Evidence map›Paper›PMID 15740118›Full record

ArticleJournal of the American Chemical Society2005

Catalytic asymmetric synthesis of chiral allylic esters.

Stefan F Kirsch, Larry E Overman

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. A chiral Lewis acid strategy for enantioselective allylic C-H oxidation.Angewandte Chemie (International ed. in English) · 2008
    Article
  15. Catalytic asymmetric synthesis of chiral allylic esters.Journal of the American Chemical Society · 2005
    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.

Stefan F KirschDepartment of Chemistry, 516 Rowland Hall, University of California, Irvine, California 92697-2025, USA.
Larry E Overman

Funding

GENERAL METHODS FOR SYNTHESIS OF BIOACTIVE MATERIALSR01GM030859 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI OVERMAN, LARRY E. · 1985 to 2011
$4.0M
NIGMS NIH HHS R01 GM030859
6 · The paper itself

Abstract

Trichloroacetimidate derivatives of prochiral (Z)-2-alken-1-ols react at room temperature with carboxylic acids to give chiral 3-acyloxy-1-alkenes in high enantiopurity in the presence of di-mu-acetatobis[(eta5-(S)-(pR)-2-(2'-(4'-methylethyl)oxazolinyl)cyclopentadienyl,1-C,3'-N)(eta4-tetraphenylcyclobutadiene)cobalt]dipalladium (COP-OAc) or its enantiomer. This reaction has broad scope, proceeds with predictable high stereoinduction, is accomplished at room temperature using high substrate concentrations and low catalyst loadings, and likely proceeds by a novel mechanism.

Indexed as

ChloroacetatesAcetamidesAllyl CompoundsCatalysisEstersPalladiumStereoisomerismTrichloroacetic AcidAcetamidesAllyl CompoundsChloroacetatesEstersPalladiumtrichloroacetamideTrichloroacetic Acid

Identifiers

PMID15740118
PMCPMC2966826

What OpenQuestion holds

Textmetadata
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.