Taylor Mark S, Jacobsen Eric N
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA.
Proc Natl Acad Sci U S A. 2004 Apr 13;101(15):5368-73. doi: 10.1073/pnas.0307893101. Epub 2004 Mar 12.
This article describes three distinct strategies by which stereochemically complex molecules are synthesized and the ways asymmetric catalysis can impact on all three. The development of general methods to prepare synthetically useful building blocks leads to an expanded "chiral pool" of potential starting materials for asymmetric synthesis. The possibility of discovering new reactions to access new types of building blocks is particularly attractive and serves to help define the frontiers of the field. Asymmetric catalysis can also be applied to diastereoselective synthesis such that the stereochemistry of the catalyst, and not that of the substrate, determines the relative configuration of the product. Finally, in reactions where multiple stereocenters are generated simultaneously or in tandem, catalyst and substrate control can operate in a complementary manner to achieve one of many possible stereochemical outcomes selectively.
本文描述了三种合成立体化学复杂分子的不同策略,以及不对称催化对这三种策略可能产生影响的方式。开发制备具有合成用途的结构单元的通用方法,可使不对称合成潜在起始原料的“手性池”得到扩展。发现新反应以获取新型结构单元的可能性尤其具有吸引力,有助于界定该领域的前沿。不对称催化还可应用于非对映选择性合成,使得产物的相对构型由催化剂而非底物的立体化学决定。最后,在同时或串联生成多个立体中心的反应中,催化剂控制和底物控制可以互补的方式选择性地实现众多可能的立体化学结果之一。