1,3-Dipolar Cycloaddition of Nitroalkanes as a Tool of DOS/LOS-like Strategy for the Synthesis of Isoxazoles and Isoxazolines

An efficient and common strategy for the generation of pharmaceutically relevant functionalized molecules based on the diversity- and lead-oriented synthesis (DOS/LOS)-like concepts is presented. The approach is implemented for the case of functionalized sp3-enriched derivatives of isoxazole and isoxazoline. The key chemical transformation used was regioselective [3+2] cycloaddition of functionalized alkenes or alkynes and nitrile oxides, which were generated from nitroalkanes upon treatment with Boc2O and DMAP under mild conditions. Further functional group transformations provided a library of building blocks (amines, carboxylic acids, alcohols, amino acids, etc.) with good scaffold and appendage diversity that met LOS physicochemical parameter constraints. The proposed method was used for the successful preparation and further biological validation of isoxazole analogs of the clinically relevant JAK inhibitors Baricitinib and Ruxolitinib, thus demonstrating potential applications in medicinal chemistry.

Authors

Institutions

Publication Details

Journal
ChemRxiv
Published
2025-09-04
DOI
https://doi.org/10.26434/chemrxiv-2025-fbxm3
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

1,3-Dipolar Cycloaddition of Nitroalkanes as a Tool of DOS/LOS-like Strategy for the Synthesis of Isoxazoles and Isoxazolines

Ilona Saraieva, Oleksandr Zginnyk, Bohdan A. Chalyk, Oleksandr O. Grygorenko et al.
ChemRxiv
Chemical Synthesis and Reactions
article

1,3-Dipolar Cycloaddition of Nitroalkanes as a Tool of DOS/LOS-like Strategy for the Synthesis of Isoxazoles and Isoxazolines

Ilona Saraieva, Oleksandr Zginnyk, Bohdan A. Chalyk, Oleksandr O. Grygorenko, Bohdan S. Sosunovych, Konstantin S. Gavrilenko, Dmitriy M. Volochnyuk, Angelina V. Biitseva, Anastasiia Grynyova, Bohdan V. Vashchenko, Petro Borysko, Anna Beshtynarska, Kostiantyn O. Halos, Nataliia Shliakhtova
article en

Abstract

An efficient and common strategy for the generation of pharmaceutically relevant functionalized molecules based on the diversity- and lead-oriented synthesis (DOS/LOS)-like concepts is presented. The approach is implemented for the case of functionalized sp3-enriched derivatives of isoxazole and isoxazoline. The key chemical transformation used was regioselective [3+2] cycloaddition of functionalized alkenes or alkynes and nitrile oxides, which were generated from nitroalkanes upon treatment with Boc2O and DMAP under mild conditions. Further functional group transformations provided a library of building blocks (amines, carboxylic acids, alcohols, amino acids, etc.) with good scaffold and appendage diversity that met LOS physicochemical parameter constraints. The proposed method was used for the successful preparation and further biological validation of isoxazole analogs of the clinically relevant JAK inhibitors Baricitinib and Ruxolitinib, thus demonstrating potential applications in medicinal chemistry.

ChemRxiv
National Academy of Sciences of Ukraine (UA), Taras Shevchenko National University of Kyiv (UA), Institute of Bioorganic Chemistry and Petrochemistry V.P. Kukhar (UA), Institute of Organic Chemistry (UA), Enamine (Ukraine) (UA)
Enamine
Openalex Percentile: Top 82%
Chemical Synthesis and Reactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.