53690-65-6

Upstream product

• 53847-99-7 2-furyl 2'-methoxyphenyl ketone 
• 57999-46-9 2-(tetrahydropyran-2-yloxy)phenyl bromide 
• 95-56-7 2-hydroxybromobenzene 
• 108-95-2 phenol 
• 527-69-5 2-furancarbonyl chloride 
• 579-75-9 2-Methoxybenzoic acid 
• 2948-14-3 furan-2-carboxylic acid phenyl ester 

Downstream Products

• 97034-99-6 C₁₃H₁₁NO₄ 
• 97034-81-6 2-furyl 2'-hydroxyphenyl ketone oxime 

Relevant academic research and scientific papers

Asymmetric Transfer Hydrogenation of o-Hydroxyphenyl Ketones: Utilizing Directing Effects That Optimize the Asymmetric Synthesis of Challenging Alcohols

A systematic range of o-hydroxyphenyl ketones were reduced under asymmetric transfer hydrogenation conditions using the C3-tethered catalyst 2. Two directing effects, i.e., an o-hydroxyphenyl coupled to a bulky aromatic on the opposite side of the ketone substrate, combine in a matched manner to deliver reduction products with very high enantiomeric excess.

2-heteroaryl 2-substituted phenylketone derivatives and their inhibitory activity on platelet aggregation

R 68070 and CV-4151 are two compounds possessing both thromboxane synthetase inhibitory activity and thromboxane receptor antagonist properties. 2-Heteroaryl 2-substituted phenylketone derivatives with a partial structural similarity to R 68070 and CV-415