![A K2CO3‐Mediated Regioselective Synthesis of Indole/Pyrrole‐Fused 1,4‐Oxazines: An Unexpected Indole‐Fused Azlactone Synthesis - Vandavasi - 2014 - European Journal of Organic Chemistry - Wiley Online Library A K2CO3‐Mediated Regioselective Synthesis of Indole/Pyrrole‐Fused 1,4‐Oxazines: An Unexpected Indole‐Fused Azlactone Synthesis - Vandavasi - 2014 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/493bf79a-564e-4286-ac62-b51be03051b6/mfig000.jpg)
A K2CO3‐Mediated Regioselective Synthesis of Indole/Pyrrole‐Fused 1,4‐Oxazines: An Unexpected Indole‐Fused Azlactone Synthesis - Vandavasi - 2014 - European Journal of Organic Chemistry - Wiley Online Library
32. Nature of K2CO3 is basic because 1. K+ react with water 2. CO32 react with water 3.k+ and CO32 react with water 4.NONE OF THESE
![Proposed schematic illustration of the K2CO3-Gly DES formation mechanism | Download Scientific Diagram Proposed schematic illustration of the K2CO3-Gly DES formation mechanism | Download Scientific Diagram](https://www.researchgate.net/publication/331451510/figure/fig2/AS:941553904267301@1601495352401/Proposed-schematic-illustration-of-the-K2CO3-Gly-DES-formation-mechanism.png)
Proposed schematic illustration of the K2CO3-Gly DES formation mechanism | Download Scientific Diagram
![K2CO3‐activated Hydrosilylation: from Redistribution of Polymethylhydrosiloxane to Selectively Reduction of Aldehydes and Ketones - Zhao - 2017 - ChemistrySelect - Wiley Online Library K2CO3‐activated Hydrosilylation: from Redistribution of Polymethylhydrosiloxane to Selectively Reduction of Aldehydes and Ketones - Zhao - 2017 - ChemistrySelect - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/648226d3-9cce-4059-8d45-b3c411e8076d/slct201701592-fig-5001-m.jpg)