IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-42446-5.html
   My bibliography  Save this article

Ultra-high-throughput mapping of the chemical space of asymmetric catalysis enables accelerated reaction discovery

Author

Listed:
  • Wenjing Nie

    (Wuhan University)

  • Qiongqiong Wan

    (Wuhan University)

  • Jian Sun

    (Wuhan University)

  • Moran Chen

    (Wuhan University)

  • Ming Gao

    (Wuhan University)

  • Suming Chen

    (Wuhan University)

Abstract

The discovery of highly enantioselective catalysts and elucidating their generality face great challenges due to the complex multidimensional chemical space of asymmetric catalysis and inefficient screening methods. Here, we develop a general strategy for ultra-high-throughput mapping of the chemical space of asymmetric catalysis by escaping the time-consuming chiral chromatography separation. The ultrafast ( ~ 1000 reactions/day) and accurate (median error

Suggested Citation

  • Wenjing Nie & Qiongqiong Wan & Jian Sun & Moran Chen & Ming Gao & Suming Chen, 2023. "Ultra-high-throughput mapping of the chemical space of asymmetric catalysis enables accelerated reaction discovery," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42446-5
    DOI: 10.1038/s41467-023-42446-5
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-42446-5
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-42446-5?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Corin C. Wagen & Spencer E. McMinn & Eugene E. Kwan & Eric N. Jacobsen, 2022. "Screening for generality in asymmetric catalysis," Nature, Nature, vol. 610(7933), pages 680-686, October.
    2. Jolene P. Reid & Matthew S. Sigman, 2019. "Holistic prediction of enantioselectivity in asymmetric catalysis," Nature, Nature, vol. 571(7765), pages 343-348, July.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Shu-Wen Li & Li-Cheng Xu & Cheng Zhang & Shuo-Qing Zhang & Xin Hong, 2023. "Reaction performance prediction with an extrapolative and interpretable graph model based on chemical knowledge," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    2. Xiaoqian Wang & Yang Huang & Xiaoyu Xie & Yan Liu & Ziyu Huo & Maverick Lin & Hongliang Xin & Rong Tong, 2023. "Bayesian-optimization-assisted discovery of stereoselective aluminum complexes for ring-opening polymerization of racemic lactide," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    3. Shingo Harada & Hiroki Takenaka & Tsubasa Ito & Haruki Kanda & Tetsuhiro Nemoto, 2024. "Valence-isomer selective cycloaddition reaction of cycloheptatrienes-norcaradienes," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    4. Ahreum Kim & Chanhee Lee & Jayoung Song & Sang Kook Lee & Yongseok Kwon, 2023. "All-round catalytic and atroposelective strategy via dynamic kinetic resolution for N-/2-/3-arylindoles," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    5. Jie Ding & Runping Ye & Yanghe Fu & Yiming He & Ye Wu & Yulong Zhang & Qin Zhong & Harold H. Kung & Maohong Fan, 2023. "Direct synthesis of urea from carbon dioxide and ammonia," Nature Communications, Nature, vol. 14(1), pages 1-4, December.
    6. Allwin D. McDonald & Peyton M. Higgins & Andrew R. Buller, 2022. "Substrate multiplexed protein engineering facilitates promiscuous biocatalytic synthesis," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    7. Diandra S. Hassan & Christian Wolf, 2021. "Optical deciphering of multinary chiral compound mixtures through organic reaction based chemometric chirality sensing," Nature Communications, Nature, vol. 12(1), pages 1-10, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42446-5. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.