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Ginsenoside Rg3 attenuates myocardial ischemia/reperfusion-induced ferroptosis via the keap1/Nrf2/GPX4 signaling pathway.
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- BMC Complementary Medicine & Therapies, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12906-024-04492-4
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- Article
Stereoselective Synthesis of Complex Polyenes through Sequential α‐/β‐C−H Functionalization of trans‐Styrenes.
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- Angewandte Chemie, 2024, v. 136, n. 12, p. 1, doi. 10.1002/ange.202315273
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- Article
Stereoselective Synthesis of Complex Polyenes through Sequential α‐/β‐C−H Functionalization of trans‐Styrenes.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 12, p. 1, doi. 10.1002/anie.202315273
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- Article
Nature's Blueprint: Chelation‐Assisted C−H Functionalization for Selective and Efficient Reactions in Aqueous Media.
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- Israel Journal of Chemistry, 2023, v. 63, n. 10, p. 1, doi. 10.1002/ijch.202300048
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- Article
NHC‐Activations on α‐, β‐, γ‐, and Beyond.
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- Chemical Record, 2023, v. 23, n. 7, p. 1, doi. 10.1002/tcr.202200279
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- Article
Functionality‐Directed Regio‐ and Enantio‐Selective Olefinic C−H Functionalization of Aryl Alkenes.
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- Chemical Record, 2023, v. 23, n. 5, p. 1, doi. 10.1002/tcr.202300012
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- Article
Chiral NHC‐Catalyzed [4+2] Cycloadditions: Highly Diastereo/Enantioselective Access to Spiro[cyclohex‐4‐ene‐1,3′‐indoles] and DFT Calculations.
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- Chemistry - A European Journal, 2023, v. 29, n. 23, p. 1, doi. 10.1002/chem.202203818
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- Article
A Dynamic Kinetic Resolution Approach to Axially Chiral Diaryl Ethers by Catalytic Atroposelective Transfer Hydrogenation.
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- Angewandte Chemie, 2023, v. 135, n. 7, p. 1, doi. 10.1002/ange.202216534
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- Article
A Dynamic Kinetic Resolution Approach to Axially Chiral Diaryl Ethers by Catalytic Atroposelective Transfer Hydrogenation.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 7, p. 1, doi. 10.1002/anie.202216534
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- Article
Recent Progress of Metal Sulfide Photocatalysts for Solar Energy Conversion.
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- Advanced Materials, 2022, v. 34, n. 45, p. 1, doi. 10.1002/adma.202202929
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- Article
Nitrosobenzene‐Enabled Chiral Phosphoric Acid Catalyzed Enantioselective Construction of Atropisomeric N‐Arylbenzimidazoles.
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- Angewandte Chemie, 2021, v. 133, n. 47, p. 25092, doi. 10.1002/ange.202111251
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- Article
Nitrosobenzene‐Enabled Chiral Phosphoric Acid Catalyzed Enantioselective Construction of Atropisomeric N‐Arylbenzimidazoles.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 47, p. 24888, doi. 10.1002/anie.202111251
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- Article
Iridium Catalysed Asymmetric Allylic Substitution Reaction of Indolizine Derivatives.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 6, p. 1500, doi. 10.1002/ajoc.202100171
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- Article
Design and Atroposelective Construction of IAN analogues by Organocatalytic Asymmetric Heteroannulation of Alkynes.
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- Angewandte Chemie, 2020, v. 132, n. 51, p. 23277, doi. 10.1002/ange.202010598
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- Article
Design and Atroposelective Construction of IAN analogues by Organocatalytic Asymmetric Heteroannulation of Alkynes.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 51, p. 23077, doi. 10.1002/anie.202010598
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- Article
Catalytic Asymmetric Dearomative [3+2] Cyclisation of 1,4‐Quinone with 2,3‐Disubstituted Indoles.
