A versatile way for the synthesis of monomethylamines by reduction of N-substituted carbonylimidazoles with the NaBH4/I2 system

Lin Chen, Xuan Zhou, Zhiyong Chen, Changxu Wang, Shunjie Wang and Hanbing Teng
Beilstein J. Org. Chem. 2022, 18, 1032–1039. https://doi.org/10.3762/bjoc.18.104

Supporting Information

Supporting Information File 1: Experimental part.
Format: PDF Size: 3.2 MB Download

Cite the Following Article

A versatile way for the synthesis of monomethylamines by reduction of N-substituted carbonylimidazoles with the NaBH4/I2 system
Lin Chen, Xuan Zhou, Zhiyong Chen, Changxu Wang, Shunjie Wang and Hanbing Teng
Beilstein J. Org. Chem. 2022, 18, 1032–1039. https://doi.org/10.3762/bjoc.18.104

How to Cite

Chen, L.; Zhou, X.; Chen, Z.; Wang, C.; Wang, S.; Teng, H. Beilstein J. Org. Chem. 2022, 18, 1032–1039. doi:10.3762/bjoc.18.104

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Presentation Graphic

Picture with graphical abstract, title and authors for social media postings and presentations.
Format: PNG Size: 7.5 MB Download

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Abraham, M. L.; Hilt, G. Investigation Towards the Asymmetric CBS‐Catalysed Reduction of Aryl Methyl Ketones with Electrochemically in Situ Generated BH3. ChemElectroChem 2024, 11. doi:10.1002/celc.202400319
  • Pétry, N.; Bantreil, X.; Lamaty, F. Synthesis of Molsidomine and Mesocarb Analog via Mechanochemistry. European Journal of Organic Chemistry 2024, 27. doi:10.1002/ejoc.202400387
  • Yang, T.-C.; Chiang, Y.-J.; Chiang, P.-Y.; Chen, H.-Y.; Zhuang, K.-R.; Wang, Y.-C.; Lin, C.-H.; Lo, L.-C.; Fu, S.-L. Design, synthesis, and anti-cancer evaluation of C-14 arylcarbamate derivatives of andrographolide. Bioorganic & medicinal chemistry 2023, 98, 117582. doi:10.1016/j.bmc.2023.117582
Other Beilstein-Institut Open Science Activities