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 α,β-unsaturated carbonyl compounds, stereoselective reduction of cycloalkanones, regiose...
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Veröffentlicht in: | Bulletin of the Korean Chemical Society 2011, 32(6), , pp.1808-1846 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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 α,β-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. KCI Citation Count: 8 |
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ISSN: | 0253-2964 1229-5949 |
DOI: | 10.5012/bkcs.2011.32.6.1808 |