1147347-29-2Relevant academic research and scientific papers
Enantioselective synthesis of syn - And anti -1,3-aminoalcohols via β-aminoketones and subsequent reduction/dynamic kinetic asymmetric transformation
Millet, Renaud,Traeff, Annika M.,Petrus, Michiel L.,Baeckvall, Jan-E.
supporting information; experimental part, p. 15182 - 15184 (2011/01/05)
β-Aminoketones obtained from imines in an organocatalytic Mannich reaction were transformed to enantio- and diastereomerically pure 1,3-aminoalcohols with two stereogenic centers via a combined reduction/dynamic kinetic asymmetric transformation. Both syn and anti diastereomers were obtained in high yield, dr, and ee.
1-Amido-1-phenyl-3-piperidinylbutanes - CCR5 antagonists for the treatment of HIV: Part 2
Barber, Christopher G.,Blakemore, David C.,Chiva, Jean-Yves,Eastwood, Rachel L.,Middleton, Donald S.,Paradowski, Kerry A.
scheme or table, p. 1499 - 1503 (2009/12/07)
Optimisation of a series of 4-piperidinyltriazoles led to the identification of compound 28a which showed good whole cell antiviral activity, excellent selectivity over the hERG ion channel and complete oral absorption.
