Related Experiment Video
Updated: Aug 24, 2026

Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols
Published on: April 4, 2014
Divergent Synthesis of Ketones and Alcohols via Iron-Catalyzed Three-Component Alcohol Cross-Coupling
Dingguo Song1, Guan Wang2, Fangyuan Hu3
1Institute of Green Pharmaceutical Innovation and Functional Evaluation, School of Life Sciences, Huzhou University, Huzhou313000, P. R. China.
Abstract:
Functionalized ketones and alcohols are two privileged scaffolds widely found in natural products and biologically active compounds. They are also key synthetic intermediates in target-oriented synthesis. The divergent synthesis of ketones and alcohols from the same starting materials and catalysts via the borrowing hydrogen (BH) reaction is of great significance. Despite the significant advances in the divergent two-component alcohol transformation, recent catalytic systems show weaknesses in the selective cross-coupling of multicomponent alcohols, which can easily produce highly functionalized molecules. New, inexpensive, and readily available Fe catalysts were synthesized and successfully used for the cross-coupling of multicomponent alcohols. By regulating the reaction conditions, we achieved the divergent synthesis of β,β-methylated/alkylated alcohols and α,α-methylated/alkylated ketones with high selectivity. The use of readily available starting materials, low catalyst loading, broad substrate scope, ease of scale-up, and versatile functionalizations of the products make this approach highly practical and attractive.
More Related Videos
Related Concept Videos
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Preparation of Aldehydes and Ketones from Alcohols, Alkenes, and Alkynes
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction
Crossed Aldol Reactions: Overview
Crossed Aldol Reaction Using Strong Bases: Directed Aldol Reaction
Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview

