Diastereoselective Synthesis of (<i>R</i>)-Phenanthrenyl-9yl-[(<i>S</i>)-pyrrolidin-2yl)] Methanol
作者:Alessio Russo、Tiziana Fuoco、Alessandra Lattanzi
DOI:10.1080/00397911.2011.609303
日期:2013.2.1
Abstract A four-step synthesis of sterically demanding (R)-phenanthren-9-yl-[(S)-pyrrolidin-2-yl] methanol has been easily accomplished starting from L-proline in high diastereoselectivity. These compounds are potentially useful ligands in metal-catalyzed reactions and organocatalysts. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications®
摘要 以高非对映选择性为原料,以 L-脯氨酸为原料,可以很容易地通过四步合成空间要求高的 (R)-菲-9-基-[(S)-吡咯烷-2-基] 甲醇。这些化合物是金属催化反应和有机催化剂中潜在有用的配体。补充材料可用于本文。转至出版商的 Synthetic Communications® 在线版以查看免费的补充文件。图形概要