Rhodium-Catalyzed Intramolecular Silylcarbotricyclization (SiCaT) of Triynes was written by Ojima, Iwao;Vu, An T.;McCullagh, James V.;Kinoshita, Atsushi. And the article was included in Journal of the American Chemical Society in 1999.Quality Control of Diethyl 2-(prop-2-yn-1-yl)malonate This article mentions the following:
Intramol. silylcarbotricyclization of triynes is catalyzed by various Rhodium complexes. For example the triyne HCCCH2C(CO2Et)2CH2CCCH2C(CO2Et)2CH2CCH was reacted with PhMe2SiH in the presence Rh(acac)(CO)2 to give the cyclization products I, II, and III. A mechanism is proposed for these cyclizations which involves silicon-initiated carbometalation followed by subsequent carbocyclization and β-hydride elimination. In the experiment, the researchers used many compounds, for example, Diethyl 2-(prop-2-yn-1-yl)malonate (cas: 17920-23-9Quality Control of Diethyl 2-(prop-2-yn-1-yl)malonate).
Diethyl 2-(prop-2-yn-1-yl)malonate (cas: 17920-23-9) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Quality Control of Diethyl 2-(prop-2-yn-1-yl)malonate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics