arene and heteroarene scaffolds of therapeutic interest h...
post-printThis report examines the effect of substrate design upon the Truce‐Smiles rearrangement, a...
post-printThe requirement of aryl ring activation by strong-electron withdrawing substituents in sub...
A conceptually new and synthetically valuable radical Smiles rearrangement reaction is reported unde...
Tetraarylmethanes are molecules that contain four aryl groups bonded to a central carbon atom. They ...
The ring-opening of 3-aminocyclobutanone oximes enables easy generation of primary alkyl radicals, c...
Direct metal-free C-H functionalization of arenes with nucleophiles is a new chapter in the chemistr...
We report the first examples of radical cation Smiles rearrangements. A series of aryloxy alkylamine...