Evidence map›Paper›PMID 21405073›Full record

ArticleThe Journal of organic chemistry2011

Direct conversion of benzylic and allylic alcohols to phosphonates.

Rocky J Barney, Rebekah M Richardson, David F Wiemer

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 2011. 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. Review
  3. Article
  4. Review
  5. Synthesis of a Coumarin-Based Analogue of Schweinfurthin F.The Journal of organic chemistry · 2021
    Article
  6. Review
  7. 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

3 authors.

Rocky J BarneyDepartment of Chemistry, University of Iowa, Iowa City, Iowa 52242-1294, United States.
Rebekah M Richardson
David F Wiemer

Funding

Pawhuskins: Potential Treatments for Stimulant Abuse.R03DA026573 · NIDA · UNIVERSITY OF IOWA · PI NEIGHBORS, JEFFREY D · 2009 to 2010
$418k
NIDA NIH HHS DA026573NIDA NIH HHS R03 DA026573
6 · The paper itself

Abstract

Benzyl phosphonate esters often serve as reagents in Horner-Wadsworth-Emmons reactions. In most cases, they can be prepared from benzylic alcohols via formation of the corresponding halide followed by an Arbuzov reaction. To identify a more direct synthesis of phosphonate esters, we have developed a one-flask procedure for conversion of benzylic and allylic alcohols to the corresponding phosphonates through treatment with triethyl phosphite and ZnI(2).

Indexed as

Benzyl AlcoholCatalysisChloridesEstersMolecular StructureOrganophosphonatesPhosphitesPropanolsStereoisomerismStilbenesZinc Compoundsallyl alcoholBenzyl AlcoholChloridesEstersOrganophosphonatesPhosphitesPropanolsStilbenestriethyl phosphitezinc chlorideZinc Compounds

Identifiers

PMID21405073
PMCPMC3204863

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.