Chiral amino acid-derived formamides represent one of the most versatile components in multicomponent reactions. Herein, we describe a facile synthesis of Nß-protected amino sulfenyl methyl formamides and sulfonyl methyl formamides via the Mannich reaction of Na-protected amino alkyl thiols followed by oxidation using 3-chloroperbenzoic acid (m-CPBA). This protocol is applicable to a wide range of Fmoc- and Cbz-protected amino acids. Notably, the reaction provides high yield and retains the stereochemistry of the chiral center of the starting componen
New chiral beta-(sulfonylamino)sulfinylimidates are synthesized in high overall yield and excellent ...
Four-component reactions between amino alcohols, aldehydes, isocyanides and thiols proceed rapidly u...
In the following thesis, new methodologies which exploit sulfinylamine reagents to enable one-pot sy...
A versatile method for the synthesis of enantioenriched N–H sulfoximines is reported. The approach s...
The 1,3 amino alcohol structural unit is found in a wide variety of natural products. We have prepar...
A facile microwave assisted three-component protocol allows the synthesis of chiral aryl-1,2-mercapt...
Synthetically useful Nb-Fmoc amino alkyl isonitriles are prepared conveniently from Nb-Fmoc amino a...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
Starting from N-protected aminoalkyl iodides and thiourea, an efficient synthesis of the correspondi...
The thesis entitled “Chemistry of Tetrathiomolybdate: Applications in Organic Synthesis” is divided ...
Sulfoximines, the monoaza analogues of sulfones, have recently gained considerable recognition as a ...
A one-pot, sequential protocol is reported that involves complementary ambiphile pairing (CAP) of a ...
Les travaux présentés dans ce mémoire décrivent une nouvelle voie de synthèse d'aminoalcools 1,2 à p...
A new synthetic protocol for the alkylation of N, N\u2032-disubstituted formamidines under Mitsunobu...
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in ...
New chiral beta-(sulfonylamino)sulfinylimidates are synthesized in high overall yield and excellent ...
Four-component reactions between amino alcohols, aldehydes, isocyanides and thiols proceed rapidly u...
In the following thesis, new methodologies which exploit sulfinylamine reagents to enable one-pot sy...
A versatile method for the synthesis of enantioenriched N–H sulfoximines is reported. The approach s...
The 1,3 amino alcohol structural unit is found in a wide variety of natural products. We have prepar...
A facile microwave assisted three-component protocol allows the synthesis of chiral aryl-1,2-mercapt...
Synthetically useful Nb-Fmoc amino alkyl isonitriles are prepared conveniently from Nb-Fmoc amino a...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
Starting from N-protected aminoalkyl iodides and thiourea, an efficient synthesis of the correspondi...
The thesis entitled “Chemistry of Tetrathiomolybdate: Applications in Organic Synthesis” is divided ...
Sulfoximines, the monoaza analogues of sulfones, have recently gained considerable recognition as a ...
A one-pot, sequential protocol is reported that involves complementary ambiphile pairing (CAP) of a ...
Les travaux présentés dans ce mémoire décrivent une nouvelle voie de synthèse d'aminoalcools 1,2 à p...
A new synthetic protocol for the alkylation of N, N\u2032-disubstituted formamidines under Mitsunobu...
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in ...
New chiral beta-(sulfonylamino)sulfinylimidates are synthesized in high overall yield and excellent ...
Four-component reactions between amino alcohols, aldehydes, isocyanides and thiols proceed rapidly u...
In the following thesis, new methodologies which exploit sulfinylamine reagents to enable one-pot sy...