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Yanli Yin

Researcher at Henan University

Publications -  22
Citations -  610

Yanli Yin is an academic researcher from Henan University. The author has contributed to research in topics: Catalysis & Enantioselective synthesis. The author has an hindex of 8, co-authored 11 publications receiving 345 citations. Previous affiliations of Yanli Yin include Henan Normal University & Henan University of Technology.

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Conjugate Addition-Enantioselective Protonation of N-Aryl Glycines to α-Branched 2-Vinylazaarenes via Cooperative Photoredox and Asymmetric Catalysis.

TL;DR: An enantioselective protonation strategy has been successfully applied to the synthesis of chiral α-tertiary azaarenes and an application of this methodology to a two-step synthesis of the enantiomerically pure medicinal compound pheniramine is presented.
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All-Carbon Quaternary Stereocenters α to Azaarenes via Radical-Based Asymmetric Olefin Difunctionalization.

TL;DR: A radical-based asymmetric olefin difunctionalization strategy for rapidly forging all-carbon quaternary stereocenters α to diverse azaarenes is reported, achieving high enantio- and diastereo-selectivities for these asymmetric [3 + 2] cycloadditions.
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Chiral acid-catalysed enantioselective C−H functionalization of toluene and its derivatives driven by visible light

TL;DR: The authors report photoinduced radical-based enantioselective C(sp3) −C( sp3) coupling of activated ketones with toluenes by means of chiral acid catalysis to afford enantioenriched tertiary alcohols.
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Organocatalytic Asymmetric Vinylogous Michael Reactions

TL;DR: In this review, the advances in the area of organocatalytic asymmetric vinylogous Michael reactions on the period from 2014 to nowadays are discussed, including the current scope, limitations of the transformations and applications in asymmetric synthesis of complex and valuable compounds.
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Enantioselective reduction of azaarene-based ketones via visible light-driven photoredox asymmetric catalysis.

TL;DR: An enantioselective reduction of azaarene-based ketones through photoredox asymmetric catalysis is reported, providing valuable chiral alcohols in high yields with good to excellent enantiOSElectivities.