Substrate Reaction Research Articles

Transition Metal-Catalyzed C(sp3)-C(sp3) Coupling to Construct All-Carbon Quaternary Carbon Centers

Transition metal-catalyzed C(sp³)-C(sp³) coupling reactions represent a powerful strategy for constructing all-carbon quaternary centers. However, these reactions remain challenging due to significant steric hindrance effects and the propensity for side reactions such as elimination and isomerization. This review provides a comprehensive summary of the progress made over the past few decades in the construction of all-carbon quaternary centers, with a focus on coupling reactions involving tertiary C(sp³) and primary/secondary C(sp³) centers (as the cross coupling of two tertiary C(sp³) centers remains unsuccessful). The discussion is organized around reaction conditions, substrate scope, and reaction mechanisms, and a brief overview of transformations based on these coupling reactions is also presented.

Fabrication of thick Cr masks for reactive ion substrate etching by electron beam lithography and lift-off techniques

Fabrication of tall Cr nanostructures of different shapes by lithography and lift-off processes is demonstrated. By varying resist thickness, metal layer thickness, and diameter of holes in the resist mask, it is demonstrated that metal structures with shapes ranging from sharp-tipped conical over flat-top cones to nearly cylindrical can be fabricated. A comparison of resist layer dissolution in acetone, covered by Ag and Cr films, reveals that Cr films grow with an open structure of particles that allow rapid solvent diffusion through Cr layers that are several hundred nanometers thick. On the other hand, the 2D growth of Ag on the resist forms a barrier against acetone diffusion. The open structure of Cr enables the lift-off process to fabricate several-μm-high nanostructures using a single resist layer. As an example, high-aspect-ratio Si structures are demonstrated by reactive ion etching using thick Cr layers as a mask, fabricating nanopillars with 3 μm height at room temperature.

CdWO4 Sub‐1 nm Nanowires for Visible‐light CO2 Photoreduction

Quantum size effect usually causes energy level splitting and band broadening as material size decreases. However, this may change again by the surface adsorbents, doping and defects, which rarely attracts much attention. Herein, CdWO4 sub‐1 nm nanowires (SNWs) with oleylamine adsorption, PO43‐‐doping and oxygen defects are synthesized by combining Cd(CH3COO)2, H3PW12O40 (PW12) and oleylamine (abbreviated as PO43‐‐CdWO4‐X SNWs). Compared with bulk CdWO4, they exhibit unexpected absorption spectra (extended from 292 nm to 453 nm) and bandgap (reduced from 4.25 eV to 2.74 eV), thus bringing remarkable visible‐light CO2 photoreduction activity. Under 410 nm LED light irradiation, PO43‐‐CdWO4‐40 SNWs exhibit the highest photocatalytic performance with a CO2‐to‐CO generation rate of 1685 µmol g‐1 h‐1. Density functional theory (DFT) calculations demonstrate the adsorbed oleylamine raises the valence band and enhances the adsorption of reaction substrate and intermediates, thus decreasing their reduction energy barriers. Furthermore, PO43‐‐doping and oxygen defects will generate defect energy band below the conduction band of PO43‐‐CdWO4‐40 SNWs, resulting in remarkable visible light absorption and superior photocatalytic CO2 reduction performance. This work highlights the significant impacts of surface adsorbents, doping and defects on the physicochemical and catalytic properties of sub‐nano materials.

CdWO4 Sub-1 nm Nanowires for Visible-Light CO2 Photoreduction.

