Evidence map›Paper›PMID 30254696›Full record

ArticleBeilstein journal of organic chemistry2018

Semi-synthesis and insecticidal activity of spinetoram J and its D-forosamine replacement analogues.

Kai Zhang, Jiarong Li, Honglin Liu, Haiyou Wang, Lamusi A

Open access · diamondAbstract read
In one paragraph

Article in Beilstein journal of organic chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
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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

5 authors at 2 institutions in 1 country.

Kai ZhangSchool of Chemistry and Chemical Engineering, Beijing Institute of Technology, 5 South Zhongguancan Street, Haidian District, Beijing, P. R. China.
Jiarong LiSchool of Chemistry and Chemical Engineering, Beijing Institute of Technology, 5 South Zhongguancan Street, Haidian District, Beijing, P. R. China.
Honglin LiuInstitute of Grassland Research of CAAS, No. 120 Wulanchabu East Street, Saihan District, Hohhot, P. R. China.
Haiyou WangInstitute of Grassland Research of CAAS, No. 120 Wulanchabu East Street, Saihan District, Hohhot, P. R. China.
Lamusi AInstitute of Grassland Research of CAAS, No. 120 Wulanchabu East Street, Saihan District, Hohhot, P. R. China.
Institute of Grassland Research · CNBeijing Institute of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinetoram, a mixture of spinetoram J (XDE-175-J, major component) and spinetoram L (XDE-175-L), is a new kind of fermentation-derived insecticide with a broad range of action against many insect pests, especially Cydia pomonella, Leaf miner and Thrips. Similar to spinosad, spinetoram is friendly to the environment, and non-toxic to animals and human beings. Therefore, spinetoram has been widely applied in pest control and grain storage. In a previous study, we had reported a semi-synthesis of spinetoram J. However, in that synthesis, there were more experimental steps, and the operations were troublesome. So an improved synthesis based on a self-protection strategy was designed and discussed. In this work, 3-

Indexed as

analoguesforosamine replacementimproved semi-synthesisinsecticidenatural productsspinetoram

Identifiers

PMID30254696
PMCPMC6142758
OpenAlexW2891456351

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.