A mild and practical tandem oxidative ring-opening/cyclization reaction mediated by Ce4+ for the synthesis of 1-tetralones is presented. This rapid transformation was completed within 30 s and conducted in an open reactor at 0 °C in a water–acetonitrile mixture. Various cyclobutanol derivatives are transformed into desired products in good to high yields, and this reaction can be easily scaled up to the gram scale
An original tandem reaction consisting of a Wittig reaction–ring contraction process between α‐hydro...
This paper describes a synthetic approach to the synthesis of 1,2,4,5-tetraarylbenzene derivatives f...
Synthesis of a tetracyclic ring system (BCDE) of atropurpuran is described. Oxidative dearomatizatio...
A facile and transition-metal-free ring expansion of the cyclobutanol moiety to 4-tetralones fused t...
A mild electrochemical method for the regioselective preparation of 1‐tetralones under environmental...
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...
Advances in the transition-metal-free cyclobutanol ring expansion to 4-tetralones under N-bromosucci...
Herein we describe the first transition-metal-free ring expansion of four-membered rings to 1-tetral...
An efficient reaction protocol for the palladium-catalyzed synthesis of 2,4-diacetoxycyclopentyliden...
A series of new polysubstituted derivatives of 2-tetralones possessing two ester groups were synthes...
An original oxidative ring contraction of easily accessible cyclobutene derivatives for the selectiv...
The number of developed methodologies for the ring expansion of cyclobutanol rings to five, six and ...
An original tandem reaction consisting of a Wittig reaction–ring contraction process between α‐hydro...
AbstractConjugate reduction of ortho-substituted cinnamic esters by Stryker’s reagent to form copper...
An original tandem reaction consisting of a Wittig reaction–ring contraction process between α‐hydro...
This paper describes a synthetic approach to the synthesis of 1,2,4,5-tetraarylbenzene derivatives f...
Synthesis of a tetracyclic ring system (BCDE) of atropurpuran is described. Oxidative dearomatizatio...
A facile and transition-metal-free ring expansion of the cyclobutanol moiety to 4-tetralones fused t...
A mild electrochemical method for the regioselective preparation of 1‐tetralones under environmental...
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...
Advances in the transition-metal-free cyclobutanol ring expansion to 4-tetralones under N-bromosucci...
Herein we describe the first transition-metal-free ring expansion of four-membered rings to 1-tetral...
An efficient reaction protocol for the palladium-catalyzed synthesis of 2,4-diacetoxycyclopentyliden...
A series of new polysubstituted derivatives of 2-tetralones possessing two ester groups were synthes...
An original oxidative ring contraction of easily accessible cyclobutene derivatives for the selectiv...
The number of developed methodologies for the ring expansion of cyclobutanol rings to five, six and ...
An original tandem reaction consisting of a Wittig reaction–ring contraction process between α‐hydro...
AbstractConjugate reduction of ortho-substituted cinnamic esters by Stryker’s reagent to form copper...
An original tandem reaction consisting of a Wittig reaction–ring contraction process between α‐hydro...
This paper describes a synthetic approach to the synthesis of 1,2,4,5-tetraarylbenzene derivatives f...
Synthesis of a tetracyclic ring system (BCDE) of atropurpuran is described. Oxidative dearomatizatio...