Academic literature on the topic '2-b]furan-3-carboxamides'

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Journal articles on the topic "2-b]furan-3-carboxamides"

1

Xia, Likai, and Yong Rok Lee. "Regioselective synthesis of novel and diverse naphtho[1,2-b]furan-3-carboxamides and benzofuran-3-carboxamides by cascade formal [3 + 2] cycloaddition." RSC Adv. 4, no. 69 (2014): 36905–16. http://dx.doi.org/10.1039/c4ra07862d.

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The regioselective synthesis of diverse naphtho[1,2-b]furan-3-amides and benzofuran-3-amides was accomplished by the In(OTf)<sub>3</sub>-catalyzed cascade formal [3 + 2] cycloaddition of 1,4-naphthoquinones or benzoquinones with β-ketoamides.
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2

Xia, Likai, and Yong Rok Lee. "ChemInform Abstract: Regioselective Synthesis of Novel and Diverse Naphtho[1,2-b]furan-3-carboxamides and Benzofuran-3-carboxamides by Cascade Formal [3 + 2] Cycloaddition." ChemInform 46, no. 9 (2015): no. http://dx.doi.org/10.1002/chin.201509136.

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3

Devi, K. Shashikala, M. Ramaiah, D. L. Roopa, and V. P. Vaidya. "Synthesis and Investigation of Antimicrobial and Antioxidant Activity of 3-Nitro-N- (3-chloro-2-oxo-substituted-phenyl-azetidin-1-yl)naphtho [2,1-b]furan-2-carboxamides." E-Journal of Chemistry 7, s1 (2010): S358—S362. http://dx.doi.org/10.1155/2010/863547.

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Ethyl-3-nitronaphtho[2,1-b]furan-2-carboxylate(2)has been synthesized from ethyl naphtha [2,1-b]furan-2-carboxylate(1). This nitro product on reaction with hydrazine hydrate formed 3-nitronaphtho [2,1-b] furan-2-carbohydrazide(3). Various Schiff bases 3-nitro-N1(aryl-methylene)-substituted-naphtho [2,1-b]furan-2-carbohydrazides4(a-g)were obtained by treating hydrazide(3)with different aldehydes. These Schiff bases on reaction with chloro acetyl chloride in presence of triethylamine in dioxane yielded 3-nitro-N-(3-chloro-2-oxo-substituted-phenyl-azetidine-1-yl) naphtha [2,1-b]furan-2-carboxamid
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4

Xia, Likai, Akber Idhayadhulla, and Yong Rok Lee. "$$\hbox {Re}_{2}\hbox {O}_{7}$$ Re 2 O 7 -catalyzed formal [3 + 2] cycloaddition for diverse naphtho[1,2-b]furan-3-carboxamides and their biological evaluation." Molecular Diversity 20, no. 1 (2015): 17–28. http://dx.doi.org/10.1007/s11030-015-9630-2.

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5

M, Heravi; Majid, A. Rezvanian, F. Moradi, V. Zadsirjan, and M. Mohammadnejad. "Cascade process for direct synthesis of indeno[1,2-b]furans and indeno[1,2-b]pyrroles from diketene and ninhydrin." Molecular Diversity, October 1, 2019. https://doi.org/10.1007/s11030-019-09996-7.

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Novel and efficient multicomponent reactions (MCRs) involving diketene, ninhydrin (indane-1,2,3-trione) and one primary amine (3CR) or two different primary amines (4CR) were achieved for the successful synthesis of dihydro-4H-indeno[1,2-b]furan-3-carboxamides or tetrahydroindeno[1,2-b]pyrrole-3-carboxamides, respectively. The merits of this method are highlighted by using either commercially available or easily accessible starting materials, operational simplicity, facile workup procedure, efficient usage of all the reactants, tolerance of a variety of functional groups and ability to conduct
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