Home / Articles / Salicylaldehydes as privileged synthons in multicomponent reactions

Salicylaldehydes as privileged synthons in multicomponent reactions

Majid M Heravi 1
Majid M Heravi
, 
Vahideh Zadsirjan 1
Vahideh Zadsirjan
, 
Malihe Mollaiye 1
Malihe Mollaiye
, 
Masumeh Heydari 1
Masumeh Heydari
, 
Afsaneh Taheri Kal Koshvandi 1
Afsaneh Taheri Kal Koshvandi
1 Department of Chemistry, Alzahra University, Tehran, Iran
10.1070/RCR4780
Published 30 November 2017
Review , RCR4780, Volume 87, Issue 6, 553-585
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Heravi M. M. et al. Salicylaldehydes as privileged synthons in multicomponent reactions // Russian Chemical Reviews. 2017. Vol. 87. No. 6. pp. 553-585.
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Heravi M. M., Zadsirjan V., Mollaiye M., Heydari M., Taheri Kal Koshvandi A. Salicylaldehydes as privileged synthons in multicomponent reactions // Russian Chemical Reviews. 2017. Vol. 87. No. 6. pp. 553-585.
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TY - JOUR
DO - 10.1070/RCR4780
UR - https://rcr.colab.ws/publications/10.1070/RCR4780
TI - Salicylaldehydes as privileged synthons in multicomponent reactions
T2 - Russian Chemical Reviews
AU - Heravi, Majid M
AU - Zadsirjan, Vahideh
AU - Mollaiye, Malihe
AU - Heydari, Masumeh
AU - Taheri Kal Koshvandi, Afsaneh
PY - 2017
DA - 2017/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 553-585
IS - 6
VL - 87
ER -
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@article{2017_Heravi,
author = {Majid M Heravi and Vahideh Zadsirjan and Malihe Mollaiye and Masumeh Heydari and Afsaneh Taheri Kal Koshvandi},
title = {Salicylaldehydes as privileged synthons in multicomponent reactions},
journal = {Russian Chemical Reviews},
year = {2017},
volume = {87},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RCR4780},
number = {6},
pages = {553--585},
doi = {10.1070/RCR4780}
}
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Heravi, Majid M., et al. “Salicylaldehydes as privileged synthons in multicomponent reactions.” Russian Chemical Reviews, vol. 87, no. 6, Nov. 2017, pp. 553-585. https://rcr.colab.ws/publications/10.1070/RCR4780.
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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 \textit{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.

Funders

Alzahra Research Council
Iran National Science Foundation

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