1107653-19-9Relevant academic research and scientific papers
London Dispersion Interactions Rather than Steric Hindrance Determine the Enantioselectivity of the Corey–Bakshi–Shibata Reduction
Eschmann, Christian,Song, Lijuan,Schreiner, Peter R.
supporting information, p. 4823 - 4832 (2021/02/01)
The well-known Corey–Bakshi–Shibata (CBS) reduction is a powerful method for the asymmetric synthesis of alcohols from prochiral ketones, often featuring high yields and excellent selectivities. While steric repulsion has been regarded as the key director of the observed high enantioselectivity for many years, we show that London dispersion (LD) interactions are at least as important for enantiodiscrimination. We exemplify this through a combination of detailed computational and experimental studies for a series of modified CBS catalysts equipped with dispersion energy donors (DEDs) in the catalysts and the substrates. Our results demonstrate that attractive LD interactions between the catalyst and the substrate, rather than steric repulsion, determine the selectivity. As a key outcome of our study, we were able to improve the catalyst design for some challenging CBS reductions.
Asymmetrie tandem michael addition-wittig reaction to cyclohexenone annulation
Liu, Yan-Kal,Chao, Ma.,Jiang, Kun,Liu, Tian-Yu,Chen, Ying-Chun
supporting information; experimental part, p. 2848 - 2851 (2009/12/05)
A highly stereoselective tandem Michael addition-Wittig reaction of (3-carboxy-2-oxopropylidene)trlphenylphosphorane and α,β-unsaturated aldehydes has been developed by employing the combined catalysis of a newly designed bulky chiral secondary amine 1g,
