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Russian Chemical Reviews, 2018, Volume 87, Issue 6, Pages 553–585
DOI: https://doi.org/10.1070/RCR4780
(Mi rcr4212)
 

This article is cited in 16 scientific papers (total in 16 papers)

Salicylaldehydes as privileged synthons in multicomponent reactions

Majid M. Heravi, Vahideh Zadsirjan, Malihe Mollaiye, Masumeh Heydari, Afsaneh Taheri Kal Koshvandi

Department of Chemistry, Alzahra University, Tehran, Iran
Abstract: Salicylaldehyde (2-hydroxybenzaldehyde) bearing two different active functional groups, namely, a hydroxy group and an aldehyde group, finds wide application as a key chemical in a variety of industrial processes, especially in the large-scale production of pharmaceuticals. Salicylaldehyde and most of its derivatives are commercially available or readily accessible, and hence are ideal starting materials for multicomponent reactions (MCRs), mostly in pseudo-three and four-component ones, giving rise to a plethora of heterocyclic systems. The importance of salicylaldehyde and an impressive amount of studies concerning its applications in MCRs prompted us to highlight in this review the important role of this compound as a privileged synthon in the synthesis of heterocycles.
Bibliography — 276 references.
Funding agency Grant number
Alzahra Research Council
Iran National Science Foundation
Received: 04.09.2017
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: English
Citation: Majid M. Heravi, Vahideh Zadsirjan, Malihe Mollaiye, Masumeh Heydari, Afsaneh Taheri Kal Koshvandi, “Salicylaldehydes as privileged synthons in multicomponent reactions”, Russian Chem. Reviews, 87:6 (2018), 553–585
Citation in format AMSBIB
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\by Majid~M.~Heravi, Vahideh~Zadsirjan, Malihe~Mollaiye, Masumeh~Heydari, Afsaneh~Taheri Kal Koshvandi
\paper Salicylaldehydes as privileged synthons in multicomponent reactions
\jour Russian Chem. Reviews
\yr 2018
\vol 87
\issue 6
\pages 553--585
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\crossref{https://doi.org/10.1070/RCR4780}
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Linking options:
  • https://www.mathnet.ru/eng/rcr4212
  • https://doi.org/10.1070/RCR4780
  • https://www.mathnet.ru/eng/rcr/v87/i6/p553
  • This publication is cited in the following 16 articles:
    1. Douglas A. Klumpp, Titas Deb, Ryan Littich, Synthesis, 2025  crossref
    2. Manman Shi, Boli Li, Mingyi Kang, Peng Liu, Xiaofeng Yang, Meishan Pei, Guangyou Zhang, Luminescence, 39:5 (2024)  crossref
    3. Ruiyang Wang, Xu Feng, Boya Feng, Yu Chen, RSC Adv., 14:28 (2024), 19922  crossref
    4. Li Han, Xiaocao Quan, Xusheng Shao, Xiaoyong Xu, Zhong Li, Tetrahedron Letters, 118 (2023), 154080  crossref
    5. M. Mousazadeh, A. Sarvary, B. Notash, Tetrahedron, 138 (2023), 133415  crossref
    6. V. Zadsirjan, Advances in Heterocyclic Chemistry, 141, 2023, 1  crossref
    7. R. Hosseinpour, A. Sarvary, S. Habibzadeh, Eur. J. Org. Chem., 26:48 (2023)  crossref
    8. A. Lazic, A. Masulovic, J. Ladjarevic, N. Valentic, J. Serb. Chem. Soc., 88:9 (2023), 811  crossref
    9. H. Sepahvand, M. Heravi, M. Saber, S. Hooshmand, J. Iran Chem. Soc., 19:6 (2022), 2115–2130  crossref  isi
    10. S. Patra, S. Bhunia, D. Das, Mol. Divers., 2022  crossref  isi
    11. V. A. Chebanov, S. M. Desenko, V. V. Lipson, N. Yu. Gorobets, Multicomponent Reactions towards Heterocycles, 2022, 287  crossref
    12. Li Han, Xiaocao Quan, Xusheng Shao, Xiaoyong Xu, Zhong Li, SSRN Journal, 2022  crossref
    13. E. Enriquez-Palacios, T. Arbeloa, J. Banuelos, C. I. Bautista-Hernandez, J. G. Becerra-Gonzalez, I. Lopez-Arbeloa, E. Pena-Cabrera, Molecules, 25:4 (2020), 781  crossref  isi
    14. A. T. Kal-Koshvandi, Trac-Trends Anal. Chem., 128 (2020), 115920  crossref  isi
    15. L. I. Belen'kii, G. A. Gazieva, Yu. B. Evdokimenkova, N. O. Soboleva, Advances in Heterocyclic Chemistry, Vol 132, Adv. Heterocycl. Chem., Advances in Heterocyclic Chemistry, 132, ed. E. Scriven, C. Ramsden, Elsevier Academic Press Inc, 2020, 385–468  crossref  isi  scopus
    16. D. Koszelewski, R. Ostaszewski, Bioorganic Chem., 93 (2019), UNSP 102825  crossref  isi  scopus
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