Direct N-H/N-Me Aziridination of Unactivated Olefins Using O-(Sulfonyl)hydroxylamines as Aminating Agents
Shekh Sabir, Chandra Bhan Pandey, Ajay K. Yadav, Bhoopendra Tiwari*, Jawahar L. Jat*
*Centre of Biomedical Research, SGPGIMS-Campus, Raebareli Road, Lucknow 226014; Department of Chemistry, Baba Saheb Bhim Rao Ambedkar University, Lucknow 226025, India,
Email: btiwari
cbmr.res.in, jatjawahargmail.com
S. Sabir, C. B. Pandey, A. K. Yadav, B. Tiwari, J. L. Jat, J. Org. Chem., 2018, 83, 12255-12260.
DOI: 10.1021/acs.joc.8b01673
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Abstract
A highly efficient Rh(II)-catalyzed direct preparation of unactivated aziridines from olefins relies on O-(sulfonyl)hydroxylamines as the aminating agents. The reactions proceed with high stereospecificity.
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Metal- and Additive-Free Intermolecular Aziridination of Olefins Using N-Boc-O-tosylhydroxylamine
J. L. Jat, D. Chandra, P. Kumar, V. Singh, B. Tiwari, Synthesis, 2022, 54, 4513-4520.
Key Words
ID: J42-Y2018
