Evidence map›Paper›PMID 28753015›Full record

ArticleOrganic letters2017

Synthesis of 1,2-Bis(trifluoromethylthio)arenes via Aryne Intermediates.

Milad Mesgar, Olafs Daugulis

Abstract read
In one paragraph

Article in Organic letters, 2017. 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
–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

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.

  1. Article
  2. Cascade trifluoromethylthiolation and cyclization ofBeilstein journal of organic chemistry · 2020
    Article
  3. 1,2-Bis(arylthio)arene synthesis via aryne intermediates.Chemical communications (Cambridge, England) · 2019
    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

2 authors.

Milad MesgarDepartment of Chemistry, University of Houston , Houston, Texas 77204, United States.
Olafs DaugulisDepartment of Chemistry, University of Houston , Houston, Texas 77204, United States.ORCID 0000-0003-2642-2992

Funding

New Methods for Direct Carbon-Hydrogen Bond FunctionalizationR01GM077635 · NIGMS · UNIVERSITY OF HOUSTON · PI DAUGULIS, OLAFS · 2007 to 2020
$3.6M
NIGMS NIH HHS R01 GM077635
6 · The paper itself

Abstract

A general method for synthesis of 1,2-bis-trifluoromethylthioarenes has been developed. Arynes generated from silyl aryl triflates or halides react with bis(trifluoromethyl)disulfide to afford 1,2-bis-trifluoromethylthioarenes. Aryl, alkyl, ester, halide, and methoxy functionalities are compatible with reaction conditions. Use of bis(perfluoroaryl)disulfides gave moderate yields of aryne disulfenylation or cyclization to fluorinated dibenzothiophenes.

Indexed as

Chemistry Techniques, SyntheticCyclizationFused-Ring CompoundsMolecular StructureSpiro CompoundsStructure-Activity RelationshipSulfidesFused-Ring CompoundsSpiro CompoundsSulfides

Identifiers

PMID28753015
PMCPMC5716473

What OpenQuestion holds

Textmetadata
LicenceTDM
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.