Evidence map›Paper›PMID 26275233›Full record

ArticleAngewandte Chemie (International ed. in English)2015

Facile Enzymatic Synthesis of Ketoses.

Liuqing Wen, Kenneth Huang, Mohui Wei, Jeffrey Meisner, Yunpeng Liu, Kristina Garner, Lanlan Zang, Xuan Wang, Xu Li, Junqiang Fang and 2 more

Open access · greenAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. 2-Ketogluconate Kinase fromMolecules (Basel, Switzerland) · 2019
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. A two-step strategy for the preparation of 6-deoxy-l-sorbose.Bioorganic & medicinal chemistry letters · 2016
    Article
  11. Article
  12. Article
  13. Efficient enzymatic synthesis of L-rhamnulose and L-fuculose.Bioorganic & medicinal chemistry letters · 2016
    Article
  14. 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

12 authors at 3 institutions in 2 countries.

Liuqing WenDepartment of Chemistry and Center for Therapeutics and Diagnostics, Georgia State University, Atlanta, GA 30303 (USA).
Kenneth HuangDepartment of Chemistry and Center for Therapeutics and Diagnostics, Georgia State University, Atlanta, GA 30303 (USA).
Mohui WeiDepartment of Chemistry and Center for Therapeutics and Diagnostics, Georgia State University, Atlanta, GA 30303 (USA).
Jeffrey MeisnerDepartment of Chemistry and Center for Therapeutics and Diagnostics, Georgia State University, Atlanta, GA 30303 (USA).
Yunpeng LiuDepartment of Chemistry and Center for Therapeutics and Diagnostics, Georgia State University, Atlanta, GA 30303 (USA).
Kristina GarnerDepartment of Chemistry and Center for Therapeutics and Diagnostics, Georgia State University, Atlanta, GA 30303 (USA).
Lanlan ZangDepartment of Chemistry and Center for Therapeutics and Diagnostics, Georgia State University, Atlanta, GA 30303 (USA).
Xuan WangDepartment of Chemistry and Center for Therapeutics and Diagnostics, Georgia State University, Atlanta, GA 30303 (USA).
Xu LiDepartment of Chemistry and Center for Therapeutics and Diagnostics, Georgia State University, Atlanta, GA 30303 (USA).
Junqiang FangNational Glycoengineering Research Center, Shandong University, Jinan 250100 (China).
Houcheng ZhangNational Glycoengineering Research Center, Shandong University, Jinan 250100 (China).
Peng George WangDepartment of Chemistry and Center for Therapeutics and Diagnostics, Georgia State University, Atlanta, GA 30303 (USA). pwang11@gsu.edu.
Georgia State University · USShandong University · CNEmory University · US

Funding

Biosynthesis of PolysaccharidesR01GM085267 · NIGMS · OHIO STATE UNIVERSITY · PI WANG, PENG GEORGE · 2009 to 2017
$2.4M
NIGMS NIH HHS R01 GM085267NIGMS NIH HHS R01GM085267
6 · The paper itself

Abstract

Studies of rare ketoses have been hampered by a lack of efficient preparation methods. A convenient, efficient, and cost-effective platform for the facile synthesis of ketoses is described. This method enables the preparation of difficult-to-access ketopentoses and ketohexoses from common and inexpensive starting materials with high yield and purity and without the need for a tedious isomer separation step.

Indexed as

BiocatalysisChemistry Techniques, SyntheticFructokinasesHumansIsomerismKetosesPhosphorylationPhosphotransferases (Alcohol Group Acceptor)Protein BiosynthesisThermotoga maritimaFructokinasesKetosesPhosphotransferases (Alcohol Group Acceptor)rhamnulokinaseenzymatic synthesisketosesone-pot reactionsphosphorylationsynthetic methods

Identifiers

PMID26275233
PMCPMC4715893
OpenAlexW2155033125

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.