反応 #546549

ord-d9d97014c41746c4bf0ac17c50df2754

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The enatiomers were separated by chiral HPLC

実験手順

The title compound was prepared from 3-[3-(3-bromo-propoxy)-phenyl]-2-methoxy-propionic acid methyl ester (Example 323, Step 1) and biphenyl-3-ol via the same procedure used for the preparation of (2S)-2-methoxy-3-[4-(3-phenoxy-propoxy)-phenyl]-propionic acid (Example 285, Step 1). The enatiomers were separated by chiral HPLC. MS (ES) for C25H26O5 [M+Na]+: 429.2.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07192982B2uspto-grants-2007_03