1997 Fiscal Year Final Research Report Summary
Studies on the syntheses and properties of novel chalogenocarboxylic acid derivatives
| Project/Area Number |
08455414
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
有機工業化学
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| Research Institution | Gifu University |
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Principal Investigator |
KATO Shinzi Gifu Univ., Department of Chemistry, professor, 工学部, 教授 (40021589)
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| Co-Investigator(Kenkyū-buntansha) |
KANDA Takahiro Gifu Univ., Department of Chemistry, research associate, 工学部, 助手 (30234157)
MURAI Toshiaki Gifu Univ., Department of Chemistry, associate professor, 工学部, 助教授 (70166239)
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| Project Period (FY) |
1996 – 1997
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| Keywords | chalcogenocarboxylic acids / selenoamides / selenothioic acid S-esters / diorganoarsinic acids / selenotellurocarboxyl group |
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| Research Abstract |
The design and syntheses of organic molecules bearing new functional groups are one of the most important problem in synthetic organic chemistry. If unprecedented molecules can be made, not only new insight conserning the structure and conformations of the molecules can be studied but also new synthetic reactions can be developed. These new results further involve several new concept.
On the basis of the above background the attention has been paid to a series of chalcogenocarboxylic acid derivatives where the oxygen atom of carboxylic acids is replaced with the heavier atoms in the same low of the periodic table such as sulfur, selenium, and tellurium. Their new synthetic methods were developed, and their properties were disclosed.
For example, new and efficient synthetic methods of selenoamides and selenothioic acid S-esters have been established. The compounds having selenotellurocarboxyl group have also been synthesized for the first time. The new reactions using these compounds were tested, and synthetic reactions leading to a variety of organoselenium compounds were provided. The studies on their spectroscopic properties and stability led the general trend of the structures and stability of the compounds, although it is qualitative.
Additionally, the reactivity of selenocarboxylic acid Se-arsenic esters have been examined. As a result, new diorganoarsinic acid salts were isolated, and their structure was analyzed.
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