Evidence map›Paper›PMID 32668064›Full record

ArticleChemSusChem2020

Nucleophilic Thiols Reductively Cleave Ether Linkages in Lignin Model Polymers and Lignin.

Grace E Klinger, Yuting Zhou, Juliet A Foote, Abby M Wester, Yanbin Cui, Manar Alherech, Shannon S Stahl, James E Jackson, Eric L Hegg

Open access · hybridAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in ChemSusChem, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

4 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. The chemical logic of enzymatic lignin degradation.Chemical communications (Cambridge, England) · 2024
    Review
  3. Article
  4. 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

9 authors at 3 institutions in 1 country.

Grace E KlingerDepartment of Chemistry, Michigan State University, East Lansing, MI, 48824, USA.ORCID http://orcid.org/0000-0001-8539-0412
Yuting ZhouDepartment of Chemistry, Michigan State University, East Lansing, MI, 48824, USA.ORCID http://orcid.org/0000-0002-8751-9686
Juliet A FooteDepartment of Chemistry, Michigan State University, East Lansing, MI, 48824, USA.
Abby M WesterDepartment of Chemistry, Michigan State University, East Lansing, MI, 48824, USA.
Yanbin CuiDOE Great Lakes Bioenergy Research Center, University of Wisconsin-Madison, Madison, WI 53706, USA.ORCID http://orcid.org/0000-0003-0708-1029
Manar AlherechDOE Great Lakes Bioenergy Research Center, University of Wisconsin-Madison, Madison, WI 53706, USA.ORCID http://orcid.org/0000-0002-9913-5647
Shannon S StahlDOE Great Lakes Bioenergy Research Center, University of Wisconsin-Madison, Madison, WI 53706, USA.ORCID http://orcid.org/0000-0002-9000-7665
James E JacksonDepartment of Chemistry, Michigan State University, East Lansing, MI, 48824, USA.ORCID http://orcid.org/0000-0002-4506-7415
Eric L HeggDepartment of Biochemistry & Molecular Biology, Michigan State University, East Lansing, MI, 48824, USA.ORCID http://orcid.org/0000-0003-2055-5495
Michigan State University · USUniversity of Wisconsin–Madison · USGreat Lakes Bioenergy Research Center · US

Funding

Great Lakes Bioenergy Research Center, U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research DE-FC02-07ER64494Great Lakes Bioenergy Research Center, U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research DE-SC0018409
6 · The paper itself

Abstract

Lignin may serve as a renewable feedstock for the production of chemicals and fuels if mild, scalable processes for its depolymerization can be devised. The use of small organic thiols represents a bioinspired strategy to cleave the β-O-4 bond, the most common linkage in lignin. In the present study, synthetic β-O-4 linked polymers were treated with organic thiols, yielding up to 90 % cleaved monomer products. Lignin extracted from poplar was also treated with organic thiols resulting in molecular weight reductions as high as 65 % (M

Indexed as

etherhomogeneous catalysisligninpolymerssulfur

Identifiers

PMID32668064
PMCPMC7540407
OpenAlexW3043696592

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.