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Number of items: 7.
Hall, Thomas Howard, Adams, Hannah, Vyas, Vijyesh K., Michael Chu, K. L. and Wills, Martin (2021) Asymmetric transfer hydrogenation of unsaturated ketones ; factors influencing 1,4- vs 1,2- regio- and enantioselectivity, and alkene vs alkyne directing effects. Tetrahedron, 77 . 131771. doi:10.1016/j.tet.2020.131771 ISSN 0040-4020 .
Hall, Thomas Howard, Adams, Hannah, Vyas, Vijyesh K., Chu, K. L. Michael and Wills, Martin (2021) Data for Asymmetric transfer hydrogenation of unsaturated ketones; factors influencing 1,4- vs 1,2- regio- and enantioselectivity, and alkene vs alkyne directing effects. [Dataset]
Wills, Martin, Jolley, Katherine E., Gosiewska, Silvia, Clarkson, Guy J., Fang, Zhijia, Hall, Thomas Howard, Treloar, Ben and Knighton, Richard C. (2018) Synthesis of enantiomerically-pure and racemic benzyl-tethered Ru (II)/TsDPEN complexes by direct arene substitution : further complexes and application. Organometallics, 37 (1). pp. 48-64. doi:10.1021/acs.organomet.7b00731 ISSN 0276-7333.
Hall, Thomas Howard (2017) Applications of tethered asymmetric hydrogenation catalysts. PhD thesis, University of Warwick.
Liu, Ruixia, Zhou, Gang, Hall, Thomas Howard, Clarkson, Guy J., Wills, Martin and Chen, Weiping (2015) Practical access to planar chiral 1,2-(α-Ketotetramethylene)- ferrocene by non-enzymatic kinetic resolution and conclusive confirmation of its absolute configuration. Advanced Synthesis & Catalysis, 357 (16-17). pp. 3453-3457. doi:10.1002/adsc.201500728 ISSN 1615-4150.
Soni, Rina, Hall, Thomas Howard, Morris, David J., Clarkson, Guy J., Owen, Matthew R. and Wills, Martin (2015) N-Functionalised TsDPEN catalysts for asymmetric transfer hydrogenation; synthesis and applications. Tetrahedron Letters, 56 (46). pp. 6397-6401. doi:10.1016/j.tetlet.2015.09.135 ISSN 0040-4039.
Soni, Rina, Hall, Thomas Howard, Mitchell, Benjamin P., Owen, Matthew R. and Wills, Martin (2015) Asymmetric reduction of electron-rich ketones with tethered ru(II)/TsDPEN catalysts using formic acid/triethylamine or aqueous sodium formate. The Journal of Organic Chemistry, 80 (13). pp. 6784-6793. doi:10.1021/acs.joc.5b00990 ISSN 0022-3263.
This list was generated on Tue Apr 23 10:41:29 2024 BST.