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Er-Lei Zhang

Researcher at Wenzhou University

Publications -  5
Citations -  246

Er-Lei Zhang is an academic researcher from Wenzhou University. The author has contributed to research in topics: Catalysis & Alkylation. The author has an hindex of 3, co-authored 4 publications receiving 200 citations.

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Iron-Catalyzed Direct Synthesis of Imines from Amines or Alcohols and Amines via Aerobic Oxidative Reactions under Air

TL;DR: Abundant and cheap iron readily catalyzed the aerobic oxidative reactions of primary amines, secondary amine, benzylamines with anilines, and alcohols with amines by directly using air as the economic and safe oxidant, providing several direct, practical, and greener approaches for the preparation of useful imines.
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Selective catalytic Hofmann N-alkylation of poor nucleophilic amines and amides with catalytic amounts of alkyl halides

TL;DR: Using only catalytic amounts of alkyl halides in the reactions of poor nucleophilic amines/amides and alcohols led to a selective Hofmann N-alkylation reaction catalytic in alkyls, providing a practical and efficient method for the practical synthesis of mono- or dialkylated amines and amides in high selectivities as discussed by the authors.
Journal ArticleDOI

Iron-Catalyzed Direct Synthesis of Imines from Amines or Alcohols and Amines via Aerobic Oxidative Reactions under Air.

TL;DR: In this article, it was shown that abundant and cheap iron readily catalyzed the aerobic oxidative reactions of primary amines, secondary amines and alcohols with amines by directly using air as the economic and safe oxidant, providing several direct, practical, and greener approaches for the preparation of useful imines.
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Lysine demethylase KDM1A promotes cell growth via FKBP8–BCL2 axis in hepatocellular carcinoma

TL;DR: In this paper , the authors showed that KDM1A can interact with and demethylate FKBP8 (FKBP prolyl isomerase 8), a cytoplasmic protein that regulates cell survival through the antiapoptotic protein BCL2 (B-cell lymphoma-2).
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Selective Catalytic Hofmann N-Alkylation of Poor Nucleophilic Amines and Amides with Catalytic Amounts of Alkyl Halides.

TL;DR: Using only catalytic amounts of alkyl halides in the reactions of poor nucleophilic amines/amides and alcohols led to a selective Hofmann N-alkylation reaction catalytic in alkyls, providing a practical and efficient method for the practical synthesis of mono- or dialkylated amines and amides in high selectivities as mentioned in this paper.