57061-25-3

Upstream product

• 1191988-08-5 2-(2-phenylethyl)-3-butyne-1,2-diol 
• 249766-43-6 2-[(1-ethoxy)ethoxy]-2-[(2,2-dimethoxy)ethyl]-4-phenyl-butanol 
• 249766-38-9 2-[(1-ethoxy)ethoxy]-2-[(2,2-dimethoxy)ethyl]-4-phenyl-butanenitrile 
• 249766-41-4 3-[(1-ethoxy)ethoxy]-1,1-dimethoxy-5-phenylpentane-3-carbaldehyde 
• 249766-35-6 2-[(1-ethoxy)ethoxy]-4-phenyl-butanenitrile 
• 121054-03-3 2-hydroxy-4-phenylbutanenitrile 
• 104-53-0 3-phenyl-propionaldehyde 
• 128587-62-2 3-styryl-furan 

Relevant academic research and scientific papers

Cationic gold(I)-mediated intramolecular cyclization of 3-alkyne-1,2-diols and 1-amino-3-alkyn-2-ols: A practical route to furans and pyrroles

The intramolecular cyclizations of the 3-alkyne-1,2-diols and the 1-amlno-3-alkyn-2-ols with a low catalyst loading (0.05-0.5 mol %) of (Ph 3P)AuCl - AgNTf2 or (Ph3P)AuCl-AgOTf proceeded at room temperature to provide a variety of substituted furans and pyrroles In excellent yields (85-98% yields). This method Is also fully applicable to the conversion of several dozen grams of the substrate using only 0.05 mol % each of the Au and Ag catalysts.

Regioselective ortho lithiation of 3-aryl and 3-styryl furans

(Chemical Equation Presented) An unusual regioselectivity pattern for the ortho lithiation of 3-aryl and 3-styryl furans has been uncovered wherein lithiation occurs preferentially at the sterically encumbered 2-position. The results are attributed, at le

Synthesis and insect antifeedant activity of 2-substituted 2,3- dihydrofuran-3-ols and butenolides (Part II)

The introduction of a hydroxy group at C-13 of the clerodane skeleton is proposed as a strategy to potentially increase the antifeedant activity of simple analogs. This idea is applied to clerodane analogs with furan or butenolide type sidechains and ther