Evidence map›Paper›PMID 36320705›Full record

ArticleChemical science2022

Accelerating the end-to-end production of cyclic phosphate monomers with modular flow chemistry.

Romain Morodo, Raphaël Riva, Nynke M S van den Akker, Daniel G M Molin, Christine Jérôme, Jean-Christophe M Monbaliu

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In one paragraph

Article in Chemical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Romain MorodoCenter for Integrated Technology and Organic Synthesis, MolSys Research Unit, University of Liège B-4000 Liège Sart Tilman Belgium jc.monbaliu@uliege.be.ORCID https://orcid.org/0000-0002-4025-2523
Raphaël RivaCenter for Education and Research on Macromolecules, Cesam Research Unit, University of Liège B-4000 Liège Sart Tilman Belgium.
Nynke M S van den AkkerDepartment of Physiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University 6200 MD Maastricht The Netherlands.
Daniel G M MolinDepartment of Physiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University 6200 MD Maastricht The Netherlands.ORCID https://orcid.org/0000-0002-9646-7283
Christine JérômeCenter for Education and Research on Macromolecules, Cesam Research Unit, University of Liège B-4000 Liège Sart Tilman Belgium.ORCID https://orcid.org/0000-0001-8442-5740
Jean-Christophe M MonbaliuCenter for Integrated Technology and Organic Synthesis, MolSys Research Unit, University of Liège B-4000 Liège Sart Tilman Belgium jc.monbaliu@uliege.be.ORCID https://orcid.org/0000-0001-6916-8846

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biocompatibility, tunable degradability and broad functionalities of polyphosphoesters and their potential for biomedical applications have stimulated a renewed interest from Chemistry, Medicinal Chemistry and Polymer Sciences. Commercial applications of polyphosphoesters as biomaterials are still hampered because of the time and resource-intensive sourcing of their corresponding monomers, in addition to the corrosive and sensitive nature of their intermediates and by-products. Here, we present a groundbreaking challenge for sourcing the corresponding cyclic phosphate monomers by a different approach. This approach relies on the use of continuous flow technologies to intensify the end-to-end preparation of cyclic phosphate monomers with a semi-continuous modular flow platform. The applied flow technology mitigates both safety and instability issues related to the more classical production of cyclic phosphate monomers. The first flow module allows safe synthesis of a library of cyclic chlorophosphite building blocks and features in-line

Identifiers

PMID36320705
PMCPMC9491087

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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.