An anomalous addition of chlorosulfonyl isocyanate to a carbonyl group: the synthesis of ((3aS,7aR,E)-2-ethyl-3-oxo-2,3,3a,4,7,7a-hexahydro-1H-isoindol-1-ylidene)sulfamoyl chloride

Aytekin Köse, Aslı Ünal, Ertan Şahin, Uğur Bozkaya and Yunus Kara
Beilstein J. Org. Chem. 2019, 15, 931–936. https://doi.org/10.3762/bjoc.15.89

Supporting Information

Supporting Information File 1: Theoretical computations, experimental procedures, copies of 1H and 13C NMR spectra, X-ray diffraction and HRMS analysis.
Format: PDF Size: 1.7 MB Download

Cite the Following Article

An anomalous addition of chlorosulfonyl isocyanate to a carbonyl group: the synthesis of ((3aS,7aR,E)-2-ethyl-3-oxo-2,3,3a,4,7,7a-hexahydro-1H-isoindol-1-ylidene)sulfamoyl chloride
Aytekin Köse, Aslı Ünal, Ertan Şahin, Uğur Bozkaya and Yunus Kara
Beilstein J. Org. Chem. 2019, 15, 931–936. https://doi.org/10.3762/bjoc.15.89

How to Cite

Köse, A.; Ünal, A.; Şahin, E.; Bozkaya, U.; Kara, Y. Beilstein J. Org. Chem. 2019, 15, 931–936. doi:10.3762/bjoc.15.89

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: 140.5 KB Download

Citations to This Article

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

Scholarly Works

  • Köse, A.; Soydaş, E.; Kara, Y. Unique reaction of cyclicimides containing double bond with chlorosulfonyl isocyanate and theoretical computations: Solvent-free reactions. Journal of Molecular Structure 2023, 1274, 134428. doi:10.1016/j.molstruc.2022.134428
  • Rzhevskiy, S. A.; Bogachev, V. N.; Minaeva, L. I.; Sterligov, G. K.; Nechaev, M. S.; Topchiy, M. A.; Asachenko, A. F. Efficient synthesis of 3-arylbutadiene sulfones using the Heck–Matsuda reaction. Mendeleev Communications 2021, 31, 548–549. doi:10.1016/j.mencom.2021.07.037
Other Beilstein-Institut Open Science Activities