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Showing 1–13 of 13 results
Advanced filters: Author: Dawen Niu Clear advanced filters
  • The construction of vicinal, congested stereocenters with high selectivities is of general utility in chemistry. Here the authors report a doubly-stereoconvergent, Cu/Mg-catalyzed asymmetric propargylic substitution reaction to convert simple starting materials to products with vicinal tertiary and all-carbon quaternary stereocenters in high yields and excellent diastereo- and enantioselectivities

    • Xiang Pu
    • Qiu-Di Dang
    • Dawen Niu
    ResearchOpen Access
    Nature Communications
    Volume: 13, P: 1-9
  • Selective manipulation of one functional group, out of many repeatedly occurring in a substrate, represents a grand challenge in chemistry. Here, the authors report a Pd/Lewis acid cocatalytic system that achieves not only site-selective, but also site-switchable mono-O-allylation of polyols.

    • Hua Tang
    • Yu-Biao Tian
    • Dawen Niu
    ResearchOpen Access
    Nature Communications
    Volume: 11, P: 1-10
  • The de novo generation of benzynes—through a hexadehydro-Diels–Alder reaction—followed by their in situ elaboration is reported; the reaction is metal-free and reagent-free, and reveals new modes of intrinsic benzyne reactivity.

    • Thomas R. Hoye
    • Beeraiah Baire
    • Brian P. Woods
    Research
    Nature
    Volume: 490, P: 208-212
  • Fluorinated amides are prevalent structural motifs in pharmaceuticals and bioactive molecules, but their enantioselective synthesis is challenging. Here, the authors synthesize fluorinated amide compounds with distal chirality (γ to F) using ene-reductases and blue light irradiation.

    • Chaoqun Huang
    • Xuerui Jin
    • Yunzi Luo
    ResearchOpen Access
    Nature Communications
    Volume: 16, P: 1-11
  • Benzynes are capable of concerted removal of two vicinal hydrogen atoms from a hydrocarbon, a discovery enabled by the thermal generation of reactive benzyne intermediates through the hexadehydro-Diels–Alder cycloisomerization reaction of triyne substrates.

    • Dawen Niu
    • Patrick H. Willoughby
    • Thomas R. Hoye
    Research
    Nature
    Volume: 501, P: 531-534
  • A glycosylation platform is demonstrated that enables selective coupling between a wide range of unprotected or minimally protected donor and acceptor sugars, producing 1,2-cis-O-glycosides in a catalyst-controlled, site-selective manner.

    • Qiu-Di Dang
    • Yi-Hui Deng
    • Dawen Niu
    Research
    Nature
    Volume: 632, P: 313-319
  • The synthesis of aryl C-glycosides often requires manipulation of protecting groups. Here a general method to prepare aryl C-glycosides from unprotected and stable starting materials has been achieved by photoredox, Ni-catalysed cross-coupling. The protocol was also applied in the synthesis of several sugar–drug conjugates and gliflozin drug molecules.

    • Chen Zhang
    • Shi-Yang Xu
    • Dawen Niu
    Research
    Nature Synthesis
    Volume: 2, P: 251-260
  • Most chemical glycosylation methods operate by acid-promoted, ionic activation of donors. Now, by exploiting the formation of a halogen-bond complex, the activation of glycosyl donors was achieved via a visible light-promoted radical cascade process, resulting in a general, simple and mild way to build challenging 1,2-cis-glycosidic bonds.

    • Chen Zhang
    • Hao Zuo
    • Dawen Niu
    Research
    Nature Chemistry
    Volume: 14, P: 686-694
  • The asymmetric O-alkylation of alcohols is a useful route to chiral ethers, but aliphatic secondary alcohols have proven to be difficult substrates. Here the authors report a method to achieve this by developing conditions to avoid the decomposition of the alkylating agent.

    • Ren-Zhe Li
    • Da-Qi Liu
    • Dawen Niu
    Research
    Nature Catalysis
    Volume: 3, P: 672-680
  • An aryne intermediate produced by a hexadehydro-Diels–Alder reaction is shown to engage in an unusual — and before this work rare and inefficient — aromatic ene reaction to produce an isotoluene. This second reactive intermediate can then engage an external enophile resulting in a conjunctive cascade in which four C–C bonds and three rings are created without involvement of reagents or generation of by-products.

    • Dawen Niu
    • Thomas R. Hoye
    Research
    Nature Chemistry
    Volume: 6, P: 34-40