The reactivity of dianions of carboxylic acids towards aziridines has been studied. Although, a similar reactivity to that of enolates from ketones, esters or amides has been observed, the method directly yields g-aminoacids in one step. The method is complementary of previous results of enenediolate reactivity with other electrophiles. A comparative study with the reactivity of this enediolates with epoxides is included
Aziridines, the nitrogenous analogues of epoxides, are useful building blocks for the synthesis of v...
In this critical review, the ring opening of non-activated 2-substituted aziridines via intermediate...
Aziridine moiety represents one of the most frequently used three-membered ring systems in organic s...
An efficient ring cleavage of aziridines with acids has been studied in the absence of any catalyst....
The ring opening of aziridines with organocuprate reagents provides a new entry to amino acids
The ring opening of aziridines with organocuprate reagents provides a new entry to amino acids
Nucleophilic ring opening of optically active N-sulphonyl aziridine-2-carboxylate esters with organo...
Nucleophilic ring opening of optically active N-sulphonyl aziridine-2-carboxylate esters with organo...
Abstract: The synthesis of aziridine-2-carboxylic acid derivatives of high enantiopurity is describe...
Aziridines are three-membered cyclic heterocycles that contain a nitrogen atom in the ring. The larg...
The high synthetic usefulness of aziridines has been often confined to their electrophilic nature, ...
The high synthetic usefulness of aziridines has been often confined to their electrophilic nature, ...
Aziridines are three-membered cyclic heterocycles that contain a nitrogen atom in the ring. The larg...
Aziridines are three-membered cyclic heterocycles that contain a nitrogen atom in the ring. The larg...
A variety of activated aziridines were cleaved by sodium azide and sodium cyanide in aqueous acetoni...
Aziridines, the nitrogenous analogues of epoxides, are useful building blocks for the synthesis of v...
In this critical review, the ring opening of non-activated 2-substituted aziridines via intermediate...
Aziridine moiety represents one of the most frequently used three-membered ring systems in organic s...
An efficient ring cleavage of aziridines with acids has been studied in the absence of any catalyst....
The ring opening of aziridines with organocuprate reagents provides a new entry to amino acids
The ring opening of aziridines with organocuprate reagents provides a new entry to amino acids
Nucleophilic ring opening of optically active N-sulphonyl aziridine-2-carboxylate esters with organo...
Nucleophilic ring opening of optically active N-sulphonyl aziridine-2-carboxylate esters with organo...
Abstract: The synthesis of aziridine-2-carboxylic acid derivatives of high enantiopurity is describe...
Aziridines are three-membered cyclic heterocycles that contain a nitrogen atom in the ring. The larg...
The high synthetic usefulness of aziridines has been often confined to their electrophilic nature, ...
The high synthetic usefulness of aziridines has been often confined to their electrophilic nature, ...
Aziridines are three-membered cyclic heterocycles that contain a nitrogen atom in the ring. The larg...
Aziridines are three-membered cyclic heterocycles that contain a nitrogen atom in the ring. The larg...
A variety of activated aziridines were cleaved by sodium azide and sodium cyanide in aqueous acetoni...
Aziridines, the nitrogenous analogues of epoxides, are useful building blocks for the synthesis of v...
In this critical review, the ring opening of non-activated 2-substituted aziridines via intermediate...
Aziridine moiety represents one of the most frequently used three-membered ring systems in organic s...
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