| Literature DB >> 19618903 |
Ian K Mangion1, Ikenna K Nwamba, Michael Shevlin, Mark A Huffman.
Abstract
The unique reactivity of sulfoxonium ylides as a carbene source is described for a variety of X-H bond insertions, taking advantage of a simple, commercially available iridium catalyst. This method has applications in both intra- and intermolecular reactivity, including a practical ring-expansion strategy for lactams. The safety and stability of sulfoxonium ylides recommend them as preferable surrogates to traditional diazo ketones and esters.Entities:
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Year: 2009 PMID: 19618903 DOI: 10.1021/ol901298p
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005