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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Bibliographic Details
Published inBulletin of the Korean Chemical Society Vol. 32; no. 6; pp. 1808 - 1846
Main Author Cha, Jin-Soon
Format Journal Article
LanguageKorean
Published 2011
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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.
Bibliography:KISTI1.1003/JNL.JAKO201120956422846
ISSN:0253-2964
1229-5949