Thirty Six Years of Research on the Selective Reduction and Hydroboration
From 1975 to 2011, for thirty six years, the author and his collaborators have developed a variety of reducing and hydroborating agents, and applied them to organic synthesis, which involves the 1,2-reduction of ${\alpha}$,${\beta}$-unsaturated carbonyl compounds, stereoselective reduction of cycloa...
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Published in | Bulletin of the Korean Chemical Society Vol. 32; no. 6; pp. 1808 - 1846 |
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Main Author | |
Format | Journal Article |
Language | Korean |
Published |
2011
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Subjects | |
Online Access | Get full text |
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Summary: | From 1975 to 2011, for thirty six years, the author and his collaborators have developed a variety of reducing and hydroborating agents, and applied them to organic synthesis, which involves the 1,2-reduction of ${\alpha}$,${\beta}$-unsaturated carbonyl compounds, stereoselective reduction of cycloalkanones, regioselective ring-opening of epoxides, partial reduction of carboxylic acid derivatives to aldehydes, regioselective addition to carbon-carbon multiple bonds, etc. by utilizing metal hydrides and the newly-devised the Meerwein-Ponndorf-Verley (MPV) type reagents. Such developments provide a new synthetic methodology making possible valuable selective reductions and hydroborations, not practical previously. |
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Bibliography: | KISTI1.1003/JNL.JAKO201120956422846 |
ISSN: | 0253-2964 1229-5949 |