The addition of the SuperQuat enolate to five- and six-membered heterocyclic <i>tert</i>-butyl sulfinimines led to a high <i>syn</i>-selectivity of up to 99:1 in good to excellent yields. The reaction is tentatively proposed to proceed through an open-chain transition state with the presence of an α-heteroatom on the sulfinimine leading to high diastereoselectivities. The adducts were derivatized to β-amino esters and amides in a facile manner
The highly diastereoselective conjugate addition of lithium N-benzyl-N-α-methylbenzylamide with enoa...
The trimethylsilyl trifluoromethanesulphonate catalyzed condensation of silyl ketene acetals with im...
Easily accessible chiral sulfinamide 2 has been developed as the first highly efficient and enantios...
The addition of the SuperQuat enolate to five- and six-membered heterocyclic <i>tert</i>-butyl sulfi...
A new chiral auxiliary for the diastereoselective alkylation of amino ester enolates that takes adva...
A diastereoselective α-sulfenylation of chiral α-aryl/alkyl <i>N</i>-<i>tert</i>-butanesulfinyl imid...
We report a diastereoselective addition reaction of fluoroacetate and α-alkylated fluoroacetate to <...
The diastereoselective addition of lithiated vinyl sulfoxides to enantiopure sulfinimines provides d...
Chiral bicyclic N,O-acetal isoserine derivatives have been synthesized by an acid-catalyzed tandem N...
The addition of a broad variety of substituted aromatic and heterocyclic silanes to chiral <i>N</i>-...
New chiral beta-(sulfonylamino)sulfinylimidates are synthesized in high overall yield and excellent ...
The use of lithio tris(methylthio)methane as a hydroxy/thio/amino carbonyl anion equivalent in the s...
A highly regioselective and diastereoselective addition of 2-azaallyl anions to N-tert-butanesulfiny...
A <i>syn</i>-selective synthesis of β-branched α-amino acids has been developed based on the alkylat...
Carbamoyl anions, generated from N,N-disubstituted formamides and lithium diisopropylamide, add with...
The highly diastereoselective conjugate addition of lithium N-benzyl-N-α-methylbenzylamide with enoa...
The trimethylsilyl trifluoromethanesulphonate catalyzed condensation of silyl ketene acetals with im...
Easily accessible chiral sulfinamide 2 has been developed as the first highly efficient and enantios...
The addition of the SuperQuat enolate to five- and six-membered heterocyclic <i>tert</i>-butyl sulfi...
A new chiral auxiliary for the diastereoselective alkylation of amino ester enolates that takes adva...
A diastereoselective α-sulfenylation of chiral α-aryl/alkyl <i>N</i>-<i>tert</i>-butanesulfinyl imid...
We report a diastereoselective addition reaction of fluoroacetate and α-alkylated fluoroacetate to <...
The diastereoselective addition of lithiated vinyl sulfoxides to enantiopure sulfinimines provides d...
Chiral bicyclic N,O-acetal isoserine derivatives have been synthesized by an acid-catalyzed tandem N...
The addition of a broad variety of substituted aromatic and heterocyclic silanes to chiral <i>N</i>-...
New chiral beta-(sulfonylamino)sulfinylimidates are synthesized in high overall yield and excellent ...
The use of lithio tris(methylthio)methane as a hydroxy/thio/amino carbonyl anion equivalent in the s...
A highly regioselective and diastereoselective addition of 2-azaallyl anions to N-tert-butanesulfiny...
A <i>syn</i>-selective synthesis of β-branched α-amino acids has been developed based on the alkylat...
Carbamoyl anions, generated from N,N-disubstituted formamides and lithium diisopropylamide, add with...
The highly diastereoselective conjugate addition of lithium N-benzyl-N-α-methylbenzylamide with enoa...
The trimethylsilyl trifluoromethanesulphonate catalyzed condensation of silyl ketene acetals with im...
Easily accessible chiral sulfinamide 2 has been developed as the first highly efficient and enantios...