Aluminosilicate-mediated C(sp<sup>2</sup>)–H alkylation of furans using allylic alcohols

Aluminosilicates enable direct C–C bond formation of furans with naturally sourced allylic alcohols at room temperature. C(sp 2 )–H alkylation shows structure-dependent efficiency and selectivity.

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Publication Details

Journal
Catalysis Science & Technology
Published
2025-01-01
DOI
https://doi.org/10.1039/d4cy01320d
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Aluminosilicate-mediated C(sp2)–H alkylation of furans using allylic alcohols

Ruilian Wu, Liangliang Huang, Nilusha Sudasinghe, Peter G. N. Neate et al.
1 links
Catalysis Science & Technology
Oxidative Organic Chemistry Reactions
article

Aluminosilicate-mediated C(sp2)–H alkylation of furans using allylic alcohols

Ruilian Wu, Liangliang Huang, Nilusha Sudasinghe, Peter G. N. Neate, Margaret R. Jones, Xiaokun Yang
article en

Abstract

Aluminosilicates enable direct C–C bond formation of furans with naturally sourced allylic alcohols at room temperature. C(sp 2 )–H alkylation shows structure-dependent efficiency and selectivity.

Catalysis Science & TechnologyVol. 15(15)
Los Alamos National Laboratory (US), University of Oklahoma (US)
U.S. Department of Energy, National Nuclear Security Administration, Laboratory Directed Research and Development, Los Alamos National Laboratory
Openalex Percentile: Top 89%
Oxidative Organic Chemistry Reactions
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Aluminosilicate-mediated C(sp<sup>2</sup>)–H alkylation of furans using allylic alcohols — Ruilian Wu, Liangliang Huang, et al. · Catalysis Science & Technology (2025) | TGRS Research Map | TGRS