Efficient benzylation of chitin in ionic liquids

An efficient benzylation of chitin using benzyl bromide in the presence of LiOH and amine bases, such as tributylamine, in ionic liquids has been developed, where ammonium salts, produced in situ , capably act as effective phase-transfer catalysts.

Authors

Yuki Shigenobu
Masayasu Totani (ORCID: https://orcid.org/0000-0001-6471-3622)
Tetsushi Kawano
Jun‐ichi Kadokawa (ORCID: https://orcid.org/0000-0001-8813-1950)

Institutions

Kagoshima University (JP)

Publication Details

Journal: New Journal of Chemistry
Published: 2025-01-01
DOI: https://doi.org/10.1039/d5nj01789k
Citations: 2
Primary Topic: Carbohydrate Chemistry and Synthesis
Type: article
Field-Weighted Citation Impact: 1.87

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article

Efficient benzylation of chitin in ionic liquids

Yuki Shigenobu, Masayasu Totani, Tetsushi Kawano, Jun‐ichi Kadokawa

Jan 1, 2025

2 citations

New Journal of Chemistry

Carbohydrate Chemistry and Synthesis

1.87

article

Efficient benzylation of chitin in ionic liquids

Yuki Shigenobu, Masayasu Totani, Tetsushi Kawano, Jun‐ichi Kadokawa

January 1, 2025article en

2 citations

Abstract

New Journal of ChemistryVol. 49(27)

Kagoshima University (JP)

Openalex Percentile: Top 15%

Carbohydrate Chemistry and Synthesis

1.87

DOI Source OpenAlex

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Efficient benzylation of chitin in ionic liquids — Yuki Shigenobu, Masayasu Totani, et al. · New Journal of Chemistry (2025) | TGRS Research Map | TGRS