Research output: Contribution to journal › Article › peer-review
Mn aminopyridine oxidase mimics : Switching between biosynthetic-like and xenobiotic regioselectivity in C–H oxidation of (-)-ambroxide. / Ottenbacher, Roman V.; Samsonenko, Denis G.; Nefedov, Andrey A. et al.
In: Journal of Catalysis, Vol. 399, 07.2021, p. 224-229.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Mn aminopyridine oxidase mimics
T2 - Switching between biosynthetic-like and xenobiotic regioselectivity in C–H oxidation of (-)-ambroxide
AU - Ottenbacher, Roman V.
AU - Samsonenko, Denis G.
AU - Nefedov, Andrey A.
AU - Talsi, Evgenii P.
AU - Bryliakov, Konstantin P.
N1 - Funding Information: This work was supported by the Russian Science Foundation (#20-13-00032). RVO, EPT and KPB gratefully acknowledge the access to the facilities of the shared research center ?National center of investigation of catalysts?, kindly provided by Boreskov Institute of Catalysis. The authors are grateful to the Collective Chemical Service Center of Siberian Branch of Russian Academy of Sciences for the HRMS measurements. Funding Information: This work was supported by the Russian Science Foundation (# 20-13-00032 ). RVO, EPT and KPB gratefully acknowledge the access to the facilities of the shared research center “National center of investigation of catalysts”, kindly provided by Boreskov Institute of Catalysis. The authors are grateful to the Collective Chemical Service Center of Siberian Branch of Russian Academy of Sciences for the HRMS measurements. Publisher Copyright: © 2021 Elsevier Inc. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/7
Y1 - 2021/7
N2 - The late-stage C–H oxofunctionalization of (-)-ambroxide with H2O2 in the presence of bioinspired honheme Mn complexes is reported. Adjusting the ligand architecture and absolute chirality, as well as tuning the reaction solvent, allows switching the catalysts’ selectivity between biosynthetic-like and bioorthogonal modes, thus directing the reaction towards either (+)-sclareolide or 2α-hydroxyambroxide, respectively. This opens the ways to 2,12-dihydroxyambroxide, 2α-hydroxysclareolide, ambroxide-2-one, ambroxide-2,12-dione, and several other, including previously unavailable, oxidized metabolites of (-)-ambroxide in synthetically meaningful yields, using the same catalyst systems.
AB - The late-stage C–H oxofunctionalization of (-)-ambroxide with H2O2 in the presence of bioinspired honheme Mn complexes is reported. Adjusting the ligand architecture and absolute chirality, as well as tuning the reaction solvent, allows switching the catalysts’ selectivity between biosynthetic-like and bioorthogonal modes, thus directing the reaction towards either (+)-sclareolide or 2α-hydroxyambroxide, respectively. This opens the ways to 2,12-dihydroxyambroxide, 2α-hydroxysclareolide, ambroxide-2-one, ambroxide-2,12-dione, and several other, including previously unavailable, oxidized metabolites of (-)-ambroxide in synthetically meaningful yields, using the same catalyst systems.
KW - Biomimetic chemistry
KW - C–H activation
KW - Late-stage functionalization
KW - Natural products
KW - Steroids
UR - http://www.scopus.com/inward/record.url?scp=85107021758&partnerID=8YFLogxK
U2 - 10.1016/j.jcat.2021.05.014
DO - 10.1016/j.jcat.2021.05.014
M3 - Article
AN - SCOPUS:85107021758
VL - 399
SP - 224
EP - 229
JO - Journal of Catalysis
JF - Journal of Catalysis
SN - 0021-9517
ER -
ID: 28764587