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- Advanced Synthesis & Catalysis, 2019, v. 361, n. 23, p. 5449, doi. 10.1002/adsc.201901035
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- Article
Geminal group-directed olefinic C-H functionalization via four- to eight-membered exo-metallocycles.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-13098-1
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- Article
Palladium Catalyzed Controllable Mono‐ or Di‐Allylic Substitution Reaction of Benzothiazolylacetate with Allylic Alcohols.
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- Advanced Synthesis & Catalysis, 2019, v. 361, n. 6, p. 1322, doi. 10.1002/adsc.201801351
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- Article
Roles of Autophagy in Ischemic Heart Diseases and the Modulatory Effects of Chinese Herbal Medicine.
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- American Journal of Chinese Medicine, 2017, v. 45, n. 7, p. 1401, doi. 10.1142/S0192415X17500768
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- Article
Enantioselective Dearomatization of Naphthol Derivatives with Allylic Alcohols by Cooperative Iridium and Brønsted Acid Catalysis.
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- Angewandte Chemie, 2017, v. 129, n. 12, p. 3290, doi. 10.1002/ange.201609693
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- Article
Enantioselective Dearomatization of Naphthol Derivatives with Allylic Alcohols by Cooperative Iridium and Brønsted Acid Catalysis.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 12, p. 3242, doi. 10.1002/anie.201609693
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- Article
Ruthenium(II)-Catalyzed Oxidant-Free C-H Olefination of Aromatic Carboxamides with Allyl Acetate.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 24, p. 3932, doi. 10.1002/adsc.201600569
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- Article
Assembly of Enantioenriched cis-3a,8a-Hexahydropyrrolo[2,3- b]indole Scaffolds by Silver(I)-Catalyzed Asymmetric Domino Reaction of Isocyanoacetates in the Presence of Cinchona-Derived Chiral Phosphorus Ligands.
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- 2016
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- Publication type:
- Other
Protecting-group directed stereospecific organocatalytic [3+2] cycloadditions: a facile access to chiral spirocyclic oxindoles.
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- ARKIVOC: Online Journal of Organic Chemistry, 2014, p. 124
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- Publication type:
- Article
[4+2] Annulation of Vinyl Ketones Initiated by a Phosphine-Catalyzed Aza-Rauhut-Currier Reaction: A Practical Access to Densely Functionalized Tetrahydropyridines.
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- Chemistry - A European Journal, 2012, v. 18, n. 32, p. 9802, doi. 10.1002/chem.201201318
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- Article
Catalytic Asymmetric [4+2] Annulation Initiated by an Aza-Rauhut-Currier Reaction: Facile Entry to Highly Functionalized Tetrahydropyridines.
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- Angewandte Chemie, 2012, v. 124, n. 31, p. 7945, doi. 10.1002/ange.201203316
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- Article
Innenrücktitelbild: Catalytic Asymmetric [4+2] Annulation Initiated by an Aza-Rauhut-Currier Reaction: Facile Entry to Highly Functionalized Tetrahydropyridines (Angew. Chem. 31/2012).
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- Angewandte Chemie, 2012, v. 124, n. 31, p. 7983, doi. 10.1002/ange.201205173
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- Article
Catalytic Asymmetric [4+2] Annulation Initiated by an Aza-Rauhut-Currier Reaction: Facile Entry to Highly Functionalized Tetrahydropyridines.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 31, p. 7825, doi. 10.1002/anie.201203316
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- Article
Inside Back Cover: Catalytic Asymmetric [4+2] Annulation Initiated by an Aza-Rauhut-Currier Reaction: Facile Entry to Highly Functionalized Tetrahydropyridines (Angew. Chem. Int. Ed. 31/2012).
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- Angewandte Chemie International Edition, 2012, v. 51, n. 31, p. 7861, doi. 10.1002/anie.201205173
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- Article
Corrigendum: Core Structure-Based Design of Organocatalytic [3+2]-Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles.
