A new method was developed to synthesize polyfunctionalized dihydrofuran and tetrahydrofuran derivatives from the three-component [2 + 2 + 1] cycloaddition of the diazoesters with aryl/alkenyl aldehydes and alkyne/olefin dipolarophiles by using a Ag(I) <i>N</i>-heterocyclic carbene complex as the catalyst. A carbonyl ylide intermediate was generated, which undertook an <i>endo</i>-type 1,3-dipolar cycloaddition to provide the desired dihydro-/tetrahydrofurans in high regio- and diastereoselectivities by using α-aryl or α-alkenyl diazoesters
A range of tetracyclic dibenzofuran derivatives bearing a variety of functional groups was readily s...
Polysubstituted tetrahydrofurans appear in a large variety of bioactive structures of both natural a...
A gold(I)-catalyzed formal [4 + 1] cycloaddition of α-diazoesters and propargyl alcohols is disclos...
A new method was developed to synthesize polyfunctionalized dihydrofuran and tetrahydrofuran derivat...
The Rh(II)-catalyzed reaction of dimethyl diazomalonate with aryl aldehydes and β-nitrostyrenes resu...
Polysubstituted tetrahydrofurans appear in a large variety of bioactive structures of both natural a...
A novel formal [4 + 1]-cycloaddition of readily available homopropargyl alcohols with diazo dicarbon...
The reaction of 1:1 zwitterionic species, generated in situ by the addition of dimethoxycarbene to d...
Copper or rhodium catalyzed reaction of diazocarbonyl compounds with β-hydroxyketones gives highly s...
Copper or rhodium catalyzed reaction of diazocarbonyl compounds with β-hydroxyketones gives highly s...
The effects of including metal salts for three-component reactions involving α-alkyl-α-diazo esters,...
A range of tetracyclic dibenzofuran derivatives bearing a variety of functional groups was readily s...
Copper or rhodium catalyzed reaction of diazocarbonyl compounds with β-hydroxyketones gives highly s...
Copper or rhodium catalyzed reaction of diazocarbonyl compounds with β-hydroxyketones gives highly s...
The effects of including metal salts for three-component reactions involving α-alkyl-α-diazo esters,...
A range of tetracyclic dibenzofuran derivatives bearing a variety of functional groups was readily s...
Polysubstituted tetrahydrofurans appear in a large variety of bioactive structures of both natural a...
A gold(I)-catalyzed formal [4 + 1] cycloaddition of α-diazoesters and propargyl alcohols is disclos...
A new method was developed to synthesize polyfunctionalized dihydrofuran and tetrahydrofuran derivat...
The Rh(II)-catalyzed reaction of dimethyl diazomalonate with aryl aldehydes and β-nitrostyrenes resu...
Polysubstituted tetrahydrofurans appear in a large variety of bioactive structures of both natural a...
A novel formal [4 + 1]-cycloaddition of readily available homopropargyl alcohols with diazo dicarbon...
The reaction of 1:1 zwitterionic species, generated in situ by the addition of dimethoxycarbene to d...
Copper or rhodium catalyzed reaction of diazocarbonyl compounds with β-hydroxyketones gives highly s...
Copper or rhodium catalyzed reaction of diazocarbonyl compounds with β-hydroxyketones gives highly s...
The effects of including metal salts for three-component reactions involving α-alkyl-α-diazo esters,...
A range of tetracyclic dibenzofuran derivatives bearing a variety of functional groups was readily s...
Copper or rhodium catalyzed reaction of diazocarbonyl compounds with β-hydroxyketones gives highly s...
Copper or rhodium catalyzed reaction of diazocarbonyl compounds with β-hydroxyketones gives highly s...
The effects of including metal salts for three-component reactions involving α-alkyl-α-diazo esters,...
A range of tetracyclic dibenzofuran derivatives bearing a variety of functional groups was readily s...
Polysubstituted tetrahydrofurans appear in a large variety of bioactive structures of both natural a...
A gold(I)-catalyzed formal [4 + 1] cycloaddition of α-diazoesters and propargyl alcohols is disclos...