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General Enantioselective C-H Activation with Efficiently Tunable Cyclopentadienyl Ligands.
Angew Chem Int Ed Engl. 2017 02 20; 56(9):2429-2434.AC

Abstract

Cyclopentadienyl (Cp) ligands enable efficient steering of various transition-metal-catalyzed transformations, in particular enantioselective C-H activation. Currently only few chiral Cp ligands are available. Therefore, a conceptually general approach to chiral Cp ligand discovery would be invaluable as it would enable the discovery of applicable Cp ligands and to efficiently and rapidly vary and tune their structures. Herein, we describe the three-step gram-scale synthesis of a structurally diverse and widely applicable chiral Cp ligand collection (JasCp ligands) with highly variable and adjustable structures. Their modular nature and their amenability to rapid structure variation enabled the efficient discovery of ligands for three enantioselective RhIII -catalyzed C-H activation reactions, including one unprecedented transformation. This novel approach should enable the discovery of efficient chiral Cp ligands for various further enantioselective transformations.

Authors+Show Affiliations

Max-Planck-Institut für Molekulare Physiologie, Abteilung Chemische Biologie, Otto-Hahn-Strasse 11, 44227, Dortmund, Germany. Technische Universität Dortmund, Fakultät Chemie und Chemische Biologie, Chemische Biologie, Otto-Hahn-Strasse 4a, 44227, Dortmund, Germany.Ruhr-Universität Bochum, Lehrstuhl für Organische Chemie II, Universitätsstrasse 150, 44801, Bochum, Germany.Max-Planck-Institut für Molekulare Physiologie, Abteilung Chemische Biologie, Otto-Hahn-Strasse 11, 44227, Dortmund, Germany.Westfälische Wilhelms-Universität Münster, Organisch-Chemisches Institut, Corrensstrasse 40, 48149, Münster, Germany.Max-Planck-Institut für Molekulare Physiologie, Abteilung Chemische Biologie, Otto-Hahn-Strasse 11, 44227, Dortmund, Germany. Technische Universität Dortmund, Fakultät Chemie und Chemische Biologie, Chemische Biologie, Otto-Hahn-Strasse 4a, 44227, Dortmund, Germany.Max-Planck-Institut für Molekulare Physiologie, Abteilung Chemische Biologie, Otto-Hahn-Strasse 11, 44227, Dortmund, Germany. Technische Universität Dortmund, Fakultät Chemie und Chemische Biologie, Chemische Biologie, Otto-Hahn-Strasse 4a, 44227, Dortmund, Germany.

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

28124831

Citation

Jia, Zhi-Jun, et al. "General Enantioselective C-H Activation With Efficiently Tunable Cyclopentadienyl Ligands." Angewandte Chemie (International Ed. in English), vol. 56, no. 9, 2017, pp. 2429-2434.
Jia ZJ, Merten C, Gontla R, et al. General Enantioselective C-H Activation with Efficiently Tunable Cyclopentadienyl Ligands. Angew Chem Int Ed Engl. 2017;56(9):2429-2434.
Jia, Z. J., Merten, C., Gontla, R., Daniliuc, C. G., Antonchick, A. P., & Waldmann, H. (2017). General Enantioselective C-H Activation with Efficiently Tunable Cyclopentadienyl Ligands. Angewandte Chemie (International Ed. in English), 56(9), 2429-2434. https://doi.org/10.1002/anie.201611981
Jia ZJ, et al. General Enantioselective C-H Activation With Efficiently Tunable Cyclopentadienyl Ligands. Angew Chem Int Ed Engl. 2017 02 20;56(9):2429-2434. PubMed PMID: 28124831.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - General Enantioselective C-H Activation with Efficiently Tunable Cyclopentadienyl Ligands. AU - Jia,Zhi-Jun, AU - Merten,Christian, AU - Gontla,Rajesh, AU - Daniliuc,Constantin G, AU - Antonchick,Andrey P, AU - Waldmann,Herbert, Y1 - 2017/01/26/ PY - 2016/12/09/received PY - 2017/1/27/pubmed PY - 2017/1/27/medline PY - 2017/1/27/entrez KW - C−H activation KW - asymmetric synthesis KW - cycloadditions KW - cyclopentadienyl ligands KW - rhodium SP - 2429 EP - 2434 JF - Angewandte Chemie (International ed. in English) JO - Angew Chem Int Ed Engl VL - 56 IS - 9 N2 - Cyclopentadienyl (Cp) ligands enable efficient steering of various transition-metal-catalyzed transformations, in particular enantioselective C-H activation. Currently only few chiral Cp ligands are available. Therefore, a conceptually general approach to chiral Cp ligand discovery would be invaluable as it would enable the discovery of applicable Cp ligands and to efficiently and rapidly vary and tune their structures. Herein, we describe the three-step gram-scale synthesis of a structurally diverse and widely applicable chiral Cp ligand collection (JasCp ligands) with highly variable and adjustable structures. Their modular nature and their amenability to rapid structure variation enabled the efficient discovery of ligands for three enantioselective RhIII -catalyzed C-H activation reactions, including one unprecedented transformation. This novel approach should enable the discovery of efficient chiral Cp ligands for various further enantioselective transformations. SN - 1521-3773 UR - https://www.unboundmedicine.com/medline/citation/28124831/General_Enantioselective_C_H_Activation_with_Efficiently_Tunable_Cyclopentadienyl_Ligands_ DB - PRIME DP - Unbound Medicine ER -