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Nitroenediamines (EDAMs), and N -methyl-1-(methylthio)-2-nitroethenamine (NMSM) derivatives: scaffolds for heterocycle molecular diversity (update from 2012 to 2021) . Fahimeh Abedinifar, Bagher Larijani, Mohammad Mahdavi
, RSC Adv.
, 2022
, 12
, 30436
Synthesis of spiroimidazopyridineoxindole, spiropyridopyrimidineoxindole and spiropyridodiazepineoxindole derivatives based on heterocyclic ketene aminals via a four-component reaction . Fatemeh Rahimi, Mohammad Bayat, Hajar Hosseini
, RSC Adv.
, 2019
, 9
, 16384
Synthesis of highly functionalized thiazolo[3,2-a ]pyridine derivatives via a five-component cascade reaction based on nitroketene N ,S -acetal . Zohreh Sahhaf Razavi, Mohammad Bayat, Hajar Hosseini
, RSC Adv.
, 2020
, 10
, 31039
Synthetic strategies of heterocycle-integrated pyridopyrimidine scaffolds supported by nano-catalysts . Mohamed M. Hammouda, Marwa M. Rashed, Khaled M. Elattar, Amany M. A. Osman
, RSC Adv.
, 2023
, 13
, 11600
An efficient synthesis of new imidazo[1,2-a ]pyridine-6-carbohydrazide and pyrido[1,2-a ]pyrimidine-7-carbohydrazide derivatives via a five-component cascade reaction . Hajar Hosseini, Mohammad Bayat
, RSC Adv.
, 2019
, 9
, 7218
Synthesis of 5-amino-N ′-(9H -fluoren-9-ylidene)-8-nitro-7-aryl-1,2,3,7-tetrahydroimidazo[1,2-a ]pyridine-6-carbohydrazide derivatives based on heterocyclic ketene aminals . Hajar Hosseini, Mohammad Bayat
, RSC Adv.
, 2018
, 8
, 41218
Multicomponent reactions in unconventional solvents: state of the art . Yanlong Gu
, Green Chem.
, 2012
, 14
, 2091
p -Toluenesulfonic acid-promoted organic transformations for the generation of molecular complexity . Sanchari Pal, Debjit Das, Sabyasachi Bhunia
, Org. Biomol. Chem.
, 2024
, 22
, 1527
Pseudo-multicomponent reactions . Julio C. Flores-Reyes, Vanesa del C. Cotlame-Salinas, Ilich A. Ibarra, Eduardo González-Zamora, Alejandro Islas-Jácome
, RSC Adv.
, 2023
, 13
, 16091
Part II: nitroalkenes in the synthesis of heterocyclic compounds . Azim Ziyaei Halimehjani, Irishi N. N. Namboothiri, Seyyed Emad Hooshmand
, RSC Adv.
, 2014
, 4
, 51794