Quantum size effect usually causes energy level splitting and band broadening as material size decreases. However, this may change again by the surface adsorbents, doping and defects, which rarely attracts much attention. Herein, CdWO4 sub-1 nm nanowires (SNWs) with oleylamine adsorption, PO4 3--doping and oxygen defects are synthesized by combining Cd(CH3COO)2, H3PW12O40 (PW12) and oleylamine (abbreviated as PO4 3--CdWO4-X SNWs). Compared with bulk CdWO4, they exhibit unexpected absorption spectra (extended from 292 nm to 453 nm) and band gap (reduced from 4.25 eV to 2.74 eV), thus bringing remarkable visible-light CO2 photoreduction activity. Under 410 nm LED light irradiation, PO4 3--CdWO4-40 SNWs exhibit the highest photocatalytic performance with a CO2-to-CO generation rate of 1685 μmol g-1 h-1. Density functional theory (DFT) calculations demonstrate the adsorbed oleylamine raises the valence band and enhances the adsorption of reaction substrate and intermediates, thus decreasing their reduction energy barriers. Furthermore, PO4 3--doping and oxygen defects will generate defect energy band below the conduction band of PO4 3--CdWO4-40 SNWs, resulting in remarkable visible light absorption and superior photocatalytic CO2 reduction performance. This work highlights the significant impacts of surface adsorbents, doping and defects on the physicochemical and catalytic properties of sub-nano materials.

Lignin-based monophenolic model compounds in L-tyrosine derivative synthesis via tyrosine phenol lyase

Tyrosine phenol lyase (TPL) synthesises L-tyrosine derivatives from monophenols, pyruvate and ammonia. Production of such high-value aromatic chemicals from biomass-derived raw materials is of great interest. In this study, six monophenols (guaiacol, phenol, o-cresol, m-cresol, catechol and syringol) were chosen based on the structure of lignin and were studied as substrates in the enzymatic reaction. Single monophenol reactions (SMR) and binary monophenol reactions (BMR) with guaiacol were carried out. TPL-M379V was found to be selective towards guaiacol (84.5 % conv.). The highest single activity was measured towards phenol (93.9 % conv.). However, the enzyme preferred guaiacol over phenol in the BMRs. Syringol was found to be inert in the reaction, whereas catechol had an inhibitory effect on the enzymatic reaction, in addition to causing degradation of all the substrates in the medium. Doubling the guaiacol concentration in the SMR did not significantly increase the production of 3-O-methyldopa (conv. 45.9 %). However, in the binary reaction systems the total monophenol conversions were higher with guaiacol and phenol (total 62.4 %) or o-cresol (total 57.1 %). This indicates possible substrate/product specific inhibition. The study provides new data on activity, selectivity and inhibitory effects of monophenols in the synthetic reaction catalysed by TPL-M379V, especially in mixed-substrate reactions.

Alkali‐Mediated/Catalyzed Transition‐Metal‐Free Tandem Reaction Triggered by the Borrowing Hydrogen and Aerobic Dehydrogenation Processes of Alcohols

AbstractThe transformation of alcohols to important classes of compounds is a central topic in chemistry because they are abundant, renewable, and attractive building blocks. The alkali‐mediated/catalyzed borrowing hydrogen and aerobic dehydrogenation processes of alcohols open a new and sustainable access for the alcohol conversion under transition‐metal‐free conditions. In this review, we summarize the recent alkali‐mediated/catalyzed sequential reactions involving the borrowing hydrogen and aerobic dehydrogenation processes of alcohols. Furthermore, this review not only introduces the tentative pathways of these transformations, but also discusses the role of alkali, solvent effects, and substrate reactivity on these reactions.

Multidimensional Engineering to Construct Ru/TiO2 Catalysts Enriched with Pores and Ti3+ Defects for Highly Efficient Selective Hydrogenation of Benzene

