Evidence map›Paper›PMID 42268563›Full record

ArticleChemistry, an Asian journal2026

Catalyst-Free Green Synthesis of Dithiocarbamate and Rhodanine Derivatives via C─S and C─N Bond Formation Using N-Substituted Maleimides.

Piyushkumar Satani, Sudha Soliya, Subrata Dutta, Togati Naveen

Abstract read
In one paragraph

Article in Chemistry, an Asian journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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5 · Who and what money

Authors and funding

4 authors.

Piyushkumar SataniDepartment of Chemistry, Sardar Vallabhbhai National Institute of Technology, Surat, Gujarat, India.
Sudha SoliyaDepartment of Chemistry, Sardar Vallabhbhai National Institute of Technology, Surat, Gujarat, India.
Subrata DuttaDepartment of Chemistry, Sardar Vallabhbhai National Institute of Technology, Surat, Gujarat, India.
Togati NaveenDepartment of Chemistry, Sardar Vallabhbhai National Institute of Technology, Surat, Gujarat, India.ORCID https://orcid.org/0000-0003-3424-4348

Funding

CSIR-HRDG 02(0449)/21/ EMR-II
6 · The paper itself

Abstract

A novel, eco-friendly synthesis method for producing dithiocarbamates and rhodanines is presented, offering a greener alternative to conventional methods. This one-pot, three-component reaction involves the reaction of simple cyclic and acyclic aliphatic amines, carbon disulfide, and N-substituted maleimides under mild, ambient conditions. Importantly, the method proceeds without metal catalysts, bases, or additional additives, helping to minimize waste and reduce environmental impact. It delivers excellent efficiency, rapidly producing biologically relevant dithiocarbamate and rhodanine derivatives in high yields and with much shorter reaction times. Using commercially available starting materials further enhances accessibility and lowers costs, making this approach highly suitable for both research and industrial applications. This study highlights how green chemistry principles can enable sustainable and convenient routes for synthesizing important dithiocarbamate and rhodanine derivatives.

Indexed as

catalyst‐freeC─N bondC─S bondmaleimidess

Identifiers

PMID42268563
PMCPMC13355110

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.