@article{a2b34b42cd1742f5a9545505422bff9a,
title = "Probing subtle ligand effects in the enantioselective transfer hydrogenation of ketones",
abstract = "The rational modification of an established amino-alcohol scaffold has revealed new, highly effective ligands for the enantioselective transfer hydrogenation of acetophenone that affords the product in up to 95% ee. Copyright (C) 2000 Elsevier Science Ltd.",
author = "Frost, {Christopher G.} and Paul Mendon{\c c}a",
note = "Funding Information: We are grateful to the University of Bath for funding a studentship (P.M.) and to Johnson Matthey for the loan of transition metal salts and generous support of our research group. We would particularly like to thank Dr. Barry Murrer, Dr. Chris Barnard and Dr. Liz Slade (Sonning Common) for many useful discussions and advice with experimental techniques.",
year = "2000",
month = may,
day = "19",
doi = "10.1016/S0957-4166(00)00150-6",
language = "English",
volume = "11",
pages = "1845--1848",
journal = "Tetrahedron Asymmetry",
issn = "0957-4166",
publisher = "Elsevier Limited",
number = "9",
}