95517-85-4

Upstream product

• 95517-92-3 8-Methyl-3-phenyl-5,6,7,8-tetrahydro-chromen-2-one 
• 824-42-0 2-methoxy-3-methylbenzaldehyde 
• 114-70-5 sodium phenylacetate 
• 2912-62-1 α-chlorophenylacetyl chloride 
• 583-60-8 2-Methylcyclohexanone 
• 4638-79-3 2-chloro-2-phenylacetaldehyde 
• 100-52-7 benzaldehyde 
• 201230-82-2 carbon monoxide 
• 100-44-7 benzyl chloride 
• 50978-45-5 3-oxobenzo[d]isothiazole-2(3H)-carbaldehyde 1,1-dioxide 
• 1333483-14-9 N-methyll-N-(phenylethylnyl)methanesulfonamide 
• 860768-70-3 4-methyl-phenanthrene-9-carboxylic acid 
• 932-87-6 1-Bromo-2-phenylacetylene 
• 95517-90-1 3-Chloro-4-methoxy-8-methyl-3-phenyl-3,4,5,6,7,8-hexahydro-chromen-2-one 

Downstream Products

• 212515-89-4 8-bromomethyl-3-phenyl-2H-chromen-2-one 
• 212515-91-8 8-formyl-3-phenyl-2H-chromen-2-one 

Relevant academic research and scientific papers

Zn(II)-Catalyzed One-Pot Synthesis of Coumarins from Ynamides and Salicylaldehydes

A highly efficient and straightforward synthesis of diversely substituted coumarins from ynamides and salicylaldehydes in the presence of Zn(II) catalyst has been developed. The sulfonamide moiety of ynamides was successfully recycled in this process, serving as an effective traceless directing group for high regioselectivity in the bond-forming event. The advantages of this protocol are good functional group tolerance, broad substrate scope, simple and high-yielding reaction, recovery/reuse of the sulfonamides, low catalyst loading of inexpensive catalyst, and, by these merits, a more cost-effective and greener process.

Pd-catalysed carbonylative annulation of salicylaldehydes with benzyl chlorides using N-formylsaccharin as a CO surrogate

A convenient and highly efficient Pd-catalysed carbonylative annulation of salicylaldehydes with benzyl chlorides to afford the corresponding 3-arylcoumarins in good to excellent yields has been developed. Importantly, the protocol utilizes a commercially available, low cost, solid and easy to handle N-formylsaccharin as an alternative to the highly toxic CO gas.

A general palladium-catalyzed carbonylative synthesis of chromenones from salicylic aldehydes and benzyl chlorides

Cute CO! An interesting and straightforward procedure for the carbonylative synthesis of chromenones from readily available salicylic aldehydes and benzyl chlorides has been developed (see scheme; DPPP=1,3-bis(diphenylphosphino) propane). In the presence of a palladium catalyst, various coumarins were produced in good to excellent yields. Copyright

Synthesis of 3-arylcoumarins through N-heterocyclic carbene catalyzed condensation and annulation of 2-chloro-2-arylacetaldehydes with salicylaldehydes

The condensation reaction of 2-chloro-2-arylacetaldehyde with salicylaldehyde catalyzed by N-heterocyclic carbene (NHC) leading to 3-arylcoumarin was studied. A number of 3-arylcoumarin derivatives were obtained in good to excellent yields via this umpolung reaction. This reaction is facile and experimentally simple and mild.

Coumarin 1,4-dihydropyridine derivatives

A series of 1,4-dihydropyridines bearing a coumarin moiety in 4-position was synthesized. The compounds were evaluated for inotropic, chronotropic and calcium antagonist activities. The replacement of the o-nitrophenyl moiety of nifedipine with a coumarin