Evidence map›Paper›PMID 21510632›Full record

ArticleOrganic letters2011

Stereoselective synthesis of a model C(18)-C(35) spiroketal fragment of integramycin.

Huikai Sun, Jason R Abbott, William R Roush

Abstract read
In one paragraph

Article in Organic letters, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. (Chemical science · 2019
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Synthesis of the spiroketal core of integramycin.Beilstein journal of organic chemistry · 2013
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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.

Huikai SunDepartment of Chemistry, Scripps Florida, Jupiter, Florida 33458, United States.
Jason R Abbott
William R Roush

Funding

NATURAL PRODUCT SYNTHESIS VIA CYCLOADDITION REACTIONSR37GM026782 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROUSH, WILLIAM R · 1998 to 2007
$2.2M
Natural Products Synthesis via Cycloaddition ReactionsR01GM026782 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROUSH, WILLIAM R · 1985 to 2011
$1.6M
NIGMS NIH HHS GM026782NIGMS NIH HHS R01 GM026782NIGMS NIH HHS R37 GM026782
6 · The paper itself

Abstract

A highly stereoselective synthesis of a model C(18)-C(35) spiroketal unit (7) of integramycin has been accomplished via an enantioselective stannyl-crotylboration reaction and an N-iodosuccinimide-mediated spiroketalization of 19a.

Indexed as

Models, MolecularFuransMolecular StructureNaphthalenesSpiro CompoundsStereoisomerismFuransintegramycinNaphthalenesSpiro Compoundsspiroketal

Identifiers

PMID21510632
PMCPMC3094501

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.