On the Mechanism and Selectivity of Palladium Catalyzed C(sp3)–H Arylation of Pyrrolidines and Piperidines at Unactivated C4 Positions: Discovery of an Improved Dimethylaminoquinoline (DMAQ) Amide Directing Group
DOI: 10.14469/hpc/11771 Metadata
Created: 2022-11-10 13:48
Last modified: 2024-11-11 10:06
License: Creative Commons: Public Domain Dedication 1.0
Funding: (none given)
Description
Raw and processed characterisation data for compounds reported in this work.
Members
DOI | Description |
---|---|
10.14469/hpc/11807 | Pyrrolidine- and piperidine-DMAQ amide substrates |
10.14469/hpc/11810 | Extra characterization data for N-Cbz pyrrolidine 3b |
10.14469/hpc/11811 | Directing group screening - arylated pyrrolidines |
10.14469/hpc/11814 | DMAQ removal |
10.14469/hpc/11808 | Deuterated pyrrolidine substrates |
10.14469/hpc/11804 | Extra characterization data for N-Cbz pyrrolidine 2 |
10.14469/hpc/11805 | Pyrrolidine amide substrates |
10.14469/hpc/11815 | Late-stage functionalization |
10.14469/hpc/11813 | 4-Arylated piperidine-3-DMAQ amides |
10.14469/hpc/11812 | 4-Arylated pyrrolidine-3-DMAQ amides |
10.14469/hpc/11809 | Palladacycles |