AbstractStructural engineering, coupled with crystalline phase engineering and surface engineering, serves as a practical and effective strategy for enhancing catalytic performance through the fine design of catalysts in terms of their structure, physical phases and surface defects. In this work, a set of strategies were employed for structural transformation and crystalline phase transition of Ru/TiO2 catalysts, utilizing multidimensional regulation. Ru nanoparticles loaded on a unique TiO2 nanosheet flowers (Ru/TSFs) enriched with pores and Ti3+ defects were prepared by solvothermal and impregnation‐chemical reduction methods. The Ru/TSFs exhibited an outstanding catalytic performance in the reaction of selective hydrogenation of benzene for the preparation of cyclohexene, with a selectivity of 79 % and a maximum yield of 52.8 % along with a benzene conversion of 45.9 % and a good stability. The excellent catalytic performance attributes to the distinctive structure of three‐dimensional nanosheet flowers, which offers a high specific surface area and improvs the effective contact between the catalyst and the reaction substrate. Meanwhile, the porous Ru/TSFs exhibit exceptional hydrophilicity and abundant Ti3+ defects on their surface, which is quite favorable for the desorption of cyclohexene from the reaction system, thus improving the selectivity of cyclohexene. The multidimensional engineering may provide an efficient approach for constructing high‐performance loaded catalysts for potential industrial applications.

The Assembly of Cerium(III)-Containing Silicotungstate with Lewis Acid-Base Sites Enables the Selective C3-Alkenylation of Oxindole.

A cerium(III)-containing silicotungstate, [H2N(CH3)2]10NaK[KCe(SiW11O39)2(H2O)]·18.5H2O (CeSiW), was successfully synthesized and characterized. Structure analysis reveals that CeSiW is composed of two {SiW11O39} units connected by one cerium(III) cation to form a typical 1:2 sandwich structure, which is further expanding into a 1D chain linked by K+ ions. The oxygen-enriched surfaces of {SiW11O39} units and open cerium sites provide abundant Lewis base and acid sites in CeSiW. As a result, CeSiW efficiently catalyzed the C3-alkenylation of oxindoles with aldehydes through the simultaneous activation of both reaction substrates on its crystal framework. Various 3-benzylidene-oxindoles are synthesized with excellent yields and high E-selectivity under solvent-free conditions.

Biomimetic supported polyoxometalate structures designed and its applications for the ultra-deep oxidative desulfurization of fuels

Inspired by the fact that human nose cilia can effectively contact with particles to prevent their entry into our body, this kind novel biomimetic structures are designed and synthesized to enable the loading efficiency between the polyoxometalate catalytic species (POMs) and the carrier, thereby improving their loading rate and promoting their catalytic performance. The mullite whiskers-uniformed cordierite (CMW) is used as a carrier to support POMs, in which mullite whiskers regarding as the cilia in our nose, this kind catalyst could not only overcome the shortcomings of simple POMs with low specific surface and easy to self-agglomerate, but also could greatly increase their contact probability with the carrier. At the same time, the advantage of the cordierite block structure also greatly conducive to their actual application value on the reusing operation. A series of Keggin-type POM-loaded bulk materials, POM@CMW, [VimAm]Br@POM@CMW, [DVim]Br@POM@CMW, have been developed with various ionic liquid-based POMs (ionic liquid = ILs, chosen these two kinds of [VimAm]Br and [DVim]Br) to a comparative study. The oxidative desulfurization reaction (ODS) for fuels was performed using the obtained materials as catalysts and H2O2 as oxidant, without the additional extractants for the existing of ILs in catalyst. Through experimental evaluations, [DVim]Br@POM@CMW was found the excellent efficiency on the Sulfur removal, with an DBT removal of 96.34 % at 70 °C for 120 min. According to the FT-IR and SEM results after the reaction, the catalyst could retain their original structure and the dibenzothiophene (DBT) removal could still be maintained above 95 % after 7 reuses. Furthermore, the oxidation reactivity of different substrates was in the following order: DBT > 4,6-dimethyldibenzothiophene (4,6-DMDBT) > thiophene (BT) and the high activity in actual diesel oil could be also exhibited. The enhanced reaction activity, excellent structural stability, and recyclability can be attributed to the abundance of active sites and outstanding mechanical properties provided by cordierite/mullite whiskers as a carrier, indicating their potential in the novel biomimetic-structured POMs-loaded catalysts.

