![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
Ru-TsDPEN with Formic Acid/Hünig's Base for Asymmetric Transfer Hydrogenation, a Practical Synthesis of Optically Enriched N-Propyl Pantolactam | The Journal of Organic Chemistry
![DIPEA (N,N-diisopropylethylamine, Hunig's Base) Molecule. Skeletal Formula. Royalty Free SVG, Cliparts, Vectors, and Stock Illustration. Image 149287710. DIPEA (N,N-diisopropylethylamine, Hunig's Base) Molecule. Skeletal Formula. Royalty Free SVG, Cliparts, Vectors, and Stock Illustration. Image 149287710.](https://previews.123rf.com/images/molekuul/molekuul2006/molekuul200600262/149287710-dipea-n-n-diisopropylethylamine-hunig-s-base-molecule-skeletal-formula.jpg)
DIPEA (N,N-diisopropylethylamine, Hunig's Base) Molecule. Skeletal Formula. Royalty Free SVG, Cliparts, Vectors, and Stock Illustration. Image 149287710.
![Ru-TsDPEN with Formic Acid/Hünig's Base for Asymmetric Transfer Hydrogenation, a Practical Synthesis of Optically Enriched N-Propyl Pantolactam | The Journal of Organic Chemistry Ru-TsDPEN with Formic Acid/Hünig's Base for Asymmetric Transfer Hydrogenation, a Practical Synthesis of Optically Enriched N-Propyl Pantolactam | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/jo802380j/asset/images/medium/jo-2008-02380j_0008.gif)
Ru-TsDPEN with Formic Acid/Hünig's Base for Asymmetric Transfer Hydrogenation, a Practical Synthesis of Optically Enriched N-Propyl Pantolactam | The Journal of Organic Chemistry
![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/3c974f939a32262aeed197ab08f1ab631c012982/3-Table1-1.png)
PDF] A SIMPLE AND HIGHLY EFFICIENT SYNTHESIS OF QUINOLINE TERTIARY AMINES CATALYZED BY HUNIG'S BASE | Semantic Scholar
![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://l450v.alamy.com/450v/2c5ntjt/dipea-nn-diisopropylethylamine-hunigs-base-molecule-stylized-skeletal-formula-chemical-structure-atoms-are-shown-as-color-coded-circles-hydrogen-hidden-carbon-grey-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
Supporting Information Continuous-flow synthesis of primary amines: Metal-free reduction of aliphatic and aromatic nitro derivat
![7087-68-5 | N,N-Diisopropylethylamine | 1,1'-Dimethyltriethylamine; Bis(1-methylethyl)ethylamine; DIEA; DIPEA; Diisopropylethylamine; Ethyl-N,N-diisopropylamine; Ethyldiisopropylamine; Huenig's base; Hunig's base; Hunig's reagent; N,N-Bis(1-methylethyl ... 7087-68-5 | N,N-Diisopropylethylamine | 1,1'-Dimethyltriethylamine; Bis(1-methylethyl)ethylamine; DIEA; DIPEA; Diisopropylethylamine; Ethyl-N,N-diisopropylamine; Ethyldiisopropylamine; Huenig's base; Hunig's base; Hunig's reagent; N,N-Bis(1-methylethyl ...](https://www.trc-canada.com/prod-img/D493340.png)
7087-68-5 | N,N-Diisopropylethylamine | 1,1'-Dimethyltriethylamine; Bis(1-methylethyl)ethylamine; DIEA; DIPEA; Diisopropylethylamine; Ethyl-N,N-diisopropylamine; Ethyldiisopropylamine; Huenig's base; Hunig's base; Hunig's reagent; N,N-Bis(1-methylethyl ...
![A Homage to Siegfried Hünig and His Research - Reissig - 2021 - Angewandte Chemie International Edition - Wiley Online Library A Homage to Siegfried Hünig and His Research - Reissig - 2021 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/895fb2da-f86f-410a-a275-c1db73cb3166/anie202101550-fig-5001-m.png)