Evidence map›Paper›PMID 32351014›Full record

ArticleAngewandte Chemie (International ed. in English)2020

Total Syntheses of (-)-Minovincine and (-)-Aspidofractinine through a Sequence of Cascade Reactions.

Szilárd Varga, Péter Angyal, Gábor Martin, Orsolya Egyed, Tamás Holczbauer, Tibor Soós

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Enantioselective construction ofChemical science · 2022
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Total Syntheses of DihydroindoleOrganic letters · 2020
    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

6 authors.

Szilárd VargaInstitute of Organic Chemistry, Research Centre for Natural Sciences, 2 Magyar tudósok krt., 1117, Budapest, Hungary.ORCID 0000-0001-9611-5168
Péter AngyalInstitute of Organic Chemistry, Research Centre for Natural Sciences, 2 Magyar tudósok krt., 1117, Budapest, Hungary.ORCID 0000-0003-4514-2187
Gábor MartinInstitute of Organic Chemistry, Research Centre for Natural Sciences, 2 Magyar tudósok krt., 1117, Budapest, Hungary.
Orsolya EgyedInstrumentation Center, Research Centre for Natural Sciences, 2 Magyar tudósok krt., 1117, Budapest, Hungary.
Tamás HolczbauerInstitute of Organic Chemistry, Research Centre for Natural Sciences, 2 Magyar tudósok krt., 1117, Budapest, Hungary.
Tibor SoósInstitute of Organic Chemistry, Research Centre for Natural Sciences, 2 Magyar tudósok krt., 1117, Budapest, Hungary.ORCID 0000-0002-2872-4313

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report 8-step syntheses of (-)-minovincine and (-)-aspidofractinine using easily available and inexpensive reagents and catalyst. A key element of the strategy was the utilization of a sequence of cascade reactions to rapidly construct the penta- and hexacyclic frameworks. These cascade transformations included organocatalytic Michael-aldol condensation, a multistep anionic Michael-S

Indexed as

alkaloidsasymmetric catalysisbiomimetic synthesisorganocatalysistotal synthesis

Identifiers

PMID32351014
PMCPMC7497198

What OpenQuestion holds

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Registered trials

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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.