A highly selective Lewis acid catalyzed annulation of three-membered heterocycles with nitrones has been developed. Oxiranes, aziridines, and thiiranes were used as substrates for the synthesis of various six-membered heterocycles using Al or In catalysts. This catalytic protocol demonstrates a broad substrate scope and provides access to new structural motifs in high yields and in excellent selectivity under mild reaction conditions
A facile preparation of benz-annulated heterocycles were achieved at rt involving a Lewis acid/Brön...
The Lewis acid promoted (4+2) cycloaddition of nitrostyrenes with various dienophiles was examined a...
Aziridines are useful intermediates for the synthesis of the amino alcohols, amino acids, and nitrog...
A highly selective Lewis acid catalyzed annulation of three-membered heterocycles with nitrones has ...
A highly selective Lewis acid catalyzed annulation of three-membered heterocycles with nitrones has ...
In the field of organic chemistry, the development of new catalytic methods for the synthesis of com...
A novel Lewis acid catalyzed [3 + 3]-annulation process for the efficient syntheses of both tetrahyd...
This thesis describes our attempts towards realising new chemistry involving methyleneaziridines, fo...
A detailed investigation on the different reactivity patterns shown by phosphorus- and nitrogen-cont...
A diverse approach toward the catalytic regioselective nucleophilic addition of nitrogen heterocycle...
An efficient Lewis acid catalyzed S<sub>N</sub>2-type ring opening of substituted aziridines with el...
A Lewis acid-promoted annulation of azadienes and cyclobutamines was developed. This reaction procee...
A catalytic [3 + 1]-annulation reaction between cyclopropane 1,1-diester and aromatic amine is devel...
A novel early and late transition-metal relay catalysis has been developed by combining a gold-catal...
The cycloaddition of azomethine ylide N-oxides (nitrone ylides) with aldehydes provides 3-oxazolines...
A facile preparation of benz-annulated heterocycles were achieved at rt involving a Lewis acid/Brön...
The Lewis acid promoted (4+2) cycloaddition of nitrostyrenes with various dienophiles was examined a...
Aziridines are useful intermediates for the synthesis of the amino alcohols, amino acids, and nitrog...
A highly selective Lewis acid catalyzed annulation of three-membered heterocycles with nitrones has ...
A highly selective Lewis acid catalyzed annulation of three-membered heterocycles with nitrones has ...
In the field of organic chemistry, the development of new catalytic methods for the synthesis of com...
A novel Lewis acid catalyzed [3 + 3]-annulation process for the efficient syntheses of both tetrahyd...
This thesis describes our attempts towards realising new chemistry involving methyleneaziridines, fo...
A detailed investigation on the different reactivity patterns shown by phosphorus- and nitrogen-cont...
A diverse approach toward the catalytic regioselective nucleophilic addition of nitrogen heterocycle...
An efficient Lewis acid catalyzed S<sub>N</sub>2-type ring opening of substituted aziridines with el...
A Lewis acid-promoted annulation of azadienes and cyclobutamines was developed. This reaction procee...
A catalytic [3 + 1]-annulation reaction between cyclopropane 1,1-diester and aromatic amine is devel...
A novel early and late transition-metal relay catalysis has been developed by combining a gold-catal...
The cycloaddition of azomethine ylide N-oxides (nitrone ylides) with aldehydes provides 3-oxazolines...
A facile preparation of benz-annulated heterocycles were achieved at rt involving a Lewis acid/Brön...
The Lewis acid promoted (4+2) cycloaddition of nitrostyrenes with various dienophiles was examined a...
Aziridines are useful intermediates for the synthesis of the amino alcohols, amino acids, and nitrog...