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Showing 1–4 of 4 results
Advanced filters: Author: Shū Kobayashi Clear advanced filters
  • Diazo compounds are invaluable intermediates in organic synthesis, however, traditional C–H diazotization methods often face environmental and safety challenges due to the use of azide compounds and excessive acid/base. Here, the authors introduce a protocol using 2-methoxyethyl nitrite, achieving efficient diazotization of 2-substituted indoles with high reactivity and selectivity.

    • Airu Hashidoko
    • Taku Kitanosono
    • Shū Kobayashi
    ResearchOpen Access
    Communications Chemistry
    P: 1-9
  • The synthesis of chiral amines is of crucial importance for the pharmaceutical industry, but it remains a challenging task and is often inefficient. Now, a heterogeneous iridium complex is developed for the asymmetric hydrogenation of imines and the asymmetric reductive amination of carbonyl compounds in continuous flow with high yields and enantioselectivities.

    • Tomohiro Yasukawa
    • Ryusuke Masuda
    • Shū Kobayashi
    Research
    Nature Catalysis
    Volume: 2, P: 1088-1092
  • Benzylic functionalisation of unactivated toluenes remains a challenge in asymmetric catalysis. Here a chiral Brønsted base catalyses the enantioselective C(sp3)-H functionalization of unactivated alkylarenes, enabling carbon-carbon bond formation at benzylic positions of toluene derivatives.

    • Tsubasa Hirata
    • Io Sato
    • Shū Kobayashi
    ResearchOpen Access
    Communications Chemistry
    Volume: 4, P: 1-8