ReviewChemSusChem2026
Toward Sustainable Carbonylation Reactions Enabled by CO Surrogates in Green Solvents.
Review in ChemSusChem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
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Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Carbonylation reactions represent a powerful strategy in synthetic chemistry, because they enable the straightforward incorporation of carbonyl functionalities into organic substrates through transition-metal catalysis in the presence of various nucleophiles. Traditionally, these transformations have been conducted under high pressures of carbon monoxide (CO), a lethal gas, and have relied on volatile organic solvents (VOCs) that are often toxic and derived from petroleum resources, thereby raising significant environmental and safety concerns. In line with the principle of green chemistry, this review summarizes recent advances in carbonylation reactions based on organic and inorganic CO surrogates that safely generate CO on demand within the reaction system, with a specific focus on strategies combining safer CO sources and green solvents classified as more sustainable alternatives to conventional VOCs according to the GSK solvent selection guide.
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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.