Solved 57. DBU (diazabicycloundecene) shown below, is an | Chegg.com
![1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU): A Versatile Reagent in Organic Synthesis | Bentham Science](https://www.eurekaselect.com/images/graphical-abstract/coc/19/9/0005D.gif "1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU): A Versatile Reagent in Organic Synthesis | Bentham Science")
1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU): A Versatile Reagent in Organic Synthesis | Bentham Science
DBU‐Promoted Nucleophilic Activation of Carbonic Acid Diesters - Carafa - 2011 - European Journal of Organic Chemistry - Wiley Online Library
DBU: A Reaction Product Component - Muzart - 2020 - ChemistrySelect - Wiley Online Library
DBU: A Reaction Product Component - Muzart - 2020 - ChemistrySelect - Wiley Online Library
organic chemistry - Reaction of chloroform with DBU - Chemistry Stack Exchange
![1,8-Diazabicyclo[5.4.0]undec-7-ene | C9H16N2 - PubChem](https://pubchem.ncbi.nlm.nih.gov/image/imgsrv.fcgi?cid=81184&t=l "1,8-Diazabicyclo[5.4.0]undec-7-ene | C9H16N2 - PubChem")
1,8-Diazabicyclo[5.4.0]undec-7-ene | C9H16N2 - PubChem
Mechanistic investigation-inspired activation mode of DBU and the function of the α-diazo group in the reaction of the α-amino ketone compound and EDA ... - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QO00602H
Proposed mechanisms for the DBU catalyzed urea-synthesis reaction from... | Download Scientific Diagram
![Facile synthesis of 2-arylimidazo[1,2-a]pyridines catalysed by DBU in aqueous ethanol | Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences](https://royalsocietypublishing.org/cms/asset/51bddc39-45b7-4fc6-865b-a440147711d1/rspa20190238f03.gif "Facile synthesis of 2-arylimidazo[1,2-a]pyridines catalysed by DBU in aqueous ethanol | Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences")
Facile synthesis of 2-arylimidazo[1,2-a]pyridines catalysed by DBU in aqueous ethanol | Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences
Optimization of DBU-Catalyzed Cyclization Reaction Condi- | Download Table
Full article: A review on DBU-mediated organic transformations
![The Dual Role of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) in the Synthesis of Terminal Aryl- and Styryl-Acetylenes via Umpolung Reactivity | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.5b02398/asset/images/medium/ol-2015-02398j_0006.gif "The Dual Role of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) in the Synthesis of Terminal Aryl- and Styryl-Acetylenes via Umpolung Reactivity | Organic Letters")
The Dual Role of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) in the Synthesis of Terminal Aryl- and Styryl-Acetylenes via Umpolung Reactivity | Organic Letters
SciELO - Brasil - Mechanistic Investigation of DBU-Based Ionic Liquids for Aza-Michael Reaction: Mass Spectrometry and DFT Studies of Catalyst Role Mechanistic Investigation of DBU-Based Ionic Liquids for Aza-Michael Reaction: Mass Spectrometry
DBU coupled ionic liquid-catalyzed efficient synthesis of quinazolinones from CO 2 and 2-aminobenzonitriles under mild conditions - RSC Advances (RSC Publishing) DOI:10.1039/D0RA00194E
![Controlled Reactivity of 1,8‐Diazabicyclo[5.4.0]undec‐7‐ene (DBU) in the Selective Synthesis of 1‐(Bromoethynyl)arenes - Krishna Moodapelly - 2017 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/da071cf8-eee0-4e2f-8e22-5b6f6a0f91e7/adsc201601279-fig-5004-m.jpg "Controlled Reactivity of 1,8‐Diazabicyclo[5.4.0]undec‐7‐ene (DBU) in the Selective Synthesis of 1‐(Bromoethynyl)arenes - Krishna Moodapelly - 2017 - Advanced Synthesis & Catalysis - Wiley Online Library")
Controlled Reactivity of 1,8‐Diazabicyclo[5.4.0]undec‐7‐ene (DBU) in the Selective Synthesis of 1‐(Bromoethynyl)arenes - Krishna Moodapelly - 2017 - Advanced Synthesis & Catalysis - Wiley Online Library
DBU
![The Dual Role of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) in the Synthesis of Terminal Aryl- and Styryl-Acetylenes via Umpolung Reactivity | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.5b02398/asset/images/large/ol-2015-02398j_0001.jpeg "The Dual Role of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) in the Synthesis of Terminal Aryl- and Styryl-Acetylenes via Umpolung Reactivity | Organic Letters")
The Dual Role of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) in the Synthesis of Terminal Aryl- and Styryl-Acetylenes via Umpolung Reactivity | Organic Letters
1,8-Diazabicyclo(5.4.0)undec-7-ene - Wikipedia
1,8-Diazabicyclo(5.4.0)undec-7-ene - Wikipedia
Structure of the PILs' precursors: DBU base (a) and the three acids... | Download Scientific Diagram
