17213-89-7

Upstream product

• 84-65-1 9,10-phenanthrenequinone 
• 1004-22-4 (phenylethynyl)sodium 
• 4440-01-1 lithium phenylacetylide 
• 536-74-3 phenylacetylene 

Downstream Products

• 17213-97-7 10-methoxy-10-phenylethynyl-9-anthrone 
• 14825-85-5 9,10-bis(phenylethynyl)-9,10-dihydroanthracene-9,10-diol 
• 17214-04-9 trans-10-Hydroxy-9-methoxy-9,10-diphenylethinyl-9,10-dihydro-anthracen 
• 17214-05-0 cis-10-Hydroxy-9-methoxy-9,10-diphenylethinyl-9,10-dihydro-anthracen 
• 80364-62-1 9,9'-di(phenylethynyl)<9,9'-bianthracene>-10,10'(9H,9'H)-dione 
• 854706-64-2 (10-phenethyl-[9]anthryl)-phenyl-ethanedione 
• 872788-85-7 1-(10-phenethyl-[9]anthryl)-2-phenyl-ethanone 
• 17368-50-2 trans-9,10-dihydro-9,10-diphenethylanthracene-9,10-diol 
• 101905-49-1 9-(trans-2-phenylethenyl)-10-phenylethylanthracene 
• 879124-35-3 9-phenethyl-10-cis-styryl-anthracene 
• 18532-00-8 9-cis-styryl-10-trans-anthracene 
• 96376-94-2 9-phenethyl-10-phenylethynyl-anthracene 

Relevant academic research and scientific papers

Synthesis of 2-(Isoquinolin-1-yl)prop-2-en-1-ones via Silver(I)-Catalyzed One-Pot Tandem Reaction of ortho-Alkynylbenzaldoximes with Propargylic Alcohols

The silver(I)-catalyzed reaction of ortho-alkynylbenzaldoximes with propargylic alcohols represents a new strategy for the divergent one-pot synthesis of 2-(isoquinolin-1-yl) prop-2-en-1-ones via tandem 6-endo-cyclization, 1,3-dipolar cycloaddition, and intramolecular dehydrative opening of the 2,3-dihydroisoxazole ring. This synthetic protocol tolerates a wide variety of ortho-alkynylbenzaldoximes and propargylic alcohols and affords the corresponding products in excellent yields.

Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols

A new and convenient strategy for the synthesis of functionalized tropone derivatives based on the gold-catalyzed oxidative ring expansion of alkynyl quinols has been developed. The reaction proceeds via gold-catalyzed highly regioselective oxidation foll

Synthesis and Evaluation of Fluorescent Materials for Colour Control of Peroxyoxalate Chemiluminescence. I. The Phenylethynylation of Anthraquinone

The synthesis of 9,10-bis(phenylethynyl)anthracene has been examined in detail prior to the synthesis of a series of phenylethynyl substituted aromatic compounds which are of interest as fluorescent materials for peroxyoxalate chemiluminescence.Reductions of the 9,10-bis(phenylethynyl)-9,10-dihydroanthracene-9,10-diol precursor by stannous chloride and by sodium hypophosphite-potassium iodide both gave a series of byproducts, in addition to 9,10-bis(phenylethynyl)anthracene.The formation of these compounds is interpreted in terms of a free-radical process.The interaction of 10-hydroxy-10-(phenylethynyl)anthrone with both the reducing systems has been rationalized and the reaction with concentrated sulfuric acid reinterpreted.