Otera’s distannoxane catalyst was found to promote the cleavage of carbamate groups from N-protected aziridines. This method enables the chemoselective cleavage of an aziridinyl N-carbobenzyloxy (Cbz) group in the presence of other N-Cbz groups. The selectivity is due to the longer, weaker N–C bond of aziridinyl carbamates, as inferred through IR and crystallographic analyses
Allene aziridination generates useful bicyclic methylene aziridine scaffolds that can be flexibly tr...
The catalytic potential of a large series of easily available metal carbamates (based on thirteen di...
A stereodivergent protocol for the aziridination of a range of cyclic allylic amine derivatives has ...
A variety of N-activated aziridines were opened with water, primary, allylic, and propargyl alcohols...
N,N-Dimethylaziridine-2-carboxamides react with organolithium reagents yielding 2-aziridinylketones....
Intramolecular aziridination remains a novel method for the creation of three-membered heterocyclic ...
Aziridines, the nitrogen analog of epoxides, are an important class of compounds. They are present i...
A general study is undertaken to examine the scope of the reductive ring opening of aziridine-2-carb...
Nitrene insertion reactions are arguably the most atom-economical method for the creation of carbon-...
The work described in this thesis is an investigation into the reactivity and possible synthetic app...
An efficient ring cleavage of aziridines with acids has been studied in the absence of any catalyst....
A novel electron poor protection group for amines has been developed. It undergoes rapid cleavage by...
Allene aziridination generates useful bicyclic methylene aziridine scaffolds that can be flexibly tr...
A variety of aziridines were opened in an efficient manner with aromatic amines using silica gel und...
Ring cleavage of a variety of N-substituted aziridines has been studied with hydroxyl compounds (pri...
Allene aziridination generates useful bicyclic methylene aziridine scaffolds that can be flexibly tr...
The catalytic potential of a large series of easily available metal carbamates (based on thirteen di...
A stereodivergent protocol for the aziridination of a range of cyclic allylic amine derivatives has ...
A variety of N-activated aziridines were opened with water, primary, allylic, and propargyl alcohols...
N,N-Dimethylaziridine-2-carboxamides react with organolithium reagents yielding 2-aziridinylketones....
Intramolecular aziridination remains a novel method for the creation of three-membered heterocyclic ...
Aziridines, the nitrogen analog of epoxides, are an important class of compounds. They are present i...
A general study is undertaken to examine the scope of the reductive ring opening of aziridine-2-carb...
Nitrene insertion reactions are arguably the most atom-economical method for the creation of carbon-...
The work described in this thesis is an investigation into the reactivity and possible synthetic app...
An efficient ring cleavage of aziridines with acids has been studied in the absence of any catalyst....
A novel electron poor protection group for amines has been developed. It undergoes rapid cleavage by...
Allene aziridination generates useful bicyclic methylene aziridine scaffolds that can be flexibly tr...
A variety of aziridines were opened in an efficient manner with aromatic amines using silica gel und...
Ring cleavage of a variety of N-substituted aziridines has been studied with hydroxyl compounds (pri...
Allene aziridination generates useful bicyclic methylene aziridine scaffolds that can be flexibly tr...
The catalytic potential of a large series of easily available metal carbamates (based on thirteen di...
A stereodivergent protocol for the aziridination of a range of cyclic allylic amine derivatives has ...