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Chiral Manganese Aminopyridine Complexes : The Versatile Catalysts of Chemo- and Stereoselective Oxidations with H2O2. / Ottenbacher, Roman V.; Talsi, Evgenii P.; Bryliakov, Konstantin P.
в: Chemical Record, Том 18, № 1, 01.01.2018, стр. 78-90.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Chiral Manganese Aminopyridine Complexes
T2 - The Versatile Catalysts of Chemo- and Stereoselective Oxidations with H2O2
AU - Ottenbacher, Roman V.
AU - Talsi, Evgenii P.
AU - Bryliakov, Konstantin P.
N1 - © 2018 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2018/1/1
Y1 - 2018/1/1
N2 - In the last decade, manganese(II) complexes with N-donor tetradentate aminopyridine ligands emerged as efficient catalysts of enantioselective epoxidation of olefins and direct selective oxidation of C-H groups in complex organic molecules, with environmentally benign oxidant hydrogen peroxide. In this personal account, we summarize the progress of these catalysts with regard to ligands design, structure-reactivity correlations, evaluation of the substrate scope, as well as mechanistic studies, shedding light on the nature of active sites and the mechanisms of selective oxygenations. Several practically promising catalytic syntheses with the aid of Mn aminopyridine catalysts are exemplified.
AB - In the last decade, manganese(II) complexes with N-donor tetradentate aminopyridine ligands emerged as efficient catalysts of enantioselective epoxidation of olefins and direct selective oxidation of C-H groups in complex organic molecules, with environmentally benign oxidant hydrogen peroxide. In this personal account, we summarize the progress of these catalysts with regard to ligands design, structure-reactivity correlations, evaluation of the substrate scope, as well as mechanistic studies, shedding light on the nature of active sites and the mechanisms of selective oxygenations. Several practically promising catalytic syntheses with the aid of Mn aminopyridine catalysts are exemplified.
KW - Asymmetric epoxidation
KW - C-H oxidation
KW - Hydrogen peroxide
KW - Manganese
KW - Mechanism
KW - C−H oxidation
KW - asymmetric epoxidation
KW - hydrogen peroxide
KW - mechanism
KW - manganese
KW - UNFUNCTIONALIZED OLEFINS
KW - HIGHLY ENANTIOSELECTIVE SYNTHESIS
KW - NONHEME FE
KW - N-4 LIGANDS
KW - EFFICIENT OXIDATION
KW - ASYMMETRIC EPOXIDATION
KW - C-H OXIDATION
KW - HYDROGEN-PEROXIDE
KW - MN COMPLEXES
KW - ELECTRON-DEFICIENT OLEFINS
UR - http://www.scopus.com/inward/record.url?scp=85025171244&partnerID=8YFLogxK
U2 - 10.1002/tcr.201700032
DO - 10.1002/tcr.201700032
M3 - Article
C2 - 28707370
AN - SCOPUS:85025171244
VL - 18
SP - 78
EP - 90
JO - Chemical Record
JF - Chemical Record
SN - 1527-8999
IS - 1
ER -
ID: 9048879