Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Advanced Synthesis & Catalysis called Synthesis of β2,2-Amino esters via Rh-Catalysed Regioselective Hydroaminomethylation, Author is Cunillera, Anton; Ruiz, Aurora; Godard, Cyril, which mentions a compound: 97739-46-3, SMILESS is CC1(C2)OC(C3)(C)OC2(C)OC3(C)P1C4=CC=CC=C4, Molecular C16H21O3P, Computed Properties of C16H21O3P.
The synthesis of β2,2-amino esters was successfully achieved via Rh-catalyzed regioselective hydroaminomethylation of Me methacrylate with secondary amines using the neutral precursor Rh(acac)(CO)2. In this process, the presence of mol. sieves was crucial in order to access the final amino ester. For the synthesis of products containing aniline derivatives, the use of the cationic precursor [Rh(COD)2]BF4 and MeCgPPh phosphine I as ligand was necessary in a mixture of toluene/DCE as solvent. Effects of the steric and electronic properties of the amines were observed Interestingly, the poisoning effect of CO in the hydrogenation of the imine intermediate was observed when benzyl amine was used.
In some applications, this compound(97739-46-3)Computed Properties of C16H21O3P is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.
Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics