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Synthesis of chiral pinopyridines using catalysis by metal complexes. / Ustimenko, Yuliya P.; Agafontsev, Alexander M.; Tkachev, Aleksey V.

In: Chemistry of Heterocyclic Compounds, Vol. 58, No. 2-3, 02.2022, p. 135-143.

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Ustimenko YP, Agafontsev AM, Tkachev AV. Synthesis of chiral pinopyridines using catalysis by metal complexes. Chemistry of Heterocyclic Compounds. 2022 Feb;58(2-3):135-143. doi: 10.1007/s10593-022-03066-x

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Ustimenko, Yuliya P. ; Agafontsev, Alexander M. ; Tkachev, Aleksey V. / Synthesis of chiral pinopyridines using catalysis by metal complexes. In: Chemistry of Heterocyclic Compounds. 2022 ; Vol. 58, No. 2-3. pp. 135-143.

BibTeX

@article{f758d9d593dc48f8909b6673a9c47106,
title = "Synthesis of chiral pinopyridines using catalysis by metal complexes",
abstract = "Methods for the preparation of pinopyridines from pinocarvone oxime or its ethers and alkenes (alkynes) using the C–H activation reaction were studied. Palladium complexes and Wilkinson's catalyst were chosen as the catalytic systems.",
keywords = "chiral pyridines, C–H activation, pinopyridines, pyridine synthesis, Wilkinson's catalyst",
author = "Ustimenko, {Yuliya P.} and Agafontsev, {Alexander M.} and Tkachev, {Aleksey V.}",
note = "Funding Information: This study was carried out with the financial support from the Russian Foundation for Basic Research, (grant No. 19-313-50081 mol_nr) and also within the framework of the State Assignment of the NIOCh SB RAS No. 1021051403061-8-1.4.1 “Design and synthesis of new carbo- and heterocyclic organic compounds with desired functional properties.” Publisher Copyright: {\textcopyright} 2022, Springer Science+Business Media, LLC, part of Springer Nature.",
year = "2022",
month = feb,
doi = "10.1007/s10593-022-03066-x",
language = "English",
volume = "58",
pages = "135--143",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer New York",
number = "2-3",

}

RIS

TY - JOUR

T1 - Synthesis of chiral pinopyridines using catalysis by metal complexes

AU - Ustimenko, Yuliya P.

AU - Agafontsev, Alexander M.

AU - Tkachev, Aleksey V.

N1 - Funding Information: This study was carried out with the financial support from the Russian Foundation for Basic Research, (grant No. 19-313-50081 mol_nr) and also within the framework of the State Assignment of the NIOCh SB RAS No. 1021051403061-8-1.4.1 “Design and synthesis of new carbo- and heterocyclic organic compounds with desired functional properties.” Publisher Copyright: © 2022, Springer Science+Business Media, LLC, part of Springer Nature.

PY - 2022/2

Y1 - 2022/2

N2 - Methods for the preparation of pinopyridines from pinocarvone oxime or its ethers and alkenes (alkynes) using the C–H activation reaction were studied. Palladium complexes and Wilkinson's catalyst were chosen as the catalytic systems.

AB - Methods for the preparation of pinopyridines from pinocarvone oxime or its ethers and alkenes (alkynes) using the C–H activation reaction were studied. Palladium complexes and Wilkinson's catalyst were chosen as the catalytic systems.

KW - chiral pyridines

KW - C–H activation

KW - pinopyridines

KW - pyridine synthesis

KW - Wilkinson's catalyst

UR - http://www.scopus.com/inward/record.url?scp=85126850193&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/7e550d61-a12b-3e5b-a66d-1602eb2f4d09/

U2 - 10.1007/s10593-022-03066-x

DO - 10.1007/s10593-022-03066-x

M3 - Article

AN - SCOPUS:85126850193

VL - 58

SP - 135

EP - 143

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 2-3

ER -

ID: 35769804