852211-39-3

Upstream product

• 96-09-3 styrene oxide 
• 766-97-2 4-n-methylphenylacetylene 
• 624-31-7 4-tolyl iodide 
• 1743-36-8 1-phenylbut-3-yn-1-ol 
• 100-52-7 benzaldehyde 

Downstream Products

• 1644562-97-9 (Z)-4-phenyl-4-(p-tolyl)-3-(trifluoromethyl)but-3-enal 
• 1376770-94-3 4-hydroxy-4-phenyl-1-(p-tolyl)butan-1-one 
• 58144-64-2 (4-methylphenyl)(5-phenyl-1,2-oxazol-3-yl)methanone 
• 1366416-86-5 (Z)-tert-butyldimethyl{[4-(4-methylphenyl)-1-phenylbut-1-en-3-yn-1-yl]oxy}silane 
• 1366416-78-5 (E)-tert-butyldimethyl{[4-(4-methylphenyl)-1-phenylbut-1-en-3-yn-1-yl]oxy}silane 
• 1366416-71-8 2,2-difluoro-4-(4-methylphenyl)-1-phenyl-but-3-yn-1-one 
• 119492-83-0 2-(4-Methoxyphenyl)-5-phenylfuran 
• 852211-44-0 4-(4-methylphenyl)-1-phenylbut-3-yn-1-one 

Relevant academic research and scientific papers

Fe-Catalyzed tandem cyclization for the synthesis of 3-nitrofurans from homopropargylic alcohols and Al(NO3)3·9H2O

Al(NO3)3·9H2O as a nitro source for the synthesis of 3-nitrofurans from homopropargylic alcohols through Fe-catalyzed tandem cyclization is described. In this transformation, the substituted nitrofurans are obtained throug

A method for accessing sulfanylfurans from homopropargylic alcohols and sulfonyl hydrazides

A sulfenylation/cyclization reaction has been developed for the synthesis of sulfanylfurans in the presence of iodine. These processes provide facile strategies to construct C-S/O bonds, and expand the methods of synthesizing sulfanylfurans. In this trans

Copper-catalyzed one-pot trifluoromethylation/aryl migration/carbonyl formation with homopropargylic alcohols

A novel copper-catalyzed one-pot functionalization of homopropargylic alcohols that involves trifluoromethylation, aryl migration, and formation of a carbonyl moiety has been developed. This reaction constitutes the first direct conversion of homopropargy

Alternate mode of palladium-catalyzed alkynyliminium ion cyclizations affording stereodefined N-alkyl-3-alkylidenepyrrolidines

Pd/P(c-C6H11)3-catalyzed alkynyliminium ion cyclization in the presence of organoboronic acids affords stereodefined N-alkyl-3-alkylidenepyrrolidines. The distinctive cis-selective addition of the boronic acids and the imi

Microwave-assisted zinc chloride-catalyzed synthesis of substituted pyrroles from homopropargyl azides

Ligand-free 5-endo-dig cyclization of 1,4- and 1,2,4-substituted but-3-yn-1-yl (homopropargyl) azides in the presence of zinc chloride (usually 20 mol %) in dichloroethane at elevated temperature provides 2,5-di- and 2,3,5-trisubstituted pyrroles in high

5-Endo-dig electrophilic cyclization of 1,4-disubstituted but-3-yn-1-ones: Regiocontrolled synthesis of 2,5-disubstituted 3-bromo- and 3-iodofurans

(Chemical Equation Presented) 5-Endo-dig electrophilic cyclization of 1,4-diaryl but-3-yn-1-ones with N-bromosuccinimide or N-iodosuccinimide/acetone and iodine monochloride/ CH2Cl2, at room temperature, in the absence of base, provi