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Chemistry

D-Index
49
Citations
6971
World Ranking
14994
National Ranking
1096

Overview

Xiulan Xie is affiliated with Philipp University of Marburg in Germany. Their research primarily focuses on materials science and chemistry, with significant contributions in the subfields of materials chemistry, organic chemistry, and inorganic chemistry. The scientist's work also extends to molecular biology and pharmacology.

The main topics covered in their research include:

  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Asymmetric Hydrogenation and Catalysis
  • Catalytic C-H Functionalization Methods
  • Synthesis and Catalytic Reactions
  • Microbial Natural Products and Biosynthesis
  • Synthesis and characterization of novel inorganic/organometallic compounds

Xiulan Xie's publications appear frequently in several established scientific journals. The primary venues include:

  • The Cambridge Structural Database
  • Angewandte Chemie International Edition
  • Angewandte Chemie
  • Organic Letters
  • Chemistry - A European Journal

Recent papers authored or co-authored by Xiulan Xie are as follows:

  • Atroposelective Synthesis of Axially Chiral N-Arylpyrroles by Chiral-at-Rhodium Catalysis (2020, Angewandte Chemie International Edition)
  • Enantioselective Ring-Closing C-H Amination of Urea Derivatives (2020, Chem)
  • Au@SiO2 SERS nanotags based lateral flow immunoassay for simultaneous detection of aflatoxin B1 and ochratoxin A (2023, Talanta)
  • Asymmetric Ring-Closing Aminooxygenation of Alkenes en Route to 2-Amino-1,3-Diols with Vicinal Stereocenters (2020, Organic Letters)
  • Increasing cytochrome P450 enzyme diversity by identification of two distinct cyclodipeptide dimerases (2020, Chemical Communications)

The scientist collaborates frequently with several peers, indicating a network of ongoing research partnerships. Frequent co-authors include:

  • Eric Meggers
  • Sergei I. Ivlev
  • Florian Weigend
  • Crispin Lichtenberg
  • Jörg Sundermeyer

Best Publications

  • Lasso Peptides: An Intriguing Class of Bacterial Natural Products

    Julian D. Hegemann;Marcel Zimmermann;Xiulan Xie;Mohamed A. Marahiel

  • Synthesis, characterization and cytotoxicity of poly(ethylene glycol)-graft-trimethyl chitosan block copolymers.

    Shirui Mao;Xintao Shuai;Florian Unger;Matthias Wittmar

  • Asymmetric NH Insertion Reaction Cooperatively Catalyzed by Rhodium and Chiral Spiro Phosphoric Acids

    Bin Xu;Shou-Fei Zhu;Xiu-Lan Xie;Jun-Jie Shen

  • Isolation and structural characterization of capistruin, a lasso peptide predicted from the genome sequence of Burkholderia thailandensis E264.

    Thomas A Knappe;Uwe Linne;Séverine Zirah;Sylvie Rebuffat

  • Catalytic Asymmetric Dearomatization by Visible-Light-Activated [2+2] Photocycloaddition.

    Naifu Hu;Hoimin Jung;Yu Zheng;Juhyeong Lee

  • The Cofactor of the Iron–Sulfur Cluster Free Hydrogenase Hmd: Structure of the Light-Inactivation Product

    Seigo Shima;Erica J. Lyon;Melanie Sordel-Klippert;Manuela Kauss

  • Insights into the Unique Phosphorylation of the Lasso Peptide Paeninodin

    Shaozhou Zhu;Julian D. Hegemann;Christopher D. Fage;Marcel Zimmermann

  • Introducing Lasso Peptides as Molecular Scaffolds for Drug Design: Engineering of an Integrin Antagonist

    Thomas A. Knappe;Florian Manzenrieder;Carlos Mas-Moruno;Uwe Linne

  • Enantioselective palladium-catalyzed insertion of α-aryl-α-diazoacetates into the O-H bonds of phenols.