Digital model of biochemical reactions in lactic acid bacterial fermentation of simple glucose and biowaste substrates

As concerns about the environmental impacts of biowaste disposal increase, lactic acid bacterial fermentation is becoming increasingly popular. Current academic research is aimed at the process optimization by developing digital bioreactors. The primary focus is to develop a digital model mimicking the biochemical reactions. In the light of this, this paper intended to build a digital model of biochemical reactions during the fermentation process of both glucose and biowaste substrates, including white pasta and organic municipal waste. For this purpose, near-infrared (NIR) and mid-infrared (MIR) spectroscopy techniques were used to collect spectral information during the fermentation process. Next, the samples were analyzed by High Pressure Liquid Chromatography (HPLC) to measure their glucose, fructose, arabinose, xylose, disaccharide, lactic acid, and acetic acid contents. The results showed that learning algorithms trained on MIR spectra accurately estimated the biochemical reactions for both glucose and biowaste substrates. For the glucose substrate, the results showed R-squared of 0.97 and RMSE of 4.69 g/L for glucose, and R-squared of 0.98 and RMSE of 2.74 g/L for lactic acid. In the case of biowaste substrate, estimations included glucose (R-squared = 0.97, RMSE = 4.69 g/L), fructose (R-squared = 0.88, RMSE = 1.47 g/L), arabinose (R-squared = 0.98, RMSE = 0.55 g/L), xylose (R-squared = 0.93, RMSE = 1.11 g/L), disaccharide (R-squared = 0.90, RMSE = 0.55 g/L), total sugar (R-squared = 0.98, RMSE = 3.79 g/L), lactic acid (R-squared = 0.98, RMSE = 2.74 g/L), and acetic acid (R-squared = 0.97, RMSE = 0.36 g/L). Regarding NIR spectral data, the predictive models were accurate when the substrate was glucose, however, they failed to accurately estimate the chemical reactions in the case of biowaste substrate. The findings of this study can be used to fulfill the requirements for a continuous fermentation process with the objective of maximizing lactic acid production.

Phytochemical and Antioxidant Analysis of Artocarpus heterophyllus Peel Extracts

BACKGROUND: Plants have a diverse variety of bioactive compounds such as tannins, alkaloids, flavonoids, carbohydrates and steroids among many others that can offer significant physiological actions in the human body. Phytochemicals are naturally occurring chemical, biological and active compounds found in plants that are of benefit to human health apart from those that act as macronutrients and micronutrients. A. heterophyllus (Jackfruit) belongs to the family Moraceae. Jackfruit tree is native to India and is popular in several tropical and sub-tropical Countries. OBJECTIVE: The aim of this study is to determine the phytochemical constituents, antioxidant properties and gas chromatography mass spectroscopy (GC-MS) of the fruit peel of A. heterophyllus extracts using three different solvents. METHODS: Artocarpus heterophyllus fruits were collected from University of Ibadan botanical garden, identified at the Forestry Research Institute of Nigeria, Oyo State. The peel was extracted and dried at 35 ℃. Qualitative method and Gas Chromatography Mass Spectroscopy were used to determine the phytochemical and bioactive compounds present in the plant, whereas¬¬¬¬¬¬ 2, 2, Diphenylpicryl-1-hydrazyl (DPPH) was used for the antioxidant analysis. RESULTS: Secondary metabolites such as flavonoids, phenols, alkaloids, glycosides, saponins, tannins, steroids, and Terpenoids were present based on the solvents while anthraquinnes were absent. Flavonoid and phenol were abundant in the three extracts while saponin was moderate. Eight chemical compounds were observed in the plant extracts. Major bioactive components with highest and lowest retention peak were (65.55 %) bis(2- ethyl hexyl) phthalate and (6.06 %) Cis- 13(2- ethylhexyl)phthalate respectively. Antioxidant activity increased with increase in concentration of which acetone extract had the highest DPPH (75.00 %) at 100 μg/ml. CONCLUSION: The fundamental means of the usage of medicinal plants for medicine is due to their bioactive properties which are used as substrates for biochemical and enzymatic reactions. Phytochemical derivatives have antiviral, anti-inflammatory, anti-oxidant, immunomodulatory, anticancer, antimicrobial, antitumor, analgesic and many other properties harbor in them.

