Evidence map›Paper›PMID 41584128›Full record

ArticleRSC advances2026

High-yielding and scalable synthesis of furfural acetals using protonated κ-carrageenan as a biorenewable acid catalyst.

Rachitha S Natraj, Saikat Dutta

Abstract read
In one paragraph

Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Rachitha S NatrajDepartment of Chemistry, National Institute of Technology Karnataka (NITK) Surathkal Mangalore 575025 Karnataka India sdutta@nitk.edu.in.
Saikat DuttaDepartment of Chemistry, National Institute of Technology Karnataka (NITK) Surathkal Mangalore 575025 Karnataka India sdutta@nitk.edu.in.ORCID https://orcid.org/0000-0003-3310-348X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The acetals of carbohydrate-derived furfurals have potential applications as fuel oxygenates and chemical intermediates. This work reports the use of protonated κ-carrageenan (kCH) as a marine biomass-derived renewable acid catalyst for the acetalization of furfural and 5-methylfurfural with ethylene glycol, 1,2-propanediol, and 1,3-propanediol. Since these glycols have promising catalytic production routes from biomass, the corresponding acetals are biorenewable to their entirety. Cyclohexane was used as the water removal agent by azeotropic distillation in a Dean-Stark apparatus. The isolated yields of the acetals were excellent (>90%), and the 2-(furan-2-yl)-1,3-dioxolane was conveniently prepared on a 10 g scale. The broad substrate scope of the catalyst was demonstrated by the successful preparation of acetals from benzaldehyde in excellent isolated yields. The kCH catalyst was conveniently recovered after the reaction and reused without catastrophic loss in catalytic activity. The effect of the extent of proton exchange on the activity, thermal stability, and recyclability of the kCH catalyst was also explored.

Identifiers

PMID41584128
PMCPMC12825003

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.