Evidence map›Paper›PMID 29963678›Full record

ArticleOrganic & biomolecular chemistry2018

Copper-catalyzed oxidative cross-dehydrogenative coupling of 2H-chromenes and terminal alkynes.

Fei Yang, Yangshan Li, Paul E Floreancig, Xiaoyan Li, Lei Liu

Abstract read
In one paragraph

Article in Organic & biomolecular chemistry, 2018. 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
1.5field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 2 countries.

Fei YangSchool of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China. xli63@sdu.edu.cn leiliu@sdu.edu.cn.
Yangshan Li
Paul E Floreancig
Xiaoyan Li
Lei Liu
Shandong University · CNUniversity of Pittsburgh · US

Funding

Stereoselective Synthesis through Allylic Alcohol Transposition and TrappingR01GM103886 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FLOREANCIG, PAUL E · 2015 to 2018
$1.1M
NIGMS NIH HHS R01 GM103886
6 · The paper itself

Abstract

An efficient copper-catalyzed cross-dehydrogenative coupling of 2H-chromenes and terminal alkynes mediated by DDQ has been established. A protic additive, EtOH, proved to be crucial for harmonizing the oxidation with a subsequent alkynylation step by retaining the oxidation state of an oxocarbenium ion in the form of acetal. The CDC reaction exhibits a good substrate scope, with a range of terminal aryl- and alkyl alkynes being well tolerated. The copper-catalyzed alkynylation of 2H-chromene acetals with terminal alkynes was also explored.

Indexed as

AlkynesBenzopyransCatalysisCopperHydrogenationOxidation-ReductionAlkynesBenzopyransCopper

Identifiers

PMID29963678
PMCPMC6051884
OpenAlexW2810032276

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.