NMR line-broadening and transverse relaxation time measurements support a di-radical intermediate for the reaction of chlorosulfonyl isocyanate with electron-rich alkenes
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference19 articles.
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2. Recent developments in the synthetic uses of chlorosulfonyl isocyanate;Rasmussen;Chem. Rev.,1976
3. Reduction of N-chlorosulfonyl β-lactams to β-lactams with sodium sulfite;Durst;J. Org. Chem.,1970
4. Synthesis and biological studies of novel β-lactams, a review;Banik,2013
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