The process for synthesis of statins is presented where the intermediate intermediate (4R,6S)-6-(dialkoxymethyl)tetrahydro-2H-pyran-2,4-diol which already possesses the desired stereochemistry corresponding to final statin is prepared by an aldolaze.
介绍了合成他汀的过程,其中通过
醛缩酶制备了中间体(4R,6S)-6-(二烷氧甲基)四氢-
2H-吡喃-2,4
-二醇,该中间体已经具有与最终他汀对应的所需立体
化学。