57573-53-2

Upstream product

• 100632-32-4 1-(tert-Butyl-dimethyl-silanyl)-2-methyl-3-methylene-2-phenyl-aziridine 
• 100589-91-1 3-[(tert-Butyl-dimethyl-silanyl)-methyl]-2-methyl-2-phenyl-2H-azirine 
• 75406-60-9 N,N,N-Trimethyl-N'-[1-methyl-2-phenyl-prop-(E)-ylidene]-hydrazinium; iodide 

Downstream Products

• 100589-85-3 C₁₀H₁₀⁽²⁾HN 
• 100589-88-6 2-(3-Methyl-3-phenyl-3H-azirin-2-yl)-1-phenyl-ethanol 
• 100632-32-4 1-(tert-Butyl-dimethyl-silanyl)-2-methyl-3-methylene-2-phenyl-aziridine 
• 110775-40-1 4-but-3-enyl-2,3-dimethyl-2,5-diphenyl-2H-pyrrole 
• 100589-86-4 methyl-2,phenyl-2,ethyl-3 aziridine 
• 73475-46-4 3-Ethyl-2-methyl-2-phenyl-aziridine 
• 100589-96-6 methyl-2,phenyl-2(buthenyl-3')-3 aziridine 

Relevant academic research and scientific papers

ALKYLATION ET SILYLATION DE 2H-AZIRINES.

Alkylation and silylation of 2H-azirines are reported.Methylation of lithiated azirines is always observed at the carbon atom.N- or C-silyated azirines can be obtained depending on the silyl reagents or substrates.

Synthese d'aziridines: Action d'organomagnesiens sur des iodures de N,N,N-trimethylhydrazonium

The reaction of Grignard reagents with N,N,N-trimethyl hydrazonium iodides provides a good method for the synthesis of secondary aziridines and specialy for aziridines 17a, b, 22, 24 and 25 which cannot be prepared by the Hoch-Campbell procedure (1) (reac