ArticleBeilstein journal of organic chemistry2015
Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides.
Article in Beilstein journal of organic chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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Who cites it
7 citing papers in PubMed, 36 citations in OpenAlex.
- Water as a green solvent for sustainable sample preparation: single drop microextraction of N-nitrosamines from losartan tablets.Analytical and bioanalytical chemistry · 2025Article
- Article
- Towards More Practical Methods for the Chemical Synthesis of Thioamides Using Sulfuration Agents: A Decade Update.Molecules (Basel, Switzerland) · 2023Review
- A genome-wide portrait of pervasive drug contaminants.Scientific reports · 2021Article
- Direct synthesis of 2-oxo-acetamidines from methyl ketones, aromatic amines and DMFRSC advances · 2019Article
- Recent Uses ofMolecules (Basel, Switzerland) · 2018Review
- Beyond a solvent: triple roles of dimethylformamide in organic chemistry.RSC advances · 2018Review
Corrections and comments
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
An improved and efficient method for the synthesis of thioamides is presented. For this transformation, dimethylamine as the key intermediate is generated in situ from dimethylformamide (DMF). All the tested substrates produced the desired products with excellent isolated yields.
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Registered trials
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.