4124-81-6

Upstream product

• 124-41-4 sodium methylate 
• 3580-38-9 2-Benzoylcyclohexanone 
• 113340-87-7 1-methoxy-3-phenyl-2-azacycloocta-1,3-diene 
• 66800-56-4 N-methoxycarbonyl-6-aminohexanoic acid 
• 67-56-1 methanol 
• 7472-43-7 6-benzoylhexanoic acid 
• 98-86-2 acetophenone 
• 627-91-8 adipic acid monomethyl ester 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 94803-44-8 7a-(1-pyrrolidinyl)-3-phenyl-3a,4,5,6,7,7a-hexahydro-1,2-benzoisoxazole 
• 70288-80-1 6-methoxycarbonylaminohexanoic acid methyl ester 
• 100-52-7 benzaldehyde 

Downstream Products

• 507278-26-4 methyl (R)-7-hydroxy-7-phenylheptanoate 
• 1242279-46-4 C₂₁H₂₆N₂O₄S 

Relevant academic research and scientific papers

Photoredox-Catalyzed Decarboxylative Alkylation of Silyl Enol Ethers to Synthesize Functionalized Aryl Alkyl Ketones

Photoredox-catalyzed decarboxylative alkylation of silyl enol ethers has been developed. Diverse functionalized aryl alkyl ketones were afforded in modest to good yields using N-(acyloxy)phthalimide as an easy access alkyl radical source under mild and operationally simple conditions. The excellent performance of drug molecules such as fenbufen and indomethacin and naturally occurring carboxylic acids such as stearic acid and dehydrocholic acid further demonstrated the practicability of the reaction.

Effect of carbon chain length in the substituent of PCBM-like molecules on their photovoltaic properties

A series of [6,6]-phenyl-C61-butyric acid methyl ester (PCBM)-like fullerene derivatives with the butyl chain in PCBM changing from 3 to 7 carbon atoms, respectively (F1-F5), are designed and synthesized to investigate the relationship between

Photoreactions of Benzonitrile with Cyclic Enol Ethers

Upon irradiation cyclic enol ethers such as 1-methoxy-cyclopentene (4) mainly add across the cyano group of benzonitrile (1) under formation of 2-azabutadienes of an imidoester type.This is in agreement with the so-called ΔG-correlation which was reported

Nonacarbonyldiiron-, Pentacarbonyliron-, or Hexacarbonylmolybdenum-induced Reactions of 4,5-Polymethylene-substituted 2-Isoxazolines

The reaction of 4,5-polymethylene-substituted 2-isoxazolines, 3-phenyl-3a,5,6,7a-tetrahydro-4H-pyranoisoxazole or 3-phenyl-3a,4,5,6a-tetrahydrofuroisoxazole, with , , or resulted in the formation of 5-hydroxy-1-phenyl-1-pentanone or 4-hydroxy-1-phenyl-1-butanone, via the N-O and C-C bond cleavage of the 2-isoxazoline ring and the subsequent hydrolysis.The similar reaction of 7a-morpholino- and 7a-(1-pyrrolidinyl)-3-phenyl-3a,4,5,6,7,7a-hexahydro-1,2-benzoisoxazoles undergoes the N-O bond cleavage and, the subsequent elimination of the amino group or the C-3a-C-7a bond fission.Although the reaction of 6a-morpholino- and 6a-(1-pyrrolidinyl)-3-phenyl-3a,4,5,6a-tetrahydro-4H-cyclopentisoxazoles with undergoes the N-O bond cleavage, and the subsequent elimination of the amino group or the C-3a-C-6a bond fission, the reaction of those 2-isoxazolines with proceeds very slowly.The mechanisms are proposed for these reactions.