仿形(计算机编程)
催化作用
化学
组合化学
模块化设计
配体(生物化学)
立体化学
药物化学
有机化学
计算机科学
生物化学
操作系统
受体
作者
Felix Spindler,Christophe Malan,Matthias Lotz,Martin Kesselgruber,Ulrich Pittelkow,Andreas Rivas‐Nass,Oliver Briel,Hans‐Ulrich Blaser
标识
DOI:10.1016/j.tetasy.2004.06.033
摘要
A set of 11 ferrocenyl based diphosphine ligands (eight Mandyphos and three Taniaphos) was tested in more than 150 experiments using 20 test reactions. For the assessment of new ligands, a two-pronged strategy was developed consisting of a basic and an extended profiling. The basic profiling showed that the choice of the substituents at the P atoms has a significant effect on the catalyst performance. In the extended profiling it was confirmed that the Mandyphos ligands, in particular M4 with two bis(3,5-dimethyl-4-methoxyphenyl)phosphino groups, and the Taniaphos ligands, especially the all-phenyl derivative T1, showed good to outstanding performances in the hydrogenation of selected α- and β-enamides, acrylic acid derivatives, itaconates, β-ketoesters and 1,3-diketones yielding the corresponding products with up to 99% ee and at substrate/catalyst ratios up to 25,000.
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