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Repurposing the novel DATB catalyst for the direct catalytic cross-coupling of carboxylic acids

Research Project

Project/Area Number 20K15292
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 33020:Synthetic organic chemistry-related
Research InstitutionMicrobial Chemistry Research Foundation

Principal Investigator

Opie Christopher  公益財団法人微生物化学研究会, 微生物化学研究所, 研究員 (90858531)

Project Period (FY) 2020-04-01 – 2023-03-31
Project Status Completed (Fiscal Year 2022)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2021: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2020: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
KeywordsDATB / Catalyst / Boron / Amide bond / Synthesis / Amide Bond / catalyst / boron / amide bond / heterocycle / Catalysis / C-C Bond Formation / Carboxylic Acids / Direct
Outline of Research at the Start

We are seeking to expand the already broad chemical reactivity of carboxylic acids in order to provide rapid access to useful building blocks for chemical synthesis. To mediate this process, the novel catalyst 'DATB' will be re-purposed from amide bond synthesis to C-C bond formation reactions.

Outline of Final Research Achievements

We had initially anticipated that the DATB catalyst could be used in tandem with transition metals to access novel reaction pathways. However. despite countless attempts over the course of a year, we we never successful in achieving this goal. As such, we changed modified our plan to exploring how changes to the structure of DATB could alter its reactivity. One of our ideas was to synthesize, characterize and test the catalytic activity of N(BOH)2-containing molecules. While this moiety is structurally similar to DATB, no synthetic pathways to produce it were present in the literature. Fortunately, we were successful in our endevour, producing a shelf-stable compound that was even more catalytically active than the DATB catalyst. The work was published in Org. Lett. (2023, 25, 4, 694-697). This novel catalytically-active moiety likely
provides a novel mode of action for amide activation, which warrants further investigation.

Academic Significance and Societal Importance of the Research Achievements

One of the most frequently encountered reactions in chemistry, especially in medicinal chemistry, is that of amide bond formation. The 'traditional' methods to achieve this transformation necessarily occur with concurrent production of waste materials. This project uncovered a new catalytic method.

Report

(4 results)
  • 2022 Annual Research Report   Final Research Report ( PDF )
  • 2021 Research-status Report
  • 2020 Research-status Report
  • Research Products

    (4 results)

All 2023 2022 Other

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (1 results) Remarks (2 results)

  • [Journal Article] Less Is More: N(BOH)2 Configuration Exhibits Higher Reactivity than the B3NO2 Heterocycle in Catalytic Dehydrative Amide Formation2023

    • Author(s)
      Opie Christopher R.、Noda Hidetoshi、Shibasaki Masakatsu、Kumagai Naoya
    • Journal Title

      Organic Letters

      Volume: 25 Issue: 4 Pages: 694-697

    • DOI

      10.1021/acs.orglett.2c04382

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed
  • [Presentation] The Synthesis and Isolation of Novel Bis-Hydroxyboranes and DATB-containing molecules2022

    • Author(s)
      ○Christopher Roderick Opie, Nobuaki Kashiwagi, Hidetoshi Noda, Ryosuke Tsutsumi, Masakatsu Shibasaki, Naoya Kumagai
    • Organizer
      The 142nd Annual Meeting of the Pharmaceutical Society of Japan (Nagoya)
    • Related Report
      2022 Annual Research Report
  • [Remarks] 微化研HP

    • URL

      https://www.bikaken.or.jp/

    • Related Report
      2022 Annual Research Report
  • [Remarks] 微生物化学研究所HP

    • URL

      https://www.bikaken.or.jp/

    • Related Report
      2021 Research-status Report

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Published: 2020-04-28   Modified: 2024-01-30  

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