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Synthesis of Chiral Building Blocks for Use in Drug Discovery

机译:用于药物发现的手性构件的合成

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摘要

In the past decade there has been a significant growth in the sales of pharmaceutical drugs worldwide, but more importantly there has been a dramatic growth in the sales of single enantiomer drugs. The pharmaceutical industry has a rising demand for chiral intermediates and research reagents because of the continuing imperative to improve drug efficacy. This in turn impacts on researchers involved in preclinical discovery work. Besides traditional chiral pool and resolution of racemates as sources of chiral building blocks, many new synthetic methods including a great variety of catalytic reactions have been developed which facilitate the production of complex chiral drug candidates for clinical trials. The most ambitious technique is to synthesise homochiral compounds from non-chiral starting materials using chiral metal catalysts and related chemistry. Examples of the synthesis of chiral building blocks from achiral materials utilizing asymmetric hydrogenation and asymmetric epoxidation are presented.
机译:在过去的十年中,世界范围内药物的销售有了显着的增长,但是更重要的是单一对映体药物的销售也有了显着的增长。由于持续需要提高药物功效,因此制药行业对手性中间体和研究试剂的需求不断增长。反过来,这会影响从事临床前发现工作的研究人员。除了传统的手性库和消旋体作为手性结构单元的来源外,还开发了许多新的合成方法,包括多种催化反应,这些方法促进了复杂手性药物候选物的生产,可用于临床试验。最雄心勃勃的技术是使用手性金属催化剂和相关化学方法,从非手性起始原料合成同手性化合物。给出了利用不对称氢化和不对称环氧化由非手性材料合成手性结构单元的实例。

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