Analyzing the synthesis route of 707-61-9

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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: 707-61-9, is researched, SMILESS is CC1=CP(CC1)(C2=CC=CC=C2)=O, Molecular C11H13OPJournal, Article, Journal of the American Chemical Society called A Phosphetane Catalyzes Deoxygenative Condensation of α-Keto Esters and Carboxylic Acids via PIII/PV=O Redox Cycling, Author is Zhao, Wei; Yan, Patrick K.; Radosevich, Alexander T., the main research direction is phosphetane catalyst preparation oxygenative condensation ketoester carboxylic acid.Application of 707-61-9.

A small-ring phosphacycle is found to catalyze the deoxygenative condensation of α-keto esters and carboxylic acids. The reaction provides a chemoselective catalytic synthesis of α-acyloxy ester products with good functional group compatibility. Based on both stoichiometric and catalytic mechanistic experiments, the reaction is proposed to proceed via catalytic PIII/PV=O cycling. The importance of ring strain in the phosphacyclic catalyst is substantiated by an observed temperature-dependent product selectivity effect. The results point to an inherent distinction in design criteria for organophosphorus-based catalysts operating via PIII/PV=O redox cycling as opposed to Lewis base (nucleophilic) catalysis.

Compounds in my other articles are similar to this one(4-Methyl-1-phenyl-2,3-dihydro-1H-phosphole 1-oxide)Application of 707-61-9, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Reference:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem