Paper
Highly cis-selective synthesis of iodo-aziridines using diiodomethyllithium and in situ generated N-Boc-imines.
Published Nov 21, 2012 · J. Bull, Tom Boultwood, T. Taylor
Chemical communications
Q1 SJR score
24
Citations
0
Influential Citations
Abstract
The first preparation of iodoaziridines is described. The addition of diiodomethyllithium to N-Boc-imines affords these novel aziridines in high yields. The reaction proceeds in one-pot via a highly diastereoselective cyclisation of an amino gem-diiodide intermediate.
Study Snapshot
This study presents a novel one-pot synthesis of iodoaziridines using diiodomethyllithium and N-Boc-imines, enabling the rapid and efficient preparation of novel aziridines.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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