https://nova.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:21973 Wed 11 Apr 2018 15:31:36 AEST ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:28469 Wed 11 Apr 2018 10:47:35 AEST ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:49939 Wed 06 Mar 2024 14:38:23 AEDT ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:17426 Sat 24 Mar 2018 08:01:40 AEDT ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:26323 NAr coupling with 1-fluoro-4-nitrobenzene. Microwave coupling of 4-morphilinoaniline 8 and 4-(piperazine-1-yl)aniline 9 with 2-(2,5-dichloropyrimidine-4-ylamino)-N-methylbenzamide 10, proved to be the most efficacious route to the target analogues 6 and 7. This hybrid methodology reduced the number of synthetic steps, gave enhanced overall yields and increased atom economy through step reduction and minimal requirement for chromatographic purification, relative to the original batch synthesis approach.]]> Sat 24 Mar 2018 07:24:11 AEDT ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:36694 Mon 26 Jul 2021 11:07:06 AEST ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:27906 Mon 23 Sep 2019 12:18:54 AEST ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:31967 Mon 23 Sep 2019 11:01:41 AEST ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:36503 3 catalysed microwave ring opening with amines afforded a select range of β-amino alcohols, but with lower levels of aminolysis regiocontrol than the sequential flow approach.]]> Fri 22 May 2020 16:51:41 AEST ]]>