4.5 Review

Recent progress in the catalytic synthesis of tertiary alcohols from ketones with organometallic reagents

Journal

SYNTHESIS-STUTTGART
Volume -, Issue 11, Pages 1647-1675

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-2008-1067046

Keywords

asymmetric catalysis; ate complexes; ketones; organometallic reagents; tertiary alcohols

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Efficient tertiary alcohol synthesis is currently one of the most rapidly advancing fields in organic chemistry, and recent powerful catalytic methodologies can provide versatile tertiary alcohols, even with enantioselective properties. This review summarizes work on the highly efficient catalytic synthesis of tertiary alcohols from ketones and organometallic reagents. New trends in the catalytic synthesis of tertiary alcohols, including functionalized ones, such as tertiary cyanohydrins and tertiary aldols, are examined from the frontier viewpoints that use typical or transition-metal catalysts, organocatalysts, and metal ate complexes, among others.

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