![DIPEA (N,N-diisopropylethylamine, Hünig's base) molecule. Skeletal formula Stock Vector Image & Art - Alamy DIPEA (N,N-diisopropylethylamine, Hünig's base) molecule. Skeletal formula Stock Vector Image & Art - Alamy](https://c8.alamy.com/comp/MNGPX1/dipea-nn-diisopropylethylamine-hnigs-base-molecule-skeletal-formula-MNGPX1.jpg)
DIPEA (N,N-diisopropylethylamine, Hünig's base) molecule. Skeletal formula Stock Vector Image & Art - Alamy
![PDF] A SIMPLE AND HIGHLY EFFICIENT SYNTHESIS OF QUINOLINE TERTIARY AMINES CATALYZED BY HUNIG'S BASE | Semantic Scholar PDF] A SIMPLE AND HIGHLY EFFICIENT SYNTHESIS OF QUINOLINE TERTIARY AMINES CATALYZED BY HUNIG'S BASE | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/3c974f939a32262aeed197ab08f1ab631c012982/4-Table2-1.png)
PDF] A SIMPLE AND HIGHLY EFFICIENT SYNTHESIS OF QUINOLINE TERTIARY AMINES CATALYZED BY HUNIG'S BASE | Semantic Scholar
![Hunig's base catalyzed synthesis of new 1-(2,3-dihydro-1H-inden-1-yl)-3-aryl urea/thiourea derivatives as potent antioxidants and 2HCK enzyme growth inhibitors - ScienceDirect Hunig's base catalyzed synthesis of new 1-(2,3-dihydro-1H-inden-1-yl)-3-aryl urea/thiourea derivatives as potent antioxidants and 2HCK enzyme growth inhibitors - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0045206819316803-ga1.jpg)
Hunig's base catalyzed synthesis of new 1-(2,3-dihydro-1H-inden-1-yl)-3-aryl urea/thiourea derivatives as potent antioxidants and 2HCK enzyme growth inhibitors - ScienceDirect
Supporting Information Continuous-flow synthesis of primary amines: Metal-free reduction of aliphatic and aromatic nitro derivat
![DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Stylized skeletal formula (chemical structure): Atoms are shown as color-coded circles: hydrogen (hidden), carbon (grey Stock Photo - Alamy DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Stylized skeletal formula (chemical structure): Atoms are shown as color-coded circles: hydrogen (hidden), carbon (grey Stock Photo - Alamy](https://c8.alamy.com/zooms/6/92a47d9e82bf42a5be725e509c804409/2c5ntjt.jpg)
DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Stylized skeletal formula (chemical structure): Atoms are shown as color-coded circles: hydrogen (hidden), carbon (grey Stock Photo - Alamy
![Table 1 from Ru-TsDPEN with formic acid/Hunig's base for asymmetric transfer hydrogenation, a practical synthesis of optically enriched N-propyl pantolactam. | Semantic Scholar Table 1 from Ru-TsDPEN with formic acid/Hunig's base for asymmetric transfer hydrogenation, a practical synthesis of optically enriched N-propyl pantolactam. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/4410a317bdfb3b2058b782e32ec4926377d819c2/2-Table1-1.png)