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Dec 18, 2024 | 
mdpi.com | Bo Zhou
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Oct 24, 2024 | 
nature.com | Li-Gao Liu |Xin Hong |Xin Lu |Bo Zhou
AbstractThe asymmetric Büchner reaction and related arene cyclopropanations represent one type of the powerful methods for enantioselective dearomatization. However, examples of asymmetric Büchner reactions via a non-diazo approach are quite scarce, and the related arene cyclopropanation based on alkynes has not been reported.
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Sep 30, 2024 | 01032-8&sz=64)
cell.com | Bo Zhou |Huck Institutes |Bulgarian Academy
1Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305, USA 2Department of Genetics, Stanford University, Stanford, CA 94305, USA 3Maternal and Child Health Research Institute, Stanford University School of Medicine, Stanford, CA 94305, USA 4Department of Statistics, Stanford University, Stanford, CA 94305, USA 5Department of Biomedical Data Science, Stanford University, Stanford, CA 94305, USA 6School of Computer Science and Engineering, Pusan National...
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Jun 28, 2024 | 
mdpi.com | Wenjia Liang |Bo Zhou |Xi Liu |Zhongyan Miao
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Apr 26, 2024 | 
mdpi.com | Bo Zhou |Yu Li |Tariq Ali
All articles published by MDPI are made immediately available worldwide under an open access license. No specialpermission is required to reuse all or part of the article published by MDPI, including figures and tables. Forarticles published under an open access Creative Common CC BY license, any part of the article may be reused withoutpermission provided that the original article is clearly cited. For more information, please refer tohttps://www.mdpi.com/openaccess.
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Mar 11, 2024 | 
nature.com | Xin Lu |Bo Zhou
AbstractSite- and stereoselective C–H functionalization is highly challenging in the synthetic chemistry community. Although the chemistry of vinyl cations has been vigorously studied in C(sp3)–H functionalization reactions, the catalytic enantioselective C(sp3)–H functionalization based on vinyl cations, especially for an unactivated C(sp3)–H bond, has scarcely explored.
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Oct 30, 2023 | 00468-x&sz=64)
cell.com | Yunnan Normal |Bo Zhou
SummaryIsoxazoles and their derivatives have been verified to be versatile building blocks and crucial intermediates for the synthesis of a range of useful N-containing molecules, especially valuable N-heterocycles. However, the catalytic asymmetric reaction of isoxazole derivatives has been rarely explored, and there is no systematic summary to date.
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Aug 30, 2023 | 
nature.com | Xiaowei Zhu |Bo Zhou |Steven Sloan |Anna-Sophie Fiston-Lavier |Laramie Duncan |Alexej Abyzov | +1 more
Correction to: Nature Neuroscience https://www.nature.com/articles/s41593-020-00767-4. Published online 11 January 2021. In the version of the article originally published, Eric Courchesne was incorrectly listed as a contributing member of the Brain Somatic Mosaicism Network. This has been amended in the HTML and PDF versions of the article. About this articleZhu, X., Zhou, B., Pattni, R. et al.
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Aug 2, 2023 | 00180-7&sz=64)
cell.com | Byrska-Bishop M |Stephanie U. Greer |Bo Zhou |Alexander E. Urban
Highlights•A framework for identifying ultra-conserved sequences in human pangenome assemblies•Pan-conserved segment tags (PSTs) from 94 pangenome and two reference genome assemblies•PSTs connect pangenome and reference genome coordinates, enabling comparative analysis•Distances between PSTs reflect preserved and variable genome regions in assembliesMotivationThe human pangenome reference addressed the limitation of the current reference by incorporating assemblies from diverse backgrounds.
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Jun 25, 2023 | 
arxiv.org | Lu Zheng |Bo Zhou
arXiv:2306.14244 (math) Download a PDF of the paper titled Largest and Least H-Eigenvalues of Symmetric Tensors and Hypergraphs, by Hongying Lin and 2 other authors Download PDF Submission history From: Bo Zhou [ view email] [v1] Sun, 25 Jun 2023 13:32:10 UTC (19 KB) Bibliographic Tools Bibliographic Explorer Toggle Bibliographic Explorer () Litmaps Toggle Litmaps (What is Litmaps?) scite.ai Toggle scite Smart Citations (What are Smart Citations?) Code, Data, Media Links to Code Toggle...
