147165-84-2

Upstream product

• 69739-34-0 t-butyldimethylsiyl triflate 
• 147165-82-0 *,S^*)>-N-hydroxy-2,2-dimethyl-N-(phenylmethyl)-α-(2-propenyl)-1,3-dioxolane-4-methanamine 
• 91190-38-4 N-benzyl-2,3-O-isopropylidene-D-glyceraldehyde nitrone 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 943227-69-8 C₂₅H₄₁NO₅Si 
• 147165-98-8 <3R-<3β(4S^*),5β>>-5-(acetoxymethyl)-3-(2,2-dimethyl-1,3-dioxolan-4-yl)-2-(phenylmethyl)isoxazolidine 
• 943227-92-7 C₁₉H₂₇NO₅ 
• 147165-94-4 <3R-<3β(4S^*),5β>>-3-(2,2-dimethyl-1,3-dioxolan-4-yl)-5-(iodomethyl)-2-(phenylmethyl)isoxazolidine 

Relevant academic research and scientific papers

Hydroxylamine oxygen as nucleophile in palladium(0)- and palladium(II)-catalyzed allylic alkylation: A novel access to isoxazolidines

In search for novel heterocyclization processes, the intramolecular Pd-mediated allylic alkylation of homoallyl hydroxylamines is described. Depending on both the reaction conditions and the substrates, cis- or trans-3-substituted-5-vinyl isoxazolidines a

Iodocyclization of Homoallylic Hydroxylamines Derived from D-Glyceraldehyde

The reaction of allylmagnesium chloride with nitrone 1 derived from D-glyceraldehyde affords two diastereoisomeric homoallylic hydroxylamines 2a and 3a which, after separation and O-silylation, are subjected to iodocyclization using N-iodosuccinimide.The