| Literature DB >> 27158802 |
Julien Buendia1, Gwendal Grelier1, Benjamin Darses1, Amanda G Jarvis1, Frédéric Taran2, Philippe Dauban3.
Abstract
Iodine(III) reagents are used in catalytic one-pot reactions, first as both oxidants and substrates, then as cross-coupling partners, to afford chiral polyfunctionalized amines. The strategy relies on an initial catalytic auto C(sp(3) )-H amination of the iodine(III) oxidant, which delivers an amine-derived iodine(I) product that is subsequently used in palladium-catalyzed cross-couplings to afford a variety of useful building blocks with high yields and excellent stereoselectivities. This study demonstrates the concept of self-amination of the hypervalent iodine reagents, which increases the value of the aryl moiety.Entities:
Keywords: C−H amination; cross-coupling; homogeneous catalysis; hypervalent iodine; tandem synthesis
Year: 2016 PMID: 27158802 DOI: 10.1002/anie.201602022
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336