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File:Use of Hunig's base for alkylating secondary amines.png - Wikimedia Commons
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. Skeletal formula.:: tasmeemME.com
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How are neutral amines effective bases in organic chemistry? - Chemistry Stack Exchange
DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Stylized skeletal formula (chemical structure). Atoms are shown as Stock Photo - Alamy
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Hunig's base | Sigma-Aldrich
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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
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N,N-Diisopropylethylamine - Wikipedia
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
diisopropylethylamine | C8H19N | ChemSpider
DIPEA (N,N-diisopropylethylamine, Hunig's base) molecule. Skeletal formula Stock Photo - Alamy
Advanced ChemTech - DIPEA (N,N'-Diisopropylethylamine) – Used in organic chemistry as a base
