Evidence map›Paper›PMID 22564056›Full record

ArticleOrganic letters2012

A formal synthesis of (-)-englerin A by relay ring closing metathesis and transannular etherification.

Jungyong Lee, Kathlyn A Parker

Abstract read
In one paragraph

Article in Organic letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Englerins: A Comprehensive Review.Journal of natural products · 2017
    Review
  7. Synthesis of a stable and orally bioavailable englerin analogue.Bioorganic & medicinal chemistry letters · 2016
    Article
  8. Article
  9. 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.

Jungyong LeeDepartment of Chemistry, Stony Brook University, Stony Brook, New York 11733, USA.
Kathlyn A Parker

Funding

Natural Product Leads for Drug DevelopmentR01GM074776 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI PARKER, KATHLYN A · 2006 to 2009
$1.3M
NIGMS NIH HHS GM74776NIGMS NIH HHS R01 GM074776
6 · The paper itself

Abstract

A bicyclization approach to englerin A has culminated in a formal asymmetric total synthesis. Key transformations in the 10-step sequence are a regiospecific epoxide opening and a relay ene-yne-ene metathesis that converts linear substrates specifically to Δ(4,6)-guaiadiene-9,10 diol derivatives. Regiospecific functionalization of the diene moiety installs the oxygen bridge required for the englerin tricyclic core.

Indexed as

CyclizationMolecular StructurePhyllanthusPlants, MedicinalSesquiterpenes, GuaianeStereoisomerismenglerin ASesquiterpenes, Guaiane

Identifiers

PMID22564056
PMCPMC3390928

What OpenQuestion holds

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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.