Evidence map›Paper›PMID 32510795›Full record

ReviewChemistry (Weinheim an der Bergstrasse, Germany)2020

Total Synthesis of Anti-MRSA Active Diorcinols and Analogues.

G Jacob Boehlich, Jessica de Vries, Olivia Geismar, Mirja Gudzuhn, Wolfgang R Streit, Sebastian G Wicha, Nina Schützenmeister

Open access · hybridAbstract readReview
In one paragraph

Review in Chemistry (Weinheim an der Bergstrasse, Germany), 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
0.5field-weighted citation impact, top 41% 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, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Total Synthesis of Anti-MRSA Active Diorcinols and Analogues.Chemistry (Weinheim an der Bergstrasse, Germany) · 2020
    Review
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

7 authors at 1 institution in 1 country.

G Jacob BoehlichFachbereich Chemie, Institut für Pharmazie, Universität Hamburg, Bundesstraße 45, 20146, Hamburg, Germany.
Jessica de VriesFachbereich Chemie, Institut für Pharmazie, Universität Hamburg, Bundesstraße 45, 20146, Hamburg, Germany.
Olivia GeismarFachbereich Chemie, Institut für Pharmazie, Universität Hamburg, Bundesstraße 45, 20146, Hamburg, Germany.
Mirja GudzuhnDepartment of Microbiology and Biotechnology, Universität Hamburg, Ohnhorststrasse 18, 22609, Hamburg, Germany.
Wolfgang R StreitDepartment of Microbiology and Biotechnology, Universität Hamburg, Ohnhorststrasse 18, 22609, Hamburg, Germany.ORCID http://orcid.org/0000-0001-7617-7396
Sebastian G WichaFachbereich Chemie, Institut für Pharmazie, Universität Hamburg, Bundesstraße 45, 20146, Hamburg, Germany.ORCID http://orcid.org/0000-0002-8773-4845
Nina SchützenmeisterFachbereich Chemie, Institut für Pharmazie, Universität Hamburg, Bundesstraße 45, 20146, Hamburg, Germany.ORCID http://orcid.org/0000-0001-9608-0057
Universität Hamburg · DE

Funding

Rahn-Quade FoundationUniversität Hamburg HamburgstipendiumVerband der Chemischen Industrie
6 · The paper itself

Abstract

Diorcinols and related prenylated diaryl ethers were reported to exhibit activity against methicillin-resistant clinical isolates of Staphylococcus aureus (MRSA). Within these lines, we report the first total synthesis of diorcinol D, I, J, the proposed structure of verticilatin and recently isolated antibacterial diaryl ether by using an efficient and highly divergent synthetic strategy. These total syntheses furnish the diaryl ethers in only five to seven steps employing a Pd-catalyzed diaryl ether coupling as the key step. The total synthesis led to the structural revision of the natural product verticilatin, which has been isolated from a plant pathogenic fungus. Furthermore, these structures were tested in order to determine their antibacterial activities against different MRSA strains as well as further Gram-positive and -negative bacteria.

Indexed as

Anti-Bacterial AgentsHumansMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsPhenolsPhenyl EthersStaphylococcal InfectionsAnti-Bacterial Agentsdiorcinol DPhenolsPhenyl EthersbiofilmMRSAnatural productsstructure elucidationtotal synthesis

Identifiers

PMID32510795
PMCPMC7497275
OpenAlexW3033528451

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.