Abstract
Sulfonylimino-λ3-bromane functions as a reactive nitrenoid, because of the hyperleaving group ability of aryl- λ3-bromanyl groups, and undergoes transimidations to iodobenzenes at room temperature under metal-free conditions probably via an SN2-type nitrenoid transition state, yielding sulfonylimino- λ3-iodanes.
Original language | English (US) |
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Pages (from-to) | 959-961 |
Number of pages | 3 |
Journal | Chemical Communications |
Issue number | 8 |
DOIs | |
State | Published - 2009 |
Externally published | Yes |