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4-(N,N-Dimethylamino)pyridine Hydrochloride as a Recyclable Catalyst for Acylation of Inert Alcohols: Substrate Scope and Reaction Mechanism | Organic Letters
![Scheme 3. Reagents and conditions: (a) Ac2O, DMAP, NEt3, THF, RT, 1 h,... | Download Scientific Diagram Scheme 3. Reagents and conditions: (a) Ac2O, DMAP, NEt3, THF, RT, 1 h,... | Download Scientific Diagram](https://www.researchgate.net/publication/343667418/figure/fig1/AS:933594616836099@1599597710961/Scheme-3-Reagents-and-conditions-a-Ac2O-DMAP-NEt3-THF-RT-1-h-77-b-i.png)
Scheme 3. Reagents and conditions: (a) Ac2O, DMAP, NEt3, THF, RT, 1 h,... | Download Scientific Diagram
![SOLVED: Select the single best answer: Which nitrogen atom in the following compound is more basic? DMAP 4-(N,N-dimethylamino)pyridine left nitrogen right nitrogen SOLVED: Select the single best answer: Which nitrogen atom in the following compound is more basic? DMAP 4-(N,N-dimethylamino)pyridine left nitrogen right nitrogen](https://cdn.numerade.com/ask_images/c60f0a29f913414ab624179ff663fe5a.jpg)
SOLVED: Select the single best answer: Which nitrogen atom in the following compound is more basic? DMAP 4-(N,N-dimethylamino)pyridine left nitrogen right nitrogen
![Steric Effects in the Uncatalyzed and DMAP‐Catalyzed Acylation of Alcohols—Quantifying the Window of Opportunity in Kinetic Resolution Experiments - Fischer - 2006 - Chemistry – A European Journal - Wiley Online Library Steric Effects in the Uncatalyzed and DMAP‐Catalyzed Acylation of Alcohols—Quantifying the Window of Opportunity in Kinetic Resolution Experiments - Fischer - 2006 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/2bba7a84-32ba-4dc1-90fc-aeabd9bf9348/mcontent.jpg)
Steric Effects in the Uncatalyzed and DMAP‐Catalyzed Acylation of Alcohols—Quantifying the Window of Opportunity in Kinetic Resolution Experiments - Fischer - 2006 - Chemistry – A European Journal - Wiley Online Library
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Access to pyridines via DMAP-catalyzed activation of α-chloro acetic ester to react with unsaturated imines - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C3QO00045A
![Full article: DMAP-catalyzed cyclization of Schiff bases with α-halo ketones: Synthesis of 1,4-benzoxazines Full article: DMAP-catalyzed cyclization of Schiff bases with α-halo ketones: Synthesis of 1,4-benzoxazines](https://www.tandfonline.com/action/showGraphicalAbstractImage?doi=10.1080%2F00397911.2017.1293107&type=img_lg&id=lsyc_a_1293107_uf0001_oc.jpeg)
Full article: DMAP-catalyzed cyclization of Schiff bases with α-halo ketones: Synthesis of 1,4-benzoxazines
![Fluorous 4‐N,N‐Dimethylaminopyridine (DMAP) Salts as Simple Recyclable Acylation Catalysts - Vuluga - 2010 - Chemistry – A European Journal - Wiley Online Library Fluorous 4‐N,N‐Dimethylaminopyridine (DMAP) Salts as Simple Recyclable Acylation Catalysts - Vuluga - 2010 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/9308c523-7976-44d8-9044-69aabdcca8c8/mcontent.gif)
Fluorous 4‐N,N‐Dimethylaminopyridine (DMAP) Salts as Simple Recyclable Acylation Catalysts - Vuluga - 2010 - Chemistry – A European Journal - Wiley Online Library
![Widely Useful DMAP-Catalyzed Esterification under Auxiliary Base- and Solvent-Free Conditions | Journal of the American Chemical Society Widely Useful DMAP-Catalyzed Esterification under Auxiliary Base- and Solvent-Free Conditions | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja075824w/asset/images/large/ja075824wn00001.jpeg)
Widely Useful DMAP-Catalyzed Esterification under Auxiliary Base- and Solvent-Free Conditions | Journal of the American Chemical Society
![Enantioselective acyl transfer catalysis by a combination of common catalytic motifs and electrostatic interactions | Nature Communications Enantioselective acyl transfer catalysis by a combination of common catalytic motifs and electrostatic interactions | Nature Communications](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fncomms11297/MediaObjects/41467_2016_Article_BFncomms11297_Fig1_HTML.jpg)
Enantioselective acyl transfer catalysis by a combination of common catalytic motifs and electrostatic interactions | Nature Communications
![DMAP-stabilized bis(silyl)silylenes as versatile synthons for organosilicon compounds - RSC Advances (RSC Publishing) DOI:10.1039/C9RA10628F DMAP-stabilized bis(silyl)silylenes as versatile synthons for organosilicon compounds - RSC Advances (RSC Publishing) DOI:10.1039/C9RA10628F](https://pubs.rsc.org/image/article/2020/RA/c9ra10628f/c9ra10628f-f1_hi-res.gif)