Evidence map›Paper›PMID 26034334›Full record

ArticleTetrahedron letters2015

Studies on the regio- and diastereo-selective epoxidation of daphnanes and tiglianes.

Pierre-Luc Boudreault, Jennifer K Mattler, Paul A Wender

Abstract read
In one paragraph

Article in Tetrahedron letters, 2015. 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. Daphnane-Type Diterpenes fromMolecules (Basel, Switzerland) · 2022
    Article
  3. 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

3 authors.

Pierre-Luc BoudreaultDepartment of Chemistry, Department of Chemical and Systems Biology, Stanford University, Stanford, California 94305-5080, USA.
Jennifer K MattlerDepartment of Chemistry, Department of Chemical and Systems Biology, Stanford University, Stanford, California 94305-5080, USA.
Paul A WenderDepartment of Chemistry, Department of Chemical and Systems Biology, Stanford University, Stanford, California 94305-5080, USA.

Funding

SYNTHETIC STUDIES RELATED TO CANCER RESEARCH/TREATMENTR01CA031845 · NCI · STANFORD UNIVERSITY · PI PAUL Anthony WENDER · 1985 to 2026
$6.9M
SYNTHETIC STUDIES ON TUMOR PROMOTERS AND INHIBITORSR01CA031841 · NCI · STANFORD UNIVERSITY · PI WENDER, PAUL ANTHONY · 1985 to 2014
$4.8M
Synthetic Studies Related to Cancer Research/TreatmentR37CA031845 · NCI · STANFORD UNIVERSITY · PI WENDER, PAUL ANTHONY · 2006 to 2015
$4.5M
SYNTHETIC STUDIES ON TUMOR PROMOTERS AND INHIBITORSR37CA031841 · NCI · STANFORD UNIVERSITY · PI WENDER, PAUL · 1993 to 1999
–
NCI NIH HHS R01 CA031841NCI NIH HHS R01 CA031845NCI NIH HHS R37 CA031841NCI NIH HHS R37 CA031845
6 · The paper itself

Abstract

Daphnanes and tiglianes are diterpenes with a shared tricyclic 5-7-6 ring system. Many members exhibit significant biological activities often associated with protein kinase C signaling. Many of these natural products (~100) have a C6-C7 α-epoxide whose influence on biological activity is little studied. Using the more readily available phorbol ester PDBu as a test substrate, we report an efficient, and potentially general, α-epoxidation method based on a vanadium-catalyzed asymmetric epoxidation with bishydroxamic acid (BHA) ligands.

Indexed as

DaphnaneEpoxidationProtein kinase CTigliane

Identifiers

PMID26034334
PMCPMC4449265

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.