| Terminal Alkynes as One‐Carbon Donors in [5+ 1] Heteroannulation: Synthesis of Pyridines via Ynimine Intermediates and Application in the Total Synthesis of Anibamine B R Lavernhe, Q Wang, J Zhu Angewandte Chemie International Edition, e202303537, 2023 | | 2023 |
| Divergent Asymmetric Total Synthesis of (−)‐Voacafricines A and B R Andres, Q Wang, J Zhu Angewandte Chemie 135 (16), e202301517, 2023 | | 2023 |
| Oxidative rearrangement of 1, 1-disubstituted alkenes to ketones Q Feng, Q Wang, J Zhu Science 379 (6639), 1363-1368, 2023 | 2 | 2023 |
| Enantioselective Total Synthesis of (+)-Stephadiamine B Yang, G Li, Q Wang, J Zhu Journal of the American Chemical Society 145 (9), 5001-5006, 2023 | 1 | 2023 |
| Organocatalytic Enantioselective Diels–Alder Reaction of 2‐Trifluoroacetamido‐1, 3‐dienes with α, β‐Unsaturated Ketones XQ Zhu, Q Wang, J Zhu Angewandte Chemie 135 (1), e202214925, 2023 | 2 | 2023 |
| Organocatalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoesters: Development and Application to the Total Synthesis of (+)‐Alstratine A R Andres, F Sun, Q Wang, J Zhu Angewandte Chemie International Edition 62 (1), e202213831, 2023 | 4 | 2023 |
| Inherently chiral calixarenes by a catalytic enantioselective desymmetrizing cross-dehydrogenative coupling X Zhang, S Tong, J Zhu, MX Wang Chemical Science 14 (4), 827-832, 2023 | 7 | 2023 |
| Dual Photoredox and Copper Catalysis: Enantioselective 1, 2-Amidocyanation of 1, 3-Dienes D Forster, W Guo, Q Wang, J Zhu ACS Catalysis 13, 7523-7528, 2023 | | 2023 |
| Apparent 6‐endo‐trig Carbofluorination of Alkenes Enabled by Palladium‐Based Dyotropic Rearrangement J Gong, Q Wang, J Zhu Angewandte Chemie International Edition 61 (50), e202211470, 2022 | 3 | 2022 |
| Thiazole Boron Difluoride Dyes with Large Stokes Shift, Solid State Emission and Room‐Temperature Phosphorescence W Wang, S Tong, QQ Wang, YF Ao, DX Wang, J Zhu Chemistry–A European Journal 28 (65), e202202507, 2022 | | 2022 |
| Synthesis of 3-Acyloxyindolenines by TiCl3-Mediated Reductive Cyclization of 2-(ortho-Nitroaryl)-Substituted Enol Esters DV Boyarskaya, A Ongaro, C Piemontesi, Q Wang, J Zhu Organic Letters 24 (38), 7004-7008, 2022 | 3 | 2022 |
| Migrative carbofluorination of saturated amides enabled by Pd-based dyotropic rearrangement G Yang, H Wu, S Gallarati, C Corminboeuf, Q Wang, J Zhu Journal of the American Chemical Society 144 (31), 14047-14052, 2022 | 3 | 2022 |
| Taming the radical cation intermediate enabled one-step access to structurally diverse lignans JC Xiang, C Fung, Q Wang, J Zhu Nature Communications 13 (1), 3481, 2022 | 2 | 2022 |
| Modular Synthesis of Benzocyclobutenes via Pd (II)-Catalyzed Oxidative [2+ 2] Annulation of Arylboronic Acids with Alkenes T Fujii, S Gallarati, C Corminboeuf, Q Wang, J Zhu Journal of the American Chemical Society 144 (20), 8920-8926, 2022 | 4 | 2022 |
| Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst R Andres, Q Wang, J Zhu Angewandte Chemie International Edition 61 (19), e202201788, 2022 | 9 | 2022 |
| Two-carbon ring expansion of cyclobutanols to cyclohexenones enabled by indole radical cation intermediate: development and application to a total synthesis of uleine A Leclair, Q Wang, J Zhu Acs Catalysis 12 (2), 1209-1215, 2022 | 8 | 2022 |
| Copper‐Catalyzed Aza‐Sonogashira Cross‐Coupling To Form Ynimines: Development and Application to the Synthesis of Heterocycles R Lavernhe, RO Torres‐Ochoa, Q Wang, J Zhu Angewandte Chemie 133 (45), 24230-24235, 2021 | 15 | 2021 |
| Photoredox catalytic three-component amidoazidation of 1, 3-dienes D Forster, W Guo, Q Wang, J Zhu Acs Catalysis 11 (17), 10871-10877, 2021 | 24 | 2021 |
| Enantioselective Total Synthesis of (+)‐Nordasycarpidone,(+)‐Dasycarpidone, and (+)‐Uleine B Delayre, C Fung, Q Wang, J Zhu Helvetica Chimica Acta 104 (8), e2100088, 2021 | 7 | 2021 |
| C–C bond activation enabled by dyotropic rearrangement of Pd(iv) species J Cao, H Wu, Q Wang, J Zhu Nature chemistry 13 (7), 671-676, 2021 | 21 | 2021 |
Luc NeuvilleDirecteur de recherche, CNRS Gif-sur Yvette在 cnrs.fr 的电子邮件经过验证
