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Development of Innovative Molecular Transformations Via Cationic Rhodacycles as Active Species

Development of Innovative Molecular Transformations Via Cationic Rhodacycles as Active Species
通过阳离子铑环作为活性物质开发创新分子转化
批准号:
20675002
负责人:
TANAKA Ken
金额:
$54.41万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Young Scientists (S)
财政年份:
2008
资助国家:
日本
项目状态:
已结题
起止时间:
2008 至 2012

项目摘要

项目成果

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中文摘要
翻译
本研究详细探讨了各种高活性阳离子红戴环的生成方法,并开发了许多以这些中间体为活性物质的新型催化剂。这些发展的催化剂被扩展到不对称催化剂,能够构建轴向、平面、螺旋和多中心手性,并合成功能性有机材料。“阳离子环化学”由此成立。
英文摘要
In this research, the method of generating various highly reactive cationic rhodacycles was examined in detail , and many novel catalyses which involve these intermediates as active species were developed. These developed catalyses were expanded to the asymmetrical catalyses that are able to construct axial, planar, helical, and multiple central chiralities, and syntheses of functional organic materials. Thus, "chemistry of cationic rhodacycles " was established.
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会议论文
DOI: 10.3987/rev-12-729
发表时间: 2012-05
期刊: Heterocycles
影响因子: 0.6
作者: [Ken Tanaka]
通讯作者: Ken Tanaka
Enantioselective Synthesis of Planar Chiral Carba-Paracyclophane via Rhodium- Catalyzed [2+2+2] Cycloaddition of Cyclic Diynes with Alkynes
铑催化对映选择性合成平面手性碳-对环芳烷 [2 2 2] 环状二炔与炔烃的环加成
DOI: --
发表时间:
期刊:
影响因子: --
作者: [Tatsuya Araki, Ken Tanaka]
通讯作者: Ken Tanaka
ロジウム触媒を用いた連続分子内[2+2+2]付加環化反応による[11]ヘリセン誘導体のエナンチオ選択的合成
使用铑催化剂通过连续分子内[2+2+2]环加成反应对映选择性合成[11]螺烯衍生物
DOI: --
发表时间:
期刊:
影响因子: --
作者: [Kenro Yatake, Toshiaki Aoki, 渡辺正夫, (Keynote) Takao Someya, 高岡晃教,亀山武志,亀岡章一郎, 木村 雄貴・府川直裕・宮内祐太・田中 健]
通讯作者: 木村 雄貴・府川直裕・宮内祐太・田中 健
Rhodium-Mediated [2+2+2] Cycloaddition
铑介导的 [2 2 2] 环加成
DOI: --
发表时间: 2013
期刊:
影响因子: --
作者: [森信介, 小田裕樹, K. Tanaka]
通讯作者: K. Tanaka
共 215 条
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    • 财政年份:
      2008
    • 负责人:
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