884589-74-6

Upstream product

• 131685-53-5 (S)-4-benzyl-3-propionyl-2-oxazolidinone 
• 106-96-7 propargyl bromide 

Downstream Products

• 1259286-27-5 C₂₀H₂₉NO₄Si 
• 1259286-26-4 (R,E)-methyl 5-(benzyldimethylsilyl)-2-methylpent-4-enoate 
• 1259286-25-3 (4S)-3-[(2R,4E)-5-(benzyldimethylsilyl)-2-methyl-1-oxo-4-penten-1-yl]-4-(phenylmethyl)-2-oxazolidinone 
• 1190409-95-0 (2S,3S,4E)-1-(4-methylphenylsulfonyl)-2-carboxy-4-[(2E,5R)-5-carboxy-1-methyl-2-hexen-1-ylidene]-3-pyrrolidineacetic acid 
• 1190409-94-9 methyl (2S,3S,4E)-1-(4-methylphenylsulfonyl)-2-methoxycarbonyl-4-[(2E,5R)-5-methoxycarbonyl-1-methyl-2-hexen-1-ylidene]-3-pyrrolidineacetate 
• 1190409-91-6 (2S,3S,4Z)-1-(4-methylphenylsulfonyl)-2-carboxy-4-[(2E,5R)-5-carboxy-1-methyl-2-hexen-1-ylidene]-3-pyrrolidineacetic acid 
• 1190409-90-5 methyl (2S,3S,4Z)-1-(4-methylphenylsulfonyl)-2-methoxycarbonyl-4-[(2E,5R)-5-methoxycarbonyl-1-methyl-2-hexen-1-ylidene]-3-pyrrolidineacetate 

Relevant academic research and scientific papers

Total synthesis of (-)-xyloketal A

The first total synthesis of the C3-symmetric and biologically active natural product, (-)-xyloketal A, has been accomplished in one step from phloroglucinol (1,3,5-trihydroxybenzene) and (4R)-3-hydroxymethyl-2,4-dimethyl- 4,5-dihydrofuran. Thi

Stereoselective, Ag-Catalyzed Cyclizations to Access Polysubstituted Pyran Ring Systems: Synthesis of C1-C12 Subunit of Madeirolide A

The exploration into the scope of a silver-catalyzed cyclization (AgCC) of propargyl benzoates for accessing pyran ring systems has been reported. The impact of the degree of substitution, nature of the substitution on the carbon backbone/benzoate moiety,