Enzymatic synthesis of phosphocarnitine, phosphogabob and fosfomycinStudies on organophosphorus compounds. Part 128. For Part 127, see C. Yuan, C. Xu and Y. Zhang, Tetrahedron, 2003, 59, 6095.
Enantioselective reduction of 2-keto-3-haloalkane phosphonates by baker's yeast
作者:Cheng-ye Yuan、Ke Wang、Zu-yi Li
DOI:10.1002/hc.1084
日期:——
Bioreduction of 3-substituted-2-oxoal-kanephosphonates by baker'syeast afforded 3-substituted-2-hydroxy-alkanephosphonates in moderate to good yields and ee value. These compounds could serve as useful chirons for the stereoselective synthesis of phosphorus analogs of biologically active molecules including R-(—)-3-trimethylammonium-2-hydroxypropanoic acid and R-(—)-3- trimethylammonium-2-hydroxypropanoic