177981-87-2

Upstream product

• 81445-44-5 (S)-2-(benzyloxy)propanal 
• 622-30-0 N-benzyl hydroxylalmine 
• 29601-98-7 N-benzylhydroxylamine hydrochloride 
• 3913-64-2 2(S)-hydroxypropanal 

Downstream Products

• 1053231-48-3 (3R,3aR,6aR)-3-[(S)-2-(benzoxy)ethyl]-2-benzyl-4,5-oxathiain-4,4-dioxide[3,4-d]isoxazolidine 
• 1053231-49-4 (3S,3aS,6aS)-3-[(S)-2-(benzoxy)ethyl]-2-benzyl-4,5-oxathiain-4,4-dioxide[3,4-d]isoxazolidine 
• 1170994-36-1 C₂₀H₂₀F₃NO₂ 
• 1170994-32-7 (1R,2S)-N-benzyl-N-[2-(benzyloxy)-1-(3,3,3-trifluoroprop-1-ynyl)propyl]hydroxylamine 
• 1170994-34-9 (1S,2S)-N-benzyl-N-[2-(benzyloxy)-1-(3,3,3-trifluoroprop-1-ynyl)propyl]hydroxylamine 
• 177981-88-3 (3S,3aS,6aS)-2-Benzyl-3-((S)-1-benzyloxy-ethyl)-tetrahydro-furo[2,3-d]isoxazol-5-one 
• 178151-97-8 (3R,3aR,6aR)-2-Benzyl-3-((S)-1-benzyloxy-ethyl)-tetrahydro-furo[2,3-d]isoxazol-5-one 

Relevant academic research and scientific papers

Regio- and stereoselective synthesis of isoxazolidine derivatives by asymmetric 1,3-dipolar cycloaddition reaction of chiral nitrones with 1-propene-1,3-sultone

(Chemical Equation Presented) Asymmetric 1,3-dipolar cycloadditions of chiral nitrones to 1-propene-1,3-sultone (1) were investigated. Chiral nitrones 6a-e reacted with sultone 1 in toluene at 90°C for 24-36 h to give the corresponding isoxazolidines in m

Lewis-acid promoted addition of 2-trimethylsilyloxyfuran to nitrones: Synthesis and absolute configuration of tetrahydro-2-benzyl-3-(1-benzyloxyethyl)-furo[2,3-d]isoxazol-5(2H)ones

A straightforward synthesis of tetrahydro-2-benzyl-3-(1-benzyloxyethyl)-furo[2,3-d]isoxazol-5(2H)ones is reported, based on the Lewis acid-catalysed addition of 2-trimethylsilyloxyfuran to the N-benzyl nitrone of (S)-lactaldehyde.