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2012 Fiscal Year Final Research Report

Development of Introducing Method of Hetero-functional groups to Alkenes via Anti-Markovnikov Nucleophilic Attack as a Key Step

Research Project

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Project/Area Number 23750112
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Synthetic chemistry
Research InstitutionNara Women's University

Principal Investigator

URA Yasuyuki  奈良女子大学, 自然科学系, 准教授 (40335196)

Project Period (FY) 2011 – 2012
Keywordsパラジウム錯体 / ワッカー型酸化 / 逆マルコフニコフ求核攻撃 / 末端アルケン / ピナコール / キノン / 分子状酸素
Research Abstract

We developed a synthetic method for terminal acetals from terminal alkenes and pinacol, and environmental load-reducing synthetic methods for aldehydes from terminal alkenes under mild reaction conditions. In these reactions, control of the regioselectivity of nucleophilic attack to coordinated alkenes is the key. By using bulky oxygen nucleophiles, the selectivity was successfully controlled to anti-Markovnikov manner.

  • Research Products

    (3 results)

All 2012 Other

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

  • [Journal Article] Palladium-catalyzed Synthesis of Terminal Acetals via Highly SelectiveAnti-Markovnikov Nucleophilic Attack of Pinacol on Vinylarenes2012

    • Author(s)
      山本真由美,中岡園江,浦 康之,片岡靖隆
    • Journal Title

      Allyl Ethers, and 1,5-Dienes,Chemical Communications

      Volume: 48巻 Pages: 1165-1167

    • DOI

      DOI:10.1039/C2CC16561A

    • URL

      http://hdl.handle.net/10935/3095

    • Peer Reviewed
  • [Presentation] パラジウム触媒によるビニルアレーン類からの選択的なアリールアセトアルデヒド類の合成2012

    • Author(s)
      中岡園江,浦 康之,片岡靖隆
    • Organizer
      日本化学会第92 春季年会
    • Place of Presentation
      神奈川
    • Year and Date
      2012-03-25
  • [Remarks]

    • URL

      http://www.chem.nara-wu.ac.jp/~kataoka/index.html

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Published: 2014-08-29   Modified: 2014-10-09  

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