/ Home
/ SUBMISSION

/ The BJOC
/ Diamond Open Access
/ Journal Statistics
/ Editorial Board
/ Community
/ Call for papers

/ Latest Articles
/ Most accessed
/ Thematic issues
/ Featured collections
/ Volumes
/ Authors

/ E-Alerts

/ BlueSky
/ LINKEDIN
/ Mastodon
/ RSS FEED

Empty search

Article Type

Publication Date Range

Search Tips

This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.

Search Examples

aromatic	the word “aromatic”
aromatic aldehyde	the word “aromatic” OR “aldehyde”
+aromatic +aldehyde	both words “aromatic” AND “aldehyde”
+aromatic -aldehyde	the word “aromatic” but NOT “aldehyde”
“aromatic aldehyde”	the exact phrase “aromatic aldehyde”
benz*	words which begin with “benz”, such as “benzene” or “benzyl”
benz*yl	words that begin with “benz” and end with “yl”, such as “benzyl” or “benzoyl”
benzyl~	words that are close to the word “benzyl”, such as “benzoyl” (i.e., fuzzy search)

BROWSE
Latest Articles
Most accessed
thematic issues
Featured Collections
volumes
authors

BROWSE

Latest Articles Most Accessed Thematic Issues Featured Collections Volumes Authors

Author

1 article(s) from Medgyesi, Zoltán

Azide–alkyne cycloaddition (click) reaction in biomass-derived solvent Cyrene^TM under one-pot conditions

Zoltán Medgyesi and
László T. Mika

Beilstein J. Org. Chem. 2025, 21, 1544–1551, doi:10.3762/bjoc.21.117

PDF

Graphical Abstract

Scheme 1: Synthesis of Cyrene^TM (dihydrolevoglucosenone) from cellulose-based feeds via levoglucosenone (LG).

Jump to Scheme 1

Scheme 2: Copper-catalyzed azide–alkyne cycloaddition of benzyl azide (1a) and phenylacetylene (2a) in variou...

Jump to Scheme 2

Figure 1: Comparison of various solvents used in the CuAAC reaction. Reaction conditions: 1.15 mmol benzyl az...

Jump to Figure 1

Figure 2: Effect of the Cu source used in the click reaction of benzyl azide (1a, 1.15 mmol) and phenylacetyl...

Jump to Figure 2

Figure 3: Copper-catalyzed azide–alkyne cycloaddition of benzyl azide (1a) and various acetylenes 2a–h in Cyr...

Jump to Figure 3

Figure 4: Consecutive synthesis of various N-substituted-4-phenyl-1H-1,2,3-triazoles in Cyrene^TM. Reaction co...

Jump to Figure 4

Figure 5: “One-pot” synthesis of various 1-allyl-4-substituted-1H-1,2,3-triazoles in Cyrene^TM. Reaction condi...

Jump to Figure 5

Figure 6: Solvent recovery for the CuAAC reaction of 1a and 2a. Reaction conditions: 12.5 mL Cyrene^TM, 1 mol ...

Jump to Figure 6

Album

Supp Info

Full Research Paper

Published 30 Jul 2025

Full text

Other Beilstein-Institut Open Science Activities

/ Help / Support & Contact / E-Alerts / Privacy Policy / Terms & Conditions / Impressum

Azide–alkyne cycloaddition (click) reaction in biomass-derived solvent CyreneTM under one-pot conditions

Azide–alkyne cycloaddition (click) reaction in biomass-derived solvent Cyrene^TM under one-pot conditions