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Volume 1 Issue 11, November 2022

Stairway to a 1,080-mer

Starting from monosaccharide building blocks, a linear 1,080-mer arabinan is assembled using an automated synthesis approach. This method is used to prepare homogeneous biomacromolecules with the number of constituent units reaching 1,080, as well as a library of bioactive oligosaccharides.

See Yao et al.

Image: Wenlong Yao, Peking University. Cover Design: Amie Fernandez.

Research Highlights

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News & Views

  • Atomically thin materials have exciting physicochemical properties but multi-element and non-layered 2D materials are difficult to prepare by conventional methods. Now, a flux-assisted method is reported, enabling the synthesis of such 2D materials by confining reaction space.

    • Hyeonkyeong Kim
    • Youngdong Yoo
    News & Views
  • Inverse vulcanization uses high temperatures to form sulfur-rich polymers. Now, using a photoinduced method, polymerization occurs at ambient conditions enabling a broader selection of viable comonomers compared with existing routes, as well as eliminating the formation of toxic gas.

    • Jaclyn Dunn
    • Courtney L. Jenkins
    News & Views
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Research Briefings

  • Coordination of a photoswitchable chiral phosphate ligand to an achiral manganese(iii)-salen complex yields a catalyst that can produce either enantiomer of an epoxide from a single alkene substrate. This enantiodivergent catalysis is governed by the transfer of the chirality of the phosphate ligand to the manganese(iii)-salen complex.

    Research Briefing
  • The construction of seven-membered carbocycles through cycloaddition reactions represents a longstanding challenge in organic synthesis. A study now reports a copper-catalysed enantioselective (4 + 3) cycloaddition between 2-aminoallyl cations and dienol silyl ethers that affords structurally diverse cycloheptanoids with high stereoselectivities and shows broad substrate scope.

    Research Briefing
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Reviews

  • Nucleophiles are versatile reagents that can engage in a plethora of C–C and C–heteroatom bond-forming reactions. This Review examines their increasing role in transition metal-catalysed directed C–H functionalization, with a focus on synthetic approaches involving organometallic nucleophiles and X-based (X = N, O and S) coupling partners.

    • Sergio Barranco
    • Jiayu Zhang
    • Mónica H. Pérez-Temprano
    Review Article
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