Catalytic (2 + 2)-Cycloaddition Reactions of Silyl Enol Ethers. A Convenient and Stereoselective Method for Cyclobutane Ring Formation
journal contributionposted on 23.01.2004, 00:00 by Kiyosei Takasu, Megumi Ueno, Kazato Inanaga, Masataka Ihara
An efficient catalytic (2 + 2)-cycloaddition reaction leading to the formation of cyclobutane rings has been devised. The process transforms silyl enol ethers and α,β-unsaturated esters into polysubstituted cyclobutanes with a high degree of trans-stereoselectivity. Both the rate and stereoselectivity of the process can be controlled by the choice of the ester group and silyl substituents. The results of stereochemical studies show that the cycloaddition step in this reaction proceeds in a nonstereospecific manner and, thus, by a pathway involving sequential nucleophilic additions via a short-lived zwitterionic intermediate.
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estersCatalyticConvenientStereoselective Methodpathwaysilyl substituentsester groupcyclobutane ringszwitterionicsilyl enol ethersstereoselectivityreaction proceedsCyclobutane Ring FormationSilyl Enol Etherschoiceformationpolysubstituted cyclobutanesstereochemical studies showsequential nucleophilic additionsnonstereospecific mannertranCycloadditioncycloaddition step