Evidence map›Paper›PMID 28970940›Full record

ReviewChemical science2017

Indole diterpenoid natural products as the inspiration for new synthetic methods and strategies.

Michael A Corsello, Junyong Kim, Neil K Garg

Abstract readReview
In one paragraph

Review in Chemical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Anticancer Effect of Mycotoxins FromInternational journal of microbiology · 2024
    Review
  7. General Synthesis ofJournal of the American Chemical Society · 2023
    Article
  8. Cytotoxic Indole Diterpenoids from aMolecules (Basel, Switzerland) · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. PAngewandte Chemie (International ed. in English) · 2020
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Twelve-Step Asymmetric Synthesis of (-)-Nodulisporic Acid C.Journal of the American Chemical Society · 2018
    Article
  20. 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.

Michael A CorselloDepartment of Chemistry and Biochemistry , University of California , Los Angeles , California 90095 , USA . Email: neilgarg@chem.ucla.edu.
Junyong KimDepartment of Chemistry and Biochemistry , University of California , Los Angeles , California 90095 , USA . Email: neilgarg@chem.ucla.edu.
Neil K GargDepartment of Chemistry and Biochemistry , University of California , Los Angeles , California 90095 , USA . Email: neilgarg@chem.ucla.edu.ORCID 0000-0002-7793-2629

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Indole terpenoids comprise a large class of natural products with diverse structural topologies and a broad range of biological activities. Accordingly, indole terpenoids have and continue to serve as attractive targets for chemical synthesis. Many synthetic efforts over the past few years have focused on a subclass of this family, the indole diterpenoids. This minireview showcases the role indole diterpenoids have played in inspiring the recent development of clever synthetic strategies, and new chemical reactions.

Identifiers

PMID28970940
PMCPMC5618777

What OpenQuestion holds

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LicenceCC BY-NC
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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.