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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 50, 2020 - Issue 22
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Articles

Nickel complexes as efficient catalysts in multicomponent synthesis of tetrahydropyridine derivatives

Andrei N. Yankina Department of Physics and Engineering, ITMO University, St. Petersburg, RussiaCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0003-4221-5619
ORCID Icon &
Maksim V. Dmitrievb Departament of Organic Chemistry, Perm State National Research University, Perm, RussiaORCID Iconhttps://orcid.org/0000-0002-8817-0543
ORCID Icon
Pages 3481-3489 | Received 16 Jun 2020, Published online: 09 Aug 2020

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Amol V. Sapkal, Jaysing M. Dinore, Ajeet A. Yelwande, Manoj P. Palve & Balaji R. Madje. (2023) Ultrasound Promoted One-Pot Multicomponent Synthesis of Highly Functionalized Tetrahydropyridine Derivatives. Polycyclic Aromatic Compounds 0:0, pages 1-11.
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Ajeet A. Yelwande, Madhukar E. Navgire, Manoj Palve, Harshal S. Patil, Mazahar Farooqui & Jaysing M. Dinore. (2022) One-pot multicomponent synthesis approach for tetrahydropyridines using polyaniline-zirconium oxide composites. Synthetic Communications 52:7, pages 1039-1049.
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Articles from other publishers (4)

Vahideh Zadsirjan. 2024. 283 406 .
Dhananjay D. Gadge & Pramod S. Kulkarni. (2022) 5‐Sulfosalicylic acid an organocatalyst for the synthesis of highly functionalized piperidines through the multicomponent reaction . Journal of Heterocyclic Chemistry 59:8, pages 1320-1332.
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Ajibola Adegunloye, Ibrahim Waziri, Sarit K. Ghosh, Venkata K. Perla, Orpah Zinyemba & Kaushik Mallick. (2022) Electric field induced polarization and electrochemical sensing performance of nickel-based organic–inorganic hybrid system. Journal of Materials Science: Materials in Electronics 33:17, pages 13574-13583.
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Dhaval B. Patel, Jagruti A. Parmar, Siddharth S. Patel, Unnati J. Naik & Hitesh D. Patel. (2021) Recent Advances in Ester Synthesis by Multi-Component Reactions (MCRs): A Review. Current Organic Chemistry 25:5, pages 539-553.
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