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Anesthesia and perioperative management for cesarean section in patient with factor XI deficiency: a case report.
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- Journal of Health Sciences of Peking University / Beijing Daxue Xuebao (Yixue Ban), 2014, v. 46, n. 2, p. 329, doi. 10.3969/j.issn.1671-167X.2014.02.031
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- Article
A case of anesthesia for caesarean section in a late pregnant woman with recurrent femoral osteosarcoma.
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- Journal of Health Sciences of Peking University / Beijing Daxue Xuebao (Yixue Ban), 2011, v. 43, n. 6, p. 908
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- Article
One-step synthesis of 2,4,5-trisubstituted pyrimidines.
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- Journal of Heterocyclic Chemistry, 2011, v. 48, n. 5, p. 1073, doi. 10.1002/jhet.606
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- Article
One-step synthesis of 2-amino-5-(4,5-diphenylpyrimidin-2-ylamino)pentanoic acid from isoflavones and arginine.
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- Journal of Heterocyclic Chemistry, 2010, v. 47, n. 5, p. 1209, doi. 10.1002/jhet.466
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- Article
De Novo Synthesis of α‐Ketoamides via Pd/TBD Synergistic Catalysis.
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- Advanced Science, 2024, v. 11, n. 34, p. 1, doi. 10.1002/advs.202404266
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- Article
Early Diastolic Peak Velocity of Mitral Valve Annulus and Right Ventricular Systolic Tricuspid Annular Velocity as Predictors in Assessing Prognosis of Patients with Sepsis.
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- Risk Management & Healthcare Policy, 2023, v. 16, p. 921, doi. 10.2147/RMHP.S407929
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- Article
Trifluoromethyl Rhodium‐Carbynoid in [2+1+2] Cycloadditions.
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- Angewandte Chemie, 2024, v. 136, n. 13, p. 1, doi. 10.1002/ange.202318887
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- Article
Biocatalytic Thionation of Epoxides for Enantioselective Synthesis of Thiiranes.
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- Angewandte Chemie, 2022, v. 134, n. 52, p. 1, doi. 10.1002/ange.202212589
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- Article
Trifluoromethyl Rhodium‐Carbynoid in [2+1+2] Cycloadditions.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 13, p. 1, doi. 10.1002/anie.202318887
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- Article
Biocatalytic Thionation of Epoxides for Enantioselective Synthesis of Thiiranes.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 52, p. 1, doi. 10.1002/anie.202212589
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- Article
Front Cover Picture: Synthesis of Fluoroalkylated Pyrrolidines through Neat Reaction of Fluoroalkyl Iodides with N, N‐Diallylamines (Adv. Synth. Catal. 18/2023).
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- Advanced Synthesis & Catalysis, 2023, v. 365, n. 18, p. 2989, doi. 10.1002/adsc.202300599
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- Article
Synthesis of Fluoroalkylated Pyrrolidines through Neat Reaction of Fluoroalkyl Iodides with N, N‐Diallylamines.
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- Advanced Synthesis & Catalysis, 2023, v. 365, n. 18, p. 3063, doi. 10.1002/adsc.202300092
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- Article
Stereoselective Synthesis of Enantiopure Oxazolidinones via Biocatalytic Asymmetric Aminohydroxylation of Alkenes.
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- Advanced Synthesis & Catalysis, 2021, v. 363, n. 18, p. 4343, doi. 10.1002/adsc.202100468
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- Article
Chiral Phosphoric Acid Catalyzed (4+1) Annulation of 3‐Diazooxindoles/4‐Diazooxisoquinolines with para‐Quinone Methides to Access Chiral Spiro[dihydrobenzofuran‐2,3′‐oxindoles/2,4′‐oxisoquinolines].
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- Advanced Synthesis & Catalysis, 2021, v. 363, n. 6, p. 1702, doi. 10.1002/adsc.202001309
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- Article
Efficient Assembly of Molecular Complexity Enabled by Palladium‐Catalyzed Heck Coupling/C(sp<sup>2</sup>)−H Activation/ C(sp<sup>3</sup>)−H Activation Cascade.
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- Advanced Synthesis & Catalysis, 2020, v. 362, n. 17, p. 3655, doi. 10.1002/adsc.202000488
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- Article
Cover Picture: Recent Advances of α-Isothiocyanato Compounds in the Catalytic Asymmetric Reaction (Adv. Synth. Catal. 14-15/2015).
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 14/15, p. 2961, doi. 10.1002/adsc.201500741
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- Article
Recent Advances of α-Isothiocyanato Compounds in the Catalytic Asymmetric Reaction.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 14/15, p. 3007, doi. 10.1002/adsc.201500264
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- Article
3-Isothiocyanato Oxindoles Serving as Powerful and Versatile Precursors to Structurally Diverse Dispirocyclic Thiopyrrolidineoxindoles through a Cascade Michael/Cyclization Process with Amino-Thiocarbamate Catalysts.
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- Chemistry - A European Journal, 2013, v. 19, n. 18, p. 5551, doi. 10.1002/chem.201300206
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- Article
Organocatalytic Enantioselective Stereoablative Hydroxylation of 3-Halooxindoles: An Effective Method for the Construction of Enantioenriched 3-Substituted 3-Hydroxy-2-Oxindoles.
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- Chemistry - A European Journal, 2012, v. 18, n. 29, p. 8916, doi. 10.1002/chem.201201395
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- Article