Weijia Xie

发表

Total synthesis, structural elucidation and anti-inflammatory activity evaluation of 2-deoxy-3,6-anhydro hexofuranoside derivatives isolated from Sauropus rostratus.

Xiao-ming Wu, Jinyi Xu, G. Tanabe, 2016, Organic & biomolecular chemistry.

6,7-Seco-ent-Kauranoids Derived from Oridonin as Potential Anticancer Agents.

Zhe-Sheng Chen, Shengtao Xu, Hequan Yao, 2017, Journal of natural products.

Design, synthesis and biological evaluation of novel nitric oxide-donating protoberberine derivatives as antitumor agents.

Shengtao Xu, Hequan Yao, Jinyi Xu, 2017, European journal of medicinal chemistry.

Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor.

Xiao-ming Wu, M. Yoshikawa, G. Tanabe, 2011, Bioorganic & medicinal chemistry.

Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent α-glucosidase inhibitors.

Xiao-ming Wu, T. Morikawa, M. Yoshikawa, 2011, Bioorganic & medicinal chemistry.

Another mode of heterocyclization of an enantiopure C2-symmetric bis-epoxide leading to the symmetric dialkyl sulfide

Xiao-ming Wu, G. Tanabe, O. Muraoka, 2010 .

Probing the Anticancer Action of Oridonin with Fluorescent Analogues: Visualizing Subcellular Localization to Mitochondria.

Zhe-Sheng Chen, Dong-Hua Yang, Shanshan Luo, 2016, Journal of medicinal chemistry.

Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor. Part 2.

I. Nakanishi, Xiao-ming Wu, M. Yoshikawa, 2012, Bioorganic & medicinal chemistry.

In silico design, synthesis and evaluation of 3'-O-benzylated analogs of salacinol, a potent α-glucosidase inhibitor isolated from an Ayurvedic traditional medicine "Salacia".

I. Nakanishi, T. Morikawa, M. Yoshikawa, 2012, Chemical communications.

Hydrophobic substituents increase the potency of salacinol, a potent α-glucosidase inhibitor from Ayurvedic traditional medicine 'Salacia'.

I. Nakanishi, T. Morikawa, Shinya Nakamura, 2016, Bioorganic & medicinal chemistry.

Design, Synthesis and Biological Evaluation of Nitrate Derivatives of Sauropunol A and B as Potent Vasodilatory Agents

Rigang Cong, Xiao-ming Wu, Jinyi Xu, 2019, Molecules.

Regioselective ortho olefination of aryl sulfonamide via rhodium-catalyzed direct C-H bond activation.

J. Yang, Baiquan Wang, Weijia Xie, 2014, The Journal of organic chemistry.

Ruthenium-catalyzed regioselective C2 alkenylation of indoles and pyrroles via C-H bond functionalization.

Haibin Song, Baiquan Wang, Shansheng Xu, 2013, The Journal of organic chemistry.

Antioxidant Properties of Novel Dimers Derived from Natural β-Elemene through Inhibiting H2O2-Induced Apoptosis.

Shengtao Xu, Hequan Yao, Jinyi Xu, 2017, ACS medicinal chemistry letters.

A Novel Potent Anticancer Compound Optimized from a Natural Oridonin Scaffold Induces Apoptosis and Cell Cycle Arrest through the Mitochondrial Pathway.

Zhe-Sheng Chen, Dong-Hua Yang, Shanshan Luo, 2017, Journal of medicinal chemistry.

2-Diphenylphosphinoyl-acetyl as a remote directing group for the highly stereoselective synthesis of β-glycosides

Huiyong Sun, Biao Yu, Haopeng Sun, 2021, Chinese Journal of Chemistry.

Regioselective C2 Oxidative Olefination of Indoles and Pyrroles through Cationic Rhodium(III)-Catalyzed C-H Bond Activation.

Baiquan Wang, Shansheng Xu, Weijia Xie, 2013, Chemistry.

Novel nitric oxide-releasing isochroman-4-one derivatives: Synthesis and evaluation of antihypertensive activity.

Xiao-ming Wu, Jieyun Jiang, Hequan Yao, 2012, Bioorganic & medicinal chemistry.

Recent Advances for the Synthesis of Selenium-containing Small Molecules as Potent Antitumor Agents.

Xiao-ming Wu, Jinyi Xu, A. Lin, 2018, Current medicinal chemistry.

Ligand compatibility of salacinol-type α-glucosidase inhibitors toward the GH31 family

I. Nakanishi, T. Morikawa, Shinya Nakamura, 2021, RSC advances.

The Construction of Anhydro Monosaccharides

Xiao-ming Wu, Jinyi Xu, A. Lin, 2017 .

Facile synthesis of de-O-sulfated salacinols: revision of the structure of neosalacinol, a potent alpha-glucosidase inhibitor.

M. Yoshikawa, G. Tanabe, O. Muraoka, 2009, Bioorganic & medicinal chemistry letters.

More than a Leaving Group: N-Phenyltrifluoroacetimidate as a Remote Directing Group for Highly α-Selective 1,2-cis Glycosylation.

