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Organics, Volume 7, Issue 4

2026 December - 11 articles

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Articles (11)

  • Article
  • Open Access

6 November 2026

Three 1-pyrrolidinyl 8-halo and one 1-pyrrolidinyl 8-cyano-substituted naphthalenes are prepared. The rate of the rotation of the pyrrolidinyl group is determined through variable temperature proton NMR using line-shape analysis and EXSY. The potenti...

  • Article
  • Open Access
5 Views
15 Pages

Divergent Chiral-Pool Synthesis of the C1–C8 and C9–C13 Fragments of Pladienolide B from L-Malic Acid

  • Sai Krishna Chilaka,
  • Nerella Ashok,
  • Marumamula Hanumaiah and
  • Ramachandra Reddy Putta

4 November 2026

Pladienolide B (1), a macrocyclic polyketide isolated from Streptomyces platensis Mer-11107, displays potent antiproliferative and antitumor activities through its interaction with the SF3b subunit of the spliceosome. Herein, we report a divergent, s...

  • Article
  • Open Access
58 Views
20 Pages

Novel 1,1′-Desymmetrized Ferrocene Conjugates of Imatinib and Nilotinib: Synthesis, Cytotoxic Activity and Molecular Docking Studies

  • Irena Philipova,
  • Rositsa Mihaylova,
  • Asine Dailova-Barzeva,
  • Mariyana Atanasova and
  • Georgi Stavrakov

3 November 2026

The incorporation of ferrocene into established pharmacophores represents a promising strategy for combining targeted activity with the properties of the organometallic scaffold. Building on our previous work on ferrocene-modified tyrosine kinase inh...

  • Article
  • Open Access
105 Views
13 Pages

2 November 2026

Urolithin M7 is a gut microbial metabolite of ellagic acid, but its glucuronide conjugate has not been well characterized. We report the first total synthesis of urolithin M7 3-glucuronide through a convergent route that combines Pd-mediated intramol...

  • Article
  • Open Access
158 Views
16 Pages

29 October 2026

A series of five novel 3-methyl-1-phenyl-4-(4-thioaroyl)-pyrazol-5-ones is obtained in excellent yields by thionation of the corresponding O-analogues with Lawesson’s reagent. The products are characterized in solution and solid phase. It is fo...

  • Review
  • Open Access
282 Views
46 Pages

Functionalized Silica-Catalyzed Multicomponent Reactions for Sustainable Heterocycle Synthesis: Structure–Activity Relationships, Mechanistic Insights, Green Metrics, and Future Perspectives

  • Jayanthi Barasarathi,
  • Md. Kadeer,
  • Maher Fathalla,
  • Kasi Venkatesan and ,
  • Parasuraman Karthikeyan,
  • Potchanun Sripothong,
  • Beata Morak Młodawska and
  • Malgorzata Jeleń
  • + 3 authors+ 0 author

26 October 2026

Catalysis has been recognized as a key science in contemporary chemistry, owing to the significant potential of nanocatalysts and organic–inorganic hybrid materials, due to their high surface area and tunability properties, as well as the possi...

(This article belongs to the Special Issue Green Catalysis and Sustainable Organic Synthesis)
  • Article
  • Open Access
177 Views
10 Pages

Effect of the Counter Anion on the NHC-Catalyzed Aroylation Reaction

  • Zhaoyu Cai,
  • Yoshifumi Hirotsu,
  • Masahiro Yoshizawa-Fujita and
  • Yumiko Suzuki

22 October 2026

The influence of the counter anion and solvent on the N-heterocyclic carbene (NHC)-catalyzed nucleophilic aroylation of electron-deficient aromatic compounds was investigated using iodide, bis(trifluoromethanesulfonyl)imide (TFSA), and tetrafluorobor...

  • Article
  • Open Access
156 Views
16 Pages

Molecular Docking, ADMET Prediction, DFT, and Biological Studies of Zinc (II) Macrocyclic Complexes

  • Kushwaha Ranjan Dinesh,
  • Monika Kamboj,
  • Pooja Srivastava,
  • Sangeeta Bajpai and ,
  • Nitin Srivastava,
  • Tiwari Shashikant Ramsanehi,
  • Sukhraj Kaur,
  • Rahul Sharma,
  • Smita Rai and
  • Ajay Kumar Singh
  • + 6 authors+ 1 author

21 October 2026

The amide macrocyclic complexes of zinc [ZnMc1, ZnMc2, and ZnMc3 (1–3)] were synthesized through template condensation of oxalic acid with different diamines, p-phenylenediamine, ethylenediamine, and propylenediamine, respectively. These zinc c...

  • Article
  • Open Access
259 Views
21 Pages

Synthesis and Characterization of Ortho-Halogen-Substituted Mono- and Bisthiocarbohydrazones: Structural Comparison

  • Gorana S. Mrđan,
  • Marko V. Rodić,
  • Milica G. Bogdanović,
  • Berta Barta Holló and ,
  • Borko M. Matijević,
  • Olivera S. Marković and
  • Mirjana M. Radanović
  • + 2 authors+ 0 author

9 October 2026

Six ortho-substituted halogen derivatives (F, Cl, Br) of mono- and analog bisthiocarbohydrazones were synthesized and fully characterized. Structural characterization was performed through elemental analysis and NMR, FT-IR and UV-Vis spectroscopy. Al...

  • Article
  • Open Access
403 Views
16 Pages

Green Biginelli Synthesis of Dihydropyrimidinone Derivatives Catalyzed by Phyllanthus acidus Fruit Extract: Structural Characterization and Preliminary Biological Evaluation

  • Arif Ashari,
  • Fina Khaerunnisa Frima,
  • Irwan Sudarmanto,
  • Sendi Diana Putri and ,
  • Iwan Syahjoko Saputra,
  • Moch Abdussalam,
  • Robby Gus Mahardika,
  • Yeni Wahyuni Hartati and
  • Heru Agung Saputra
  • + 4 authors+ 0 author

9 October 2026

The development of environmentally sustainable synthetic approaches for biologically active heterocyclic compounds has become increasingly important in medicinal chemistry. In this study, two dihydropyrimidinone (DHPM) derivatives were synthesized th...

  • Review
  • Open Access
464 Views
38 Pages

Synthetic Methods and Process Approaches to Betulin 3,28-Diacetate: From Birch Bark to Semi-Synthetic Derivatives

  • Aigerim Zhaxybayeva,
  • Khava Yevloyeva,
  • Saltanat Kaliyeva,
  • Nurgul Nurmukhanbetova and ,
  • Idiya Ostretsova,
  • Nazira Kassenova,
  • Dana Kazyakhmetova and
  • Aziza Yeskendirova
  • + 3 authors+ 0 author

23 September 2026

Betulin, a lupane-type pentacyclic triterpene abundant in birch bark, is an accessible renewable scaffold for semisynthetic chemistry, while its 3,28-diacetate serves both as an isolable derivative and as a protected intermediate for further function...

(This article belongs to the Topic Biological and Pharmacological Activity of Natural Products)
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Organics - ISSN 2673-401X