| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223170 | Tetrahedron | 2009 | 6 Pages |
Abstract
The utility of N-sulfonylimines as radical acceptors was investigated under the different reaction conditions such as the stannyl radical-mediated addition reaction, the triethylborane-mediated tin-free radical reaction, and the zinc-mediated aqueous-medium radical reaction. The alkyl radical addition reaction of N-sulfonylimines proceeded effectively without the activation by Lewis acid. These reactions were successfully extended to one-pot reactions for preparing a wide range of amine derivatives.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Masafumi Ueda, Hideto Miyabe, Okiko Miyata, Takeaki Naito,