Research output: Contribution to journal › Article › peer-review
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.Research output: Contribution to journal › Article › peer-review
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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