The ring opening of aziridines with organocuprate reagents provides a new entry to amino acids
Intramolecular aziridination remains a novel method for the creation of three-membered heterocyclic ...
Contains fulltext : mmubn000001_125236069.pdf (publisher's version ) (Open Access)...
1-Benzyl-2-(bromomethyl)aziridine was successfully substituted with protected glycine esters to affo...
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...
An efficient ring cleavage of aziridines with acids has been studied in the absence of any catalyst....
Organolithium-induced ring-opening of aziridines of 2,5-dihydrofuran (5 and 8) and 1,4-dimethoxybut-...
The reactivity of dianions of carboxylic acids towards aziridines has been studied. Although, a simi...
SIGLEAvailable from TIB Hannover: DW 5776 / FIZ - Fachinformationszzentrum Karlsruhe / TIB - Technis...
A. Majee acknowledges the financial support from DST-RSF Major Research Project (Ref. № INT/RUS/RSF/...
A general study is undertaken to examine the scope of the reductive ring opening of aziridine-2-carb...
Aziridine moiety represents one of the most frequently used three-membered ring systems in organic s...
Organolithium-induced alkylative ring opening of N-sulfonyl-protected aziridinyl ethers is described...
(S)-(-)-N-acetyl-2-methoxycarbonylaziridine 1 undergoes easy ring-opening by Bronsted acids or nucle...
Intramolecular aziridination remains a novel method for the creation of three-membered heterocyclic ...
Contains fulltext : mmubn000001_125236069.pdf (publisher's version ) (Open Access)...
1-Benzyl-2-(bromomethyl)aziridine was successfully substituted with protected glycine esters to affo...
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...
An efficient ring cleavage of aziridines with acids has been studied in the absence of any catalyst....
Organolithium-induced ring-opening of aziridines of 2,5-dihydrofuran (5 and 8) and 1,4-dimethoxybut-...
The reactivity of dianions of carboxylic acids towards aziridines has been studied. Although, a simi...
SIGLEAvailable from TIB Hannover: DW 5776 / FIZ - Fachinformationszzentrum Karlsruhe / TIB - Technis...
A. Majee acknowledges the financial support from DST-RSF Major Research Project (Ref. № INT/RUS/RSF/...
A general study is undertaken to examine the scope of the reductive ring opening of aziridine-2-carb...
Aziridine moiety represents one of the most frequently used three-membered ring systems in organic s...
Organolithium-induced alkylative ring opening of N-sulfonyl-protected aziridinyl ethers is described...
(S)-(-)-N-acetyl-2-methoxycarbonylaziridine 1 undergoes easy ring-opening by Bronsted acids or nucle...
Intramolecular aziridination remains a novel method for the creation of three-membered heterocyclic ...
Contains fulltext : mmubn000001_125236069.pdf (publisher's version ) (Open Access)...
1-Benzyl-2-(bromomethyl)aziridine was successfully substituted with protected glycine esters to affo...
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