ArticleRSC advances2019
Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki-Miyaura reaction.
Article in RSC advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
7 citing papers in PubMed, 28 citations in OpenAlex.
- Recent Applications of Propylene Carbonate as a Solvent in Sustainable Organic Synthesis.ChemSusChem · 2026Review
- Dimethyl-, Diethyl-, and Propylene Carbonates: An Emerging Class of Green Solvents for Organic Synthesis.Chemical record (New York, N.Y.) · 2026Review
- Biomass-Derived Solvents and Low-GWP Refrigerants as Working Fluids for Sustainable Absorption Refrigeration.ACS sustainable chemistry & engineering · 2025Article
- Amino-Substituted Azoxybenzenes as Potential Redox-Active Catholyte Materials.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
- Ultrasonic-assisted, additive-free Pd-catalyzed Suzuki-Miyaura cross-coupling enabled synthesis of novel arylated benzofuran-triazole hybrids.Frontiers in chemistry · 2025Article
- Sustainable and SafeInternational journal of molecular sciences · 2024Article
- Suzuki-Miyaura cross coupling is not an informative reaction to demonstrate the performance of new solvents.Beilstein journal of organic chemistry · 2020Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The Suzuki-Miyaura reaction is one of the most used transformations in drug research. Thus making this reaction more sustainable is of considerable current interest. Here we show that propylene carbonate (PC) can be used as a solvent for the Suzuki-Miyaura reaction. PC is one of the greenest solvents since it is synthesized under green conditions by the use of carbon dioxide in the air. All reactions proceeded well and good or excellent yields were observed for the biaryl products. Nonetheless in the case of pyridazinones, 2-hydroxypropyl- chain containing side-products were observed. Importantly, this fact allowed the isolation of several novel compounds which were generated under prominently green conditions.
Identifiers
What OpenQuestion holds
Registered trials
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.