W. Li, Wei Liu, Huiyong Sun, 2022, Angewandte Chemie.

Design, synthesis and biological evaluation of 3'-benzylated analogs of 3'-epi-neoponkoranol as potent α-glucosidase inhibitors.

Xiao-ming Wu, G. Tanabe, O. Muraoka, 2016, European journal of medicinal chemistry.

Synthetic study on neoponkoranol and its side chain epimer as potent α-glucosidase inhibitors, optimization of protecting group

Xiao-ming Wu, Hequan Yao, Jinyi Xu, 2013 .

Synthesis and biological evaluation of 4'-[(benzimidazole-1-yl)methyl]biphenyl-2-sulfonamide derivatives as dual angiotensin II/endothelin A receptor antagonists.

Xiao-ming Wu, Jieyun Jiang, Hequan Yao, 2012, Bioorganic & Medicinal Chemistry.

Synthetic studies on naturally occurring sulfonium-type α-glucosidase inhibitors: progress and perspective

G. Tanabe, O. Muraoka, Weijia Xie, 2022, Journal of Carbohydrate Chemistry.

Recent Progress in Construction of Natural De-O-sulfonated Sulfonium Sugars with Antidiabetic Activities.

Weijia Xie, Yao Yang, Xiaoya Li, 2019, Chemistry.

Practical Route to Neokotalanol and Its Natural Analogues: Sulfonium Sugars with Antidiabetic Activities.

Xiao-ming Wu, Jinyi Xu, G. Tanabe, 2019, Angewandte Chemie.

Practical Route to Neokotalanol and Its Natural Analogues: Sulfonium Sugars with Antidiabetic Activities

Xiao-ming Wu, Jinyi Xu, G. Tanabe, 2019, Angewandte Chemie.

Facile Synthesis of Neokotalanol, a Potent α-glycosidase Inhibitor Isolated from the Ayurvedic Traditional Medicine “Salacia”

G. Tanabe, Shinsuke Marumoto, F. Ishikawa, 2019, ACS Omega.

Research Progress of Synthesis and Structure-activity Relationship Studies on Sulfonium-type α-glucosidase Inhibitors Isolated from Salacia Genus Plants

Xiao-ming Wu, Jinyi Xu, T. Morikawa, 2013 .

Characteristic alkaline catalyzed degradation of kotalanol, a potent α-glucosidase inhibitor isolated from Ayurvedic traditional medicine Salacia reticulata, leading to anhydroheptitols: another structural proof.

T. Morikawa, M. Yoshikawa, G. Tanabe, 2010 .

Facile Synthesis of De-O-sulfated Salacinols: Revision of the Structure of Neosalacinol, a Potent α-Glucosidase Inhibitor.

M. Yoshikawa, G. Tanabe, O. Muraoka, 2009 .

On the structure of the bioactive constituent from ayurvedic medicine Salacia reticulata: revision of the literature

M. Yoshikawa, G. Tanabe, O. Muraoka, 2008 .

Diastereoselective Synthesis of Salacinol-Type α-Glucosidase Inhibitors.

T. Morikawa, G. Tanabe, Shinsuke Marumoto, 2018, The Journal of organic chemistry.

Practical Synthesis of Neoponkoranol and its Related Sulfonium Salt, an Optimised Protocol using Isopropylidene as an Effective Protecting Group

Xiao-ming Wu, Hequan Yao, Jinyi Xu, 2013 .

Novel hybrids of natural β-elemene bearing isopropanolamine moieties: Synthesis, enhanced anticancer profile, and improved aqueous solubility.

Shengtao Xu, Hequan Yao, Jinyi Xu, 2017, Fitoterapia.

First total synthesis of cyclic pentadepsipeptides Hikiamides A–C

Xiao-ming Wu, Jinyi Xu, Dong-mei Fu, 2018, Tetrahedron Letters.

First Total Syntheses of Amorfrutin C and pseudo‐Amorfrutin A

Xiao-ming Wu, Jinyi Xu, G. Tanabe, 2018 .

Discovery of novel antitumor nitric oxide-donating β-elemene hybrids through inhibiting the PI3K/Akt pathway.

Shengtao Xu, Pengfei Zhang, Hequan Yao, 2017, European journal of medicinal chemistry.

Glutathione-depleted cyclodextrin pseudo-polyrotaxane nanoparticles for anti-inflammatory oxaliplatin (IV) prodrug delivery and enhanced colorectal cancer therapy

Lei Xing, G. Tanabe, O. Muraoka, 2023, Chinese Chemical Letters.

Regioselective C2 Oxidative Olefination of Indoles and Pyrroles through Cationic Rhodium(III)-Catalyzed C-H Bond Activation.

Baiquan Wang, Shansheng Xu, Weijia Xie, 2013, Chemistry.

Ruthenium-catalyzed regioselective C2 alkenylation of indoles and pyrroles via C-H bond functionalization.

Baiquan Wang, Shansheng Xu, Weijia Xie, 2013, The Journal of organic chemistry.