879879-63-7

Upstream product

• 879879-59-1 N-[(Z)-1-{tri(n-butyl)stannyl}-2-(4-methoxyphenyl)vinyl]formamide 
• 862263-47-6 {(E)-2-Isocyanato-3-(4-methoxy-phenyl)-1-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-allyl}-carbamic acid 2-trimethylsilanyl-ethyl ester 
• 862263-00-1 2,3-Bis-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-succinic acid monomethoxymethyl ester 
• 862263-41-0 2,3-Bis-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid monomethoxymethyl ester 
• 862263-35-2 (E)-3-Isocyanato-4-(4-methoxy-phenyl)-2-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-but-3-enoic acid methoxymethyl ester 
• 862263-43-2 (E)-3-Isocyanato-4-(4-methoxy-phenyl)-2-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-but-3-enoic acid methoxymethyl ester 
• 862262-88-2 (4-methoxy-phenyl)-propynoic acid methoxymethyl ester 
• 862263-08-9 C₃₂H₄₄N₂O₈Si₂ 
• 2227-57-8 3-(4-methoxyphenyl)propynoic acid 
• 862263-06-7 [(E)-3-(4-Methoxy-phenyl)-1-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-allyl]-carbamic acid 2-trimethylsilanyl-ethyl ester 
• 862263-04-5 (E)-4-(4-Methoxy-phenyl)-2-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-(2-trimethylsilanyl-ethoxycarbonylamino)-but-3-enoic acid 
• 862263-45-4 (E)-4-(4-Methoxy-phenyl)-2-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-3-(2-trimethylsilanyl-ethoxycarbonylamino)-but-3-enoic acid 
• 862262-98-4 2,3-Bis-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-succinic acid methoxymethyl ester 2-trimethylsilanyl-ethyl ester 
• 862263-18-1 2,3-Bis-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid methoxymethyl ester 2-trimethylsilanyl-ethyl ester 

Downstream Products

• 862263-10-3 1,1'-[(1E,3E)-2,3-diisocyano-1,3-butadiene-1,4-diyl]bis[methoxybenzene] 

Relevant academic research and scientific papers

ALPHA-SUBSTITUTED VINYLTIN COMPOUND

To provide α-substituted vinyltin useful for the search for function-developing substances such as pharmaceuticals/agrichemicals and functional materials and for the construction of a compound library. An α-substituted vinyltin compound represented by the

The first stereoselective total synthesis of antiviral antibiotic, xanthocillin X dimethylether and its stereoisomer

Xanthocillin X dimethylether (1) has been stereoselectively synthesized from the propiolic acid 6 through an oxidative rearrangement of the stannyl vinyl amide 27 to give the vinyl isocyanate 30 and a homocoupling of the stannyl N-formylenamine 31.