Study of Kazakhstan’s Shungite as electrocatalyst substrate in hydrogen evolution reaction in acidic media

Study of Kazakhstan’s Shungite as electrocatalyst substrate in hydrogen evolution reaction in acidic media

Rational modulation of covalent organic frameworks heterogeneous catalyst: Structural cationization effect on accelerating photocatalytic oxidation process

Photocatalytic technology has been playing a key role in energy conversion and environmental remediation. It is critical and challenging that understanding and modulating the local structure effect on accelerating each rate-dependent step during the photocatalytic process. Herein, we utilize the highly ordered and structurally tunable COFs as a favorable platform for integrating multiple modulations of photochemical properties, including light capture, exciton dissociation, charge separation, and mass transfer by structural cationization strategy. Moreover, it is found that the cationized COF has a strong enrichment ability on the sulfide substrates, exhibiting an extremely fast selective oxidation rate of sulfides even in air. The calculation results indicate that the structural cationization successfully aggregates reaction substrates and increases the molecular collision probability, generating a reaction environment to promote the photocatalytic performances. This study will be expected to facilitate the new insights for the exploration of highly active COFs heterogeneous photocatalysts.

Stability and dissolution of single-crystalline iron oxide thin films in electrochemical environments

The stability of single-crystalline monolayer FeO(111) and 10 nm thin Fe3O4(111) films on Pt(111) upon exposure to environments of increasing chemical complexity has been studied with X-ray photoelectron spectroscopy, temperature-programmed desorption, in-situ scanning tunneling microscopy, and cyclic voltammetry. The well-defined oxide films, which were prepared under ultrahigh-vacuum conditions, were exposed to aqueous solutions of different pH and electrochemical cycling in pure and catechol-containing electrolyte. The films are stable in neutral (pH 7) and alkaline (pH 13) solutions both at open circuit conditions and during electrochemical cycling within the limits of hydrogen and oxygen evolution potentials. Also in strongly acidic (pH 1) perchlorate solution the films remain intact under open circuit conditions, but they quickly dissolve on application of electrochemical potential. Especially for the ultrathin FeO(111) films, catechol enhances the dissolution at neutral pH during electrochemical cycling. A comparison of Pt(111), FeO(111) and Fe3O4(111) substrates in the electrochemical catechol oxidation reaction reveals enhanced and sustained activity of FeO in alkaline environment, while strong deactivation occurs on Pt(111) and Fe3O4(111). This is explained by the weaker interaction between catechol and FeO(111) compared to the other substrates, which hampers the formation of a barrier layer on the electrode surface.

Glycerol 3-Phosphate Dehydrogenase Catalyzed Hydride Transfer: Enzyme Activation by Cofactor Pieces.

Glycerol 3-phosphate dehydrogenase catalyzes reversible hydride transfer from glycerol 3-phosphate (G3P) to NAD+ to form dihydroxyacetone phosphate; from the truncated substrate ethylene glycol to NAD+ in a reaction activated by the phosphite dianion substrate fragment; and from G3P to the truncated nicotinamide riboside cofactor in a reaction activated by adenosine 5'-diphosphate, adenosine 5'-monophosphate, and ribose 5-phosphate cofactor fragments. The sum of the stabilization of the transition state for GPDH-catalyzed hydride transfer reactions of the whole substrates by the phosphodianion fragment of G3P and the ADP fragment of NAD+ is 25 kcal/mol. Fourteen kcal/mol of this transition state stabilization is recovered as phosphite dianion and AMP activation of the reactions of the substrate and cofactor fragments. X-ray crystal structures for unliganded GPDH, for a binary GPDH·NAD+ complex, and for a nonproductive ternary GPDH·NAD+·DHAP complex show that the ligand binding energy is utilized to drive an extensive protein conformational change that creates a caged complex for these ligands. The phosphite dianion and AMP fragments are proposed to activate GPDH for the catalysis of hydride transfer by stabilization of this active caged complex. The closure of a conserved loop [292-LNGQKL-297] during substrate binding stabilizes the G3P and NAD+ complexes by interactions, respectively, with the Q295 and K296 loop side chains. The appearance and apparent conservation of two side chains that interact with the hydride donor and acceptor to stabilize the active closed enzyme are proposed to represent a significant improvement in the catalytic performance of GPDH.

