Evidence map›Paper›PMID 42063825›Full record

ArticleJACS Au2026

Sulfur Ylide-Mediated Cascade Transformations to Access Cyclopropylallocolchicinoids with Potent Antimitotic Activity.

Dipto Mukhopadhyay, Kaushalendra Patel, Anwita Chattopadhyay, Sampurna Pal, Tejal Pathak, Indranil Banerjee, S S V Ramasastry

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Article in JACS Au, 2026. 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
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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

7 authors.

Dipto MukhopadhyayDepartment of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S A S Nagar 140306, Punjab, India.
Kaushalendra PatelDepartment of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S A S Nagar 140306, Punjab, India.
Anwita ChattopadhyayDepartment of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S A S Nagar 140306, Punjab, India.
Sampurna PalDepartment of Biological Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S A S Nagar 140306, Punjab, India.
Tejal PathakDepartment of Biological Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S A S Nagar 140306, Punjab, India.
Indranil BanerjeeDepartment of Biological Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S A S Nagar 140306, Punjab, India.
S S V RamasastryDepartment of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S A S Nagar 140306, Punjab, India.ORCID https://orcid.org/0000-0001-5814-9092

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present an efficient one-pot transformation for the synthesis of unprecedented classes of cyclopropyl-fused allocolchicinoids through the discovery of a new reactivity pattern of sulfoxonium ylides. This hybrid strategy rationally manipulates the nucleophilic character of sulfur ylides to achieve the regio- and stereoselective construction of structurally intriguing allocolchicinoids bearing multiple stereocenters. Notably, this methodology represents the first general approach to sp

Indexed as

allocolchicinesantimitotic agentscascade transformationcyclopropanesdibenzocycloheptanesinfluenza A virusmicrotubulessulfur ylides

Identifiers

PMID42063825
PMCPMC13126153

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.