ArticleNature communications2023
Asymmetric hydrogenation of 1,1-diarylethylenes and benzophenones through a relay strategy.
Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
5 citing papers in PubMed.
- Designed Synthesis of Unsymmetrical (Deuterated) 1,1-Diarylethylenes via Simple Sequential Coupling of Arenes and Aldehydes.The Journal of organic chemistry · 2026Article
- Enantioconvergent Synthesis of Diarylmethane Drugs via Privileged Benzhydrol Intermediates.The Journal of organic chemistry · 2026Article
- Transient π-coordination enables nucleophilic borylation of simple arenes.Chemical science · 2026Article
- One-Pot Synthesis of Chiral Succinate Dehydrogenase Inhibitors and Antifungal Activity Studies.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
- Extensive Studies on the Synthesis and Characterization of π-Arene Chromium Complexes and Their Performance in SChemistry, an Asian journal · 2025Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Homogenous transition-metal catalysts bearing a chiral ligand are widely used for asymmetric hydrogenation of unsaturated compounds such as olefins and ketones, providing efficient concise access to products with chiral carbon centers. However, distinguishing the re and si prochiral faces of a double bond bearing two substituents that are sterically and electronically similar is challenging for these catalysts. Herein, we report a relay strategy for constructing compounds with a chiral gem-diaryl carbon center by means of a combination of selective arene exchange between 1,1-diarylethylenes or benzophenones with (naphthalene)Cr(CO)
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Registered trials
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