Bernadyuk, Stanislav Z.’s team published research in Mendeleev Communications in 1994 | CAS: 6553-72-6

Ethyl 1-methylcyclopentanecarboxylate(cas: 6553-72-6) is a member of cyclopentanes. Although cyclopentane itself doesn’t have a single highly favoured conformation, a substituent on the cyclopentane ring can upset the balance of strains thereby favouring either the envelope or the half-chair.Name: Ethyl 1-methylcyclopentanecarboxylate

Name: Ethyl 1-methylcyclopentanecarboxylateOn September 30, 1994 ,《Carbonylation of methylcyclopentane and cyclohexane initiated by the aprotic organic superacid CBr4·2AlBr3》 was published in Mendeleev Communications. The article was written by Bernadyuk, Stanislav Z.; Akhrem, Irena S.; Vol’pin, Mark E.. The article contains the following contents:

The aprotic organic superacid CBr4·2AlBr3 initiates carbonylation of methylcyclopentane and cyclohexane with CO at atm. pressure with formation (after EtOH treatment) of various products in high yields depending on the conditions. The products are Et 1-methylcyclopentanecarboxylate (at -45°), Et cyclohexanecarboxylate (at 0°) and 2-methylcyclohexanone (at -23°). The reaction mechanism is discussed. The results came from multiple reactions, including the reaction of Ethyl 1-methylcyclopentanecarboxylate(cas: 6553-72-6Name: Ethyl 1-methylcyclopentanecarboxylate)

Ethyl 1-methylcyclopentanecarboxylate(cas: 6553-72-6) is a member of cyclopentanes. Although cyclopentane itself doesn’t have a single highly favoured conformation, a substituent on the cyclopentane ring can upset the balance of strains thereby favouring either the envelope or the half-chair.Name: Ethyl 1-methylcyclopentanecarboxylate

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Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics