Xiaolei Wang

ORCID: 0000-0002-8867-6528
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About
Contact & Profiles
Research Areas
  • Catalytic C–H Functionalization Methods
  • Carbohydrate Chemistry and Synthesis
  • Synthetic Organic Chemistry Methods
  • Chemical synthesis and alkaloids
  • Marine Sponges and Natural Products
  • Radical Photochemical Reactions
  • Advanced Synthetic Organic Chemistry
  • Synthesis and Catalytic Reactions
  • Sulfur-Based Synthesis Techniques
  • Chemical Synthesis and Analysis
  • Asymmetric Synthesis and Catalysis
  • Microbial Natural Products and Biosynthesis
  • Alkaloids: synthesis and pharmacology
  • Synthesis of Indole Derivatives
  • Oxidative Organic Chemistry Reactions
  • Chemical Synthesis and Reactions
  • Cancer-related gene regulation
  • Cyclopropane Reaction Mechanisms
  • Catalytic Cross-Coupling Reactions
  • Peptidase Inhibition and Analysis
  • Traditional and Medicinal Uses of Annonaceae
  • Catalytic Alkyne Reactions
  • Synthesis and Characterization of Pyrroles
  • Bacterial Infections and Vaccines
  • RNA modifications and cancer

Lanzhou University
2013-2025

Lanzhou Veterinary Research Institute
2022-2025

Chinese Academy of Agricultural Sciences
2024-2025

China Earthquake Administration
2024-2025

State Key Laboratory of Applied Organic Chemistry
2021-2024

Nankai University
2024

Hangzhou First People's Hospital
2022

Zhejiang University
2022

Zhejiang Chinese Medical University
2022

Shenyang University of Technology
2022

Cycloaddition is an essential tool in chemical synthesis. Instead of using light or heat as a driving force, marine sponges promote cycloaddition with more versatile but poorly understood mechanism producing pyrrole-imidazole alkaloids sceptrin, massadine, and ageliferin. Through de novo synthesis sceptrin we show that may use single-electron oxidation central to three different types cycloaddition. Additionally, provide surprising evidence that, contrast previous reports, ageliferin have...

10.1126/science.1255677 article EN Science 2014-10-09

Porcupine is a member of the membrane-bound O-acyltransferase family proteins. It catalyzes palmitoylation Wnt proteins, process required for their secretion and activity. We recently disclosed class small molecules (IWPs) as first reported Porcn inhibitors. now describe structure–activity relationship studies identification subnanomolar also report herein effects IWPs on Wnt-dependent developmental processes, including zebrafish posterior axis formation kidney tubule formation.

10.1021/jm400159c article EN Journal of Medicinal Chemistry 2013-03-11

Simple and cheap alcohols can promote the direct arylation of unactivated arenes with aryl iodides bromides in presence potassium tert-butoxide. This transition-metal-free aromatic C–H transformation offers a easy practical way to synthesize biaryls under mild conditions.

10.1039/c3cc40695d article EN Chemical Communications 2013-01-01

A platinum-catalyzed tandem reaction involving enynyl ester isomerization and subsequent intramolecular [3 + 2] cyclization has been developed. This strategy provides an efficient approach to five-, six-, or seven-membered cyclic polyfunctional compounds.

10.1021/ja910346m article EN Journal of the American Chemical Society 2010-01-25

This report describes palladium-catalyzed C-H glycosylation and retro Diels-Alder tandem reaction via structurally modified norbornadienes (smNBDs). smNBDs were proposed to regulate the reactivity of aryl-norbornadiene-palladacycle (ANP), including its high chemoselectivity regioselectivity, which key constructing C2 C3 unsubstituted C4-glycosidic indoles. The scope this substrate is extensive; halogenated six-membered five-membered glycosides applied smoothly, N-alkyl (primary, secondary...

10.1039/d1sc03569j article EN cc-by-nc Chemical Science 2021-01-01

A novel photocatalyst-free visible-light-mediated dithioacetalization of aldehydes and thiols has been developed.

10.1039/c8gc02237b article EN Green Chemistry 2018-01-01

The pyrrole-imidazole alkaloids have fascinated chemists for decades because of their unique structures. high nitrogen and halogen contents the densely functionalized skeletons make laboratory synthesis challenging. We describe herein an oxidative method accessing core two classes dimers. This synthetic strategy was inspired by putative biosynthesis pathways its development facilitated computational studies. Using this method, we successfully prepared ageliferin, bromoageliferin,...

10.1021/ja309172t article EN Journal of the American Chemical Society 2012-10-17

A strategy for the synthesis of multisubstituted hydrocarbazoles has been developed through (3 + 2)-annulation p-quinamines and arynes. In this way, new analogs with quaternary carbon center can be synthesized in satisfactory yield under mild conditions. Furthermore, easily scaled-up, products modified simple transformation.

10.1021/acs.orglett.7b01578 article EN Organic Letters 2017-06-28

Open AccessCCS ChemistryRESEARCH ARTICLE7 Nov 2022Enzyme-like C–H Oxidation of Glucosides Promoted by Visible Light Mingzhong Wu, Qian Jiang, Qiong Tian, Tianyun Guo, Feng Cai, Shouchu Tang, Jian Liu and Xiaolei Wang Wu State Key Laboratory Applied Organic Chemistry, Department Chemistry School Pharmacy, Lanzhou University, 730000 , Jiang Tian Veterinary Etiological Biology, OIE/National Foot Mouth Disease Reference Laboratory, Guo Cai The National Glycoengineering Research Center, Shandong...

10.31635/ccschem.022.202101621 article EN cc-by-nc CCS Chemistry 2022-01-13

Concise and efficient asymmetric total syntheses of three substituted α-pyrone-type natural products have been accomplished via 7−9 steps from 5b in high overall yields, which involve linchpin coupling, ring-closing metathesis, a tandem sequence deacetylation intramolecular oxa-Michael addition as the key steps.

10.1021/ol901024t article EN Organic Letters 2009-06-19

The development of a visible-light mediated bromo radical addition/spirocyclization/ester migration cascade reaction to generate 3-bromocoumarins from alkynoates is reported.

10.1039/c7ob02199b article EN Organic & Biomolecular Chemistry 2017-01-01

Abstract A series of compounds bearing quinoline‐imidazole ( 8a–e , 9a–e 10a–e 11a–e and 12a–e ) not reported previously were designed synthesized. The target evaluated for antitumor activity against A549, PC‐3, HepG2, MCF‐7 cells by the MTT method, with NVP‐BEZ235 being positive control. Most showed moderate compound 12a best PC‐3 cells, half‐maximal inhibitory concentration (IC 50 values 2.42 ± 1.02 µM, 6.29 0.99 5.11 1.00 respectively, which was equal to (0.54 0.13 0.36 0.06 0.20 0.01...

10.1002/ardp.201700407 article EN Archiv der Pharmazie 2018-05-07

The first total synthesis of Gardneria oxindole alkaloid (−)-gardmultimine A has been achieved in 19 steps from d-tryptophan a fully stereocontrolled manner. This features (1) an Ir-catalyzed regioselective C–H borylation/oxidation sequence to introduce the C12 methoxyl group, (2) oxidative rearrangement indole construct spirooxindole motif, and (3) Au(I)-catalyzed transannular Conia-ene-type 6-exo-dig cyclization establish azabicyclo[2.2.2]octane skeleton exocyclic E-alkene with exclusive...

10.1021/acs.orglett.0c00399 article EN Organic Letters 2020-02-25

Klebsiella pneumoniae found in the normal flora of human oral and intestinal tract mainly causes hospital-acquired infections but can also cause community-acquired infections. To date, most clinical trials vaccines against K. have ended failure. Furthermore, no single conserved protein has been identified as an antigen candidate to accelerate vaccine development. In this study, we five outer membrane proteins , namely, Kpn_Omp001, Kpn_Omp002, Kpn_Omp003, Kpn_Omp004, Kpn_Omp005, by using...

10.3389/fimmu.2021.730116 article EN cc-by Frontiers in Immunology 2021-10-20

Adjuvants are crucial agents that enhance the immunogenicity of vaccines, with QS-21 being particularly noteworthy for its potent immunostimulatory properties. QS-21, a saponin-based vaccine adjuvant isolated from bark Quillaja saponaria, has garnered significant attention. However, application as is limited due to scarcity, complex chemical synthesis, and inherent toxicity. This study aims develop analogues simplified structures, enhanced immunogenicity, reduced Our research findings...

10.1021/acs.jmedchem.4c02173 article EN Journal of Medicinal Chemistry 2025-01-02

Here we present a regio- and stereoselective alkylation approach for unprotected saccharides using synergistic boronic acid photoredox catalysis. Targeting the equatorial C-H bond of cis-1,2-diol motif, this method employs MeB(OH)2 as catalyst. Mechanistic investigations indicate that formation tetracoordinate boron species, resulting from interaction between cyclic diol ester free hydroxyl group in saccharide, is critical to transformation. Notably, enables efficient late-stage modification...

10.1021/acs.orglett.4c04425 article EN Organic Letters 2025-01-12

A modular total synthesis of A201E and its analogues is modeled after the previously reported biosynthetic pathway. The challenging task obtaining 1,2-cis-furanoside, a vital core structure analogues, was accomplished through strategic use remote 2-quinolinecarbonyl-assisted glycosylation. From this pivotal 1,2-cis-furanoside moiety, we successfully completed analogues. Guided by principles medicinal chemistry, evaluated antimicrobial activities A201A/E comprehensive assessment their has...

10.1021/acs.joc.4c03051 article EN The Journal of Organic Chemistry 2025-02-12

In the field of space gravitational wave detection, high-precision temperature measurement with a resolution at micro-Kelvin level in milli-Hertz frequency range is required to mitigate interference caused by fluctuations around core components. This very challenging task due resistance thermal noise and inherent 1/f electronic To overcome this problem, paper proposes low-noise, high-resolution method based on an inductive voltage divider alternating-current (AC) bridge. The proposed has...

10.3390/s25092777 article EN cc-by Sensors 2025-04-28
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