A mild electrochemical method for the regioselective preparation of 1‐tetralones under environmentally friendly conditions from readily available cyclobutanols was developed. A series of aromatic‐ and heteroaromatic‐fused 1‐tetralones was accessed through ring expansion of the functionalized cyclobutanols via electrochemical generation of alkoxy radicals and intramolecular cyclization
Herein, we report a new electrochemical method for alkoxy radical generation from alcohols using a p...
The preparation of carbocyclic medium rings by two electron processes is reviewed with particular re...
A mild and practical tandem oxidative ring-opening/cyclization reaction mediated by Ce4+ for the syn...
A mild electrochemical method for the regioselective preparation of 1‐tetralones under environmental...
A facile and transition-metal-free ring expansion of the cyclobutanol moiety to 4-tetralones fused t...
Herein we describe the first transition-metal-free ring expansion of four-membered rings to 1-tetral...
A facile and transition-metal-free ring expansion of the cyclobutanol moiety to 4-tetralones fused t...
The number of developed methodologies for the ring expansion of cyclobutanol rings to five, six and ...
Cyclobutanol ring expansions have emerged as a powerful tool to access functionalised five- and six-...
Cyclobutanol ring expansions have emerged as a powerful tool to access functionalised five- and six-...
Herein we report an electrochemical approach for the deconstructive functionalization of cycloalkano...
Herein we report an electrochemical approach for the deconstructive functionalization of cycloalkano...
Advances in the transition-metal-free cyclobutanol ring expansion to 4-tetralones under N-bromosucci...
Herein, we report a new electrochemical method for alkoxy radical generation from alcohols using a p...
Herein, we report a new electrochemical method for alkoxy radical generation from alcohols using a p...
Herein, we report a new electrochemical method for alkoxy radical generation from alcohols using a p...
The preparation of carbocyclic medium rings by two electron processes is reviewed with particular re...
A mild and practical tandem oxidative ring-opening/cyclization reaction mediated by Ce4+ for the syn...
A mild electrochemical method for the regioselective preparation of 1‐tetralones under environmental...
A facile and transition-metal-free ring expansion of the cyclobutanol moiety to 4-tetralones fused t...
Herein we describe the first transition-metal-free ring expansion of four-membered rings to 1-tetral...
A facile and transition-metal-free ring expansion of the cyclobutanol moiety to 4-tetralones fused t...
The number of developed methodologies for the ring expansion of cyclobutanol rings to five, six and ...
Cyclobutanol ring expansions have emerged as a powerful tool to access functionalised five- and six-...
Cyclobutanol ring expansions have emerged as a powerful tool to access functionalised five- and six-...
Herein we report an electrochemical approach for the deconstructive functionalization of cycloalkano...
Herein we report an electrochemical approach for the deconstructive functionalization of cycloalkano...
Advances in the transition-metal-free cyclobutanol ring expansion to 4-tetralones under N-bromosucci...
Herein, we report a new electrochemical method for alkoxy radical generation from alcohols using a p...
Herein, we report a new electrochemical method for alkoxy radical generation from alcohols using a p...
Herein, we report a new electrochemical method for alkoxy radical generation from alcohols using a p...
The preparation of carbocyclic medium rings by two electron processes is reviewed with particular re...
A mild and practical tandem oxidative ring-opening/cyclization reaction mediated by Ce4+ for the syn...