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Synthesis of Chiral Aminophenols Based on Proline and Their Application in Enantioselective Addition of Diethylzinc to Aldehydes

Synthesis of Chiral Aminophenols Based on Proline and Their Appli-cation in Enantioselective Addition of Diethylzinc to Aldehydes

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【作者】 葛健锋沈宗旋张雅文陆新华陆忠娥

【Author】 GE, Jian-Feng SHEN, Zong-Xuan ZHANG, Ya-WenLU, Xin-Hua LU, Zhong-E Department of Chemistry and Chemical Engineering , Suzhou University, Suzhou , Jiangsu 215006, China Department of Material and Engineering , Suzhou University, Suzhou, Jiangsu 215006, China

【机构】 Dapartment of Chemistry and Chemical EngineeringSuzhou UniversitySuzhouJiangsu 215006China Department of Material and EngineeringChinaDepartment of Chemistry and Chemical EngineeringChina

【摘要】 <正> Three 2-{(3R,7As)-1,1-disubstituted-tetrahydro-1 H-pyrrolo[1,2-c][1,3]oxazol-3-yl}phenols have been synthesized fromsalicylaldehyde and amino alcohols derived from L-proline,andused as ligands in enantioselective addition of diethylzinc toaldehydes,the ee values of obtained secondary alcohols werefound in the range of 0-90%.

【Abstract】 Three 2-{(3R, 7aS)-1, 1-disubstituted-tetrahydro-1H-pyrrolo [1,2-c][1,3]oxazol-3-yl} phenols have been synthesized from salicylaldehyde and amino alcohols derived from L-proline, and used as ligands hi enantioselective addition of diethylzinc to aldehydes, the ee values of obtained secondary alcohols were found in the range of 0-90%.

【基金】 Project supported by the Key Laboratory of Organic Syntheses,Jiangsu Province(No.T2109102).
  • 【文献出处】 Chinese Journal of Chemistry ,中国化学(英文版) , 编辑部邮箱 ,2003年07期
  • 【分类号】O623
  • 【下载频次】3
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