Literature DB >> 27158802

The Multiple Facets of Iodine(III) Compounds in an Unprecedented Catalytic Auto-amination for Chiral Amine Synthesis.

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.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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


  3 in total

1.  Organocatalytic nitrenoid transfer: metal-free selective intermolecular C(sp3)-H amination catalyzed by an iminium salt.

Authors:  Logan A Combee; Balaram Raya; Daoyong Wang; Michael K Hilinski
Journal:  Chem Sci       Date:  2017-11-27       Impact factor: 9.825

Review 2.  Atom-economical group-transfer reactions with hypervalent iodine compounds.

Authors:  Andreas Boelke; Peter Finkbeiner; Boris J Nachtsheim
Journal:  Beilstein J Org Chem       Date:  2018-05-30       Impact factor: 2.883

3.  Exploration of Novel Chemical Space: Synthesis and in vitro Evaluation of N-Functionalized Tertiary Sulfonimidamides.

Authors:  Flavia Izzo; Martina Schäfer; Philip Lienau; Ursula Ganzer; Robert Stockman; Ulrich Lücking
Journal:  Chemistry       Date:  2018-06-19       Impact factor: 5.236

  3 in total

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