1221289-08-2

Upstream product

• 959-33-1 3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 
• 50793-44-7 2-bromo-3-(4-methoxyphenyl)-1-phenyl-2-propen-1-one 
• 536-74-3 phenylacetylene 

Downstream Products

• 1260510-86-8 3-(methoxy(4-methoxyphenyl)methyl)-2,4,5-triphenylfuran 
• 126525-66-4 2,5-diphenyl-3-(4-methoxybenzyl)furan 
• 1221288-85-2 (2,5-dibenzyl-3-(4-methoxyphenyl)-2,3-dihydroisoxazol-4-yl)(phenyl)methanone 

Relevant academic research and scientific papers

Indium-Catalysed Transfer Hydrogenation for the Reductive Cyclisation of 2-Alkynyl Enones towards Trisubstituted Furans

Indium tribromide catalysed the transfer hydrogenation from dihydroaromatic compounds, such as the commercially available γ-terpinene, to enones, which resulted in the cyclisation to trisubstituted furan derivatives. The reaction was initiated by a Michae

Sc(OTf)3-Catalyzed Diastereoselective Formal [3+2] Cycloaddition Reactions of Alkynylcyclopropane Ketones with Electron-Rich Aromatic Aldehydes to Yield 2,5-trans-Tetrahydrofurans

In contast to the general [4+2] cycloaddition reactions of alkynylcyclopropane ketones reported in the literature, we report herein a Sc(OTf)3-catalyzed formal intermolecular [3+2] cycloaddition reaction of alkynylcyclopropane ketones with elec

Gold-Catalyzed Concomitant [3 + 3] Cycloaddition/Cascade Heterocyclization of Enynones/Enynals with Azides Leading to Furanotriazines

[Au]-catalyzed [3 + 3] cycloaddition reaction of enynones/enynals with azides, which allows the efficient regioselective synthesis of highly fused furo[3,4-d][1,2,3]triazines in good-to-excellent yields under mild conditions, has been developed. The synth