Evidence map›Paper›PMID 39242485›Full record

ReviewMolecular diversity2025

An overview: total synthesis of arborisidine, and arbornamine.

Gitanjali Yadav, Megha, Sangeeta Yadav, Ravi Tomar

Abstract readReview
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In one paragraph

Review in Molecular diversity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Gitanjali YadavDepartment of Chemistry, Indira Gandhi University, Meerpur, Rewari, Haryana, 122502, India.
MeghaDepartment of Chemistry, Indira Gandhi University, Meerpur, Rewari, Haryana, 122502, India.
Sangeeta YadavDepartment of Chemistry, Netaji Subhas University of Technology, Dwarka, Delhi, 110078, India.
Ravi TomarDepartment of Chemistry, SRM Institute of Science & Technology, Delhi-NCR Campus, Modinagar, Ghaziabad, 201204, India. ravitomar451@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arborisidine and Arbornamine are two monoterpenoid indole alkaloids that were isolated from the Malayan Kopsia arborea plant. This review provides valuable information about the total and formal syntheses of these alkaloids. The synthesis strategies discussed in this review, such as Pictet-Spengler cyclization, chemo- and stereoselective oxidative cyclization, Michael/Mannich cascade process, and intramolecular N-alkylation, can be useful for developing new methods to synthesize these and other similar compounds.

Indexed as

Secologanin Tryptamine AlkaloidsChemistry Techniques, SyntheticCyclizationMolecular StructureStereoisomerismSecologanin Tryptamine AlkaloidsAlkaloidsArborisidineArbornamineCyclizationNatural productTotal synthesis

Identifiers

PMID39242485

What OpenQuestion holds

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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.