Literature DB >> 28240440

Catalytic Enantioselective γ-Selective Additions of 2-Allylazaarenes to Activated Ketones.

Xiangbin Bai1, Guangkuo Zeng1, Tianju Shao1, Zhiyong Jiang1.   

Abstract

Reported herein is the first example of 2-allylazaarenes in asymmetric catalysis. Highly γ-selective allylation was demonstrated for activated ketones, including isatins and trifluoromethyl ketones. In the presence of either an amino-acid-based tertiary amine or quaternary ammonium salt catalyst, two series of tertiary hydroxy-containing moieties were installed at the remote δ-position of azaarenes in good chemical yields, excellent enantioselectivities, and E/Z ratios. The success of current γ-selective reactions should provide inspiration for expansion to other allylazaarene derivatives and would open up new paradigms for the synthesis of chiral γ- and/or δ-functionalized azaarenes.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  allylic compounds; arenes; heterocycles; organocatalysis; synthetic methods

Year:  2017        PMID: 28240440     DOI: 10.1002/anie.201700190

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  3 in total

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Journal:  Chemistry       Date:  2021-11-11       Impact factor: 5.020

3.  Acetic Acid Promoted Redox Annulations with Dual C-H Functionalization.

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  3 in total

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