An article Regioselective Synthesis of 4,5-Dihydro-6H-oxepino[3,2-c]chromene-2,6(3H)-diones through Palladium-Catalyzed Intramolecular Alkoxycarbonylation of 3-Allyl-4-hydroxycoumarins WOS:000476059300001 published article about 7-MEMBERED RING LACTONES; ENANTIOSELECTIVE SYNTHESIS; CYCLOCARBONYLATION; EFFICIENT; CARBONYLATION; DERIVATIVES; LACTAMS; WATER; 4-HYDROXYCOUMARINS; CONSTANT in [Sosa, D. Oliver; Almaraz, Karla; Amezquita-Valencia, Manuel] Univ Nacl Autonoma Mexico, Inst Quim, Ciudad Univ, Mexico City 04510, DF, Mexico in 2019, Cited 47. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6. Recommanded Product: 150-19-6
Seven-membered ring lactones fused to coumarin scaffolds were obtained via a palladium-catalyzed regioselective intramolecular alkoxycarbonylation under a CO atmosphere. Cyclocarbonylation of 3-allyl-4-hydroxycoumarin derivatives was accessed in the absence of hydrogen gas, acidic conditions, or any other additives. The results of the control experiments revealed the importance of pKa of the substrate for initiating the reaction.
About m-Methoxyphenol, If you have any questions, you can contact Sosa, DO; Almaraz, K; Amezquita-Valencia, M or concate me.. Recommanded Product: 150-19-6
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Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles