Evidence map›Paper›PMID 26178784›Full record

ArticleChemical communications (Cambridge, England)2015

Cascade bicyclizations of o-alkynyl aldehydes with thiazolium salts: a new access toward poly-functionalized indeno[2,1-b]pyrroles.

Peng Zhou, Wen-Juan Hao, Jin-Peng Zhang, Bo Jiang, Guigen Li, Shu-Jiang Tu

Abstract read
In one paragraph

Article in Chemical communications (Cambridge, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Peng ZhouJiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, Jiangsu Normal University, Xuzhou, 211116, P. R. China. wjhao@jsnu.edu.cn jiangchem@jsnu.edu.cn laotu@jsnu.edu.cn.
Wen-Juan Hao
Jin-Peng Zhang
Bo Jiang
Guigen Li
Shu-Jiang Tu

Funding

GAP Chemistry Approaches to Chiral Amino Acids, Peptides and PeptidomimeticsR33DA031860 · NIDA · TEXAS TECH UNIVERSITY · PI LI, GUIGEN · 2013 to 2014
$706k
NIDA NIH HHS R33 DA031860NIDA NIH HHS R33DA031860
6 · The paper itself

Abstract

A new cascade bicyclization of o-alkynyl aldehydes with thiazolium salts is described, in which 25 examples of densely functionalized indeno[2,1-b]pyrroles are achieved in a functional-group-compatible manner. Thiazole carbenes generated in situ from thiazolium salts play dual roles as reaction partners and as NHC catalysts. The synthetic utility of these bicyclization reactions results in subsequent C-C bond-forming events to rapidly build up molecular complexity.

Indexed as

AldehydesCatalysisIndenesMethaneModels, MolecularPyrrolesSaltsThiazolesAldehydescarbeneIndenesMethanePyrrolesSaltsThiazoles

Identifiers

PMID26178784
PMCPMC4547933

What OpenQuestion holds

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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.