Data

Data from: ZrCl4-catalyzed C-O bond to C-N bond formation: synthesis of 1,2,3-triazoles and their biological evaluation

RMIT University, Australia
Assoc Professor Helmut Hugel (Associated with, Aggregated by)
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=https://figshare.com/articles/ZrCl_sub_4_sub_Catalyzed_C_O_Bond_to_C_N_Bond_Formation_Synthesis_of_1_2_3_Triazoles_and_Their_Biological_Evaluation/1104372&rft.title=Data from: ZrCl4-catalyzed C-O bond to C-N bond formation: synthesis of 1,2,3-triazoles and their biological evaluation&rft.identifier=eace6d522421109974083d725ae5d3f1&rft.publisher=RMIT University, Australia&rft.description=Attached file provides supplementary data for linked article. A simple and efficient protocol was developed for the synthesis of aryl azides directly from aryl carbinols using ZrCl4 as a Lewis acid catalyst. The azides were converted to novel triazoles under click reaction conditions, which were evaluated for their antimicrobial activity against various strains.&rft.creator=Assoc Professor Helmut Hugel&rft.date=2018&rft.relation=http://dx.doi.org/10.1080/00397911.2014.910528&rft_rights=All rights reserved&rft_rights=CC BY-NC: Attribution-Noncommercial 3.0 AU http://creativecommons.org/licenses/by-nc/3.0/au&rft_subject=1,2. 3-triazole&rft_subject=Antimicrobial activity&rft_subject=Click chemistry&rft_subject=Zirconium(IV) chloride&rft_subject=Organic Chemical Synthesis&rft_subject=CHEMICAL SCIENCES&rft_subject=ORGANIC CHEMISTRY&rft.type=dataset&rft.language=English Access the data

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Attached file provides supplementary data for linked article. A simple and efficient protocol was developed for the synthesis of aryl azides directly from aryl carbinols using ZrCl4 as a Lewis acid catalyst. The azides were converted to novel triazoles under click reaction conditions, which were evaluated for their antimicrobial activity against various strains.

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  • Local : eace6d522421109974083d725ae5d3f1