The first (4 + 1)-annulation of <i>o</i>-quinone methides with α-branched allenoates as C1 synthons has been developed. This operationally simple protocol gives access to highly functionalized dihydrobenzofurans in an unprecedented fashion with excellent diastereoselectivities and high yields
A one-pot protocol for the synthesis of 2,3-diarylbenzo[<i>b</i>]furan derivatives through an <i>N...
A convergent, catalytic asymmetric formal [4 + 2] annulation for the synthesis of dihydroquinolones ...
A highly enantioselective [4 + 2] cycloaddition of allenoates with 2-olefinic benzofuran-3-ones cata...
A highly enantio- and diastereoselective [4+1] annulation between in situ generated ammonium ylides ...
A novel phosphine sequentially catalyzed domino 1, 6-addition/annulation process has been developed ...
A novel and efficient method for the generation of o-quinone methide intermediates was developed fro...
During this master thesis the enantioselective syntheses of trans-2,3,dihydrobenzofurans via in situ...
A Mild Method for Generation of o-Quinone Methide under the Basic Condition. The Facile Synthesis of...
An unprecedented [4 + 3] annulation reaction of aza-<i>ortho</i>-quinone methides with arylcarbohyd...
A new method is presented for the regioselective one-pot synthesis of 3-substituted 2,3-dihydrobenzo...
Abstract: A facile method for the stereoselective synthesis of trans-2,3-dihydrobenzofurans from ort...
Rhodium(III)-catalyzed annulation of acetophenone O-acetyl oximes with allenoates was achieved, affo...
A formal 1,6-conjugated addition-mediated [2+1] annulation to synthesize spiro[2.5]octa-4,7-dien-6-...
A simple, general route to the 1,2-dihydronaphtho[2,1-<i>b</i>]furans and 2,3-dihydrobenzofurans s...
The highly efficient and expedient route for the syntheses of 2-aroyl benzofurans has been developed...
A one-pot protocol for the synthesis of 2,3-diarylbenzo[<i>b</i>]furan derivatives through an <i>N...
A convergent, catalytic asymmetric formal [4 + 2] annulation for the synthesis of dihydroquinolones ...
A highly enantioselective [4 + 2] cycloaddition of allenoates with 2-olefinic benzofuran-3-ones cata...
A highly enantio- and diastereoselective [4+1] annulation between in situ generated ammonium ylides ...
A novel phosphine sequentially catalyzed domino 1, 6-addition/annulation process has been developed ...
A novel and efficient method for the generation of o-quinone methide intermediates was developed fro...
During this master thesis the enantioselective syntheses of trans-2,3,dihydrobenzofurans via in situ...
A Mild Method for Generation of o-Quinone Methide under the Basic Condition. The Facile Synthesis of...
An unprecedented [4 + 3] annulation reaction of aza-<i>ortho</i>-quinone methides with arylcarbohyd...
A new method is presented for the regioselective one-pot synthesis of 3-substituted 2,3-dihydrobenzo...
Abstract: A facile method for the stereoselective synthesis of trans-2,3-dihydrobenzofurans from ort...
Rhodium(III)-catalyzed annulation of acetophenone O-acetyl oximes with allenoates was achieved, affo...
A formal 1,6-conjugated addition-mediated [2+1] annulation to synthesize spiro[2.5]octa-4,7-dien-6-...
A simple, general route to the 1,2-dihydronaphtho[2,1-<i>b</i>]furans and 2,3-dihydrobenzofurans s...
The highly efficient and expedient route for the syntheses of 2-aroyl benzofurans has been developed...
A one-pot protocol for the synthesis of 2,3-diarylbenzo[<i>b</i>]furan derivatives through an <i>N...
A convergent, catalytic asymmetric formal [4 + 2] annulation for the synthesis of dihydroquinolones ...
A highly enantioselective [4 + 2] cycloaddition of allenoates with 2-olefinic benzofuran-3-ones cata...
DOI
Add to ORKG