Evidence map›Paper›PMID 36448365›Full record

ArticleChemSusChem2023

Effective Production of Selected Dioxolanes by Sequential Bio- and Chemocatalysis Enabled by Adapted Solvent Switching.

Jan-Dirk Spöring, Jan Wiesenthal, Victoria S Pfennig, Jochem Gätgens, Kassem Beydoun, Carsten Bolm, Jürgen Klankermayer, Dörte Rother

Open access · greenAbstract read
In one paragraph

Article in ChemSusChem, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 32% of its field
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

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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

8 authors at 2 institutions in 1 country.

Jan-Dirk SpöringInstitute of Bio- and Geosciences 1, Forschungszentrum Jülich GmbH, 52428, Jülich, Germany.ORCID http://orcid.org/0000-0002-5656-3537
Jan WiesenthalInstitute of Technical and Macromolecular Chemistry, RWTH Aachen University, 52056, Aachen, Germany.ORCID http://orcid.org/0000-0002-6101-4399
Victoria S PfennigInstitute of Organic Chemistry, RWTH Aachen University, 52056, Aachen, Germany.ORCID http://orcid.org/0000-0002-7460-5446
Jochem GätgensInstitute of Bio- and Geosciences 1, Forschungszentrum Jülich GmbH, 52428, Jülich, Germany.
Kassem BeydounInstitute of Technical and Macromolecular Chemistry, RWTH Aachen University, 52056, Aachen, Germany.ORCID http://orcid.org/0000-0003-0979-8277
Carsten BolmInstitute of Organic Chemistry, RWTH Aachen University, 52056, Aachen, Germany.ORCID http://orcid.org/0000-0001-9415-9917
Jürgen KlankermayerInstitute of Technical and Macromolecular Chemistry, RWTH Aachen University, 52056, Aachen, Germany.ORCID http://orcid.org/0000-0003-2143-9402
Dörte RotherInstitute of Bio- and Geosciences 1, Forschungszentrum Jülich GmbH, 52428, Jülich, Germany.ORCID http://orcid.org/0000-0002-2339-4431
RWTH Aachen University · DEForschungszentrum Jülich · DE

Funding

Deutsche Forschungsgemeinschaft 390919832
6 · The paper itself

Abstract

Most combinations of chemo- and biocatalysis take place in aqueous media or require a solvent change with complex intermediate processing. Using enzymes in the same organic solvent as the chemocatalyst eliminates this need. Here, it was shown that a complete chemoenzymatic cascade to form dioxolanes could be carried out in a purely organic environment. The result, including downstream processing, was compared with a classical mode, shifting solvent. First, a two-step enzyme cascade starting from aliphatic aldehydes to chiral diols (3,4-hexanediol and 4,5-octanediol) was run either in an aqueous buffer or in the potentially biobased solvent cyclopentyl methyl ether. Subsequently, a ruthenium molecular catalyst enabled the conversion to dioxolanes [e. g., (4S,5S)-dipropyl-1,3-dioxolane]. Importantly, the total synthesis of this product was not only highly stereoselective but also based on the combination of biomass, CO

Indexed as

DioxolanesBiocatalysisCatalysisSolventsStereoisomerismWaterDioxolanesSolventsWaterasymmetric catalysisbiocatalysiscascade reactionchiralityunconventional media

Identifiers

PMID36448365
PMCPMC10107191
OpenAlexW4310377205

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.