Evidence map›Paper›PMID 38601429›Full record

ArticleEuropean journal of organic chemistry2023

Cooperative Chiral Lewis Base/Palladium-Catalyzed Asymmetric Syntheses of Methylene-Containing δ-Lactams.

Paul Zebrowski, Uwe Monkowius, Mario Waser

Open access · hybridAbstract read
In one paragraph

Article in European journal of organic chemistry, 2023. 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
1.0field-weighted citation impact, top 26% of its field
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, 7 citations in OpenAlex.

  1. Article
  2. Determination of the pEuropean journal of organic chemistry · 2025
    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 at 1 institution in 1 country.

Paul ZebrowskiInstitute of Organic Chemistry Johannes Kepler University Linz Altenbergerstrasse 69 4040 Linz Austria.
Uwe MonkowiusSchool of Education Chemistry Johannes Kepler University Linz Altenbergerstrasse 69 4040 Linz Austria.ORCID https://orcid.org/0000-0003-0662-2866
Mario WaserInstitute of Organic Chemistry Johannes Kepler University Linz Altenbergerstrasse 69 4040 Linz Austria.ORCID https://orcid.org/0000-0002-8421-8642
Johannes Kepler University of Linz · AT

Funding

Austrian Science Fund FWF P 31784
6 · The paper itself

Abstract

We herein report a two-step approach for the enantioselective synthesis of novel chiral δ-lactams. By using a cooperative chiral ITU/achiral Pd-catalyst system, this protocol proceeds via an asymmetric α-allylation of activated aryl esters first, followed by an acid-mediated lactam formation. A variety of differently substituted products could be obtained with usually high levels of enantioselectivities and in reasonable yields (16 examples, up to 98 : 2 er and 73 % yield over two steps). In addition, further utilizations of the products via transformations of the exocyclic double bond were successfully carried out as well.

Indexed as

asymmetric organocatalysiscyclizationslactamsLewis base catalysisPd-catalysis

Identifiers

PMID38601429
PMCPMC11005102
OpenAlexW4387770987

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.