847548-22-5

Upstream product

• 3129-98-4 (S)-N-benzylidene(1-phenylethylamine) 
• 847981-54-8 2-bromohex-2-enoyl chloride 

Downstream Products

• 847981-57-1 (S)-3-[(R)-2-Azido-but-(E)-ylidene]-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one 
• 876726-80-6 (3R,4R)-3-((R)-2-Amino-butyl)-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one 
• 917110-41-9 (3S,4S)-3-((1S,2S)-2-Azido-1-hydroxy-butyl)-3-bromo-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one 
• 917110-38-4 (3S,4S)-3-((1R,2R)-2-Azido-1-hydroxy-butyl)-3-bromo-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one 
• 917110-44-2 (2R,3R,6S)-2-((R)-1-Azido-propyl)-6-phenyl-5-((S)-1-phenyl-ethyl)-1-oxa-5-aza-spiro[2.3]hexan-4-one 
• 917110-47-5 (2S,3R,6S)-2-((S)-1-Azido-propyl)-6-phenyl-5-((S)-1-phenyl-ethyl)-1-oxa-5-aza-spiro[2.3]hexan-4-one 
• 917110-32-8 (3S,4S)-3-Bromo-3-((2R,3S)-3-ethyl-oxiranyl)-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one 
• 917110-35-1 (3S,4S)-3-Bromo-3-((2S,3R)-3-ethyl-oxiranyl)-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one 
• 847548-39-4 (1'S,1''S,3R,4S)-3-but-1-enyl-3-(hydroxyphenylmethyl)-4-phenyl-1-(1'-phenylethyl)azetidin-2-one 

Relevant academic research and scientific papers

Zinc metal-promoted nucleophilic addition of azetidin-2-ones to aldehydes and nitriles

The reactivity of in situ generated organozinc reagents of 3-alkenyl-3-bromoazetidin-2-ones with aromatic and aliphatic aldehydes to give the corresponding alcohol derivatives has been studied. The effect of solvent and Lewis acids has been explored in or

Highly diastereoselective allylic azide formation and isomerization. Synthesis of 3(2′-amino)-β-lactams

(Chemical Equation Presented) The stereoselective anti S N2′ attack of NaN3 to 3-alkenyl-3-bromo-azetidin-2- ones gave a mixture of diastereomeric azides in fast equilibrium. The [3,3]-sigmatropic rearrangement of allylic azides occu