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The first catalytic asymmetric addition of diethylzinc to aldehyde promoted by chiral thiourea

The first catalytic asymmetric addition of diethylzinc to aldehyde promoted by chiral thiourea
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摘要 A series of C_2-symmetric and asymmetric chiral thiourea derivatives were synthesized from commercial L-phenylalanine.All of the new compounds have been fully characterized by IR,~1H NMR,^(13)C NMR,MS spectra and elemental analyses.The chiral thioureas were used as chiral ligands in the catalytic enantioselective ethylation of aldehydes with diethylzinc,the corresponding sec-alcohols were gained with excellent enantioselectivities(up to 87.1%ee) and high yields(up to 76.7%) after the conditions were optimized. A series of C_2-symmetric and asymmetric chiral thiourea derivatives were synthesized from commercial L-phenylalanine.All of the new compounds have been fully characterized by IR,~1H NMR,^(13)C NMR,MS spectra and elemental analyses.The chiral thioureas were used as chiral ligands in the catalytic enantioselective ethylation of aldehydes with diethylzinc,the corresponding sec-alcohols were gained with excellent enantioselectivities(up to 87.1%ee) and high yields(up to 76.7%) after the conditions were optimized.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2011年第11期1265-1268,共4页 中国化学快报(英文版)
基金 Open-Ended Fund of the State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology
关键词 Chiral thiourea DIETHYLZINC Amino alcohol C_2-symmetric Enantioselective addition Chiral thiourea Diethylzinc Amino alcohol C_2-symmetric Enantioselective addition
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