Pickering Emulsion Promoted Interfacial Sequential Chemo-Biocatalytic Reaction for the Synthesis of Chiral Alcohols from Styrene.

Chemo-biocatalytic cascades have emerged as a promising approach in the realm of advanced synthesis. However, reconciling the incompatible reaction conditions among distinct catalytic species presents a significant challenge. Herein, we introduce an innovative solution using an emulsion system stabilized by Janus silica nanoparticles, which serve as a bridge for both chemo-catalysts and biocatalysts at the interface. The chemo-catalyst is securely anchored within a hydrophobic polymer matrix, ensuring its residence in an organic environment. Meanwhile, the negatively charged E. coli cells containing enzymes are attracted to the aqueous phase at the interface, facilitating their optimal positioning. We demonstrate the efficacy of this system through a two-step cascade reaction. Initially, the oxidation of styrene to acetophenone using palladium as a chemocatalyst achieves a 6-fold increase in yield compared to the control system. Subsequently, the reduction of achiral acetophenone to its chiral alcohol derivative presents a 17-fold yield enhancement relative to that of the control reaction. Importantly, our system exhibits versatility, accommodating a wide range of substrates for both individual and sequential reactions. This work not only validates the concept but also paves the way for the integration of chemo- and biocatalysts in the synthesis of a broader array of high-value chemical compounds.

A Wurster-Type Covalent Organic Framework with Internal Electron Transfer-Enhanced Catalytic Capacity for Tumor Therapy.

The low immunogenicity of tumors, along with the abnormal structural and biochemical barriers of tumor-associated vasculature, impedes the infiltration and function of effector T cells at the tumor site, severely inhibiting the efficacy of antitumor immunotherapy. In this study, a cobaloxime catalyst and STING agonist (MSA-2)-coloaded Wurster-type covalent organic framework (Co-TB COF-M) with internal electron transfer-enhanced catalytic capacity was developed as a COF-based immune activator. The covalently anchored cobaloxime adjusts the energy band structure of TB COF and provides it with good substrate adsorption sites, enabling it to act as an electron transmission bridge between the COF and substrate in proton reduction catalytic reactions. This property significantly enhances the sonodynamic catalytic performance. Under sono-irradiation, Co-TB COF-M can produce a substantial amount of reactive oxygen species (ROS) to induce Gasdermin D-mediated pro-inflammatory pyroptosis, thereby effectively enhancing the immunogenicity of tumors. Furthermore, MSA-2 is specifically released in response to ROS at the tumor site, minimizing the off-target side effects. More importantly, Co-TB COF-induced STING activation normalizes tumor vasculature and increases the expression of endothelial T cell adhesion molecules, which greatly enhance the infiltration and function of effector T cells. Thus, Co-TB COF-M as an immune activator could remold the tumor microenvironment, leading to increased infiltration and an improved function of T cells for immunotherapy.

