A highly enantio- and diastereoselective [4+1] annulation between in situ generated ammonium ylides and o-quinone methides for the synthesis of a variety of 2,3-dihydrobenzofurans has been developed. The key factors controlling the reactivity and stereoselectivity were systematically investigated by experimental and computational means and the energy profiles obtained provide a deeper insight into the mechanistic details of this reaction
A convergent, catalytic asymmetric formal [4 + 2] annulation for the synthesis of dihydroquinolones ...
The enantioselective alpha-addition of deconjugated butenolides has rarely been exploited, in contra...
Asymmetric organocatalytic domino type Michael-S(N)2 reactions give access to enantiomerically enric...
During this master thesis the enantioselective syntheses of trans-2,3,dihydrobenzofurans via in situ...
A novel and efficient method for the generation of o-quinone methide intermediates was developed fro...
A highly straightforward route to enantiomerically highly enriched cis-2,3-dihydrobenzofurans has be...
The first (4 + 1)-annulation of <i>o</i>-quinone methides with α-branched allenoates as C1 synthons ...
The first organocatalyzed asymmetric method for the synthesis of dihydrodibenzofurans based on a die...
Abstract: A facile method for the stereoselective synthesis of trans-2,3-dihydrobenzofurans from ort...
The first asymmetric insertion reactions of donor–donor carbenoids, i.e., those with no pendant elec...
A new method is presented for the regioselective one-pot synthesis of 3-substituted 2,3-dihydrobenzo...
ABSTRACT: A convergent, catalytic asymmetric formal [4 + 2] annulation for the synthesis of dihydroq...
The synthesis of useful chiral skeletons from simple achiral starting materials is always the dream ...
A simple, general route to the 1,2-dihydronaphtho[2,1-<i>b</i>]furans and 2,3-dihydrobenzofurans s...
An asymmetric [3+2] cycloaddition of quinone esters with 2,3-dihydrofuran has been realized via a ne...
A convergent, catalytic asymmetric formal [4 + 2] annulation for the synthesis of dihydroquinolones ...
The enantioselective alpha-addition of deconjugated butenolides has rarely been exploited, in contra...
Asymmetric organocatalytic domino type Michael-S(N)2 reactions give access to enantiomerically enric...
During this master thesis the enantioselective syntheses of trans-2,3,dihydrobenzofurans via in situ...
A novel and efficient method for the generation of o-quinone methide intermediates was developed fro...
A highly straightforward route to enantiomerically highly enriched cis-2,3-dihydrobenzofurans has be...
The first (4 + 1)-annulation of <i>o</i>-quinone methides with α-branched allenoates as C1 synthons ...
The first organocatalyzed asymmetric method for the synthesis of dihydrodibenzofurans based on a die...
Abstract: A facile method for the stereoselective synthesis of trans-2,3-dihydrobenzofurans from ort...
The first asymmetric insertion reactions of donor–donor carbenoids, i.e., those with no pendant elec...
A new method is presented for the regioselective one-pot synthesis of 3-substituted 2,3-dihydrobenzo...
ABSTRACT: A convergent, catalytic asymmetric formal [4 + 2] annulation for the synthesis of dihydroq...
The synthesis of useful chiral skeletons from simple achiral starting materials is always the dream ...
A simple, general route to the 1,2-dihydronaphtho[2,1-<i>b</i>]furans and 2,3-dihydrobenzofurans s...
An asymmetric [3+2] cycloaddition of quinone esters with 2,3-dihydrofuran has been realized via a ne...
A convergent, catalytic asymmetric formal [4 + 2] annulation for the synthesis of dihydroquinolones ...
The enantioselective alpha-addition of deconjugated butenolides has rarely been exploited, in contra...
Asymmetric organocatalytic domino type Michael-S(N)2 reactions give access to enantiomerically enric...