Article
Chemistry, Physical
Abdullah Bicer, Ramazan Altundas
Summary: The Vilsmeier Haack formylation reactions of 4-phenyl-N-N'-benzoyl and 4-phenyl-N-substituted (N-sulphonyl and N-phenyl)-2-aminothiazole molecules with POCl3/DMF were studied. The Crystal (6) ((E)-N'-(5-formyl-4phenylthiazol-2-yl)-N,N-dimethylformimid amide) and crystal (14) (N-phenyl-N-(4-phenylthiazol-2-yl)formamide) molecules were obtained in the formylating reactions of N,N'-benzoyl, N-sulphonyl protecting group 4phenyl thiazole molecules. All compounds have been synthesized and characterized by FT-IR, 1H NMR, 13C NMR techniques, and X-ray structure analysis. These molecules demonstrate O,S-syn conformation.
JOURNAL OF MOLECULAR STRUCTURE
(2023)
Review
Chemistry, Organic
Aditi Arora, Sumit Kumar, Vinod Khatri, Ashok K. Prasad, Rajni Johar Chhatwal, Sandeep Kumar
Summary: C-2-formyl glycals have been of sustained interest in carbohydrate chemistry as they provide valuable chiral building blocks for numerous biological, pharmaceutical, and industrial compounds. They are a class of carbohydrates incorporating an α,β-unsaturated aldehyde, which can serve as the core in many organic reactions. This review compiles a literature survey on the synthesis of C-2-formyl glycals from 2013 to 2022 and discusses their importance for the synthesis of medicinal, supramolecular, biological, organic, and material chemistry based molecules.
SYNTHESIS-STUTTGART
(2023)
Article
Chemistry, Organic
Yu-Rong Zhu, Jin-Hong Lin, Ji-Chang Xiao
Summary: This study presents a method for the formylation of indoles using Ph(3)P/ICH(2)CH(2)I-promoted DMF, which allows for a convenient one-step process for electron-rich indoles under mild conditions.
Review
Biochemistry & Molecular Biology
Vladimir S. S. Tyurin, Alena O. O. Shkirdova, Oscar I. I. Koifman, Ilya A. A. Zamilatskov
Summary: This review presents a strategy for obtaining various functional derivatives of tetrapyrrole compounds based on transformations of unsaturated carbon-oxygen and carbon-carbon bonds of the substituents at the meso position. First, synthetic approaches to the preparation of these precursors are described. Then diverse pathways for the transformations of the multipotent synthons are discussed, revealing a variety of products of such reactions. The structures, electronic, and optical properties of the compounds obtained by the methods under consideration are analyzed. In addition, there is an overview of the applications of the products obtained, with biomedical use being among the most important. Finally, the advantages of using the reviewed synthetic strategy to obtain dyes with targeted properties are highlighted.
Review
Chemistry, Organic
Ameen A. Abu-Hashem, Ahmed A. M. Abdelgawad, Moustafa A. Gouda
Summary: This article presents a systematic and comprehensive survey of the method of preparation and the chemical reactivity of thieno[2,3-b]quinolines through the Vilsmeier-Haack reaction. Substituted Tqs have been shown to be useful building blocks for the synthesis of polyfunctionalized heterocyclic compounds.
LETTERS IN ORGANIC CHEMISTRY
(2023)
Review
Chemistry, Organic
Moustafa A. Gouda, Ghada G. El-Bana
Summary: This review discusses the synthesis of 2-(piperidin-1-yl) and/or 2-(morpholin-1-yl) quinoline-3-carbaldehyde derivatives through Vilsmeier-Haack formylation and their reactions with various reagents to produce corresponding quinoline derivatives. The review emphasizes the potential of these compounds as precursors and building blocks for the synthesis of diverse heterocyclic systems of pharmacological interest.
MINI-REVIEWS IN ORGANIC CHEMISTRY
(2023)
Article
Chemistry, Organic
Geeta Devi Yadav, Pooja Chaudhary, Balaram Pani, Surendra Singh
Summary: Chiral transition metal complexes with privileged ligands are efficient catalysts for various asymmetric organic transformations. Transition metal complexes of C1-symmetric pyrrolidine-based ligands have been widely used in asymmetric organic reactions. However, a comprehensive review article on the transition metal complexes of chiral C1-symmetric pyrrolidine-based ligands derived from (L)-proline has not been published.
TETRAHEDRON LETTERS
(2024)