Variously substituted 2,3-dihydrobenzofurans have been synthesized according to a sequential one-pot oxidation/cyclization procedure between para-aminophenol derivatives and an azadiene.Variously substituted 2,3-dihydrobenzofurans have been synthesized according to a sequential one-pot oxidation/cyclization procedure between para-aminophenol derivatives and an azadiene. © 2011 Elsevier Ltd. All rights reserved
A range of tetracyclic dibenzofuran derivatives bearing a variety of functional groups was readily s...
Abstract: A facile method for the stereoselective synthesis of trans-2,3-dihydrobenzofurans from ort...
The enantioselective synthesis of 2,3-dihydrobenzofurans was achieved by using two sequential C–H fu...
Variously substituted 2,3-dihydrobenzofurans have been synthesized according to a sequential one-pot...
A new method is presented for the regioselective one-pot synthesis of 3-substituted 2,3-dihydrobenzo...
A series of functionalized 2,5-dihydrofurans were efficiently synthesized via an amine-promoted Peta...
A tandem S<sub>N</sub>Ar/5-<i>exo</i>-<i>trig</i> cyclization reaction is reported that converts <i>...
The first synthesis of 4-, 5-, and 6-nitrobenzo[b]furans has been achieved via the Sonogashira cross...
This review gives an overview on recent developments in methods for the construction of compounds wi...
During this master thesis the enantioselective syntheses of trans-2,3,dihydrobenzofurans via in situ...
An oxidative route to N-substituted sulfonamidic azobenzene derivatives is reported. A mechanism, ba...
<div><p></p><p>Efficient syntheses of new 2,2′-disubstituted-2,3-dihydrofuran(5H)-4-one,spiro{benzof...
A Mild Method for Generation of o-Quinone Methide under the Basic Condition. The Facile Synthesis of...
Propargyl amines 4, where R3 is aryl, undergo 5-exo-dig cyclization reactions under relatively mild ...
Palladium-catalyzed oxidative annulations between phenols and alkenylcarboxylic acids produced a lib...
A range of tetracyclic dibenzofuran derivatives bearing a variety of functional groups was readily s...
Abstract: A facile method for the stereoselective synthesis of trans-2,3-dihydrobenzofurans from ort...
The enantioselective synthesis of 2,3-dihydrobenzofurans was achieved by using two sequential C–H fu...
Variously substituted 2,3-dihydrobenzofurans have been synthesized according to a sequential one-pot...
A new method is presented for the regioselective one-pot synthesis of 3-substituted 2,3-dihydrobenzo...
A series of functionalized 2,5-dihydrofurans were efficiently synthesized via an amine-promoted Peta...
A tandem S<sub>N</sub>Ar/5-<i>exo</i>-<i>trig</i> cyclization reaction is reported that converts <i>...
The first synthesis of 4-, 5-, and 6-nitrobenzo[b]furans has been achieved via the Sonogashira cross...
This review gives an overview on recent developments in methods for the construction of compounds wi...
During this master thesis the enantioselective syntheses of trans-2,3,dihydrobenzofurans via in situ...
An oxidative route to N-substituted sulfonamidic azobenzene derivatives is reported. A mechanism, ba...
<div><p></p><p>Efficient syntheses of new 2,2′-disubstituted-2,3-dihydrofuran(5H)-4-one,spiro{benzof...
A Mild Method for Generation of o-Quinone Methide under the Basic Condition. The Facile Synthesis of...
Propargyl amines 4, where R3 is aryl, undergo 5-exo-dig cyclization reactions under relatively mild ...
Palladium-catalyzed oxidative annulations between phenols and alkenylcarboxylic acids produced a lib...
A range of tetracyclic dibenzofuran derivatives bearing a variety of functional groups was readily s...
Abstract: A facile method for the stereoselective synthesis of trans-2,3-dihydrobenzofurans from ort...
The enantioselective synthesis of 2,3-dihydrobenzofurans was achieved by using two sequential C–H fu...