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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 49, 2019 - Issue 1
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Articles

One-pot facile synthesis, crystal structure and antifungal activity of 1,2,3-triazoles bridged with amine-amide functionalities

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Pages 118-128 | Received 19 Sep 2018, Published online: 14 Jan 2019

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Mohamed G. Badrey, Sobhi M. Gomha, Magdi E.A. Zaki, Basant Farag & Ahmed A.M. El-Reedy. (2024) Cyanauric Chloride as a key precursor and a core component for Three-Armed Triazolopyrimidines: Recent finding about SARs and docking analyses. Results in Chemistry 7, pages 101337.
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Guimiao Tian, Qiuyi Song, Ziwei Liu, Ju Guo, Shuang Cao & Sihui Long. (2023) Recent advances in 1,2,3- and 1,2,4-triazole hybrids as antimicrobials and their SAR: A critical review. European Journal of Medicinal Chemistry 259, pages 115603.
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Atamjit Singh, Karanvir Singh, Aman Sharma, Kaustubh Joshi, Brahmjeet Singh, Sambhav Sharma, Kevin Batra, Kirandeep Kaur, Dilpreet Singh, Renu Chadha & Preet Mohinder Singh Bedi. (2023) 1,2,3‐Triazole Derivatives as an Emerging Scaffold for Antifungal Drug Development against Candida albicans : A Comprehensive Review . Chemistry & Biodiversity 20:5.
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Nada Y. Tashkandi, Zahra M. Al-Amshany & Nasser A. Hassan. (2022) Design, synthesis, molecular docking and antimicrobial activities of novel triazole‐ferulic acid ester hybrid carbohydrates. Journal of Molecular Structure 1269, pages 133832.
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Arnab Chakraborty, Chitra Jaiswal, Atikur Hassan, Saurabh Kumar, Khushwant Singh, Biman B. Mandal & Neeladri Das. (2022) Tunable and improved antiproliferative activity of Pt (II)‐based organometallics bearing alkynyls and 1,2,3‐triazole moieties. Applied Organometallic Chemistry 36:7.
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Mahrokh Marzi, Mojtaba Farjam, Zahra Kazeminejad, Abolfazl Shiroudi, Amin Kouhpayeh & Elham Zarenezhad. (2022) A Recent Overview of 1,2,3-Triazole-Containing Hybrids as Novel Antifungal Agents: Focusing on Synthesis, Mechanism of Action, and Structure-Activity Relationship (SAR). Journal of Chemistry 2022, pages 1-50.
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C. P. Kaushik & Manisha Chahal. (2021) Synthesis, antimalarial and antioxidant activity of coumarin appended 1,4-disubstituted 1,2,3-triazoles. Monatshefte für Chemie - Chemical Monthly 152:8, pages 1001-1012.
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Adinath D. Badar, Shubham M. Sulakhe, Mahesh B. Muluk, Naziya N. M. A. Rehman, Prashant P. Dixit, Prafulla B. Choudhari, Giribala M. Bondle & Kishan P. Haval. (2021) Synthesis, Antimicrobial Evaluation and Docking Study of Novel Thiosemicarbazone Clubbed with 1,2,3-Triazoles. Current Bioactive Compounds 17:6.
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Sogand Mirshafiee, Arefe Salamatmanesh & Akbar Heydari. (2021) A sustainable approach for efficient one‐pot synthesis of 1‐aryl 1,2,3‐triazoles using copper iodide supported on 3‐thionicotinyl‐urea‐modified magnetic nanoparticles in DES. Applied Organometallic Chemistry 35:7.
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Serigne Abdou Khadir Fall, Sara Hajib, Oumaima Karai, Younas Aouine, Salaheddine Boukhssas, Hassane Faraj & Anouar Alami. (2021) Tetramethyl 1,1′-(2-[{4,5-bis(Methoxycarbonyl)-1H-1,2,3-triazol-1-yl}methyl]-2-[(4-methylphenyl)sulfonamido]propane-1,3-diyl)bis(1H-1,2,3-triazole-4,5-dicarboxylate). Molbank 2021:1, pages M1186.
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Caibao Jiang, Jinguo Shi, Liping Liao, Liantao Zhang, Jiayong Liu, Yang Wang, Yaoqiang Lao & Jingxia Zhang. (2020) 5‐[2‐(N‐(Substituted phenyl)acetamide)]amino‐1,3,4‐thiadiazole‐2‐sulfonamides as Selective Carbonic Anhydrase II Inhibitors with Neuroprotective Effects. ChemMedChem 15:8, pages 705-715.
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Tamer El Malah, Hany F. Nour, Amira A. E. Satti, Bahaa A. Hemdan & Wael A. El-Sayed. (2020) Design, Synthesis, and Antimicrobial Activities of 1,2,3-Triazole Glycoside Clickamers. Molecules 25:4, pages 790.
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Satish V. Akolkar, Amol A. Nagargoje, Vagolu S. Krishna, Dharmarajan Sriram, Jaiprakash N. Sangshetti, Manoj Damale & Bapurao B. Shingate. (2019) New N -phenylacetamide-incorporated 1,2,3-triazoles: [Et 3 NH][OAc]-mediated efficient synthesis and biological evaluation . RSC Advances 9:38, pages 22080-22091.
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Péter Szuroczki, Judit Sámson & László Kollár. (2019) Synthesis of 5‐Carboxamidotriazoles via Azide‐Alkyne Cycloaddition–Aminocarbonylation Sequence. ChemistrySelect 4:19, pages 5527-5530.
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