Asymmetric reduction of prochiral ketones with chiral hydride reagents prepared from lithium aluminium hydride and (S)-2-(N-substituted aminomethyl)pyrrolidines.

スポンサーリンク

概要

• 論文の詳細を見る

• Asymmetric reduction of prochiral ketones with various hydride reagents prepared from lithium aluminium hydride and (<I>S</I>)-2-(<I>N</I>-substituted aminomethyl) pyrrolidines, derived easily by four steps from commercially available (<I>S</I>)-proline, yields optically active alcohols with 13–92% optical purity having the <I>S</I>-configuration.

• 公益社団法人 日本化学会の論文

著者

• Asami Masatoshi

  The University of Tokyo

• Ohno Hiroyasu

  The University of Tokyo

• Kobayashi Susumu

  The University of Tokyo

• Mukaiyama Teruaki

  The University of Tokyo

関連論文

• Asymmetric reduction of prochiral ketones with chiral hydride reagents prepared from lithium aluminium hydride and (S)-2-(N-substituted aminomethyl)pyrrolidines.

スポンサーリンク