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Anhydrous tertiary alkanolamines as hybrid chemical and physical CO 2 capture reagents with pressure-swing regeneration - Energy & Environmental Science (RSC Publishing) DOI:10.1039/C0EE00506A
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Kinetics screening of the N -alkylation of organic superbases using a continuous flow microfluidic device: basicity versus nucleophilicity - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB25215E
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Synthesis of Highly Oxygenated Dinaphthyl Ethers via SNAr Reactions Promoted by Barton's Base | Organic Letters
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2-tert-Butyl-1,1,3,3-tetramethylguanidine - Wikipedia
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Organic liquid CO2 capture agents with high gravimetric CO2 capacity
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![Bases investigated in this study. I, diazabicyclo[5.4.0]-undec7-ene... | Download Scientific Diagram](https://www.researchgate.net/publication/228508616/figure/fig4/AS:668842074333185@1536475785337/Bases-investigated-in-this-study-I-diazabicyclo540-undec7-ene-DBU-II-1-1-3-3.png "Bases investigated in this study. I, diazabicyclo[5.4.0]-undec7-ene... | Download Scientific Diagram")
Bases investigated in this study. I, diazabicyclo[5.4.0]-undec7-ene... | Download Scientific Diagram
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CAS#:29166-72-1 | 2-tert-butyl-1,1,3,3-tetramethylguanidine | Chemsrc
2-tert-Butyl-1,1,3,3-tetramethylguanidine = 97.0 GC 29166-72-1
