Purposeful regioselectivity control of the Birch reductive alkylation of biphenyl-4-carbonitrile › Research Explorer

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Purposeful regioselectivity control of the Birch reductive alkylation of biphenyl-4-carbonitrile

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

DOI

https://doi.org/10.1016/j.tet.2017.12.046
Final published version

Pavel A. Fedyushin
Roman Yu Peshkov
Elena V. Panteleeva
Evgeny V. Tretyakov
Irina V. Beregovaya
Yuri V. Gatilov
Vitalij D. Shteingarts

Original language	English
Pages (from-to)	842-851
Number of pages	10
Journal	Tetrahedron
Volume	74
Issue number	8
DOIs	https://doi.org/10.1016/j.tet.2017.12.046
Publication status	Published - 22 Feb 2018

Research areas

Biphenyl-4-carbonitrile, Cyclohexadienyl anions, Dianion, Nucleophilic substitution, Reductive alkylation, METAL-AMMONIA REDUCTION, NATURAL-PRODUCTS, ELECTROCHEMICAL REDUCTION, AROMATIC-COMPOUNDS, LIQUID-AMMONIA, ANIONIC PRODUCTS, 2-ELECTRON REDUCTION, CROSS-COUPLING REACTIONS, SYNTHETIC APPLICATIONS, ELECTRONIC-STRUCTURE

OECD FOS+WOS

ID: 12100297