Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 37943-90-1, is researched, SMILESS is P(C1=CC=CC=C1)(C2=CC=CC=C2)C3=NC=CC=C3, Molecular C17H14NPJournal, Applied Organometallic Chemistry called The intriguing methoxycarbonylation of trimethylsilylacetylene in the presence of Drent’s catalytic system, Author is Sole, Roberto; Scrivanti, Alberto; Alam, Mahbubul Md.; Beghetto, Valentina, the main research direction is palladium phosphine catalyzed methoxycarbonylation trimethyl silylacetylene Drent catalysis; acrylate trimethylsilyl preparation.COA of Formula: C17H14NP.
The alkoxycarbonylation of trimethylsilylacetylene has been studied in order to develop an atom economic sustainable synthesis of 2-(trimethylsilyl)acrylates, a family of valuable intermediates. Pd(OAc)2 in combination with CH3SO3H and diphenyl-(pyridin-2-yl)phosphine or diphenyl-(6-methyl-pyridin-2-yl)phosphine is an active catalyst for the reaction affording mixtures of the sought 2-(trimethylsilyl)acrylate and the isomeric 3-(trimethylsilyl)acrylate. The phosphine ligand has a dramatic effect on the reaction. When employing diphenyl-(pyridin-2-yl)phosphine, it is necessary to carry out the reaction at 80° in order to observe a modest catalytic activity, and the product is an almost equimol. mixture of the two isomeric esters. On the contrary, when employing diphenyl-(6-methyl-pyridin-2-yl)phosphine, the reaction proceeds under much milder conditions affording with high rate (turnover frequency [TOF] up to 1200 h-1) and selectivity (>95%) of the sought 2-(trimethylsilyl)acrylate. The reaction conditions have been optimized, and the effects of phosphine/palladium, acid/palladium, reaction time, temperature, and CO pressure have been investigated.
Although many compounds look similar to this compound(37943-90-1)COA of Formula: C17H14NP, numerous studies have shown that this compound(SMILES:P(C1=CC=CC=C1)(C2=CC=CC=C2)C3=NC=CC=C3), has unique advantages. If you want to know more about similar compounds, you can read my other articles.
Reference:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem