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
Les travaux présentés dans ce mémoire décrivent une nouvelle voie de synthèse d'aminoalcools 1,2 à p...
Les travaux présentés dans ce mémoire décrivent une nouvelle voie de synthèse d'aminoalcools 1,2 à p...
A one-pot, sequential protocol is reported that involves complementary ambiphile pairing (CAP) of a ...
A versatile method for the synthesis of enantioenriched N–H sulfoximines is reported. The approach s...
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...
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 ...
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...
Les travaux présentés dans ce mémoire décrivent une nouvelle voie de synthèse d'aminoalcools 1,2 à p...
A one-pot, sequential protocol is reported that involves complementary ambiphile pairing (CAP) of a ...
A versatile method for the synthesis of enantioenriched N–H sulfoximines is reported. The approach s...
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...
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 ...
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...
Les travaux présentés dans ce mémoire décrivent une nouvelle voie de synthèse d'aminoalcools 1,2 à p...
A one-pot, sequential protocol is reported that involves complementary ambiphile pairing (CAP) of a ...