Home > Publications database > Asymmetric synthesis of C–N axially chiral carbazoles via axial-to-axial chirality transfer > print |
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100 | 1 | _ | |a Myllek, Sebastian |b 0 |
245 | _ | _ | |a Asymmetric synthesis of C–N axially chiral carbazoles via axial-to-axial chirality transfer |
260 | _ | _ | |a Cambridge |c 2025 |b Royal Society of Chemistry |
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520 | _ | _ | |a C–N axially chiral carbazole derivatives were synthesised by an intramolecular Buchwald–Hartwig amination starting from C–C axially chiral biaryls utilising an axial-to-axial chirality transfer with enantiospecificities up to 91%. The mechanism of the chirality transfer was investigated via DFT calculations. |
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700 | 1 | _ | |a Klischan, Moritz K. T. |0 P:(DE-Juel1)180402 |b 2 |
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700 | 1 | _ | |a Neudecker, Philipp |0 P:(DE-Juel1)144510 |b 4 |
700 | 1 | _ | |a Breugst, Martin |0 0000-0003-0950-8858 |b 5 |
700 | 1 | _ | |a Pietruszka, Jörg |0 P:(DE-Juel1)128906 |b 6 |e Corresponding author |u fzj |
773 | _ | _ | |a 10.1039/D5OB00587F |g Vol. 23, no. 20, p. 4888 - 4892 |0 PERI:(DE-600)2097583-1 |n 20 |p 4888 - 4892 |t Organic & biomolecular chemistry |v 23 |y 2025 |x 1477-0520 |
856 | 4 | _ | |u https://juser.fz-juelich.de/record/1043734/files/d5ob00587f.pdf |y OpenAccess |
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