首页> 外文期刊>The Journal of Organic Chemistry >Highly enantioselective phenyl transfer to aryl aldehydes catalyzed by easily accessible chiral tertiary aminonaphthol
【24h】

Highly enantioselective phenyl transfer to aryl aldehydes catalyzed by easily accessible chiral tertiary aminonaphthol

机译:易于手性叔氨基氨基萘酚催化的高对映选择性苯基转移至芳醛

获取原文
获取原文并翻译 | 示例
       

摘要

A new chiral tertiary aminonaphthol ligand 3b served as a highly efficient ligand for the asymmetric catalytic phenyl transfer to aromatic aldehydes and a variety of chiral diarylmethanols was prepared in high ee values (ee up to 99%) and chemical yields. The straightforward syntheses of both 3b and its enantiomer provide an excellent opportunity for large-scale applications.
机译:一种新的手性叔氨基萘配体3b可作为不对称催化苯基转移到芳族醛的高效配体,并以高ee值(ee高达99%)和化学收率制备了各种手性二芳基甲醇。 3b及其对映异构体的直接合成为大规模应用提供了极好的机会。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号