Visible-Light-Mediated Regioselective Organophotocatalytic C3–H Phosphonylation of Pyrazolo[1,5- <i>a</i> ]pyrimidines

In this work, we have developed an approach for direct regioselective phosphonylation of pyrazolo[1,5-<i>a</i>]pyrimidines in the presence of organophotocatalyst 4CzIPN under visible light irradiation to obtain a series of (pyrazolo[1,5-<i>a</i>]pyrimidin-3-yl)phosphonates. The discovered reaction represents the first example of direct phosphonylation of pyrazolo[1,<i>5-a</i>]pyrimidines. Various (pyrazolo[1,<i>5-a</i>]pyrimidine-3-yl)phosphonates containing both alkyl and aryl substituents at different positions were obtained in yields ranging from 39 to 95%. The use of commercially available 4CzIPN as a photocatalyst along with simple and mild reaction conditions, a wide range of substrates, the absence of heavy metals, as well as the use of clean energy, available oxidant, and a common solvent are all attractive features of this method.

Authors

Institutions

Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-10-21
DOI
https://doi.org/10.1021/acs.joc.5c01957
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Visible-Light-Mediated Regioselective Organophotocatalytic C3–H Phosphonylation of Pyrazolo[1,5- a ]pyrimidines

I. P. Beletskaya, А.Н. Ефремов, Alexander Yu. Mitrofanov
The Journal of Organic Chemistry
Radical Photochemical Reactions
article

Visible-Light-Mediated Regioselective Organophotocatalytic C3–H Phosphonylation of Pyrazolo[1,5- a ]pyrimidines

I. P. Beletskaya, А.Н. Ефремов, Alexander Yu. Mitrofanov
article en

Abstract

In this work, we have developed an approach for direct regioselective phosphonylation of pyrazolo[1,5-<i>a</i>]pyrimidines in the presence of organophotocatalyst 4CzIPN under visible light irradiation to obtain a series of (pyrazolo[1,5-<i>a</i>]pyrimidin-3-yl)phosphonates. The discovered reaction represents the first example of direct phosphonylation of pyrazolo[1,<i>5-a</i>]pyrimidines. Various (pyrazolo[1,<i>5-a</i>]pyrimidine-3-yl)phosphonates containing both alkyl and aryl substituents at different positions were obtained in yields ranging from 39 to 95%. The use of commercially available 4CzIPN as a photocatalyst along with simple and mild reaction conditions, a wide range of substrates, the absence of heavy metals, as well as the use of clean energy, available oxidant, and a common solvent are all attractive features of this method.

The Journal of Organic ChemistryVol. 90(47)
Lomonosov Moscow State University (RU)
Openalex Percentile: Top 77%
Radical Photochemical 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.