![Scheme 2. Preparation of alkene 14 (DIPEA = N,N-diisopropylethylamine). | Download Scientific Diagram Scheme 2. Preparation of alkene 14 (DIPEA = N,N-diisopropylethylamine). | Download Scientific Diagram](https://www.researchgate.net/publication/236921786/figure/fig8/AS:267859049840651@1440873982345/Scheme2-Preparation-of-alkene-14-DIPEA-N-N-diisopropylethylamine.png)
Scheme 2. Preparation of alkene 14 (DIPEA = N,N-diisopropylethylamine). | Download Scientific Diagram
![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://us.123rf.com/450wm/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.
![SOLVED: Predict the minor and major product DIPEA-diisopropylethylamina or Hunig s base DcJe malc prcducl rnE prcducl Predict products and indicate which one major product 4meducl ShowIne machansm oline lollowing reaclions Clearly SOLVED: Predict the minor and major product DIPEA-diisopropylethylamina or Hunig s base DcJe malc prcducl rnE prcducl Predict products and indicate which one major product 4meducl ShowIne machansm oline lollowing reaclions Clearly](https://cdn.numerade.com/ask_images/a2f1cafde6ec4b419903fdfa7e1a3cab.jpg)
SOLVED: Predict the minor and major product DIPEA-diisopropylethylamina or Hunig s base DcJe malc prcducl rnE prcducl Predict products and indicate which one major product 4meducl ShowIne machansm oline lollowing reaclions Clearly
![Electrochemical Formation of Cinnamaldehyde by the Electrolyte System N,N‐ Diisopropylethylamine and 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol - Imada - 2020 - ChemElectroChem - Wiley Online Library Electrochemical Formation of Cinnamaldehyde by the Electrolyte System N,N‐ Diisopropylethylamine and 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol - Imada - 2020 - ChemElectroChem - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/bc92a293-42f8-4eee-ad78-fc52203605c6/celc202000275-toc-0001-m.jpg)
Electrochemical Formation of Cinnamaldehyde by the Electrolyte System N,N‐ Diisopropylethylamine and 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol - Imada - 2020 - ChemElectroChem - Wiley Online Library
![DIPEA-induced activation of OH − for the synthesis of amides via photocatalysis - RSC Advances (RSC Publishing) DOI:10.1039/D2RA02107B DIPEA-induced activation of OH − for the synthesis of amides via photocatalysis - RSC Advances (RSC Publishing) DOI:10.1039/D2RA02107B](https://pubs.rsc.org/image/article/2022/RA/d2ra02107b/d2ra02107b-f1_hi-res.gif)
DIPEA-induced activation of OH − for the synthesis of amides via photocatalysis - RSC Advances (RSC Publishing) DOI:10.1039/D2RA02107B
![Dipea Nndiisopropylethylamine Hunigs Base Molecule Skeletal Stock Vector (Royalty Free) 1093026992 | Shutterstock Dipea Nndiisopropylethylamine Hunigs Base Molecule Skeletal Stock Vector (Royalty Free) 1093026992 | Shutterstock](https://www.shutterstock.com/image-vector/dipea-nndiisopropylethylamine-hunigs-base-molecule-260nw-1093026992.jpg)
Dipea Nndiisopropylethylamine Hunigs Base Molecule Skeletal Stock Vector (Royalty Free) 1093026992 | Shutterstock
![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
![Diisopropylethylamine-triggered, highly efficient, self-catalyzed regioselective acylation of carbohydrates and diols - ScienceDirect Diisopropylethylamine-triggered, highly efficient, self-catalyzed regioselective acylation of carbohydrates and diols - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1477052022068100-c8ob01464g-ga.jpg)
Diisopropylethylamine-triggered, highly efficient, self-catalyzed regioselective acylation of carbohydrates and diols - ScienceDirect
![Scheme 4 Reagents and conditions: a) aryl alkyne, CuI, DIPEA, THF; b)... | Download Scientific Diagram Scheme 4 Reagents and conditions: a) aryl alkyne, CuI, DIPEA, THF; b)... | Download Scientific Diagram](https://www.researchgate.net/profile/Marcos-Garcia-4/publication/5843446/figure/fig3/AS:669153312657426@1536549990260/Scheme-4-Reagents-and-conditions-a-aryl-alkyne-CuI-DIPEA-THF-b-base-solvent_Q320.jpg)