Hexafluoroisopropanol‐Enabled One‐Step Access to Oxetanol and Azetidinol Scaffolds from Unprotected Indoles and Heteroarenes

This work reports a direct, hexafluoroisopropanol (HFIP)‐enabled, one‐step construction of oxetanol and azetidinol scaffolds from unprotected indoles and other electron‐rich (hetero)arenes via selective activation of strained four‐membered heterocyclic ketones. The method operates under mild, protecting‐group‐free conditions, shows broad functional‐group tolerance (e.g., halides, ester, boronate), and accommodates diversely substituted indoles. Compared with metal–halogen activation routes, this approach streamlines access to valuable strained tertiary‐alcohol frameworks with strong potential for late‐stage functionalization in medicinal chemistry.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2026-02-03
DOI
https://doi.org/10.1002/adsc.70304
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Hexafluoroisopropanol‐Enabled One‐Step Access to Oxetanol and Azetidinol Scaffolds from Unprotected Indoles and Heteroarenes

J. Satyanarayana Reddy, Shu‐Yu Lin, Y J Lin, Wen‐Chieh Huang et al.
Advanced Synthesis & Catalysis
Catalytic C–H Functionalization Methods
article

Hexafluoroisopropanol‐Enabled One‐Step Access to Oxetanol and Azetidinol Scaffolds from Unprotected Indoles and Heteroarenes

J. Satyanarayana Reddy, Shu‐Yu Lin, Y J Lin, Wen‐Chieh Huang, Sheng‐Ju Hsu
article en

Abstract

This work reports a direct, hexafluoroisopropanol (HFIP)‐enabled, one‐step construction of oxetanol and azetidinol scaffolds from unprotected indoles and other electron‐rich (hetero)arenes via selective activation of strained four‐membered heterocyclic ketones. The method operates under mild, protecting‐group‐free conditions, shows broad functional‐group tolerance (e.g., halides, ester, boronate), and accommodates diversely substituted indoles. Compared with metal–halogen activation routes, this approach streamlines access to valuable strained tertiary‐alcohol frameworks with strong potential for late‐stage functionalization in medicinal chemistry.

Advanced Synthesis & CatalysisVol. 368(3)
National Health Research Institutes (TW)
Shanghai Educational Development Foundation, National Health Research Institutes, National Science and Technology Council
Openalex Percentile: Top 64%
Catalytic C–H Functionalization Methods
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Hexafluoroisopropanol‐Enabled One‐Step Access to Oxetanol and Azetidinol Scaffolds from Unprotected Indoles and Heteroarenes — J. Satyanarayana Reddy, Shu‐Yu Lin, et al. · Advanced Synthesis & Catalysis (2026) | TGRS Research Map | TGRS