Evidence map›Paper›PMID 24679218›Full record

ArticleOrganic letters2014

A chemoselective route to β-enamino esters and thioesters.

Dongyue Xin, Kevin Burgess

Abstract read
In one paragraph

Article in Organic letters, 2014. 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. Article
  3. Selective hydrolysis of α-oxo keteneBeilstein journal of organic chemistry · 2024
    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.

Dongyue XinTexas A & M University , Chemistry Department, P.O. Box 30012, College Station, Texas 77842, United States.
Kevin Burgess

Funding

Development of an Optimized System for Non-covalent Delivery of Proteins into CelR01GM087981 · NIGMS · TEXAS A&M UNIVERSITY · PI BURGESS, KEVIN · 2009 to 2012
$1.3M
NIGMS NIH HHS GM087981NIGMS NIH HHS R01 GM087981
6 · The paper itself

Abstract

Conditions were developed for syntheses of β-enamino esters, thioesters, and amides. These reactions involve hydroxybenzotriazole derivatives in buffered media. Illustrative syntheses of some heterocyclic systems are given, including some related to protein-protein interface mimics.

Indexed as

AmidesCatalysisEstersMolecular StructureStereoisomerismSulfur CompoundsTriazoles1-hydroxybenzotriazoleAmidesEstersSulfur CompoundsTriazoles

Identifiers

PMID24679218
PMCPMC4203388

What OpenQuestion holds

Textmetadata
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.