    Xiu-Lan Xie;Shou-Fei Zhu;Jun-Xia Guo;Yan Cai

  • Caulosegnins I–III: A Highly Diverse Group of Lasso Peptides Derived from a Single Biosynthetic Gene Cluster

    Julian D. Hegemann;Marcel Zimmermann;Xiulan Xie;Mohamed A. Marahiel

  • The Astexin-1 Lasso Peptides: Biosynthesis, Stability, and Structural Studies

    Marcel Zimmermann;Julian D. Hegemann;Xiulan Xie;Mohamed A. Marahiel

  • Metal-Templated Design: Enantioselective Hydrogen-Bond-Driven Catalysis Requiring Only Parts-per-Million Catalyst Loading

    Weici Xu;Marcus Arieno;Henrik Löw;Kaifang Huang

  • Biochemical characterization of indole prenyltransferases: filling the last gap of prenylation positions by a 5-dimethylallyltryptophan synthase from Aspergillus clavatus.

    Xia Yu;Yan Liu;Yan Liu;Xiulan Xie;Xiao-Dong Zheng

  • Structure-function analysis of an enzymatic prenyl transfer reaction identifies a reaction chamber with modifiable specificity.

    Marco Jost;Georg Zocher;Sylwia Tarcz;Marco Matuschek

  • Solid-State NMR Spectroscopy of Paramagnetic Metallocenes

    Henrike Heise;Frank H Köhler;Xiulan Xie

  • Rational improvement of the affinity and selectivity of integrin binding of grafted lasso peptides.

    Julian D. Hegemann;Mariarosaria De Simone;Mariarosaria De Simone;Marcel Zimmermann;Thomas A. Knappe

  • The glucagon receptor antagonist BI‐32169 constitutes a new class of lasso peptides

    Thomas A. Knappe;Uwe Linne;Xiulan Xie;Mohamed A. Marahiel

  • Enantioselective Iron-Catalyzed Intramolecular Cyclopropanation Reactions†

    Jun-Jie Shen;Shou-Fei Zhu;Yan Cai;Huan Xu

  • Asymmetric NH Insertion Reaction Cooperatively Catalyzed by Rhodium and Chiral Spiro Phosphoric Acids

    Unknown

  • Xanthomonins I-III: a new class of lasso peptides with a seven-residue macrolactam ring.

    Julian D. Hegemann;Marcel Zimmermann;Shaozhou Zhu;Holger Steuber

  • Effects of cell-penetrating peptides and pegylation on transfection efficiency of polyethylenimine in mouse lungs.

    Juliane Nguyen;Xiulan Xie;Michael Neu;Rio Dumitrascu

  • Catalytic asymmetric synthesis of a nitrogen heterocycle through stereocontrolled direct photoreaction from electronically excited state

    Xiaoqiang Huang;Xinyao Li;Xiulan Xie;Klaus Harms

  • An Organometallic Inhibitor for the Human Repair Enzyme 7,8-Dihydro-8-oxoguanosine Triphosphatase.

    Manuel Streib;Katja Kräling;Kristin Richter;Xiulan Xie

  • Structure and catalytic mechanism of a cyclic dipeptide prenyltransferase with broad substrate promiscuity.

    Jan Michael Schuller;Georg Zocher;Mike Liebhold;Xiulan Xie

  • Ergot alkaloid biosynthesis in Aspergillus fumigatus: Conversion of chanoclavine-I aldehyde to festuclavine by the festuclavine synthase FgaFS in the presence of the old yellow enzyme FgaOx3†

    Christiane Wallwey;Marco Matuschek;Xiu-Lan Xie;Shu-Ming Li

Frequent Co-Authors

Shu-Ming Li
Shu-Ming Li Philipp University of Marburg
Mohamed A. Marahiel
Mohamed A. Marahiel Philipp University of Marburg
Eric Meggers
Eric Meggers Philipp University of Marburg
Uwe Linne
Uwe Linne Philipp University of Marburg
Klaus Harms
Klaus Harms Philipp University of Marburg
Florian Weigend
Florian Weigend Philipp University of Marburg
Seigo Shima
Seigo Shima Max Planck Society
Jörg Sundermeyer
Jörg Sundermeyer Philipp University of Marburg
Stefanie Dehnen
Stefanie Dehnen Karlsruhe Institute of Technology
Ulrich Ermler
Ulrich Ermler Max Planck Society

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