carbodiimide
Also known as methanediimine
thumb|right|General structure of trans-carbodiimides: The core functional group is shown in blue with attached Substituent|R groups
Research
8,958 papers- Theoretical and Experimental Study on Carbodiimide Formation.International journal of molecular sciences · 2024
- Synthesis and characterization of chemically fueled supramolecular materials driven by carbodiimide-based fuels.Nature protocols · 2021
- Carbodiimide inactivation of matrix metalloproteinases in radicular dentine.Journal of dentistry · 2019
- Immobilized Carbodiimide Assisted Flow Combinatorial Protocol to Facilitate Amide Coupling and Lactamization.ACS combinatorial science · 2020
- Substituent Effects on Transient, Carbodiimide-Induced Geometry Changes in Diphenic Acids.The Journal of organic chemistry · 2021
via PubMed
~7 min read
Article
15 sectionsContents
- Structure and bonding
- Synthesis
- From thioureas and ureas
- From isocyanates
- Reactions
- Moffatt oxidation
- Coupling agents
- Amide formation pathway
- Examples
- DCC
- DIC
- EDC
- CMCT or CMC
- See also
- References
thumb|right|General structure of trans-carbodiimides: The core functional group is shown in blue with attached Substituent|R groups
In organic chemistry, a carbodiimide (systematic IUPAC name: methanediimine) is a functional group with the formula RN=C=NR. On Earth they are exclusively synthetic, but in interstellar space the parent compound HN=C=NH has been detected by its maser emissions.