The focus of our study is the synthesis and biological activity evaluation of a series of 4H-Pyran compounds and schiff bases fused 4H-Pyran derivatives which are known to possess a wide variety of biological activities. In this paper at first a simple and efficient one-pot synthesis of 4H-Pyran s from the three-component reaction between malononitrile, aldehydes, and active methylene compounds...

Introduction The number of natural and synthetic 2H-pyran-2-one derivatives has been reported to exert notably the potential biological activity [1] and medicinal application such as: anticancer activity [2] hepatoprotective activity [3]. On the other hand, catechol derivatives are promising group of compounds worthwhile for further investigation, which may lead to the discovery of selective ac...

The synthesis of C2-symmetrical bis(β-enamino-pyran-2,4-dione) derivative 3 connected via 1,6-hexylene linker was reported for the first time. X-ray structures and Hirshfeld studies new bis- β-enamino-pyran-2,4-dione along with two structurally related pyran-2,4-dione derivatives 2a,b were discussed. A comparative analysis different intermolecular contacts affecting crystal stability presented....

A novel bicyclization of 2-(2-(hydroxymethyl)-1-methylene-2,3-dihydro-1H-inden-2-yl)ethanol with aldehydes in the presence of 10 mol% BF3·OEt2 in dichloromethane at 0-25 °C affords the biologically relevant indeno[2,1-c]pyran scaffolds in good yields with high selectivity. Similarly the bicyclization of 2-(1-(hydroxymethyl)-2-methylenecyclopentyl)ethanol with aldehydes generates the correspondi...

Through the studies on structure-activity relationships o f 5-acyl-3-(l-aminoalkylidene)4-hydroxy-2 H-pyran-2,6(3 H)-dione derivatives in photosystem II (PS II) inhibition, overall lipophilicity o f the molecule was found to be a major determinant for the activity. In the sub­ stituted N-benzyl derivatives, not only the lipophilicity but also the electronic and steric char­ acters o f the subst...

An easy, effective and eco-friendly one-pot process for the preparation of 4H-pyran compounds has been established by using a catalytic amount reduced graphene oxide functionalized with diethylenetriamine (rGO-DETA) in water under mild conditions. The catalyst was very this reaction provided desired products 1a–t good to high yields (87%–97%) short times. Moreover, rGO-DETA composite could be r...

An atom-economical stereoselective synthesis of [{1-acetyl-5-methyl-6,8-dioxabicyclo(3.2.1)octane}-7-spiro-3'-(indolin-2'-one)] derivatives, containing both the oxindole and 6,8-dioxabicyclo(3.2.1)octane moieties via TiCl(4) catalyzed coupling of 2-acetyl-6-methyl-2,3-dihydro-4H-pyran with isatin derivatives is described.

An efficient and convenient method for synthesis of 2,6-bis (4-(dialkylamino) styryl)-4H-pyran-4-one starting from 4- (dialkylamino) benzaldehyde with 2,6-dimethyl-4H-pyran-4-onein the presence of MeONa as the base was described. Additionally, preparation of novel compounds with bis-DCM-type skeleton for application in organic light-emitting diodes was developed via reactio...

Intra and intermolecular interactions found in the developed crystals of synthesized py-ron-2,4-dione derivatives play crucial rules molecular conformations crystal stabili-ties, respectively. In this regard, Hirshfeld calculations were used to quantitatively analyze different structures some functionalized py-ran-2,4-dione derivatives. The X-ray structure pyran-2,4-dione derivative namely (3E,...

An operationally simple and efficient protocol for the construction of dihydrofuran derivatives has been accomplished via a sequential addition of N-chlorosuccinimide and a base to 2-amino-4H-pyran derivatives in alcohol medium. The one-pot protocol proceeding via tandem oxidative difunctionalization and ring contraction provides an entirely new strategy for the construction of the dihydrofuran...