1366331-54-5

Upstream product

• 4510-34-3 (Z)-cinnamyl alcohol 
• 530-62-1 1,1'-carbonyldiimidazole 

Downstream Products

• 1366331-38-5 C₁₇H₁₇NO₅S 
• 129217-18-1 (2-oxooxazolidin-4-yl)(phenyl)methyl benzoate 
• 129217-19-2 4(R*)-<(S*)-hydroxy(phenyl)methyl>-1,3-oxazolin-2-one 
• 1424055-61-7 (Z)-3-phenylallyl benzoyloxycarbamate 
• 1609548-84-6 (Z)-3-phenylallyl (3,5-bis(trifluoromethyl)benzoyl)oxycarbamate 

Relevant academic research and scientific papers

Iron(II)-catalyzed intramolecular aminohydroxylation of olefins with functionalized hydroxylamines

A diastereoselective aminohydroxylation of olefins with a functionalized hydroxylamine is catalyzed by new iron(II) complexes. This efficient intramolecular process readily affords synthetically useful amino alcohols with excellent selectivity (dr up to > 20:1). Asymmetric catalysis with chiral iron(II) complexes and preliminary mechanistic studies reveal an iron nitrenoid is a possible intermediate that can undergo either aminohydroxylation or aziridination, and the selectivity can be controlled by careful selection of counteranion/ligand combinations.

Intramolecular iron(ii)-catalyzed aminobromination of allyl N-tosyloxycarbamates

Allyl N-tosyloxycarbamates are found to be catalytically transformed into β-brominated oxazolidinones with FeBr2/n-Bu4NBr in t-BuOH. The Royal Society of Chemistry 2012.