Hydroformylation of Protected Propargylic Alcohols

A rhodium catalyst modified with a self-assembling pyridone-based phosphine ligand enables a chemoselective hydroformylation of protected propargylic alcohols to furnish either 4-siloxy enals or protected 4-hydroxy aldehydes depending on the reaction conditions.

Authors

Felix Bauer (ORCID: https://orcid.org/0000-0003-2370-6711)
Vladislav Agabekov
Bernhard Breit (ORCID: https://orcid.org/0000-0002-2514-3898)
Adrian Veith

Institutions

University of Freiburg (DE)

Publication Details

Journal: Synlett
Published: 2025-09-18
DOI: https://doi.org/10.1055/a-2694-6852
Primary Topic: Catalytic Alkyne Reactions
Type: article
Field-Weighted Citation Impact: 0.00

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article

Hydroformylation of Protected Propargylic Alcohols

Felix Bauer, Vladislav Agabekov, Bernhard Breit, Adrian Veith

Sep 18, 2025

Synlett

Catalytic Alkyne Reactions

article

Hydroformylation of Protected Propargylic Alcohols

Felix Bauer, Vladislav Agabekov, Bernhard Breit, Adrian Veith

September 18, 2025article en

Abstract

SynlettVol. 36(20)

University of Freiburg (DE)

Openalex Percentile: Top 81%

Catalytic Alkyne Reactions

DOI Source OpenAlex

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Hydroformylation of Protected Propargylic Alcohols — Felix Bauer, Vladislav Agabekov, et al. · Synlett (2025) | TGRS Research Map | TGRS