Nickel-Catalyzed Dehydrogenation–Condensation–Rehydrogenation (DCR) Approach toward the Synthesis of Branched Primary Alcohols

We demonstrated the first Ni-catalyzed dehydrogenation-condensation-rehydrogenation (DCR) approach for the cross-coupling of two primary alkyl alcohols to β-alkylated primary alcohols. A wide variety of primary alkyl, aryl, and heteroaryl alcohols efficiently coupled with aliphatic primary and secondary alkyl alcohols and released water as a green byproduct (44 entries and up to 96% yield). Straightforward synthesis to chromane and sequential one-pot coupling to C3-substituted quinolines was enabled by nickel catalysis. Initial mechanistic studies including deuterium labeling experiments establish the sequential DCR strategy.

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Publication Details

Journal
Organic Letters
Published
2025-12-19
DOI
https://doi.org/10.1021/acs.orglett.5c04659
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
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article

Nickel-Catalyzed Dehydrogenation–Condensation–Rehydrogenation (DCR) Approach toward the Synthesis of Branched Primary Alcohols

Debasis Banerjee, Adrija Ghosh
Organic Letters
Asymmetric Hydrogenation and Catalysis
article

Nickel-Catalyzed Dehydrogenation–Condensation–Rehydrogenation (DCR) Approach toward the Synthesis of Branched Primary Alcohols

Debasis Banerjee, Adrija Ghosh
article en

Abstract

We demonstrated the first Ni-catalyzed dehydrogenation-condensation-rehydrogenation (DCR) approach for the cross-coupling of two primary alkyl alcohols to β-alkylated primary alcohols. A wide variety of primary alkyl, aryl, and heteroaryl alcohols efficiently coupled with aliphatic primary and secondary alkyl alcohols and released water as a green byproduct (44 entries and up to 96% yield). Straightforward synthesis to chromane and sequential one-pot coupling to C3-substituted quinolines was enabled by nickel catalysis. Initial mechanistic studies including deuterium labeling experiments establish the sequential DCR strategy.

Organic LettersVol. 28(1)
Indian Institute of Technology Roorkee (IN), Institute of Organic Synthesis (RU), Laboratoire de Synthèse Organique (FR), Chemical Synthesis Lab (SG)
Openalex Percentile: Top 65%
Asymmetric Hydrogenation and Catalysis
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