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- Chemistry - A European Journal, 2012, v. 18, n. 21, p. 6414, doi. 10.1002/chem.201201323
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- Article
Core Structure-Based Design of Organocatalytic [3+2]-Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles.
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- Chemistry - A European Journal, 2012, v. 18, n. 1, p. 63, doi. 10.1002/chem.201103449
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- Publication type:
- Article
Chiral Brønsted Acid Catalyzed Enantioselective α-Aminoxylation of Enecarbamates.
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- Angewandte Chemie, 2010, v. 122, n. 46, p. 8770, doi. 10.1002/ange.201002640
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- Article
Chiral Brønsted Acid Catalyzed Enantioselective α-Aminoxylation of Enecarbamates.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 46, p. 8588, doi. 10.1002/anie.201002640
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- Publication type:
- Article
Water-More Than Just a Green Solvent: A Stereoselective One-Pot Access to All-Chiral Tetrahydronaphthalenes in Aqueous Media.
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- Chemistry - A European Journal, 2010, v. 16, n. 12, p. 3842, doi. 10.1002/chem.200902932
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- Article
Highly Stereoselective One-Pot Synthesis of Bicyclic Isoxazolidines with Five Stereogenic Centers by an Organocatalytic Process.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 33, p. 6089, doi. 10.1002/anie.200901249
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- Article
Unusual Domino Michael/Aldol Condensation Reactions Employing Oximes as N-Selective Nucleophiles: Synthesis of N-Hydroxypyrroles.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 4, p. 758, doi. 10.1002/anie.200805205
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- Publication type:
- Article
Organocatalytic Asymmetric α-Aminoxylation/Aza-Michael Reactions for the Synthesis of Functionalized Tetrahydro-1,2-oxazines.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 52, p. 10013, doi. 10.1002/anie.200890274
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- Article
Organocatalytic Asymmetric α-Aminoxylation/Aza-Michael Reactions for the Synthesis of Functionalized Tetrahydro-1,2-oxazines.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 52, p. 10187, doi. 10.1002/anie.200803731
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- Article
The Scope of the Direct Proline-Catalyzed Asymmetric Addition of Ketones to Imines.
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- Advanced Synthesis & Catalysis, 2004, v. 346, n. 9/10, p. 1131, doi. 10.1002/adsc.200404114
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- Article
A Facile and Rapid Route to Highly Enantiopure 1,2-Diols by Novel Catalytic Asymmetric α-Aminoxylation of AldehydesWe gratefully acknowledge Prof. R. Lerner and The Scripps Research Institute for support. We thank R. M. Gordley for helpful discussions.
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- Angewandte Chemie International Edition, 2003, v. 42, n. 35, p. 4247, doi. 10.1002/anie.200352097
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- Publication type:
- Article
A Facile and Rapid Route to Highly Enantiopure 1,2-Diols by Novel Catalytic Asymmetric α-Aminoxylation of AldehydesWe gratefully acknowledge Prof. R. Lerner and The Scripps Research Institute for support. We thank R. M. Gordley for helpful discussions.
- Published in:
- Angewandte Chemie, 2003, v. 115, n. 35, p. 4379, doi. 10.1002/ange.200352097
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- Publication type:
- Article
Broadening the Aldolase Catalytic Antibody Repertoire by Combining Reactive Immunization and Transition State Theory: New Enantio- and Diastereoselectivities.
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- Angewandte Chemie International Edition, 1999, v. 38, n. 24, p. 3738, doi. 10.1002/(SICI)1521-3773(19991216)38:24<3738::AID-ANIE3738>3.0.CO;2-2
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- Article
Catalytic Enantioselective Retro-Aldol Reactions: Kinetic Resolution of β-Hydroxyketones with Aldolase Antibodies.
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- Angewandte Chemie International Edition, 1998, v. 37, n. 18, p. 2481, doi. 10.1002/(SICI)1521-3773(19981002)37:18<2481::AID-ANIE2481>3.0.CO;2-T
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- Article