Lewis base catalyzed asymmetric hydrosilylation of α-substituted β-enamino esters: facile access to enantioenriched β2-amino esters via dynamic kinetic resolution was written by Shu, Chang;Hu, Xiao-Yan;Li, Shuai-Shuai;Yuan, Wei-Cheng;Zhang, Xiao-Mei. And the article was included in Synlett in 2014.Name: Ethyl 2-(4-fluorophenyl)acetate This article mentions the following:
A chiral Lewis base organocatalyzed asym. hydrosilylation of α-substituted β-enamino esters H5C2C(O)OC(R):CHNH(PMP) [R = 3,4-(OCH3)2C6H3, piperonyl, 2-naphthyl, 2-thienyl, etc.] was presented. The reactions proceeded through dynamic kinetic resolution and mild synthesis of various enantioenriched β2-amino ester derivatives H5C2COC(O)C(R)CH2NH(PMP) with high yields (up to 98%) in moderate enantioselectivities (up to 77% ee). In the experiment, the researchers used many compounds, for example, Ethyl 2-(4-fluorophenyl)acetate (cas: 587-88-2Name: Ethyl 2-(4-fluorophenyl)acetate).
Ethyl 2-(4-fluorophenyl)acetate (cas: 587-88-2) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. 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. Name: Ethyl 2-(4-fluorophenyl)acetate
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