Enhancement of the activity of a porphyranase by fusing a polymerization-inducing domain

Porphyra is one of the most economically valuable species of red algae, with porphyran being its primary bioactive polysaccharide. Highly active enzymes play a significant role in the research and development of porphyran. This study identified a PKD domain within a polysaccharide-binding protein, displaying an apparent molecular weight (Mw) of 20.20 kDa that is approximately twice the theoretical value, thereby suggesting the possibility of self-aggregation. By fusing it with porphyranase Por16B_Wf, a chimeric enzyme PKD-Por16B was constructed. It was confirmed that the fusion enzyme successfully assembles into an aggregation under the mediation of PKD domain, with its apparent Mw (65.13 kDa) significantly higher than theoretical Mw (46.02 kDa). The activity of PKD-Por16B was remarkably enhanced from 65.31 U/mg to 325.69 U/mg, accompanied by an improvement in enzymatic stability. Meanwhile, the hydrolysis pattern of PKD-Por16B remained unaltered in comparison to that of Por16B_Wf, indicating no significant deviation in its substrate specificity or reaction mechanism. These results suggest the feasibility of a strategy based on domain-induced aggregation to enhance enzyme activity, which is easy and economical.

Computational Investigation of the Ru‐Mediated Preparation of Benzothiazoles From N‐Arylthioureas: Elucidation of the Reaction Mechanism and the Origin of Differing Substrate Reactivity

ABSTRACTSynthesis of novel benzothiazoles via intramolecular CS bond formation reactions is increasingly being explored since they have been found in a wide range of natural products and pharmaceutical agents. Sharma et al. reported the ruthenium‐catalyzed preparation of novel benzothiazole derivatives from N‐arylthiourea precursors, with a range of reaction yields and selectivity being observed. We have employed a density functional theory‐based computational model to investigate the reaction mechanism leading to the benzothiazole product and help uncover the origin of the differing experimental yields and substrate specificities. We proposed a modified mechanistic scheme where the rate‐determining step to be the synchronized breaking of the peroxide bond of the oxidizing agent with the concomitant proton‐coupled electron transfer from the haloarene urea and a Ru‐bound water molecule, not electrophilic RuC bond activation. Evidence for this being the rate‐determining step is (a) the barrier is consistent with a lack of kinetic isotope effects associated with the ortho‐H atom and (b) the computed rate‐determining barriers for 10 N‐arylthiourea substrates show good correlation with the observed yield.

Linear and Angular Heteroannulated Pyridines Tethered 6-Hydroxy-4,7-Dimethoxybenzofuran: Synthesis and Antimicrobial Activity.

2-Chloropyridine-3-carbonitrile derivative 1 was utilized as a key precursor to build a series of linear and angular annulated pyridines linked to a 6-hydroxy-4,7-dimethoxybenzofuran moiety. Reaction of substrate 1 with various hydrazines afforded pyrazolo[3,4-b]pyridines. Treatment of substrate 1 with 1,3-N,N-binucleophiles including 3-amino-1,2,4-triazole, 5-amino-1H-tetrazole, 3-amino-6-methyl-1,2,4-triazin-5(4H)-one and 2-aminobenzimidazole produced the novel angular pyrido[3,2-e][1,2,4]triazolo[4,3-a]pyrimidine, pyrido[3,2-e][1,2,4]tetrazolo[1,5-a]pyrimidine, pyrido[3',2':5,6] pyrimido[2,1-c][1,2,4]triazine and benzo[4,5]imidazo[1,2-a]pyrido[3,2-e]pyrimidine, respectively. Reaction of substrate 1 with 1,3-C,N-binucleophiles including cyanoacetamides and 1H-benzimidazol-2-ylacetonitrile furnished 1,8-naphthyridines and benzoimidazonaphthyridine. Moreover, reacting substrate 1 with 5-aminopyrazoles gave pyrazolo[3,4-b][1,8]naphthyridines. Finally, reaction of compound 1 with 6-aminouracils as cyclic enamines yielded pyrimido[4,5-b][1,8]naphthyridines. Some of the synthesized products showed noteworthy antimicrobial efficiency against all types of microbial strains. Structures of the produced compounds were established using analytical and spectroscopic tools.