58010-00-7

Upstream product

• 100-46-9 benzylamine 
• 108-94-1 cyclohexanone 
• 58010-00-7 (+/-)-1-benzyl-3,3-cyclohexylidenediaziridine 

Downstream Products

• 58010-00-7 (-)-1-benzyl-3,3-cyclohexylidenediaziridine 
• 58010-00-7 (+)-1-benzyl-3,3-cyclohexylidenediaziridine 
• 1337979-01-7 benzyl 1-benzyl-3-(thiophen-3-yl)-1,2-diazaspiro[4.5]dec-3-ene-2-carboxylate 
• 1337978-98-9 benzyl 1-benzyl-3-(4-(trifluoromethyl)phenyl)-1,2-diazaspiro[4.5]dec-3-ene-2-carboxylate 
• 1337978-96-7 benzyl 3-([1,1'-biphenyl]-4-yl)-1-benzyl-1,2-diazaspiro[4.5]dec-3-ene-2-carboxylate 
• 1337978-94-5 benzyl 1-benzyl-3-(4-methoxyphenyl)-1,2-diazaspiro[4.5]dec-3-ene-2-carboxylate 
• 1337978-92-3 benzyl 1-benzyl-3-(4-bromophenyl)-1,2-diazaspiro[4.5]dec-3-ene-2-carboxylate 
• 1337978-90-1 benzyl 1-benzyl-3-(p-tolyl)-1,2-diazaspiro[4.5]dec-3-ene-2-carboxylate 
• 1337978-86-5 benzyl 1-benzyl-3-phenyl-1,2-diazaspiro[4.5]dec-3-ene-2-carboxylate 
• 1337978-88-7 C₂₉H₃₀N₂O₂ 
• 1337979-07-3 benzyl 1-benzyl-3-pentyl-1,2-diazaspiro[4.5]dec-3-ene-2-carboxylate 
• 1337979-05-1 benzyl 1-benzyl-3-(6-methoxynaphthalen-2-yl)-1,2-diazaspiro[4.5]dec-3-ene-2-carboxylate 
• 1337979-03-9 benzyl 1,3-dibenzyl-1,2-diazaspiro[4.5]dec-3-ene-2-carboxylate 
• 1337978-84-3 1-benzyl-2-carboxybenzyl-1,2-diazaspiro[2,5]octane 

Relevant academic research and scientific papers

Gold(I)-catalyzed formation of 3-pyrazolines through cycloaddition of diaziridine to alkynes

This work reports the high-yield formation of pyrazoline derivatives mediated by gold(I) catalysts. The reaction utilizes a diaziridine, which has seen only limited usage in organic methodology. Mechanistic studies suggest a gold-mediated opening of the d

PREPARATIVE SEPARATIONS AND RACEMIZATIONS OF ENANTIOMERIC DIAZIRIDINES

Preparative separations or enrichments of enantiomers of diaziridines 1, 2, and 5 were achieved by liquid chromatography on triacetylcellulose, (+)-1 and (+)-2 being isolated almost pure (Table 1).Enantiomeric purities were determined by 1H NMR in the pre