Selective amine de-alkylation enables the conversion of Sommelet–Hauser rearrangement products into 2-aryl-2-bromoacetic acid derivatives. These compounds are valuable synthetic intermediates in the synthesis of α-aryl-α-amino or α-aryl-β-amino acid derivatives. The method presented herein is a formal de-N,N-dialkylation of Sommelet–Hauser rearrangement products
N-Alkylation is conceptually the most straightforward disconnection towards secondary and tertiary a...
International audienceVarious protected β2-amino acids can be prepared by radical addition of β-phth...
This thesis deals with the development and application of new synthetic methodology in organic chemi...
An aryne induced transition-metal-free and mild Sommelet-Hauser rearrangement of tertiary benzylamin...
A unique and simple preparative method for N-cyano--aryl pipecolinic acid esters via base-induced S...
γ-Chloro-α-(N-alkylimino)esters were reduced by sodium cyanoborohydride in methanol in the presence ...
The Stevens rearrangement of N-allylic α-aryl amino acid-derived ammonium salts and the Sommelet–Hau...
<p>Synthetic procedure for β,γ–diamino esters by reductive amination of Phe-derived β–ketoester 1.</...
A new protecting group, 1,2-dimethoxy-4,5-dimethylene, for acyclic amino acid derivatives could be i...
Primary aromatic amines 1 with a variety of ring substituents are easily converted to their N-monoal...
The Brønsted acid-catalyzed synthesis of primary amines from acetyl arenes and alkanes with C–C bond...
2-endo-Hydroxy-2-phenyl-3-endo-aminonorbornane-5,6-exo-d2 was synthesized and subjected to nitrous a...
The reductive cleavage of cyclic aminol ethers to give N-alkylamino- derivatives in very high yields...
An efficient method for N-alkylation of diethyl acetamidomalonate (DEAM) is reported. C-Alkenylation...
A novel route has been developed for the solid-phase synthesis of N-carboxyalkyl unnatural amino aci...
N-Alkylation is conceptually the most straightforward disconnection towards secondary and tertiary a...
International audienceVarious protected β2-amino acids can be prepared by radical addition of β-phth...
This thesis deals with the development and application of new synthetic methodology in organic chemi...
An aryne induced transition-metal-free and mild Sommelet-Hauser rearrangement of tertiary benzylamin...
A unique and simple preparative method for N-cyano--aryl pipecolinic acid esters via base-induced S...
γ-Chloro-α-(N-alkylimino)esters were reduced by sodium cyanoborohydride in methanol in the presence ...
The Stevens rearrangement of N-allylic α-aryl amino acid-derived ammonium salts and the Sommelet–Hau...
<p>Synthetic procedure for β,γ–diamino esters by reductive amination of Phe-derived β–ketoester 1.</...
A new protecting group, 1,2-dimethoxy-4,5-dimethylene, for acyclic amino acid derivatives could be i...
Primary aromatic amines 1 with a variety of ring substituents are easily converted to their N-monoal...
The Brønsted acid-catalyzed synthesis of primary amines from acetyl arenes and alkanes with C–C bond...
2-endo-Hydroxy-2-phenyl-3-endo-aminonorbornane-5,6-exo-d2 was synthesized and subjected to nitrous a...
The reductive cleavage of cyclic aminol ethers to give N-alkylamino- derivatives in very high yields...
An efficient method for N-alkylation of diethyl acetamidomalonate (DEAM) is reported. C-Alkenylation...
A novel route has been developed for the solid-phase synthesis of N-carboxyalkyl unnatural amino aci...
N-Alkylation is conceptually the most straightforward disconnection towards secondary and tertiary a...
International audienceVarious protected β2-amino acids can be prepared by radical addition of β-phth...
This thesis deals with the development and application of new synthetic methodology in organic chemi...