144027-22-5

Upstream product

• 915127-49-0 N-phenylselenosaccharin 
• 83-33-0 inden-1-one 
• 645-96-5 Benzeneselenol 
• 1666-13-3 diphenyl diselenide 
• 95-13-6 1-indene 
• 34837-55-3 Phenylselenyl bromide 
• 5707-04-0 Phenylselenyl chloride 

Downstream Products

• 99706-09-9 2-allyl-2,3-dihydro-1H-inden-1-one 
• 83-33-0 inden-1-one 
• 1303532-59-3 (R)-[2-((S)-1-(2-fluorophenyl)2-nitroethyl)-2-(phenylselanyl)-2,3-dihydro-1H-inden-1-one] 
• 1303532-60-6 (R)-[2-((S)-1-(3,4-dichlorophenyl)2-nitroethyl)-2-(phenylselanyl)-2,3-dihydro-1H-inden-1-one] 
• 1303532-54-8 (R)-2-[(S)-2-nitro-1-[(4-nitrophenyl)ethyl]-2-(phenylselanyl)-2,3-dihydro-1H-inden-1-one] 
• 1303532-56-0 (R)-[2-((S)-1-(4-methoxyphenyl)2-nitroethyl)-2-(phenylselanyl)]-2,3-dihydro-1H-inden-1-one 
• 1303532-55-9 4-[((S)-2-nitro-1-[((R)1-oxo-2-(phenylselanyl)-2,3-dihydro-1H-inden-2-yl)]ethyl)]benzonitrile 
• 1303532-58-2 (R)-[2-((S)-1-(2-fluorophenyl)2-nitroethyl)-2-(phenylselanyl)-2,3-dihydro-1H-inden-1-one] 
• 1303532-53-7 (R)-[2-((S)-2-nitro-1-phenylethyl)-2-(phenylselanyl)-2,3-dihydro-1H-inden-1-one] 
• 1303532-70-8 (S)-2-[((R)-2-nitro-1-phenylethyl)-2-(phenylselanyl)-2,3-dihydro-1H-inden-1-one] 
• 1303532-57-1 C₂₁H₁₇NO₄Se 

Relevant academic research and scientific papers

Visible-light-induced oxidative coupling of vinylarenes with diselenides leading to α-aryl and α-alkyl selenomethyl ketones

A visible-light-induced oxidative coupling of diselenides with readily available vinylarenes is demonstrated. This benign protocol allows one to access a wide range of α-aryl and α-alkyl selenomethyl ketones in good yields with excellent functional group compatibility. The distinct advantages of this protocol over all previous methods include the use of a green solvent and air as an oxidant and the lack of a photocatalyst, a base, and an oxidant as well as better green chemistry matrices. Furthermore, the title reaction can be performed with natural sunlight, the most sustainable energy source imaginable. Additionally, the mild reaction conditions, easy operation and suitability for the modification of styrene-functionalized biomolecules make the current reaction system a more attractive method for the synthesis of a variety of medicinal and agrochemical compounds of interest.

N-Phenylselenosaccharin (NPSSac): a new electrophilic selenium-containing reagent

A new reagent N-phenylselenosaccharin (NPSSac) was simply prepared and used as a source of the electrophilic phenylselenyl group. This relatively stable new compound was able to react with a series of electron rich organic molecules like alkenes in the pr