Evidence map›Paper›PMID 31258206›Full record

ArticleTetrahedron2019

Synthetic studies towards the penicisulfuranols: Synthesis of an advanced spirocyclic diketopiperazine intermediate.

Kevin M Gayler, Kyle M Lambert, John L Wood

Abstract read
In one paragraph

Article in Tetrahedron, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. A Ring Expansion Approach ToTetrahedron letters · 2022
    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

3 authors.

Kevin M GaylerDepartment of Chemistry and Biochemistry, Baylor University, Waco, TX, 76798, USA.
Kyle M LambertDepartment of Chemistry and Biochemistry, Baylor University, Waco, TX, 76798, USA.
John L WoodDepartment of Chemistry and Biochemistry, Baylor University, Waco, TX, 76798, USA.

Funding

Ring Expansions to Access Structurally-Diverse Diketopiperazine AlkaloidsF32GM129969 · NIGMS · BAYLOR UNIVERSITY · PI LAMBERT, KYLE M. · 2018 to 2019
$112k
NIGMS NIH HHS F32 GM129969
6 · The paper itself

Abstract

The 2,5-diketopiperazine (DKP) moiety is a core feature of many natural products and medicinally relevant scaffolds. As part of our efforts directed towards a total synthesis of penicisulfuranol B, we have developed and report herein: (1) the preparation of an

Indexed as

DiketopiperazineHydroxamic acidOxidationPenicisulfuranolsSpirocycle

Identifiers

PMID31258206
PMCPMC6599588

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.